The SF-Chem transaction is part of Clariant's strategy to sell
businesses that are outside its core activities. Last year the company
began a far-reaching Transformation Program that includes selling
several non-strategic businesses, cutting costs and making
sustainable competitiveness improvements.
Syngenta announced today that it is selling its 75
per cent stake in the Swiss chemical company SF-Chem to the Zurich-based
private equity firm Capvis. The remaining 25 per cent
stake held by Clariant is also being sold to Capvis. The total consideration
for the transaction is CHF81 million ($64 million), of which
Syngenta’s share is CHF59 million
($46 million), plus an additional performance-related component.
“It has become increasingly clear that our
investment in SF-Chem is no longer core“, said Christoph Mader,
responsible for Syngenta in Switzerland.
SF-Chem supplies customers in the chemical industry, in
particular in the pharmaceutical, agrochemical and speciality
chemicals industries. The company, founded in 1917, has its head
office and production facilities at Pratteln in Basel,
Switzerland.
SF-Chem is pursuing a growth strategy with its independently
operated business units Chemicals and Custom Manufacturing in
order to ensure an independent worldwide market position.
・
Chemicals: sulfur- and
chlorine-based intermediates.
・
Custom Manufacturing: development
of custom-tailored, specific solutions for the
pharmaceutical, agrochemical and speciality chemicals
industries.
With this move, Dyneon continues to build on its long-term
commitment to the worldwide fluoropolymer business, effectively
strengthening its product availability and reinforcing its
ability to supply product globally. Under this arrangement, which
is the first of a series of cooperative projects planned between
the companies, Dyneon will be able to better serve and support
its customers.
Dyneon, a 3M company, is one of the world's leading fluoropolymer
producers with operations or representation in more than 50
countries. Headquartered in Oakdale, Minn., Dyneon employs more
than 800 people globally who are dedicated to customer service,
technical and sales support, marketing, research, application
development, and production.
Transformational merger
of Hexal and Eon Labs with Sandoz strengthens market
positions globally, achieving top positions in key
markets, particularly US and Germany
・
Significantly broadened
product portfolio
・
One of the largest
pipelines in industry covering most generic opportunities
・
Best-in-class
development teams with proven record of being first to
market
・
Leadership in high-value
delivery technologies and biogenerics
・
Hexal and 67.7% of Eon
Labs acquired for EUR 5.65 billion
・
Tender offer for
remaining Eon Labs shares to be launched for USD 31.00
per share
・
Cost synergies of USD
200 million per year expected within three years after
closing, 50% of which to be realized within 18 months
・
Transactions to be
accretive to earnings within 12 months of closing
Quadrant has signed an
agreement with Menasha
Corporation
to purchase its Poly Hi Solidur, Inc. business, the world's leading
manufacturer of ultra-high molecular weight
polyethylene (UHMW-PE) semi-finished products for machining and fabrication.
The purchase price of approximately US$ 82 million in cash plus
the assumption of US$ 3 million of capitalized leases will be
financed from existing liquid funds and by increasing bank
borrowings by about 90 million Swiss francs. An increase in share
capital is not planned. The transaction will be completed in
August of this year. This external growth step is the
second-largest in Quadrant’s history and significantly
extends the company’s product range and its global
leadership in the market for engineering plastic products.
Poly Hi Solidur, based in Fort Wayne, Ind., US, operates
production facilities in the USA, Germany, France, the UK, Japan
and South Africa, and has dedicated R&D, sales and business
development resources among its workforce of over 1000 employees
worldwide. In 2004, the company posted total sales of US$ 169
million, approximately two-thirds of which were generated in the
US.
UHMW-PE products display very high non-stick characteristics
similar to Teflon(R) and high resistance to corrosion from
chemicals and to abrasive environments such as sand and slurries.
In machined and fabricated part form, their uses include
applications in material handling, agricultural, power
transmission and food processing machinery, as well as in medical
devices, shipping and recreational equipment. Poly Hi Solidur’s branded UHMW-PE products include
the well-known TIVAR(R) and QuickSilver(R) trademarks.
STERLING CHEMICALS, INC.
announced that it was exiting the acrylonitrile business
and related derivative operations. The Company's decision was based
on a history of operating losses incurred by its acrylonitrile
and derivatives business, and was made after a full review and
analysis of the Company's strategic alternatives.
Based in Houston, Texas, Sterling Chemicals, Inc. manufactures a
variety of petrochemical products at its facilities in Texas City,
Texas.
Sterling
Chemicals
We manufacture styrene, acetic acid and plasticizers at our
Texas City, Texas facility.
Styrene
Percent of Total North American Capacity 11%
North American Market Position by Capacity 4
Acetic Acid
Percent of Total North American Capacity 17%
North American Market Position by Capacity 3
Plasticizers
Percent of Total North American Capacity 9%
North American Market Position By Capacity 3
Canada seeks
investment in oil, petrochemicals from Alberta sands
Aromatics would be
extracted from raw bitumen contained in the oil sands, while
olefins would be cracked from naphtha to be produced from
synthetic crude oil, which in turn would come from bitumen as
well.
In a feasibility
study presented at a seminar to a group of Japanese delegates,
Plessis estimated that a production capacity of 300,000 b/d of
bitumen could support a worldscale steam cracker with ethylene,
propylene and butadiene capacities of 2,800 mt/day (1 million
mt/year), 1,600 mt/day, and 270 mt/day, respectively.
BOC, one of the world's
largest industrial gases companies, is expanding its carbon
dioxide (CO2) capacity with a new plant in Volney, New York. The
plant will be the first CO2 plant built in the Northeast in
nearly two decades and will be the only CO2 plant in the region.
BOC will build the
600 ton a day plant at the Permolex International/NEB ethanol
plant,
expected to begin operating in December 2007, and which will be
housed in a former brewery in the Riverview Business Park, some
25 miles north of Syracuse.
When BOC’s plant comes online next year it
will capture
ethanol’s by-product, CO2,
purify it and liquefy it for sale to BOC customers. Those
customers, major food and beverage companies and chemicals
manufacturers are located throughout New York, New Jersey,
Pennsylvania and New England.
2006/3/6 Linde
Recommended cash offer by
Linde for BOC
Linde AG, Wiesbaden/Germany, has agreed to make a pre-conditional
offer to acquire the entire share capital of The
BOC Group plc,
Windlesham/UK, for 1,600 pence in cash per share. The board of
directors of BOC intends to recommend BOC shareholders to accept
the offer.
The making of the offer is subject to the satisfaction or waiver
of European and US competition authority clearance pre-conditions
and the offer is subject to the requisite approval of BOC's
shareholders and the English Courts. Given the complementary
product portfolios of both companies, Linde expects that the
pre-conditions can be satisfied. Linde currently anticipates this
will occur by the end of May 2006. If the pre-conditions are
satisfied by that time, the transaction is expected to be
completed in the third quarter of 2006.
Following the acquisition, Linde will be one of the world's
leading industrial gases and engineering groups with combined gas
and engineering sales of approximately Euro 11.9 billion.
The funds necessary for the acquisition will be provided under a
credit facility entered into with Commerzbank AG, Deutsche Bank
AG, Dresdner Bank AG, Morgan Stanley International Limited and
The Royal Bank of Scotland plc. The credit facility will be
refinanced through a combination of a capital increase in an
amount of Euro 1,4 to 1,8 billion, hybrid capital (1,2 to 1,6
Euro billion), the issue of bonds, bank loans and the divestment
of selected activities. It is Linde's intention to maintain an
investment grade rating for the combined group.
2006/6/6 Linde
European Commission
approves Linde’s acquisition of BOC
The European Commission has approved the acquisition by Linde
AG, Wiesbaden, of The BOC Group plc, Windlesham, UK. The
approval is subject to certain conditions. The conditions
require the divestiture of Linde’s gas business in the UK, BOC’s gas activities in Poland and
contracts with Linde’s ethylene oxide customers in
the UK and Ireland. These divestitures correspond to a sales
volume of approximately 160 million euros.
In addition, Linde committed to transfer certain contracts
with helium suppliers and to sever, to an extent agreed with
the Commission, joint ventures between BOC and Air Liquide in
the Asia/Pacific region, either by selling BOC’s shareholding or by acquiring
Air Liquide’s shareholding.
“The approval from the European
Commission is a key step towards a merger with BOC,”
confirmed Prof.
Wolfgang Reitzle, President and CEO of Linde AG. “We expect the transaction to
be closed in the course of the third quarter of 2006. The
extent of the Commission’s conditions is in line with
our expectations and we will comply promptly with these
conditions.”
2006/7/18 Linde
U.S. Federal Trade
Commission clears Linde’s proposed acquisition of BOC
The U.S. Federal Trade Commission (FTC) has cleared the
proposed acquisition by Linde AG, Wiesbaden, of The BOC Group
plc, Windlesham, UK.
The clearance is subject to certain divestitures to address
FTC concerns relating to atmospheric gases and wholesale bulk
liquid helium. As a condition to FTC clearance, Linde has
agreed to divest eight air separation units in the United
States. It has also agreed to divest
three liquid helium purchase agreements with suppliers in the
United States, Russia, and Poland as well as associated
assets. These
divestitures correspond to a sales volume of approximately
180 million euro in the year ended December 31, 2005.
"We are pleased to confirm that each of the
pre-conditions to the making of the Offer has now been
satisfied," said Prof. Wolfgang Reitzle, President and
CEO of Linde AG. "This is a milestone on our way towards
the merger with BOC. We will swiftly take the next steps to
implement the transaction and look forward to our joint
integration process with BOC."
The Offer to the BOC shareholders will shortly be launched,
by means of the posting of the scheme document. The consent
of the High Court to the despatch of the scheme document has
been obtained. Completion of the Offer is expected in
September 2006.
Teknor Apex Company is a
privately-held company founded in 1924 and headquartered in
Pawtucket, Rhode Island. Our seven divisions and two subsidiaries
employ over 2000 people in 10 locations in the United States, one
in Singapore, and one in the United Kingdom.
Teknor Apex
entered the Far Eastern market in 2001 when it bought
Singapore Polymer Corporation, which now compounds the
full range of TPEs in Singapore.
The company's aim is to be able to supply
global companies anywhere in the world with locally
produced materials to identical
specifications. To that end it plans to open
its European plant in 2008 - it is being coy about
where the plant will be, and the Chem Polymer Oldbury
site is not the only possibility - and says that at about
the same time it will start up a
TPE plant in China.
Teknor Apex supplies TPE compounds under six trade names
that represent different technologies, including di- and
tri-block hydrogenated styrene block copolymers (Tekron,
Elexar, and Monprene), thermoplastic polyolefin blends
(Telcar), thermoplastic vulcanisates (Uniprene), and
over-moulding compositions designed to bond to diverse
polar substrates (Tekbond).
--------
Teknor Apex
Company traces its origins to Apex Tire
Company
which was started in Providence, Rhode Island in 1924.
Alfred A. Fain, a retired wholesale grocery executive,
and his son-in-law, Albert Pilavin, grew this tire sales
and recapping business until it had expanded to include
16 retail tire stores along the East Coast.
Today the Rubber Division of Teknor Apex has a healthy
business mixing rubber compounds for outside customers
and molding its own products such as rubber floor mats.
In 1949 the Company began the production of vinyl
compounds
as a result of a shift in the wire and cable industry
from rubber to vinyl materials. Apex Rubber also began
manufacturing vinyl resin and plasticizers as the vinyl
compounding part of the business grew.
Today Teknor Apex is a leading custom compounder of PVC
and thermoplastic elastomer products used in many
industries such as wire and cable, medical, automotive,
building materials and appliances.
Vinyl garden hose production was begun in the Pawtucket,
RI plant in the late 50s as an outgrowth of the company's
vinyl production. The Lawn and Garden
business at
Teknor Apex has also grown over the years and Teknor Apex
is now one of the major manufacturers of garden hose in
the United States.
The Massachusetts
plant produced chemicals and PVC resin.
In 1959 Teknor Apex began selling colorants
for plastics
to customers buying its vinyl compounds.
Through acquisitions over the years, in 1981 this
operation became Teknor Color Company, a wholly owned
subsidiary of Teknor Apex Company.
Vinyl
Thermoplastic
Elastomer
Teknor Color Company
Chemicals
Specialty
Compounding
Lawn & Garden
Commercial Products
The Vinyl
Division of
Teknor Apex is one of the world's leading suppliers of specialty
PVC compounds.
The
Thermoplastic Elastomer Division of Teknor Apex has built its
worldwide TPE leadership on more than 75 years experience with
flexible and elastomeric polymers.
Headquartered in Pawtucket, Rhode Island, Teknor Apex also
operates thermoplastic elastomer facilities in St. Albans,
Vermont; Brownsville, Tennessee; Henderson, Kentucky; and in
Singapore.
With strategically
located plants across North America and one in Singapore, Teknor Color
Company provides
colorants for the plastics industry worldwide. We offer a full
line of custom and standard colors and additives as well as
special effects for all processes.
Chem Polymer is an engineering
thermoplastics compounder which produces reinforced, filled
and specially modified compounds of nylon 6 and 66, acetal, PBT
and PET for automotive, appliance, electrical, electronic and
other applications.
Teknor
Specialty Compounding is a diversified toll and custom
manufacturer of thermoplastic compounds and additive blends. We
are a resource for customers requiring an independent,
confidential provider of production capacity, formulating
experience and process expertise.
Teknor Apex Acquires Chem
Polymer, International Supplier of Engineering Plastics Compounds
with Plants in UK and USA
Teknor Apex Company today
purchased the UK and US engineering thermoplastics compounding
businesses of Chem Polymer, which is a leading supplier to
customers throughout Europe and the Americas and has a growing
presence in Asia. Chem Polymer will operate under its existing
management as a distinct entity within Teknor Apex, retaining the
Chem Polymer name and a workforce of 150.
Until now a member of the UK-based Chem Polymer Group (formerly
BIP Group), Chem Polymer produces reinforced, filled, and
specially modified compounds of nylon 6 and 66, acetal, PBT, and
PET for automotive, appliance, electrical, electronic, and other
applications. It operates two plants in the UK and one in the
USA, with combined annual capacity of 30,000 metric tons
(66,000,000 lb.).
Teknor Apex Co., a
U.S.-based compounder of specialty PVC, thermoplastic elastomers
and color concentrates, plans to start a European TPE compounding
operation in 2008, officials said at Fakuma 2006.
Teknor Apex plans
to install a small compounding operation next year in the
Oldbury, England, factory of Chem Polymer, according to Andre Toczek, sales
and marketing manager of the European operation.
Teknor officials have not
decided the location of the full-scale TPE production, although
Oldbury is one option, Toczek said Oct. 19 at the show.
January 9, 2007 RTP
RTP Company Announces Long Fiber Thermoplastics Availability at
China Facility
RTP Company, a global leader in specialty compounds, has added
multiple long fiber-reinforced
thermoplastic (LFRT)
production lines at its Suzhou, China manufacturing facility. The
long glass fiber compounds are based on various resin systems
including nylon and polypropylene.
“The
new LFRT lines will support our rapidly-growing automotive and
industrial customer base in China along with offering long fiber
technology to other markets for applications requiring higher
strength at lighter weights,” said Joe Kluck, Executive Vice
President at RTP Company.
RTP Company’s 16,000 square meter (170,000
square feet) manufacturing plant in Suzhou, China was opened in
December 2005. The state-of-the-art facility offers a full
complement of customer support, product development, and
technical service.
RTP Company significantly expanded its LFRT capabilities earlier
this year with the opening of a long fiber facility near its
Winona, Minnesota headquarters. RTP Company also installed
additional long fiber lines at several of its worldwide
operations in 2006 and introduced a broader long fiber product
offering.
Long Fiber Compounds are often used to replace metals and
consequently have become one of the fastest-growing materials in
the thermoplastic industry. They offer excellent mechanical
properties and their high strength-to-weight ratios result in
parts that can withstand heavy loads over long periods of time,
even in elevated temperatures.
ABOUT RTP COMPANY
RTP Company, headquartered in Winona, Minnesota, is a global
leader in specialty thermoplastic compounding. The company has
eight manufacturing plants on three continents, plus sales
representatives throughout North America, Europe, and
Asia/Pacific. RTP Company's engineers develop and produce custom
compounds in over 60 different engineering resin systems for
applications requiring color, conductivity, flame retardancy,
high temperature, structural, elastomeric and wear resistant
properties.
Mexico's PVC producer
Mexichem eyes takeover of Pemex's VCM plant
Mexico City-based
chemicals group, Mexichem, whose recent acquisitions have
made it the biggest producer of PVC in
Latin America,
aims to break a production bottleneck by taking control of state Pemex's VCM plant, Enrique Ortega, Mexichem's
investor relations manager said Monday.
"We supply the plant with 90% of the
chlorine it
uses and buy 70% of its VCM output," Ortega told Platts.
"It's natural that we would want to acquire it and the law
allows us to do so." VCM is classified as a secondary
petrochemical to which Pemex's state monopoly does not apply.
The
Pajaritos VCM plant has
been a thorn in Mexichem's flesh for some time. In 2002, Pemex
announced the award to Spain's Duro Felguera of a $74 million
contract for an expansion of the plant's capacity from 200,000
metric tons/year to 405,000 mt/year. The expansion project took
much longer than programmed, forcing Mexichem and others to
import VCM in the meanwhile, and the expansion of production
capacity appears to have fallen far short of target. Last year
the plant produced 209,000 mt/year of VCM.
In February, Mexichem announced the acquisition of two Latin
American companies -- Costa Rica-based Grupo Amanco, which makes PVC piping for water
systems, and Petroquimica Colombiana (Petco), a Colombia-based producer of PVC
resins. The addition of Amanco and Petco to Mexichem's
fast-growing portfolio of affiliates should double the group's
revenues to $2.4 billion this year, Ortega said.
Clariant sells Custom Manufacturing Business to International
Chemical Investors Group
Clariant today announced the sale of its Custom
Manufacturing Business to International Chemical Investors Group
(ICIG) for
an undisclosed transaction value. The sale is the latest step in
Clariant’s strategy to focus on its core
competencies in colors, surfaces and performance chemicals.
Clariant’s Customer Manufacturing Business
supplies a wide range of intermediates and actives ingredients
for the agrochemicals, pharmaceuticals and polymers industries.
At closing, the new autonomous entity will be one of the world’s leading suppliers to the
agrochemicals industry with production sites in Germany and the
US. In 2006, the Custom
About International Chemical Investors
International Chemical Investors is an investment group focusing
on mid-sized chemical businesses, preferably subsidiaries of
large corporations, which are considered non-core, with leading
positions in niche markets, operating in competitive
environments. Including the newly acquired Clariant businesses,
ICIG will operate 14 production facilities located in Germany,
the United States, France, Belgium, Ireland and Poland with total
sales of close to Euro 500 million and more than 2,500 employees.
CVC to Buy Chemical
Seller Univar for EU1.52 Billion
CVC Capital Partners Ltd.
agreed to buy Univar NV of the Netherlands for 1.52 billion euros ($2.07 billion) to gain the largest distributor
of chemicals in the U.S.
Europe's No. 2 buyout
firm will purchase Univar for 53.50 euros a share, the companies
said in a statement today. That's 37 percent more than Friday's
closing price for Univar, which buys bulk chemicals and then
sells them to 250,000 industrial users.
CVC's bid comes less than
three months after Rotterdam- based Univar bought
Chemcentral Corp. of Illinois to boost U.S. sales 40 percent.
London-based CVC said it backs expansion in the world's biggest
economy, which grew at its slowest pace since the end of 2002 in
the first quarter, and also plans to fund further acquisitions in
Europe, Asia and the Middle East.
Univar has 8,000 employees and more than
200 chemical- distribution centers in the U.S., Canada, Europe
and Asia, it said in the statement. The majority of the company's
products are commodity chemicals bought in bulk and then processed,
blended and sold to clients in industries ranging from
agriculture and drugs to forestry, food and electronics.
CVC is investing 10
billion euros it has amassed in the past two years. The Univar
deal comes five days after the 800 million-euro
purchase of Taminco NV, a Belgian maker of chemical ingredients
for the pharmaceutical industry. Dutch investment firm AlpInvest
Partners NV sold Taminco in an auction.
CVC was founded in 1981
as Citicorp's European private- equity arm before its managers
bought their independence in 1993. Run by Michael Smith, who
joined from Citibank in 1982, the firm has about $24 billion of
funds. It already owns more than 40 companies with more than
300,000 employees and revenue in excess of 38.5 billion euros,
according to its Web site.
Hexcel Corporation, in
conjunction with Tianjin Xeda Administrative Committee, has today
announced further details of its plans to build a new prepreg
plant in China.The new facility is intended to
meet the strong demand for composites used in wind turbines.China is
experiencing major growth in its wind energy market and the
country plans to double the amount of energy it obtains from
renewable sources by 2020; a strategy that will require a major
increase in the number of wind power plants in the country.
With the support of Xeda,
Hexcel has secured a total floor area of 30 000m2 site in
Tianjin, close to the facilities of major wind power customers.
The plant building area will occupy approximately 8,000m2 and
manufacture HexPly® epoxy resin
prepregs,
primarily for wind energy and industrial applications.Production at the
new facility will commence in summer 2008.
Prepreg is
fiber-reinforced resin system that cures under heat and pressure
to produce structures with a very high strength to weight ratio.Prepreg is widely
used in the wind energy industry where its outstanding strength
and low weight have enabled turbine blades to grow to today’s giant proportions.
HexPly® prepregs are specially
formulated resin matrix systems, that are reinforced
with man-made fibers such as carbon, glass and aramid.When cured at
elevated temperatures, the themoset resin undergoes a
chemical reaction that transforms the prepreg into a solid
structural material that is highly durable, temperature
resistant, exceptionally stiff andlightweight.
Rio Tinto notes the
recent announcement from BHP Billiton involving a proposed
acquisition of Rio Tinto. Under this proposal each Rio Tinto
share would be exchanged for three BHP Billiton shares.
The Boards of Rio Tinto
have given the proposal careful consideration and concluded that it significantly
undervalues Rio Tinto and its prospects. Accordingly, the Boards have
unanimously rejected the proposal as not being in the best
interests of shareholders.
Rio Tinto will continue
to focus on the implementation of its well articulated strategy,
including integrating Alcan operations.
A merger would create
a base metals colossus with powerful positions in coking
coal, iron ore, copper and aluminium. BHP's offer - three BHP
shares for every Rio share, which values the bid at more than $140
billion
on current prices - was rejected by Rio at a board meeting
held earlier this week to consider the proposal. Rio shares
gained 956p, or 22 per cent, to £52.96 in response to news of
BHP's interest, while BHP fell 100p, or 5.6 per cent, to £16.56.
Albemarle to Expand
Antioxidant Production in China
Strategic move will
further strengthen position in the China plastics additives
marketplace
Albemarle Corporation, a
leading global supplier of antioxidants for polymers, lubricants,
fuels and biofuels, announced today that its Board of Directors
has approved a project to more than double the
antioxidant production capacity of Shanghai Jinhai Albemarle Fine
Chemicals Co., Ltd.,
part of the "Jinhai Albemarle" manufacturing joint
venture in which Albemarle gained a majority ownership stake last
year.
This strategic expansion
will allow Jinhai Albemarle to maintain its market position as
the leading manufacturer and supplier of polymer antioxidants in
China.
2008/6/22
polymer-age.co.uk
Cabot
to manufacture in the Middle East
Carbon
black masterbatch producer Cabot Corporation is to start making
masterbatch in the Arabian Gulf. It is to build a plant in the
Jebel Ali Free Zone, Dubai with an
initial capacity of 25,000tonnes
with provision to expand to
75,000tonnes.
Output
from the plant will be sold in the Middle East, Europe and Asia
Pacific. The key markets for black masterbatch are in PE and PP
compounds for building infrastructure, water supply, electricity,
and telecommunications.
By
2010 the Middle East is expected to produce one-fifth of the
world's polyethylene and polypropylene.
2008/5/28 Cabot
Cabot Corporation to
Build Masterbatch Facility in Dubai
Cabot Corporation
announced today that it intends to build a carbon black
masterbatch manufacturing facility in the Jebel Ali Free Zone,
Dubai. The plant will have an initial production capacity of
25,000 tons per year with provision to expand to 75,000 tons in
the future. Cabot has secured a plot of land and construction
will begin later this calendar year, with production scheduled to
start in the fall of 2009.
The state-of-the-art
manufacturing facility will include the latest environmental and
manufacturing technologies to ensure production of high-quality
masterbatch products. Laboratories, administration offices,
production and packaging will all be located within the building.
The Dubai plant will
allow Cabot to better meet the increasing demand of its customers
in the Middle East, Europe, and Asia Pacific regions. In recent
years, the Middle East has become a major producer of polyolefins
and downstream compounds and by 2010 is expected to produce
one-fifth of the world's polyethylene (PE) and polypropylene
(PP).
Cabot Vice President and
General Manager for the Performance Segment, Sean Keohane said,
"Within the Middle East there is already strong demand for
PE and PP compounds for use in building infrastructure for water
supply, electricity, and telecommunications projects. These are
key markets for carbon black masterbatch. This new site will
offer significant quality and service advantages to Middle East
producers who are global exporters of masterbatch
compounds."
2008/10/3 Ferro
Ferro Announces Agreement
to Sell Fine Chemical Business
Ferro Corporation (NYSE:
FOE) announced today that it has signed an asset purchase
agreement with Novolyte Technologies LP, an affiliate of Arsenal
Capital Management LP, to sell its Fine Chemicals business for
$66 million in cash.
"This sale is
consistent with our vision of focusing Ferro's businesses around
our core capabilities of particle engineering, formulation, color
and glass science, and our deep understanding of customer
applications," said Ferro Chairman, President and Chief
Executive Officer James F. Kirsch. "The decision to sell the
business is a result of a regular review of our business
portfolio. Fine Chemicals consists of a number of smaller
businesses that do not effectively leverage the scale of Ferro's
core performance materials operations. I am confident that the
Fine Chemicals business will continue to pursue many exciting
opportunities under its new owners. At the same time, Ferro will
benefit from additional liquidity and balance sheet flexibility
as proceeds from the sale are used to reduce debt."
The Fine Chemicals
business produces electrolytes used in the manufacture of lithium
batteries, specialty solvents, and phosphines and also does
contract manufacturing of fine chemicals. It recorded 2007
revenues of approximately $55 million and currently employs
approximately 140 employees who will be transferred to Novolyte
as a result of the sale. The business includes manufacturing
facilities in Baton Rouge, Louisiana and Suzhou, China.
The agreement is subject
to normal closing conditions and the sale is expected to close in
the fourth quarter of 2008. KeyBanc Capital Markets served as
Ferro's financial advisor and investment banker for this
transaction.
About Ferro Corporation
Ferro Corporation
(http://www.ferro.com) is a leading global supplier of
technology-based performance materials for manufacturers. Ferro
materials enhance the performance of products in a variety of end
markets, including electronics, solar energy, telecommunications,
pharmaceuticals, building and renovation, appliances, automotive,
household furnishings, and industrial products.
Headquartered in
Cleveland, Ohio, the Company has approximately 6,300 employees
globally and reported 2007 sales of $2.2 billion.
Lilly to Acquire ImClone
Systems in $6.5 Billion Transaction Creates a Global Leader in
Oncology Biopharmaceuticals Boosts Oncology Pipeline With Up
to Three Promising Targeted Therapies in Phase III in 2009
Eli Lilly
and Company and ImClone Systems Inc. today announced that the boards
of directors of both companies have approved a definitive merger
agreement under which Lilly will acquire ImClone through an all
cash tender offer of $70.00 per share, or approximately $6.5 billion. The offer represents a premium of
51 percent to ImClone's closing stock price on July 30, 2008, the
day before an acquisition offer for ImClone was made public.
ImClone's board recommends that ImClone's shareholders tender
their shares in the tender offer. Additionally, certain entities
associated with ImClone's chairman, Carl C. Icahn, holding
approximately 14 percent of ImClone's outstanding common stock,
have agreed to tender their shares in the tender offer.
Sep 22, 2011 (Datamonitor via COMTEX)
Williams to expand Geismar olefins production
facility
Williams, an integrated
natural gas company focused on exploration and production, midstream
gathering and processing, and interstate natural gas transportation, has
announced that its board of directors has approved an expansion of its
Geismar olefins production facility.
The expansion will increase the facility's ethylene production capacity
by 600 million pounds per year to a new annual
capacity of 1.95 billion pounds. It is expected to
be placed into service in the third quarter of 2013, the company said.
Located south of Baton Rouge, La., the Geismar facility is a
light-end natural gas liquid (NGL) cracker with current volumes of 37,000
barrels per day (bpd) of ethane and 3,000 bpd of
propane and annual production of
1.35 billion pounds of ethylene. The facility also
produces propylene, butadiene and debutanized aromatic
concentrate (DAC). Williams owns 83.3 percent of the Geismar facility and
operates the plant.
"The shale gas revolution in the US, coupled with continued strong crude oil
prices, has given US-based ethylene manufacturing a tremendous cost advantage
over many other supply regions," said Rory Miller, president of Williams'
midstream business. "The results are a revitalized North American petrochemical
business and a US ethylene market short of supply.
"This expansion will serve petrochemical companies by adding 600 million pounds
per year of new ethylene supply to the market," Miller said. "It will also add
to Williams' growing large-scale infrastructure serving the petrochemical
industry in the Gulf Coast region and help balance our lengthening ethane
position."
The expected capital spending on the Geismar expansion is a range of $350
million to $400 million in 2012-13. These amounts will be included in the
company's 2012-13 capital expenditure guidance to be released in conjunction
with third-quarter 2011 financial results, the company added.
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An integrated natural gas company, Williams
produces, gathers, processes and transports clean-burning natural gas to
heat homes and power electric generation across the country.
Williams' olefins business provides
customers in the petrochemical industry a full suite of products and
services.
Gulf Coast Olefins
The Geismar, La. facility annually produces approximately 1.3 billion pounds
of ethylene and 90 million pounds of polymer grade propylene. Also in
Louisiana, the olefins team is responsible for the ethane transportation
business consisting of approximately 200 miles of pipelines, as well as a
refinery-grade propylene splitter.
Canadian Olefins
Williams’ Canadian olefins business extracts natural gas liquids and
olefins from oil sands refining near Fort
McMurray, Alberta. The liquids are then fractionated into various products
at a Williams facility near Redwater, Alberta. Williams also has a business
office in Calgary.
Cryogenic Liquids Extraction Plant
Located Near Fort McMurray
An environmentally-friendly project
as it reduces sulphur emissions and other green house gases
Extracts natural gas liquids (NGLs)
from coker off-gas produced from an oil sands plant
Coker off-gas includes olefins such
as propylene which is typically produced through ethane or propane
cracking
Olefins Fractionation Plant Located
Near Edmonton
Only olefinic fractionator in
Western Canada
Fractionates NGL mix from Fort
McMurray
On a yearly basis, produces
approximately 2.4MM bbls of propane, 140MM lbs of polymer grade
propylene, 1.10MM bbls of butane/butylene mix and 230K bbls of olefinic
condensate
October 17, 2011 PolyOne
PolyOne Expands Globalization with New Middle
East Joint Venture
PolyOne Corporation, a premier global provider of specialized polymer materials,
services and solutions, today announced an agreement with
E.A. Juffali & Brothers Company Limited to form a joint venture that will
enable PolyOne to expand its Global Color, Additives and Inks business into the
Middle East. The new joint venture will be 51% owned by PolyOne and will be
based in Jeddah, Saudi Arabia.
“I am pleased to announce our new agreement, which strengthens our relationship
with a key business partner to drive profitable growth in the Middle East,” said
Stephen D. Newlin, chairman, president and chief executive officer of PolyOne.
“Juffali brings local expertise and years of running successful businesses in
the region, while PolyOne is providing the formulating technology and material
science to market new, innovative solutions.”
The joint venture will be investing in a new manufacturing facility focused on
the production of specialty color concentrates with the potential for expansion
into other product lines in future phases. The initial investment is expected to
be approximately $14 million and will take place over the next nine to twelve
months with local production forecasted to come on-line in late 2012.
The agreement follows PolyOne’s October 3, 2011 announcement that it will
acquire ColorMatrix Group, a
leading global innovator of additives, liquid colorants and fluoropolymers.
About PolyOne
PolyOne Corporation, with 2010 revenues of $2.6 billion, is a premier provider
of specialized polymer materials, services and solutions. Headquartered outside
of Cleveland, Ohio USA, PolyOne has operations around the world. For additional
information on PolyOne, visit our Web site at www.polyone.com.
About E.A. Juffali & Brothers Company Limited
E.A. Juffali & Brothers Company Limited is an established conglomerate in Saudi
Arabia participating in numerous joint venture relationships with multi-national
companies who are leaders in their respective industries such as Dow Chemical
and DuPont.
---------
October 03, 2011 PolyOne
PolyOne Accelerates Specialty Growth with
Agreement to Acquire ColorMatrix Group
PolyOne Corporation, a premier global provider of specialized polymer materials,
services and solutions, today announced an agreement to acquire
ColorMatrix Group, Inc., the leading global
innovator in liquid colorants, additives and fluoropolymers.
“I am extremely pleased to announce we’ve reached an agreement to acquire
ColorMatrix, an exceptional and unique specialty company,” said Stephen D.
Newlin, chairman, president and chief executive officer, PolyOne Corporation.
“Much like our acquisition of GLS in 2008, ColorMatrix is a game-changer for
PolyOne. With the addition of ColorMatrix, more than 50 percent of PolyOne’s
operating income will now be derived from our specialty businesses, compared to
only 2 percent in 2005.”
ColorMatrix is the leading manufacturer of performance-enhancing specialty
additives, liquid colorant and dosing technologies that serve diverse niche
markets, such as rigid beverage and food packaging, performance molding and
fiber. The company’s leadership position in technology is evidenced by an IP
portfolio of 162 patents and 107 pending applications worldwide. Its solutions
in packaging, in particular, offer customers exceptional performance attributes
such as increased product shelf life, taste preservation and improved
recyclability.
Further, ColorMatrix is a leading global provider of colorant for fluoropolymers
and provides specialty additives that support fluoropolymers’ unique
high-performance properties such as lubricity, high-level heat insulation,
static dissipation and x-ray opaqueness. Through its April 2011 acquisition of
Gayson, ColorMatrix expanded its portfolio to include short turnaround, custom
color dispersions used in silicone processing for a broad range of medical,
consumer and automotive applications.
Under the leadership of CEO John Gelp and a strong management team, ColorMatrix
achieved sales and EBITDA of approximately $196.8 million and $43.6 million
respectively for the 12 months ended June 30, 2011.
“Since 2002, ColorMatrix has organically increased EBITDA at an annualized
growth rate of 16 percent, and our purchase price of $486 million recognizes the
earnings and growth potential of this specialty business,” said Newlin. “We
believe we can accelerate this growth by leveraging our global scale and through
additional investment in commercial resources, just as we’ve done with GLS.”
“Not only will the acquisition of ColorMatrix accelerate our specialization
strategy, it also expands our geographic presence in Asia and Brazil and creates
an entry point into Russia,” said Robert M. Patterson, executive vice president
and chief financial officer. Approximately 70 percent of ColorMatrix’s revenues
are outside North America.
PolyOne intends to finance the purchase price of $486 million, which includes
transaction tax benefits of $10 million, with a combination of cash on hand and
the addition of approximately $300 million of long term debt. The acquisition is
being made on a cash free, debt free basis, and the purchase price is subject to
a customary working capital adjustment and other closing conditions.
“Net of interest expense on the long term debt, and the incremental investments
in commercial resources, we expect ColorMatrix to be modestly accretive to
earnings in 2012 ($0.02-$0.03 per share) and to add approximately $0.10-$0.12
per share in 2013,” added Patterson.
This acquisition is subject to regulatory approvals and is expected to close
late this year. PolyOne management will discuss the acquisition in more detail
during its regularly scheduled third quarter earnings conference call to be held
on October 26, 2011.
About ColorMatrix
ColorMatrix Group Inc., based in Berea, Ohio, is a leading specialty provider of
innovative liquid colorants and additives business that serves diverse segments,
including rigid beverage and food packaging, industrial extrusion, performance
molding, wire, cable, fiber, and silicone rubber markets. ColorMatrix has
operations, R&D capabilities and customer reach throughout the globe. For
additional information on ColorMatrix, visit its Web site at www.colormatrix.com.
December 2, 2013
Rockwood to Acquire 49%
Interest in Talison Lithium through a Joint Venture with Chengdu Tianqi Industry
Group
Provides ownership in the
world’s largest and richest spodumene sourceリチア輝石
of lithium リチウムとアルミニウムを含む単斜輝石
Strengthens further ROC’s #1
position as a leading global integrated producer of lithium compounds and
chemicals
Delivers immediate and
significant accretion to ROC’s 2014 earnings per share
Enables a partnership with
Tianqi, China’s leading lithium company
Rockwood Holdings, Inc.
announced today that it entered into a joint venture ("JV") with Chengdu Tianqi
Industry Group ("Tianqi"成都天齊實業集團) giving Rockwood a 49%
ownership interest and Tianqi a 51% interest in
Talison Lithium Pty Ltd. This transaction is expected to close during the
first quarter of 2014, following receipt of regulatory approvals.
Rockwood (49%) and Chinese
lithium producer Chengdu Tianqi Group (51%) will form a joint venture to
acquire Talison from its current owners (Windfield is the Holdco of Talison
Lithium Pty Ltd.)
At close, it is expected that
Rockwood and Tianqi will contribute equity of $196 million and $204 million,
respectively. In addition, Rockwood will also provide to the joint venture a
two-year secured loan of up to $670 million at 8% interest. Rockwood will grant
Tianqi a three-year call option to invest from 20% to 30% in the equity of
Rockwood Lithium GmbH, the European arm of
Rockwood’s global lithium business, which will be valued at 14x the last twelve
months Adjusted EBITDA.
Proceeds to the joint venture
will be used to pay off existing debt and equity holders including Tianqi Group
HK Co., Limited (a subsidiary of Tianqi) and Leader Investment Corporation (a
subsidiary of China Investment Corporation). Rockwood is expected to fund its
investment in the joint venture from cash on hand.
"With this acquisition, we have
secured access to another significant lithium reserve, in addition to our
current resources in the U.S. and Chile," said Seifi Ghasemi, Chairman and Chief
Executive Officer. "Further, not only does this complement our core lithium
business, but it also meets with all of our prior stated financial and strategic
objectives for allocation of capital in a disciplined manner to enhance economic
value for shareholders."
Lazard acted as Rockwood’s
financial advisor and Clifford Chance as legal advisor.
Talison Lithium Pty Ltd
Talison is a leading global
producer of lithium for over 25 years. Talison mines and processes lithium
bearing mineral spodumene at its operations located at Greenbushes, Western
Australia (the "Greenbushes Lithium Operations"), located approximately 250
kilometers from Perth, Western Australia. Greenbushes Lithium Operations is
estimated to be the world’s largest known reserves of lithium spodumene minerals
with a current mine life of 40 years.
Talison has a leading position
in the growing Chinese lithium concentrates market. Talison produces two
categories of lithium concentrates: (i) technical-grade lithium concentrates
which have low iron content for use in the manufacture of, among other
applications, glass, ceramics and heat-proof cookware; and (ii) a high-yielding
chemical-grade lithium concentrate which is used to produce lithium chemicals
which form the basis for manufacture of, among other applications, lithium-ion
batteries for laptop computers, mobile phones, electric bicycles and electric
vehicles.
Chengdu Tianqi Industry
Group Co., Ltd ("Tianqi")
Tianqi is a privately held
Chinese company founded in 2003. Tianqi and its subsidiaries conduct their
operations mainly from China, but have customers, business partners and
suppliers in various countries around the world, including Europe, Australia,
the United States and Japan. Its business activities are primarily conducted
through the following subsidiaries:
Sichuan Tianqi Lithium
Industries, Inc. – a Chinese company listed on the Shenzhen Stock Exchange,
engaged in the production of lithium carbonate and other lithium products
from chemical-grade lithium concentrates sourced from
Talison;
Sichuan Tianqi Industry Co.,
Ltd. – a distributor of technical grade lithium concentrates, as the sole
distributor for Talison in China;
Chengdu Tianqi Machinery –
provides spare parts and accessories for machinery and electrical equipment
used in the construction, packing and agriculture sectors; and
Chengdu Sendasun
Agricultural Machinery Co., Ltd. – undertakes research, development,
manufacturing and sales of agricultural equipment.
In June 2012, Talison
completed and commissioned a new chemical-grade concentrate processing plant
to double Talison’s production capacity to 740,000 tons per year of
concentrate (~100,000 tones lithium carbonate equivalent per annum)
Langelsheim is the largest and most
diverse production location operated by the Chemetall Group. Today's
production range covers chemicals for the surfact treatment of metals,
inorganic and organic lithium compounds and lithium metal, aircraft
sealants as well as high-purity metals and metal compounds of the elements
caesium, barium, titanium and zirkonium.
Talison Lithium is a leading global
producer of lithium.
Talison Lithium’s headquarters are in
Perth, Western Australia and the Company has over 140 employees located in
Australia, Canada, Chile and China.
Talison Lithium currently produces
lithium concentrate at its lithium mineral project in Western Australia
located in the town of Greenbushes. The lithium orebody at Greenbushes is
unique in that it contains large zones of high grade lithium ore. Lithium
has been produced from the Greenbushes operations for over 25 years and
Talison Lithium currently exports over 350,000 tonnes of lithium products
annually to a global customer base.
Talison Lithium also has a lithium brine
project located in the Atacama Region III, in Chile.
This prospective exploration project consists of seven salars (brine lakes
and surrounding concessions). Five of the salars are clustered within a
radius of approximately 30kms and are 100% owned by Talison Lithium and its
Chilean partners.
The Salares 7 Project
consists of seven salars (salt lakes) and playas located in the
Atacama Region of Northern Chile. Five of the seven salars are
100% owned by Talison Lithium and its Chilean partners, and
these five are clustered within a radius of approximately 30
kilometres. The salars are largely underlain and surrounded by
volcanic rocks of andesitic to basaltic affinity that make up
some of the 800 volcanoes located in the Andes Mountains of
northern Chile.
The salars are salt filled
closed basins, confined by a sequence of volcanic rocks. The
brines in the salars were formed by leaching of the host
volcanic rocks by snowmelt and rainwater run-off that
accumulated in the closed basins. Evaporation concentrated the
waters and precipited the salts which are commonly gypsum and
halite.
Talison Lithium’s exploration
program at Salares 7 has included initial drilling, transient
electromagnetic geophysical surveys and regional surface water
geochemical sampling programs. Talison Lithium has also
undertaken process test work studies to assist in designing a
processing facility for the project and collecting environmental
data.
------
August 23, 2012
Rockwood Holdings Agrees to Acquire Talison Lithium
Rockwood Holdings Inc. announced today that it has entered
into a definitive agreement with Talison Lithium Limited to
acquire all of the outstanding shares of Talison in an all-cash
transaction for C$6.50 per share for an equity purchase price of
approximately C$724 million, on a fully diluted basis (US$732, based
on an exchange rate of C$1 = US$1.011635). The Board of Directors of
Talison has unanimously recommended the transaction to Talison
shareholders. The transaction is subject to the approval of Talison
shareholders and other customary closing conditions.
Rockwood intends to finance the acquisition using existing cash on
its balance sheet and new debt financing.
Commenting on the transaction, Seifi Ghasemi, Chairman and CEO of
Rockwood, "The acquisition of Talison is the logical next step in
further strengthening our lithium business and enhancing our
capabilities. This acquisition will enable us to better serve both
our existing global customers as well as Talison's current lithium
concentrate customers in China and the rest of the world".
Lazard is acting as exclusive financial advisor to Rockwood, and
Gilbert & Tobin is acting as Rockwood's legal counsel.
In a C$724 million
cash-ready deal for Talison, Rockwood aimed
to dominate about half the world’s
lithium market, adding, roughly speaking, Talison's
30 percent market share to its 20 percent.
But Talison's chief customer in China,
Chengdu Tianqi, usurped Rockwood’s plans, eventually
making what Talison’s board deemed a superior offer worth
$847 million.
Rockwood declined to enter a bidding war.
Nov 13, 2012
Chengdu Tianqui Proposes Talison
Bid to Trump Rockwood
Chengdu Tianqi Industry Group Co., a closely held Chinese battery maker, said it
will make an offer for Australian mining company Talison Lithium Ltd. that will
exceed an agreed takeover bid from Rockwood Holdings Inc. (ROC)
Chengdu Tianqi’s Windfield Holdings unit agreed to buy or has already purchased
an aggregate 15 percent stake in Talison, the Chengdu, Sichuan province-based
company said yesterday in a statement. Chengdu Tianqi plans to submit a proposal
for the rest of the shares at a higher price than Rockwood’s bid of C$6.50
($6.50) a share, according to the statement.
Talison, based in Perth, Australia, mines ore to produce battery-grade lithium,
which analysts at Dahlman Rose & Co. say may double in demand during the next
eight years on its use in electric vehicles. Talison has the largest open-pit
mine for lithium with the highest grade ore in the world, according to Jonathan
Lee, an analyst at Toronto-based Byron Capital Markets Ltd. Chengdu Tianqi
purchases more than 90 percent of its lithium raw material from Talison, he
said.
“It’s basically vertical integration for them and securing their source of
supply,” Lee said in a telephone interview yesterday.
Talison rose 7.9 percent to C$6.96 in Toronto yesterday.
Talison dominates the market for technical-grade lithium used in the glass and
ceramics industries, he said. Tianqi is the only distributor of Talison’s
technical-grade lithium in China, according to the statement.
Australian Approval
“There’s a limited number of competitors in that space that are vastly smaller
than Talison,” Lee said.
Talison said yesterday in a statement it hasn’t received a proposal from Chengdu
Tianqi and recommends shareholders vote for Rockwood’s bid. A voicemail message
left with Princeton, New Jersey-based Rockwood wasn’t immediately returned.
Talison will be able to grow its business and continue its track record of
innovation and development in Australia, Joshua Goldman-Brown, a spokesman for
Chengdu Tianqi from public relations company Kreab Gavin Anderson, said
yesterday in an interview.
A takeover by Chengdu Tianqi would have to be approved by Australia’s Foreign
Acquisitions and Takeovers Act and may be blocked because of the uniqueness of
Talison’s resources, Lee said. Goldman-Brown declined to comment on the details
of the approval process.
Chengdu Tianqi, which also makes agricultural machinery, owns a 20 percent stake
in Quebec City-based exploration company Nemaska Lithium Inc., according to a
Nov. 1 statement from Nemaska.
Separately, Toronto-based Canada Lithium Corp. said
yesterday it agreed to a five-year agreement to supply China’s Tianjin Products
and Energy Resources Development Co. with 12,000 metric tons of battery-grade
lithium carbonate annually.
Chengdu
Tianqi Industry (Group) Co., Ltd. today announced that Windfield Holdings
Pty Ltd, a wholly-owned subsidiary of Tianqi, has entered into a definitive
agreement with Talison Lithium Limited to acquire all of the shares in
Talison that it does not already own in an all cash transaction at a price
of C$7.50 per share, by way of a scheme of arrangement (the "Transaction").
The aggregate consideration to be paid to Talison securityholders under the
Transaction is approximately C$847 million.
December 12, 2012
Tallison Lithium and Rockwood
terminate agreement
Talison Lithium Limited
and Rockwood Holdings, Inc. have agreed to terminate the scheme implementation
agreement for the proposed schemes of arrangement between Talison and its
Shareholders and Optionholders that would have resulted in all Talison
Securities being acquired by a wholly owned subsidiary of Rockwood, as announced
on August 23, 2012. Talison will pay Rockwood a C$7 million break fee.
The termination of the Rockwood
Proposal was foreshadowed in Talison’s announcement on December 6, 2012
regarding the proposed schemes of arrangement between Talison and its
Shareholders and Optionholders that would result in all Talison Securities being
acquired by Windfield Holdings Pty Ltd, an Australian incorporated wholly-owned
subsidiary of Chengdu Tianqi Industry (Group) Co., Ltd
.
17 Oct 2014 Pirelli
Pirelli and Rosneft, agreement
in the synthetic ruber sector in Nakhodka to extend to new technological partner
Pirelli and Rosneft, in the context of the agreement signed last May for the
production and supply of synthetic rubber in Nakhodka,
today reached a new agreement which calls for, on the basis of a short list, the
identification within three months of a new technological partner for the
further development of activities in the rubber sector, including
Styrene-Butadiene Rubber (SBR), in that region.
Under the terms of the MOU, Rosneft and future partner will analyze the ways in
which the joint production of synthetic rubber could be launched in Nakhodka,
while Pirelli will collaborate in the related Research and Development
activities.
For Pirelli, the MOU also includes the possibility of entering into a long-term
supply agreement to purchase the synthetic rubber jointly produced by Rosneft
and the new technological partner being identified. SBR is of particular
interest as it is an eco-friendly material used in the production of “green
tyres”, which improves fuel efficiency and grip in both wet and dry conditions.
Marco Tronchetti Provera,
chairman and CEO of Pirelli, said: “The agreement signed today goes in the
direction of strengthening the synthetic rubber project in Nakhodka both
technologically and in terms of the already existing synergies between
Pirelli and Rosneft. It is also shows Pirelli and Rosneft beginning to
move together into new alliances which, as we
have already said, could also be a part of our future cooperation.”
Foundation Stone Laid at Ceremony to Mark
Launch of Construction of Eastern Petrochemical Company
A foundation stone laying ceremony has
been held at the construction site of the Eastern
Petrochemical Company outside Nakhodka. Construction work, which is
being carried out by Rosneft, was formally launched by Russian President
Vladimir Putin.
The petrochemical facility will produce
polypropene, high and low density polyethylene, monoethylene glycol and
other petrochemical products. Annually, it will process 3.4 mln
tonnes of feedstock supplied by Rosneft’s Achinsk and
Komsomolsk refineries and the Angarsk Petrochemical Company. Some of
the Eastern Petrochemical Company’s facilities will have higher capacity
than similar units elsewhere in the world. For instance, the
plant’s pyrolysis unit will produce 1.4 million tonnes
of ethylene a year. In terms of capacity, it will be unrivalled
globally.
Technologies for the plant will be
licensed from leading world-class specialist companies to ensure the
facility’s technical prowess and safety. Particular attention was paid to
environmental issues as early as at the design stage.
The complex is located close to
fast-growing South-East Asian markets and has its own sea terminal in an
ice-free port.
Construction of the facility will give a
strong boost to the regional economy with a multiplier effect increasing tax
returns at all levels. Thousands of new jobs will be created at the plant as
well as in related sectors with the region reaping corresponding social
benefits.
--------
24 May 2014
PIRELLI AND ROSNEFT FURTHER CONSOLIDATE RELATIONSHIP WITH TWO MOUs
On the industrial front, under the terms of the MOU, Pirelli will cooperate
jointly with Rosneft in activities to produce synthetic
rubbers in Nakhodka, including Styrene-Butadiene Rubber (SBR). Pirelli is
also interested in entering into a long-term supply agreement to purchase the
synthetic rubber produced. SBR is an eco-friendly material used in the
production of “green tyres” which improves fuel efficiency and grip in both wet
and dry conditions. This agreement follows an MOU signed for similar activities
in Armenia in December 2013.
Mar 4, 2015 AbbVie
AbbVie to Acquire Pharmacyclics, including
its blockbuster product Imbruvica®, Creating an Industry Leading Hematological
Oncology Franchise
- Adds Imbruvica® a first in class BTK
inhibitor approved in multiple indications for blood cancers.
- Extensive clinical program with over 50
studies ongoing evaluating Imbruvica® as a treatment for a wide range of
additional indications, including early assessments for solid tumors and
potential treatment of Graft v Host disease.
- Broadens and deepens AbbVie's already
robust pipeline, and establishes the combined company as an emerging leader
in the hematological oncology space.
- Accelerates the company's commercial
presence in oncology.
- Transaction valued at $261.25 per
Pharmacyclics' share, total transaction value of approximately $21 billion
- Highly accretive to both revenue and
earnings by 2017.
AbbVie and Pharmacyclics today announced a
definitive agreement under which AbbVie will acquire Pharmacyclics, and its
flagship asset Imbruvica® (ibrutinib), a highly effective treatment for
hematologic malignancies. The acquisition accelerates AbbVie's clinical
and commercial presence in oncology, strengthening its already robust
pipeline, and establishing its strong leadership position in hematological
oncology – an attractive and rapidly growing market, now approaching
$24 billion globally. The
acquisition adds to AbbVie's already comprehensive pipeline and strong
growth prospects.
Under the
terms of the transaction, AbbVie will pay
$261.25 per share comprised of a mix of cash and AbbVie equity. The
transaction values Pharmacyclics at approximately
$21 billion and was approved
by the Boards of Directors of both companies.
Imbruvica® is a
Bruton's tyrosine kinase (BTK) inhibitor approved for use in four
indications to treat three different types of blood cancers including
chronic lymphocytic leukemia, mantle cell lymphoma and Waldenstrom's
macroglobulinemia. Imbruvica® received initial U.S. Food and Drug
Administration (FDA) approval in 2013 and is the only therapy to have
received three Breakthrough Therapy designations by the FDA. It is
currently approved in more than 40 countries. Significant opportunity
exists with further Imbruvica® indications, including solid tumors, the
potential to leverage AbbVie's immunology expertise for the development of
Pharmacyclics' immunology program, and advance AbbVie's efforts in
hematologic malignancies.
"The acquisition of Pharmacyclics is a
strategically compelling opportunity. The addition of Pharmacyclics'
talented and innovative team will add enormous value to AbbVie," said
Richard A. Gonzalez,
chairman and chief executive officer, AbbVie. "Its flagship product,
Imbruvica®, is not only complementary to AbbVie's oncology pipeline, it has
demonstrated strong clinical efficacy across a broad range of hematologic
malignancies and raised the standard of care for patients."
"Team Pharmacyclics is honored and
enthusiastic to join the AbbVie organization. We share a common purpose.
Together and as one, our focus remains to create a remarkable difference for
patient betterment around the world," said
Bob Duggan, chairman
and chief executive officer, Pharmacyclics.
Transaction Terms AbbVie will acquire all of the outstanding shares of common stock of
Pharmacyclics through a tender offer, followed by a second-step merger. In
the tender offer, AbbVie will offer to acquire all of the outstanding shares
of Pharmacyclics' common stock for $261.25
per share, consisting of cash and AbbVie common stock. Pharmacyclics'
stockholders will be permitted to elect cash, AbbVie common stock or a
combination, subject to proration. The aggregate consideration will consist
of approximately 58% cash and 42% AbbVie common stock. The closing of the
tender offer is subject to customary closing conditions, including
regulatory approvals, and the tender of a majority of outstanding shares of
Pharmacyclics' common stock, and is expected to close in mid-2015.
AbbVie will acquire all remaining shares
of Pharmacyclics' common stock that are not tendered in the tender offer
through a second-step merger, which will be completed immediately following
the tender offer and without a vote of Pharmacyclics' stockholders.
AbbVie expects to fund the transaction
through a combination of existing cash, new debt and stock.
About
Pharmacyclics Pharmacyclics, Inc. (NASDAQ: PCYC) is a biopharmaceutical company
focused on developing and commercializing innovative small-molecule drugs
for the treatment of cancer and immune mediated diseases. The company's
mission is to build a viable biopharmaceutical company that designs,
develops and commercializes novel therapies intended to improve quality of
life, increase duration of life and resolve serious unmet medical needs. It
will do so by identifying and controlling promising product candidates based
on scientific development and administrative expertise, developing its
products in a rapid, cost-efficient manner and, pursuing commercialization
and/or development partners when and where appropriate.
Pharmacyclics markets IMBRUVICA and has
three product candidates in clinical development and several preclinical
molecules in lead optimization. The company is committed to high standards
of ethics, scientific rigor and operational efficiency as it moves each of
these programs to commercialization. Pharmacyclics is headquartered in
Sunnyvale, CA. To learn more,
please visit
www.pharmacyclics.com.
In 2013, Perrigo solidified its
global foothold by acquiring Elan Corporation plc
through formation of a new holding company, Perrigo Company plc,
now headquartered in Dublin, Ireland.
Mylan Proposes To Acquire Perrigo For $205 Per Share
Mylan N.V. today announced that Mylan has
made a proposal to acquire Perrigo Company plc in a cash-and-stock
transaction that would create a diversified, global pharmaceutical leader with
an unmatched commercial and operating platform and a unique, one-of-a-kind
profile. The combination of these highly complementary businesses would produce
a company with critical mass in specialty brands,
generics, over-the-counter (OTC) and nutritional products; a powerful
commercial platform with reach across all customer channels; an exceptional
high-quality operating platform; and opportunities to generate enhanced growth
and deliver significant immediate and long-term value and benefits for
shareholders and the other stakeholders of both companies.
Under the terms of the non-binding proposal, which was delivered to Perrigo's
Chairman on April 6, 2015, Perrigo shareholders would receive $205 in a
combination of cash and Mylan stock for each Perrigo share, which represents a
greater than 25% premium to the Perrigo trading
price as of the close of business on Friday, April 3, 2015 (the last trading
date prior to the date of Mylan's proposal), a greater than 29% premium to
Perrigo's sixty-day average share price and a greater than 28% premium to
Perrigo's ninety-day average share price.
Mylan's Executive Chairman Robert J. Coury commented, "This proposal is the
culmination of a number of prior discussions between Mylan and Perrigo about the
compelling strategic and financial logic of this combination. This combination
would result in meaningful immediate and long-term value creation, and our
proposal is designed to deliver that value to shareholders and other
stakeholders of both companies. We have great respect for Perrigo's board and
management team and what they have built. We look forward in the weeks ahead to
working with them to capitalize on this tremendous opportunity and working
together to create a unique leader with a one-of-a-kind profile in our
industry."
The proposal is subject to the pre-condition of confirmatory due diligence,
which pre-condition may be waived by Mylan at its discretion. This announcement
is not an announcement of a firm intention to make an offer under rule 2.5 of
the Irish Takeover Panel Act, 1997, Takeover Rules 2013 and there can be no
certainty that an offer will be made, even if the due diligence pre-condition is
satisfied or waived. A further statement will be made if and when appropriate.
ーーーーー
About Perrigo
Perrigo Company plc, a top five global
over-the-counter (OTC) consumer goods and pharmaceutical company, offers
consumers and customers high quality products at affordable prices. From its
beginnings in 1887 as a packager of generic home remedies, Perrigo,
headquartered in Ireland, has grown to become
the world's largest manufacturer of OTC products and supplier of infant formulas
for the store brand market. The Company is also a leading provider of
generic extended topical prescription products and
receives royalties from Multiple Sclerosis drug Tysabri®. Perrigo provides "Quality
Affordable Healthcare Products®" across a wide variety of product
categories and geographies primarily in North America,
Europe, and Australia,
as well as other key markets including Israel
and China.
Perrigo develops, manufactures and
distributes over-the-counter (OTC) and generic prescription (Rx)
pharmaceuticals, nutritional products and active pharmaceutical ingredients
(API), and receives royalties from Multiple Sclerosis 多発性硬化症drug Tysabri®.
Perrigo Consumer Healthcare (CHC) markets a
broad line of over-the-counter (OTC), diabetes and animal
healthcare products that are comparable in quality and effectiveness to
the advertised brands. Perrigo CHC supplies more than 500 formulas in nearly
every major OTC category: analgesics, pediatric analgesics, cough and cold,
gastrointestinal, nicotine replacement, allergy, feminine hygiene, as well as
blood glucose meters, test strips and supplies for the diabetes market. Perrigo
CHC also markets several animal healthcare products, pet treats and
miscellaneous pet care items. Perrigo is the store brand leader in creating
comprehensive marketing programs and campaigns that support all OTC categories –
in-store, e-commerce and digital media.
Perrigo is one of the United States' largest
manufacturers of nutrition products for the store brand market. Nutrition
products include infant formula, pediatric
nutritionals and vitamins, minerals, and supplements.
Perrigo API (formerly known as Chemagis)
provides differentiated Active Pharmaceutical Ingredients (APIs) and Finished
Dosage Forms (FDFs) for the branded and generic pharmaceutical industries.
TYSABRI® is marketed and distributed solely
by Biogen. Perrigo receives royalties on in-market sales.
May 6, 2015
Alexion to Acquire Synageva to
Strengthen Global Leadership in Developing and Commercializing
Transformative Therapies for Patients with Devastating and Rare Diseases
-- Expands
Alexion’s metabolic franchise with the addition
of Kanuma™ (sebelipase alfa) for LAL Deficiency
(LAL-D) --
-- Launches of Kanuma and
Alexion’s Strensiq™ (asfotase
alfa) expected in 2015 --
-- Creates the most robust rare disease pipeline
in biotech; adds SBC-103 for MPS IIIB to
clinical development programs --
-- Combined pipeline to have eight highly
innovative product candidates in the clinic for
eleven indications --
-- Preclinical pipeline to have more than 30
diverse programs across a range of therapeutic
modalities, including 12 from Synageva’s novel
drug discovery platform, with at least four
additional programs to enter the clinic in 2016
--
-- Transaction valued at $8.4 billion net of
cash --
-- Accelerates and diversifies Alexion’s growing
revenues starting in 2015 --
-- Accretive to non-GAAP EPS in 2018 --
-- Alexion Board increases authorized share
repurchase to a total of $1 billion --
Alexion Pharmaceuticals,
Inc. and Synageva BioPharma Corp. announced today that they
have entered into a definitive agreement pursuant to which
Alexion will acquire Synageva for consideration of $115 in
cash and 0.6581 Alexion shares, for each share of Synageva,
implying a total per share value of $230 based on the nine
day volume-weighted average closing price of Alexion stock
through May 5, 2015. The acquisition strengthens Alexion’s
global leadership in developing and commercializing
transformative therapies for patients with devastating and
rare diseases.
The transaction has been
unanimously approved by both companies’ Boards of Directors,
and is valued at approximately $8.4
billion net of Synageva’s cash. The transaction is
expected to accelerate and diversify Alexion’s growing
revenues, and Alexion expects to achieve annual cost
synergies starting this year and growing to at least $150
million in 2017. In addition, the transaction is expected to
be accretive to non-GAAP earnings per share in 2018.
“Synageva is an ideal
strategic and operational fit for Alexion that aligns with
what we know well and do well -- providing life-transforming
therapies to an increasing number of patients with
devastating and rare diseases,” said David Hallal, Chief
Executive Officer of Alexion. “With strong ongoing Soliris
growth in PNH and aHUS worldwide, and the anticipated 2015
global launches of Strensiq and Kanuma, we will accelerate
and diversify our revenue growth. We are excited to create
the most robust rare disease pipeline in biotech across a
range of therapeutic modalities. Synageva is an outstanding
company that shares Alexion’s commitment to serving patients
with rare diseases, and together we will create increasing
value for our stakeholders.”
“Alexion is uniquely
suited to advance Synageva’s mission to deliver life-saving
therapies to patients whose diseases were once considered
too rare for developing treatments,” said Sanj K. Patel,
President and Chief Executive Officer of Synageva. “As
Kanuma moves closer toward patients who suffer from LAL
Deficiency, and the other pipeline programs continue to
progress, I am confident that this transaction will help
continue to improve the lives of patients with LAL
Deficiency and other devastating, rare diseases for years to
come.”
The addition of Kanuma
expands Alexion’s premier global metabolic rare disease
franchise. Alexion will leverage its proven expertise in
rare disease education and diagnostics, and its 50-country
operating platform, to maximize the opportunity to serve
patients suffering from LAL-D. The Company expects that
these efforts will result in more infants, children and
adults with LAL-D receiving a rapid and accurate diagnosis
and, following regulatory approvals for Kanuma, enable
physicians to make better informed treatment decisions for
their patients. Kanuma is under Priority Review with the
U.S. Food and Drug Administration (FDA) and has been granted
accelerated assessment of its Marketing Authorization
Application (MAA) by the European Medicines Agency (EMA).
Kanuma has been granted Breakthrough Therapy Designation by
the FDA for LAL Deficiency presenting in infants. Regulatory
decisions in the U.S. and Europe are expected in the second
half of 2015.
Alexion developed Soliris®
(eculizumab) from the laboratory through regulatory
approvals, and currently provides Soliris to patients around
the world with paroxysmal nocturnal hemoglobinuria (PNH発作性夜間血色素尿症) and
atypical hemolytic uremic syndrome (aHUS)非典型溶血性尿毒症症候群, two
life-threatening ultra-rare disorders. Since its launch in
2007, Soliris has grown to more than $2 billion in revenues
in 2014, with additional growth anticipated as the Company
has consistently identified significant numbers of new
patients with PNH and aHUS each year. With Soliris, and
following the anticipated approvals of Kanuma and Strensiq,
Alexion will have three highly innovative and transformative
therapies serving patients with four devastating and rare
diseases in 2015.
2014/1 Alexion
はFDAが腎移植患者の移植後臓器機能障害の予防に対し、画期的な終末補体阻害薬であるSolirisをOphan
Drug 指定した。
“By every measure,
Alexion is at the strongest and most promising point in our
history given the strength of our clinical, commercial, and
operational performance and the depth of our team,” said
Leonard Bell, M.D., Chairman of Alexion’s Board of
Directors. “These strengths will enable us to accelerate the
transformation of the lives of patients suffering from LAL-D
around the world. Also, I am personally very pleased that
Dr. Felix Baker, a deeply experienced board member and
leader in the biopharmaceutical industry, will join the
Alexion Board of Directors when our transaction is
completed. I look forward to working with Felix as we pursue
our ambitions to serve more patients with more severe and
rare disorders.”
“This transaction
provides Synageva shareholders with immediate value and the
opportunity to participate in Alexion’s long-term growth
potential,” said Felix Baker, Ph.D., Chairman of Synageva’s
Board of Directors. “I am excited to be joining the board of
Alexion, a leading, global biotechnology company that is
aligned with the mission that Synageva was founded upon – to
serve patients who would otherwise be left behind.”
Acquisition Creates Most
Robust Rare Disease Pipeline in Biotech; Expands
Manufacturing Capabilities
Synageva’s pipeline is
complementary to Alexion’s growing portfolio of highly
innovative product candidates for patients with devastating
and rare diseases. Alexion will have a robust clinical
pipeline with eight product candidates in clinical trials
for eleven indications. The programs include Synageva’s
SBC-103, an investigational enzyme replacement therapy in an
ongoing Phase 1/2 trial for patients with
mucopolysaccharidosis IIIB (MPS IIIB), a genetic and
progressive rare metabolic disease. SBC-103 was granted Fast
Track designation by the FDA in January 2015.
In addition, Alexion will
have more than 30 diverse pre-clinical programs across a
range of therapeutic modalities, including 12 from
Synageva’s novel drug discovery platform. At least four
pre-clinical candidates from the combined pipelines are
expected to enter the clinic by year-end 2016.
Alexion will also have
expanded manufacturing capabilities with three Synageva
upstream facilities. Synageva brings to Alexion a
proprietary manufacturing technology, known as the
expression platform, an integrated system of proprietary
vectors that can be used to produce proteins with human-like
glycosylation patterns, creating additional therapies with
better targeting capabilities and the potential for greater
efficacy.
Drugmaker Alexion Pharmaceuticals said it
would buy Synageva BioPharma for $8.4 billion to boost its rare drug
pipeline.
Alexion's cash-and-stock offer values Synageva at $225.92 per share—more
than double of Synageva closing price of $95.87 on Tuesday.
Makers of drugs that treAugat rare diseases are attractive because they
typically charge hefty premiums for their products.
The deal will give Alexion access to Kanuma—Synageva's
treatment for a rare disease called Lysosomal Acid Lipase Deficiencyウォルマン病およびコレステロールエステル蓄積症
, where build-up of fatty material in the
blood and liver causes unexpected complications and some times early death.
Kanuma's marketing application is being reviewed in the United States and
Europe.
Shire Pharmaceuticals, the rare disease-focused drug firm based in Dublin,
Ireland, is bidding $30 billion, all of it in stock, for
Baxalta, the Deerfield, Ill. drugmaker spun out by
Baxter Laboratories last month.
This deal could have a tough time getting done.
It’s all in stock to preserve the tax-free nature of Baxter’s spin-off, but in
order to sweeten the deal further Shire is pledging to buy back shares after the
deal closes.
Baxalta told Shire it’s not interested. But Shire is going to Baxalta’s
shareholders to try and pressure it to the negotiating table. Right now, the
market doesn’t look convinced the deal will ever happen. Baxalta shares are
trading at $38, 15% below the $45 per share that Shire is offering. And Shire
shares have slumped 3%.
And the skepticism is well founded. For one thing, Shire’s offer looks low. The
average acquisition premium being offered in biotechnology deals so far this
year hovers around 30%. Shire is offering a 36% premium, all of it in stock, not
cash. That’s nice, but not knock-your-socks off nice, and it’s no sure thing
that it will lead investors to clamor for Baxalta to start talks. Consider that
when Actavis bought Allergan for $66 billion last, that represented a 54%
premium to Allergan’s share price before the company became embroiled in a nasty
takeover battle.
In fact, the logic behind this deal may be much the same as the logic behind the
Allergan one: a tax break. Allergan was originally approached with a hostile
offer by Valeant Pharmaceuticals , which has a tax domicile in Bermuda, giving
it a lower corporate tax rate than many U.S. competitors. When Allergan was
unable to fend Valeant off by other means, it
arranged for the deal with Actavis,
which has a tax domicile in Ireland. Now the resulting company, once again
called Allergan, pays taxes in Ireland.
Former Allergan boss David Pyott has been approaching members of Congress and
even testified in the Senate that U.S. tax law basically puts American companies
on sale for foreign acquirers. If this deal goes through, it will be evidence
that he’s right. But that’s also a reason that it might not happen.
Consider: Shire CEO Flemming Ornskov is already promising that layoffs, which
often are the real justification behind the mergers of big drug companies (Shire
employs 5,000 people, Baxalta 16,000) will not be a big factor here. Instead,
it’s that tax advantage, major manufacturing synergies, and Baxalta’s global
marketing heft to sell drugs in countries where Shire has no presence that will
make the numbers work.
But that’s also why investors in Shire may not be all that happy with Baxalta as
a acquisition target. Both Shire and Baxalta are attempting the same
metamorphosis: they are trying to evolve from old-line specialty pharmaceutical
firms into hot, hip, fast-growing biotechnology firms, focused on research and
development – the kind of companies investors love to reward with high stock
valuations.
Shire was a drug-delivery firm that first became a big deal thanks to Adderall,
the treatment for attention deficit hyperactivity disorder. But in 2005 it
bought Transkaryotic Therapies, a Cambridge, Mass., biotech firm, for $1.6
billion. It was a cheap and transformative deal that repositioned the company as
a maker of treatments for rare genetic disorders. Now portfolios of treatments
for rare ailments generate $2.3 billion of Shire’s $6 billion in annual 2014
sales.
Investors were probably hoping for a deal that wouldn’t add so much headcount,
and would bring innovation instead. One thing that distinguishes biotechs from
big pharma is leanness: Gilead, with a $176 billion market capitalization, has
just 7,000 employees; Celgene CELG -0.29%, worth $100 billion, has 6,000
employees; Regeneron, worth $63 billion, employs 3,000 people.
Baxalta is in a complicated business: it makes clotting factors to treat
hemophilia, which are made from blood. These are in some ways like the so-called
biologic drugs that are the mainstays of biotech companies, but they are more
difficult to make. Part of Shire’s rationale for the deal is that its own
treatments for angioedema, a deadly swelling of the lips and throat, are sourced
to some of the same suppliers for raw material.
The idea behind Baxalta is that these technologies could be the launching point
for a biotechnology company, but some of the analysts on Shire’s conference call
were concerned about the already marketed products. Ronny Gal, from Bernstein,
asked whether Shire had thought about the fact that not only are new long-acting
therapies on the way, but also gene therapies that could reduce the need for
injected clotting factors. Ornskov shrugged the question off.
Part of the challenge for Shire is simply an expectations game. The last time it
was involved in a big M&A deal, it was to be acquired, not the acquirer. AbbVie,
the North Chicago, Ill., drug giant, was going to buy it in part to get its tax
domicile, but walked away due to political pressure and regulatory moves by the
Obama administration that made the move, known as a tax inversion, less
favorable. Now, once again, Shire is planning a deal that could put it in the
crosshairs of U.S. politicians.
アイルランドの医薬品大手Shire
Pharmaceuticalsは1月11日、米バイオ医薬品のNPS Pharmaceuticals, Inc. を52億ドルで買収すると発表した。
米食品医薬品局(FDA)は8月18日、閉経前女性の性欲低下障害(HSDD:Hypoactive
Sexual Desire Disorder)に対する初の治療薬Addyi(一般名:flibanserin)を承認した。HSDDは、閉経の苦悩やパートナーとの対人関係の困難さを引き起こす性欲の低下を特徴としている。同疾患は、併存する医学的あるいは心理的状態や人間関係自体の問題、他の医薬品の影響などは関係のないものである。HSDDはいままで性欲が正常だった女性に発症し、性行動のタイプやパートナーに関係なく発症する。
Development by Boehringer Ingelheim was
halted in October 2010 following a negative evaluation by the U.S. Food and
Drug Administration.
The rights to the drug were then transferred to Sprout Pharmaceuticals,
which achieved approval of the drug by the US FDA in August 2015.
-----
08/20/2015 Valeant
Valeant Pharmaceuticals To Acquire Sprout
Pharmaceuticals
Enters Sexual Health Market with FDA-Approved Addyi™ (flibanserin 100mg)
Addyi Expected to Launch in U.S. in the Fourth Quarter of 2015
Valeant Pharmaceuticals International, Inc. and Sprout
Pharmaceuticals, Inc. today announced that they have entered into a
definitive agreement under which a wholly-owned subsidiary of Valeant will
acquire Sprout, on a debt-free basis, for approximately $1
billion in cash, plus a share of future profits based upon the
achievement of certain milestones.
On Tuesday, August 18, 2015, Sprout received approval from the U.S. Food and
Drug Administration (FDA) on its New Drug Application (NDA) for
flibanserin, which will be marketed as Addyi
in the U.S. Addyi has demonstrated improvements in desire for sex,
reducing distress from the loss of sexual desire and increasing the number of
satisfying sexual events. Sprout also has global rights for flibanserin. Valeant
will leverage its global scale to register flibanserin internationally.
Sprout is passionate about women's sexual health and has focused solely on the
delivery of a treatment option for the unmet need of premenopausal women with
acquired, generalized Hypoactive Sexual Desire Disorder (HSDD) as characterized
by low sexual desire that causes marked distress or interpersonal difficulty and
is not due to a co-existing medical or psychiatric condition, problems within
the relationship, or the effects of a medication or other drug substance.
Addyi is not indicated for use in postmenopausal women or men or to enhance
sexual function. Addyi was approved with a Boxed Warning. Use of Addyi with
alcohol increases the risk of severe hypotension and syncope; therefore, alcohol
use is contraindicated. Severe hypotension and syncope occurs when Addyi is used
with moderate or strong CYP3A4 inhibitors or in patients with hepatic
impairment; therefore use of Addyi in patients with hepatic impairment is also
contraindicated. Hypotension, syncope and central nervous system (CNS)
depression can occur with Addyi alone. The most common adverse reactions are
dizziness, somnolence, nausea, fatigue, insomnia and dry mouth.
Valeant expects Addyi to be available in the United States in the fourth quarter
of 2015 through prescribers and pharmacies that have been certified under the
U.S. FDA's comprehensive Risk Evaluation and Mitigation Strategy (REMS) program
to assure safe use. Following the closing of the transaction, Valeant, under the
REMS, will offer physicians and pharmacists the required certification programs
for prescribing and dispensing Addyi.
Following the closing of the acquisition, Sprout will remain headquartered in
Raleigh, N.C. and become a division of Valeant. Cindy Whitehead, Chief Executive
Officer of Sprout, will join Valeant to lead this division dedicated to the
introduction and global commercialization of Addyi, reporting to Anne Whitaker,
Executive Vice President and Company Group Chairman.
Valeant's Chairman and Chief Executive Officer, J. Michael Pearson, said,
"Delivering a first-ever treatment for a commonly reported form of female sexual
dysfunction gives us the perfect opportunity to establish a new portfolio of
important medications that uniquely impact women. We applaud the efforts of the
Sprout team to address this important area of unmet need and look forward to
working with them to bring the benefits of Addyi to additional markets around
the world."
Sprout Chief Executive Officer, Cindy Whitehead, said, "I am extremely proud of
the commitment and passion of our 34 employees who have been mission driven to
get to this breakthrough first for women. This partnership with Valeant allows
us the capacity to now ensure broader, more affordable access to all the women
who have been waiting for this treatment. Beyond building this in the United
States, Valeant also offers us a global footprint that could eventually bring
Addyi to women across the globe."
"The Valeant team is excited to be a part of the launch of this critically
important treatment for women, and I am personally delighted to welcome Cindy
and her colleagues at Sprout to Valeant," added Anne Whitaker, Executive Vice
President and Company Group Chairman. "The Sprout team, along with the
healthcare providers involved in the Addyi pivotal clinical trials, has
delivered on its promise to provide access to a safe and effective treatment for
a condition that affects millions of women."
Under terms of the acquisition agreement, Valeant will pay approximately
$500 million, subject to customary purchase price adjustments, upon the
closing of the transaction and an additional payment in the amount of
$500 million, payable in the first quarter of 2016,
plus a share of future profits based upon the
achievement of certain milestones. Valeant expects no impact to 2015 earnings,
and moderate accretion to 2016 earnings.
The transaction is subject to customary closing conditions and regulatory
approval, including Hart-Scott-Rodino antitrust clearance. The transaction is
expected to close in the third quarter of 2015.
Skadden, Arps, Slate, Meagher & Flom LLP served as Valeant's legal counsel.
Sprout was advised by Sullivan & Cromwell LLP as its legal counsel and Perella
Weinberg Partners as its financial advisor.
About Addyi
Addyi is a novel, non-hormonal oral pill taken once daily at bedtime.
Flibanserin has been studied in over 11,000 women. For premenopausal women with
HSDD, Addyi has demonstrated improvements in desire for sex, reducing distress
from the loss of sexual desire and increasing the number of satisfying sexual
events. The most common adverse events among patients treated with Addyi were
dizziness, somnolence, nausea, fatigue, insomnia and dry mouth. Hypotension,
syncope, and central nervous system (CNS) depression were seen with Addyi alone
and more frequently when Addyi was taken in the morning and when co-administered
with alcohol or certain other drugs. Alcohol consumption is contraindicated for
women taking Addyi. With the FDA, Sprout Pharmaceuticals developed a
comprehensive Risk Evaluation and Mitigation Strategy (REMS) program, including
prescriber and pharmacist certification, to ensure safe use of Addyi.
About Sprout Pharmaceuticals
Sprout Pharmaceuticals, Inc. is passionate about women's sexual health. With a
breakthrough concept for women, the company "sprouted" out of
Slate Pharmaceuticals in 2011. Based in Raleigh,
N.C., the company is focused solely on the delivery of a treatment option for
women with HSDD.
Sprout was founded in 2011 by CEO, Cindy
Whitehead and her husband, Robert, when they spun out of and later sold
their previous company, Slate Pharmaceuticals, to Actient Pharmaceuticals.
Slate developed and commercialized a testosterone implant for men.
Prior to Sprout Pharmaceuticals, Cindy
co-founded and led all operational functions at Slate Pharmaceuticals. Slate
Pharmaceuticals commercialized the first FDA-approved long-acting
testosterone preparation for men, Testopel 医療用テストステロン埋め込みペレット,
in the field of sexual medicine. Cindy led the sale of the Slate to GTCR/Actient
Pharmaceuticals in December 2011 spinning out Sprout Pharmaceuticals to
pursue the first ever FDA drug approval for women’s most common sexual
dysfunction.
Slate
Pharmaceuticals, Inc. acquires, develops, and commercializes products
for the diseases of maturing men and women. It offers specialized
subcutaneous pellet delivery of hormones. The company offers its products in
the United States. Slate Pharmaceuticals, Inc. was founded in 2007 and is
headquartered in Durham, North Carolina. As of December 29, 2011,
Actient
Pharmaceuticals, LLC, a therapeutics company, develops, acquires, and
markets pharmaceutical pharmaceutical products that improve patient
outcomes. It focuses on urology, as well as other specialty areas.
Rosneft and Synthos sign MOU for next phase of future
cooperation in synthetic rubber production in Nakhodka
Pirelli, Rosneft and Synthos
today signed a Memorandum of Understanding regarding the approval of the results
of the feasibility study begun in April and future cooperation in the
development of the synthetic rubber plant construction project in Nakhodka.
2015年4月16日、両社とポーランドの石油化学会社
Synthos は覚書を締結、Synthosが技術パートナーとなった。
計画名をFEPCO (Far East Petrochemical Company)
としている。
The document was signed during
the Fourth Eurasian Forum in Verona by Rosneft Chairman of the Management Board
Igor Sechin, Pirelli Executive Vice Chairman and CEO Marco Tronchetti Provera,
and Synthos majority stakeholder Michal Solowow.
The successful finalization of
this phase marks another important step in the implementation of a large-scale
project aimed at creating an advanced technology petrochemical cluster in
Russia’s Far East. By signing the MOU, the parties confirm their intention to
analyze the possibility of the creation of a joint venture between Rosneft and
Synthos in the area of synthetic rubber production in Nakhodka, and the
implementation of joint Pirelli R&D in the area of tyre materials. Ultimately,
Pirelli would become the key customer for the synthetic rubber, as indicated in
an MOU signed with Rosneft in 2014.
Following the signing Igor
Sechin said that: “We intend to create at FEPCO a cutting-edge technological and
production platform for boosting the development of the automotive and
petrochemical clusters in the Russian Far East. In particular, the agreement
that we have signed today with two recognized global leaders in high-end
technology for synthetic rubber and tire production will allow us not only to
build the most advanced synthetic rubber plants as part of our FEPCO development
in Nakhodka, but also to successfully supply Chinese and other Asian automotive
tire markets for years to come. Developing the FEPCO project is one our key
priorities. Its implementation will allow Rosneft to significantly strengthen
its position in the energy and petrochemical arena of the region, whilst at the
same time creating an unprecedented platform for a multiplicative and all-round
development of the Russian Far East region.”
Marco Tronchetti Provera said:
“We are pleased to be moving forward with Rosneft and Synthos on this project,
greatly encouraged by the positive results of feasibility study. Pirelli’s
involvement in the process of developing this advanced regional production hub,
both on the R & D side and eventually as a key customer, underlines our belief
in and commitment to the entire Russian market.”
September 9, 2014
FMC Buys Cheminova for $1.8
Billion and Revises Breakup
FMC Corp. agreed to acquire Danish pesticide maker Cheminova for $1.8 billion,
including debt, as Chief Executive Officer Pierre Brondeau builds up the crop
chemicals division and reduces the scale of a planned breakup.
The acquisition, to be completed in early 2015, will add to profit in the first
full year, Philadelphia-based FMC said today in a statement. The price for the
unit of Lemvig, Denmark-based Auriga Industries A/S includes $340 million of
debt, Brondeau, who is also chairman of FMC, said on a conference call.
Brondeau is buying Cheminova as he revises a March plan to spin off all mineral
businesses. He’ll instead sell alkali chemical assets while retaining the unit
that makes lithium, used in rechargeable batteries that power electronics. The
moves will boost agricultural chemicals to 77 percent of revenue, from 55
percent, with sales in Europe to rise the most, FMC said.
“That’s exactly where I wanted to go,” Brondeau said today by phone. “I want a
very high focus” on agriculture, health and nutrition, he said.
Proceeds from FMC’s planned sale of its alkali chemicals business, the world’s
largest maker of natural soda ash used to make paper and glass, will allow it to
pay down some of the debt needed to complete the purchase of Cheminova, Brondeau
said.
FMC rose 0.8 percent to $66.12 at the close in New York. Auriga gained 1.1
percent to 308.50 kroner in Copenhagen.
Insecticide Focus
Cheminova has 2,200 employees and sales in more than 100 countries exceeding
$1.2 billion last year. More than two-thirds of sales are in Europe and Latin
America, with insecticides ranking as the biggest business, followed by
herbicides and fungicides.
FMC is paying about 11.7 times earnings before interest, taxes, depreciation and
amortization in the past 12 months, Cheminova Chief Financial Officer Rene
Schneider said by phone. The Ebitda multiple is 11 times based on estimated
full-year results, FMC Chief Financial Officer Paul W. Graves said on the
conference call.
Cheminova’s earnings before interest and taxes will rise to a “high teens”
percentage of sales compared with a profit margin currently lower than 10
percent, Graves said. The gains will come from expanded sales opportunities and
eliminating duplicate functions, he said.
Auriga plans to hold a special meeting of shareholders in October to approve the
transaction, the company said in a separate statement.
FMC will retain its lithium unit, which makes the
metal from brine in Argentina, because of change-in-control provisions in its
mining contract with the South American country, Brondeau said.
Reverse Spin
FMC was planning a so-called reverse spin in which
the smaller minerals business would spin off the rest of the company to get
around the change-in-control provisions, he said in the interview. A reverse
spin won’t work for the lithium unit alone, as it’s too small to succeed
independently, he said.
FMC, which already supplies lithium used by Panasonic Corp. to make batteries
for Tesla Motors Inc., expects to be a supplier to Tesla’s planned gigafactory
in Nevada, Brondeau said.
“Maybe they are starting to see with the announcement from Tesla on the
gigafactory that there is more opportunity in lithium than they had thought
previously,” James Sheehan, an Atlanta-based analyst at Suntrust Robinson
Humphrey Inc. who rates FMC neutral, said by phone today.
The Cheminova deal follows Platform Specialty Products Corp.’s purchase of
Chemtura Corp.’s agrochemicals business for about $1 billion earlier this year,
in a further sign that makers of active ingredients and crop protection are
being snapped up. Platform was co-founded by Nicolas Berggruen and backed by
hedge fund manager Bill Ackman.
‘Very Competitive’
“The sale process has been very competitive, with a lot of interest,” Schneider
said. With FMC, “the strategies match, with similar ambitions in research and
development, and a good complementary in geography.”
Cheminova competes with Syngenta AG, Dow Chemical Co. and BASF SE as well as
Nufarm Ltd. and Adama Agricultural Solutions Ltd.
Alkali chemicals are “highly profitable and cash generative” and will attract
“many interested buyers,” Brondeau said in the statement. FMC is looking to
complete the disposal by mid-2015.
Goldman Sachs acted as financial adviser to FMC and Wachtell, Lipton, Rosen &
Katz acted as legal counsel. Citigroup provided additional financial advice and
committed debt facilities.
JP Morgan Chase & Co. advised Auriga. After redistributing the proceeds of the
sale to shareholders, Auriga will be dissolved, Schneider said.
Before it's here, it's on the Bloomberg Terminal.
Sanofi Comments on Medivation’s Rejection of Proposal
– Reiterates
Commitment to Consummating Transaction –
Paris, France –
April 29, 2016 –
Sanofi today commented on Medivation, Inc.’s (NASDAQ:
MDVN) rejection of Sanofi’s non-binding all-cash proposal to
acquire Medivation for $52.50 per share:
Combining Sanofi and
Medivation represents a compelling strategic and financial
opportunity to drive immediate and certain value for
Medivation’s shareholders while benefiting patients and both
companies’ respective stakeholders. Sanofi’s all-cash
proposal represents over a 50 percent premium to
Medivation’s two-month volume weighted average trading price
(VWAP) prior to takeover rumors.
Sanofi is a disciplined
acquirer and has a strong acquisition track-record. While to
date Medivation has chosen not to enter into discussions
regarding this value-creating transaction, Sanofi remains
committed to the combination and looks forward to engaging
directly with Medivation shareholders with regard to our
proposal.
- See more at: http://mediaroom.sanofi.com/sanofi-comments-on-medivations-rejection-of-proposal/#sthash.lFlvJTbn.dpuf
-----
Medivation's Board of Directors Unanimously
Rejects Sanofi's Unsolicited Proposal
Medivation, Inc. today
announced that its Board of Directors, after consultation with its financial and
legal advisors, unanimously determined that the unsolicited proposal from Sanofi
to acquire Medivation for
$52.50 per share in cash substantially undervalues
Medivation and is not in the best interests of the company and its
stockholders.
"Over the past several years, we have
established a world class oncology franchise and a unique, diversified and
highly-promising late-stage development pipeline," said
David Hung, M.D., Founder, President and Chief Executive Officer of
Medivation. "Further, we have a track record of delivering extraordinary
value to our stockholders. Sanofi's opportunistically-timed proposal, which
comes during a period of significant market dislocation, and prior to several
important near-term events for the company, is designed to seize for Sanofi
value that rightly belongs to our stockholders. We believe the continued
successful execution of our well-defined strategic plan will deliver greater
value to Medivation's
stockholders than Sanofi's substantially inadequate proposal."
The Medivation Board of Directors' unanimous
conclusion was based on the following:
The proposal
substantially undervalues
Medivation and its leading oncology franchise.
Medivation has significant scarcity
value as one of the few profitable, commercial-stage oncology companies;
it has brought a blockbuster product to market and is leveraging its
expertise to develop and bring to market additional products.
Medivation has built XTANDI® (enzalutamide) capsules into a
rapidly-growing, multi-billion dollar oncology product and remains on track to achieve its 2016 U.S. net
sales guidance, which implies approximately 28% growth (at the mid-point)
for the year.
XTANDI is one of the most successful
oncology product launches in history and just surpassed Johnson &
Johnson's Zytiga® (abiraterone) in U.S. market share, despite launching
sixteen months later.
XTANDI has achieved worldwide annual
net sales of $2.2 billion on a run rate basis, less than
four years after its initial approval.
XTANDI has significant patent life with
10+ years of remaining exclusivity.
XTANDI is poised to capitalize on a
substantial, near-term commercial opportunity in urology, enabling it to
serve a larger patient population of men with metastatic
castration-resistant prostate cancer (mCRPC) and increasing the duration of
therapy.
The
PDUFA date for TERRAIN/STRIVE label expansion on October 22, 2016,
is rapidly approaching and is anticipated to drive significantly
greater adoption by urologists.
In April, the CHMP issued a positive
opinion to include findings from the TERRAIN trial in the European
label.
Medivation
recently expanded its specialty salesforce to create dedicated urology
and oncology selling teams that are just starting to have a promotional
impact.
XTANDI has multiple opportunities beyond
mCRPC, which are not reflected in the company's current valuation.
Ongoing Phase 3 trials, i.e. PROSPER
and EMBARK, are designed to move XTANDI even earlier in the prostate
cancer treatment paradigm; PROSPER is
on track to complete enrollment of 1,560 patients in mid-2017.
Medivation
is pursuing clinical development across three major subtypes of breast
cancer, a new and significant market opportunity for XTANDI, and expects
to report top-line Phase 2 data in patients with ER/PR+ breast cancer,
which represents 50% of all breast cancers, in the second half of 2016.
A Phase 3 trial in Triple Negative
Breast Cancer, a significant unmet need, is expected to initiate later
in 2016.
The company continues to explore
XTANDI in other solid tumor indications and settings, e.g., in
hepatocellular carcinoma and in combination with immunotherapy.
Sanofi's proposal
would deny Medivation's
stockholders the value of
Medivation's wholly-owned, innovative late-stage pipeline.
Talazoparib represents another blockbuster opportunity as a
potentially best-in-class PARP inhibitor targeting a wide range of
oncology indications.
Top-line
data from the Phase 3 EMBRACA trial in germline BRCA mutated advanced
breast cancer is expected in the first half of 2017.
Recent data reported at AACR
demonstrate talazoparib's potential in tumors with defects in DNA repair
beyond BRCA deficiency and possibly in patients without evidence of
homologous recombination deficiency when used in combination with low
dose chemotherapy.
The
company is preparing to initiate several clinical trials in 2016,
including in breast cancer beyond germline BRCA mutations, prostate
cancer, ovarian cancer and small cell lung cancer, including potentially
registrational trials.
Medivation recently met with the FDA to discuss
clinical trial design and a potential accelerated approval pathway in
prostate cancer.
Talazoparib is highly synergistic
with our existing development and commercial infrastructure.
Additional clinical data
demonstrating talazoparib's potent activity is expected to be presented
at a medical meeting later in the year.
Pidilizumab has the potential to be a
novel immuno-oncology candidate supported by clinical efficacy and a strong
safety profile in several hematological malignancies.
The execution of
Medivation's business plan will deliver value to its stockholders that is
far superior to Sanofi's proposal.
Medivation has an exceptional track record for execution.
XTANDI has achieved all development
and sales milestones under
Medivation's collaboration with Astellas.
Medivation's
track record for delivering value to our stockholders is exemplified by
XTANDI, which was in-licensed as a pre-clinical asset in 2005, received full
FDA approval in seven years (better than industry average), and
achieved $2.2 billion in worldwide annual net sales on a run
rate basis in less than four years.
The company has generated a 1,440%+
total shareholder return for its stockholders since 2009.
Medivation
has already achieved two years of profitability, despite only launching
XTANDI in late 2012, and the company has pursued minimal, dilutive capital
raises.
Sanofi's timing
is designed to benefit Sanofi - not
Medivation's stockholders.
Sanofi approached
Medivation following a period of significant market dislocation in
biotech and just as the market was beginning to recover.
The "private offer" was submitted to
Medivation when the NBI index was almost 30% below its July
2015 high.
The proposal offer price is:
21% below
Medivation's 52-week trading high of $66.40
Less than a 14% premium to
Medivation's 12-month volume weighted average price, or VWAP
Only a 9% premium to
Medivation's VWAP over the last month
Medivation will provide
additional information on its financial performance, XTANDI's utilization and
the company's clinical development plans for talazoparib on next week's earnings
call.
Kim D.
Blickenstaff, Chairman of
Medivation's Board of Directors, notes that "Medivation
has a long history of producing superior growth and generating significant
value for its stockholders. Since the launch of XTANDI,
Medivation has achieved revenues of nearly $1 billion
in just over three years. There are several exciting pipeline opportunities
that will drive significant growth. The Board is determined to continue to
aggressively focus on working for, and delivering value to,
Medivation's stockholders."
ーーーーーーーー
Sanofi Comments on Medivation’s Rejection of Proposal
– Reiterates
Commitment to Consummating Transaction –
Paris, France –
April 29, 2016 –
Sanofi today commented on Medivation, Inc.’s (NASDAQ:
MDVN) rejection of Sanofi’s non-binding all-cash proposal to
acquire Medivation for $52.50 per share:
Combining Sanofi and
Medivation represents a compelling strategic and financial
opportunity to drive immediate and certain value for
Medivation’s shareholders while benefiting patients and both
companies’ respective stakeholders. Sanofi’s all-cash
proposal represents over a 50 percent premium to
Medivation’s two-month volume weighted average trading price
(VWAP) prior to takeover rumors.
Sanofi is a disciplined
acquirer and has a strong acquisition track-record. While to
date Medivation has chosen not to enter into discussions
regarding this value-creating transaction, Sanofi remains
committed to the combination and looks forward to engaging
directly with Medivation shareholders with regard to our
proposal.
- See more at: http://mediaroom.sanofi.com/sanofi-comments-on-medivations-rejection-of-proposal/#sthash.lFlvJTbn.dpuf
Sanofi Comments on Medivation’s Rejection of Proposal
– Reiterates
Commitment to Consummating Transaction –
Paris, France –
April 29, 2016 –
Sanofi today commented on Medivation, Inc.’s (NASDAQ:
MDVN) rejection of Sanofi’s non-binding all-cash proposal to
acquire Medivation for $52.50 per share:
Combining Sanofi and
Medivation represents a compelling strategic and financial
opportunity to drive immediate and certain value for
Medivation’s shareholders while benefiting patients and both
companies’ respective stakeholders. Sanofi’s all-cash
proposal represents over a 50 percent premium to
Medivation’s two-month volume weighted average trading price
(VWAP) prior to takeover rumors.
Sanofi is a disciplined
acquirer and has a strong acquisition track-record. While to
date Medivation has chosen not to enter into discussions
regarding this value-creating transaction, Sanofi remains
committed to the combination and looks forward to engaging
directly with Medivation shareholders with regard to our
proposal.
- See more at: http://mediaroom.sanofi.com/sanofi-comments-on-medivations-rejection-of-proposal/#sthash.lFlvJTbn.dpuf
Sanofi Comments on Medivation’s
Rejection of Proposal
Paris, France – April 29, 2016 – Sanofi today commented on Medivation, Inc.’s
rejection of Sanofi’s non-binding all-cash proposal to acquire Medivation for
$52.50 per share:
Combining Sanofi and Medivation represents a compelling strategic and financial
opportunity to drive immediate and certain value for Medivation’s shareholders
while benefiting patients and both companies’ respective stakeholders. Sanofi’s
all-cash proposal represents over a 50 percent premium to Medivation’s two-month
volume weighted average trading price (VWAP) prior to takeover rumors.
Sanofi is a disciplined acquirer and has a strong acquisition track-record.
While to date Medivation has chosen not to enter into discussions regarding this
value-creating transaction, Sanofi remains committed to the combination and
looks forward to engaging directly with Medivation shareholders with regard to
our proposal.
August 16, 2016
Praxair, Inc. Confirms Preliminary Talks about a Potential Merger with Linde AG
Praxair, Inc. today confirmed that it is currently in preliminary discussions
with Linde AG regarding a potential merger. These discussions are ongoing and
there can be no assurance that they will result in a transaction, or on what
terms any transaction may occur. Praxair does not intend to comment further at
this time.
------
August 16, 2016 Reuters
Gas Suppliers Praxair and Linde Are Discussing a Possible Merger
U.S. industrial gas supplier Praxair and German peer Linde have held initial
talks about a merger to create a market leader with a value of more than $60
billion, people familiar with the matter said, sending shares in Linde more than
7% higher.
An agreement would accelerate consolidation sweeping the industrial gas sector
where slower economic growth has weakened demand in the manufacturing, metals
and energy sectors and put pressure on smaller players to compete.
A combination of Praxair and Linde would face scrutiny from regulators in a year
when other major deals, such as U.S. oilfield services provider Halliburton
$34.6 billion acquisition of Baker Hughes, were shot down due to antitrust
concerns.
Details of the talks, which were first reported by the Wall Street Journal, were
not immediately clear.
One person familiar with the matter said Praxair was considering a takeover of
Linde, while two other sources said Linde wanted a merger of equals.
A fourth person, who is close to Linde, said there had been talks, but that no
agreement had been reached.
One of the sources said a share swap was one possible structure of a deal but
that talks were still very preliminary.
Linde has a market value of around 27 billion euros ($30.4 billion), compared
with about $33.7 billion for Praxair.
Representatives for Danbury, Connecticut-based Praxair could not be immediately
reached for comment. Munich, Germany-based Linde declined to comment.
Sector Shake-Out
Analysts said talks may have been spurred by French Air Liquide’s acquisition of
smaller U.S. peer Airgas for $10.3 billion this year, making the world’s leading
industrial gases group a strong second player in North America behind Praxair.
Linde has
a strong position in healthcare gases in North America, while
Praxair is more focused on industrial on-site production,
which means a market share of close to 50% resulting from a merger should not
spark opposition from U.S. anti-trust regulators, analysts said.
Baader Helvea analyst Markus Mayer said overlaps in the rest of the world could
help generate synergies of up to 800 million euros in a merger.
“Asset disposals are hardly crippling in a business of regional oligopolies, and
the transaction could fix strategic challenges for both companies,” Jefferies
analysts said in a note.
They said they estimated that Praxair could pay a 26% premium over Linde’s
market value to gain control of it and still achieve an 8% return on invested
capital in the full year and improve its free cash flow per share by $1.70.
June 29, 2018
AbbVie, Besins Owe $448M In FTC Androgel
Antitrust Case
AbbVie Inc. and an affiliate must pay $448 million in the Federal
Trade Commission’s suit alleging they netted more than $1 billion after
bringing sham patent lawsuits to stave off
generic competition to AbbVie’s AndroGel testosterone replacement
drugテストテトロン補充薬, a Pennsylvania federal court ruled Friday.
Friday’s decision by U.S. District Judge Harvey Bartle III calls for
AbbVie and Besins Healthcare Inc. to disgorge $448 million in profits
from June 2013, when competitor Perrigo Co.
would have entered the market if not for the AndroGel makers’
intervention, ・・・
June 29, 2018
AbbVie and affiliate owe $448
million in FTC antitrust case
AbbVie Inc. was
hit with a $448 million judgement late Friday to
be paid out to consumers
that were allegedly overcharged by the pharmaceutical
giant, according to the Federal Trade Commission.
In 2014, the FTC
alleged AbbVie and its partner Besins Healthcare Inc.
blocked consumer access to lower cost versions of the
testosterone replacement drug Androgel. The FTC accused
AbbVie of using "sham litigation" to maintain its
monopoly. "This decision is a double victory, both for
patients who rely on Androgel and for competition more
broadly," said FTC chairman Joe Simons. "It sends a
clear signal that pharmaceutical companies can't use
baseless litigation to forestall competition from
low-cost generics."
The decision handed
down in the U.S. District Court for Eastern Pennsylvania
is the largest monetary award in a litigated FTC
antitrust case, the agency said.
SC Johnson today announced that
it has signed an agreement to acquire Sun Bum®, a fast-growing
brand that makes quality personal care products including sun
protection, hair care and lip care products. The acquisition
also includes the Baby Bum® brand of sun protection and baby
care products.
“The Sun Bum brand is a welcome addition to our portfolio of
trusted products,” said Fisk Johnson, Chairman and CEO of SC
Johnson. “It also expands our robust selection of fast-growing,
on-trend products like Babyganics, Method, Mrs. Meyer’s Clean
Day and Caldrea that appeal to consumers and their families.”
SC Johnson expects the deal to be finalized subject to U.S.
regulatory approval.
As a private company, SC Johnson does not disclose details
regarding financial or business transactions.
About
SC Johnson
SC Johnson is a family company
dedicated to innovative, high-quality products, excellence in
the workplace and a long-term commitment to the environment and
the communities in which it operates. Based in the USA, the
company is one of the world's leading manufacturers of household
cleaning products and products for home storage, air care, pest
control and shoe care, as well as professional products. It
markets such well-known brands as GLADE®, KIWI®, OFF!®, PLEDGE®,
RAID®, SCRUBBING BUBBLES®, SHOUT®, WINDEX® and ZIPLOC® in the
U.S. and beyond, with brands marketed outside the U.S. including
AUTAN®, BAYGON®, BRISE®, KABIKILLER®, KLEAR®, MR MUSCLE® and
RIDSECT®. The 133-year-old company, which generates $10 billion
in sales, employs approximately 13,000 people globally and sells
products in virtually every country around the world.
www.scjohnson.com
8/20/2019
PolyOne to sell PP&S business
to SK Capital
PolyOne Corporation
announced it has entered into a definitive agreement to sell its Performance
Products and Solutions (PP&S) business to SK Capital
Partners for $775 million in cash.
PolyOne expects to record a pre-tax gain of
approximately $600 million at the time the sale is completed.
With sales of approximately $700 million,
PP&S is a global provider of formulated PVC and
polypropylene based solutions, as well as contract manufacturing
services, primarily serving the North American Construction and Automotive end
markets. "We conducted what became a very competitive bidding process for our
PP&S segment," said Robert M. Patterson, chairman, president and CEO, PolyOne
Corporation. "Ultimately, we determined that divesting the business to SK
Capital Partners would provide greater flexibility to accelerate our specialty
growth strategy, and is in the best interest of customers, employees and
shareholders." "In the short term, proceeds from the sale will be used to pay
down debt on our revolving line of credit and reduce our overall net debt to
EBITDA leverage from 3.2 to 2.0 by year-end," said Patterson.
"Longer term, we can further refine our focus
on investing in and growing our three remaining segments:
Specialty Engineered Materials;
Color, Additives and Inks; and
Distribution." The company noted it expects full
year 2019 adjusted earnings per share from continuing operations to expand 6-8
percent over the prior year. "We continue to benefit from recent investments
made in composites and other sustainable solutions, which is helping us to
deliver adjusted EPS growth in an otherwise challenging environment," said
Patterson. "As discussed on our second quarter conference call, margins are
expanding as a result of improved mix, pricing and cost reductions."
In accordance with U.S. GAAP, the company expects the PP&S business will be
classified as "held for sale" and reported as a discontinued operation. The
company noted that HSBC served as financial advisor and led the sale process for
PolyOne. Jones Day served as outside legal counsel. The sale is subject to
satisfaction of regulatory requirements and other customary closing conditions,
which the company expects to be completed during the fourth quarter. The company
will discuss additional details of the transaction on its third quarter 2019
conference call.
SK Capital targets investments
in the specialty materials, chemicals and pharmaceuticals sectors, working
collaboratively with management to support the realization of their strategic,
operational and financial objectives.
Diamondback Energy, Inc. and Endeavor
Energy Resources, L.P. to Merge to Create a Premier Permian Independent
Oil and Gas Company
Diamondback Energy, Inc. and
Endeavor Energy Resources, L.P., today announced that they have
entered into a definitive merger agreement under which Diamondback and
Endeavor will merge in a transaction valued at
approximately $26 billion, inclusive of Endeavor’s net
debt. The combination will create a premier Permian independent
operator.
The transaction
consideration will consist of approximately 117.3
million shares of Diamondback common stock and $8 billion
of cash, subject to customary adjustments. The cash portion of
the consideration is expected to be funded through a combination of cash
on hand, borrowings under the Company’s credit facility and/or proceeds
from term loans and senior notes offerings. As result of the
transaction, the Company’s existing stockholders are expected to own
approximately 60.5% of the combined company
and Endeavor’s equity holders are expected to own approximately
39.5% of the combined company.
The transaction was
unanimously approved by the Board of Directors of the Company and has
all necessary Endeavor approvals.
“This is a
combination of two strong, established companies merging to create a
‘must own’ North American independent oil company. The combined
company’s inventory will have industry-leading depth and quality that
will be converted into cash flow with the industry’s lowest cost
structure, creating a differentiated value proposition for our
stockholders,” stated Travis Stice, Chairman and Chief
Executive Officer of Diamondback. “This combination meets all the
required criteria for a successful combination: sound industrial logic
with tangible synergies, improved combined capital allocation and
significant near and long-term financial accretion. With this
combination, Diamondback not only gets bigger, it gets better.”
Mr. Stice
continued, “Over the past forty-five years, Mr. Stephens
and his team at Endeavor have built the highest quality private oil
company in the United States.
Our companies share a similar culture and operating philosophy and are
headquartered across the street from one another, which should allow for
a seamless integration of our two teams. As a result, we look forward to
continuing to deliver best-in-class results with a combined employee
base headquartered in
Midland, assuring Midland’s relevance in the global oil
market for the next generation.”
“I am grateful to the
Endeavor team and proud of what we have built since 1979,” said
Autry C. Stephens,
Founder and Chairman of the Board of Endeavor. “We believe
Diamondback is the right partner for Endeavor, our employees, families
and communities. Together we will create value for shareholders and our
other stakeholders.”
“As we look toward
the future, we are confident joining with Diamondback is a
transformational opportunity for us,” said Lance Robertson,
President and Chief Executive Officer of Endeavor. “Our success up to
this point is attributable to the dedication and hard work of Endeavor
employees, and today’s announcement is recognition by Diamondback of the
significant efforts from our team over the past seven years, driving
production growth, improving safety performance and building a more
sustainable company. We look forward to working together to scale our
combined business, unlock value for all of our stakeholders and ensure
our new company is positioned for long-term success as we build the
premier Permian-focused company in Midland.”
Strategic and
Financial Benefits
Combined pro forma scale of
approximately 838,000 net acres and 816 MBOE/d of net production
Best in-class inventory depth
and quality with approximately 6,100 pro forma locations with break
evens at <$40 WTI
Annual synergies of $550
million representing over $3.0 billion in
NPV10 over the next decade
Capital and operating cost
synergies: approximately $325 million
Capital allocation and land
synergies: approximately $150 million
Financial and corporate cost
synergies: approximately $75 million
Substantial near and long-term
financial accretion with ~10% free cash flow per share accretion
expected in 2025
“This combination
offers significant, tangible synergies that will accrue to the pro forma
stockholder base,” stated Travis Stice. “Diamondback
has proven itself to be a premier low-cost operator in the
Permian Basin
over the last twelve years, and this combination allows us to bring this
cost structure to a larger asset and allocate capital to a stronger pro
forma inventory position. We expect both teams will learn from each
other and implement best practices to improve combined capital
efficiency for years to come.”
2024 Diamondback
Stand-alone Guidance and Base Dividend Increase
In conjunction with
this announcement, Diamondback is releasing selected operating
information for the fourth quarter of 2023 and providing initial
production and capital guidance for 2024. Diamondback today also
announced that the Company's Board of Directors will approve a 7%
increase to its base dividend to $3.60 per share annually
($0.90 per share quarterly), effective for the fourth
quarter of 2023.
Average fourth quarter 2023
production of 273.1 MBO/d (462.6 MBOE/d)
Fourth quarter 2023 cash capital
expenditures of $649 million
On a stand-alone basis in 2024
Diamondback expects to generate oil production of 270 – 275 MBO/d
(458 – 466 MBOE/d) with a total capital budget of approximately
$2.3 - $2.55 billion
Beginning in the first quarter
of 2024, Diamondback will reduce its return of capital commitment to
at least 50% of free cash flow to stockholders from at least 75% of
free cash flow previously
“Diamondback today
released fourth quarter production that exceeded expectations and
announced a 2024 capital and operating plan that prioritizes capital
efficiency and free cash flow generation over growth,” stated
Travis Stice. “The decision to reduce our return of capital to
stockholders reflects our Board’s desire to increase financial
flexibility and pay down debt added through this combination. Our
near-term objective is to reduce pro forma net debt below $10
billion very quickly, ensuring balance sheet strength and
best-in-class credit quality. Return of capital to stockholders will
always remain a core tenet of our value proposition and capital
allocation philosophy at Diamondback.”
2024 Endeavor
Stand-alone Guidance
Endeavor is providing
stand-alone 2024 capital and operating guidance while the two companies
work to close the merger.
Expected 2024 oil production of
190 – 200 MBO/d (350 – 365 MBOE/d)
Total 2024 capital budget of
approximately $2.5 - $2.6 billion
Full pro forma
guidance will be released by Diamondback after closing of the
transaction.
2025 Pro Forma
Outlook
Diamondback expects
operational synergies to be realized in 2025 by the combined company.
Therefore, the Company is providing a preliminary look at its pro forma
2025 combined company capital and operating plan assuming Diamondback’s
cost structure and current estimated well costs. The 2025 plan is
preliminary and subject to changes, including as result of changes in
oil and gas prices, the macro environment and well costs.
On a pro forma basis in 2025,
Diamondback expects to generate oil production of 470 – 480 MBO/d
(800 – 825 MBOE/d) with a capital budget of approximately
$4.1 - $4.4 billion
This operating plan implies
significant pro forma cash flow and free cash flow per share
accretion
Endeavor Energy Resources
Endeavor is a privately-held exploration
and production company. Headquartered near operational activity in
Midland, Texas,
Endeavor has more than 1,200 valued employees and is one of the largest
private operators in the United States.
With more than 45 years of experience acquiring assets, the company is
uniquely situated holding ~470,000 Net Acres across multiple basins,
inclusive of 344,000 Net Acres in the Core 6 Midland Basin counties.
Focused on the Core 6 Midland Basin counties, Endeavor has a sustainable
horizontal drilling program for years to come.
The Midland Basin consists of
Martin, Howard, Midland, Glasscock,
Upton, and Reagan counties. These Core 6 counties are the
center of focus for Endeavor’s horizontal drilling operations.