- Neuropharm mulls voluntary liquidation as it waits for deal
Shares of U.K.'s Neuropharm shot up 33 percent this morning when the developer announced that its board will explore the possibility of a return of cash to shareholders. The company is still hoping to pull off a deal for its lead autism candidate NPL-2008, which it put up for sale in November of last year. "The company is continuing talks with a potentially interested party, which is in the advanced stages of due diligence, but no indicative offer has yet been received from that party," Neuropharm says in a statement.
Neuropharm's shares took a beating early last year after the biotech reported that its late-stage trial for an experimental autism therapy flunked its primary endpoint. But its stock was revived upon rumors that it was getting close to a deal for NPL-2008. In its release, the company notes it has significantly reduced its cash burn and had £6.18 million ($9.2 million) on hand as of Dec. 31, 2009.
- here's Neuropharm's release
- read this Reuters report for more
Related Articles:
Neuropharm shares spike on fresh deal buzz
Neuropharm shares tank on Phase III failure
Struggling UK biotechs call for support
- EKR names interim president, CEO
> EKR Therapeutics has announced that its executive chairman John Bailye has been appointed interim president and CEO replacing Howard Weisman, who is no longer with the company. Weisman will also no longer serve on EKR's board of directors. Release
> Human Genome Sciences has named David Southwell as CFO and EVP. Release
> Robert Shepard has been appointed CMO of Cornerstone Pharmaceuticals. Release
> Shengtai Pharmaceutical has appointed Hu Ye as its new CFO. Release
> Talaris Advisors has named Derek Lee as CFO and corporate development officer. Release
> Sandoz announced the appointment of Don DeGolyer as president of the company's U.S. operations and head of commercial operations for North America.
> Phillip Frost will serve as the new chairman of the board of Teva Pharmaceutical Industries after Eli Hurvitz indicated he wishes to be released from his duties. Moshe Many has stepped down from his role as interim chairman and has been appointed vice chairman. Release
> Protalix BioTherapeutics has reported that Eli Hurvitz is relinquishing his position as chairman and member of the board of directors. The board has unanimously appointed longstanding member Zeev Bronfeld to serve as interim chairman. Release
> Charles Lannon has been named vice-chairman of the board at Kinex Pharmaceuticals. Release
> China Yongxin Pharmaceutical has announced that Hal Lieberman, Laura Philips, Bing Li and Jingang Wang were appointed to its board of directors as independent directors. Release
> 3SBio has announced changes to its board of directors. Liping Xu, company founder, executive director and VP, will retire from the board and her position as a company officer. Peiguo Cong will join the board and serve as an independent, non-executive director.
- Novartis offers $955M deal to snare Transgene drug option
Novartis has put up $10 million and promised up to €700 million more in milestones in exchange for an option on Transgene's promising, late-stage cancer immunotherapy.
France's Transgene will hold on to control of the upcoming Phase IIb/III pivotal trial of TG4010 that is slated to get under way by the end of this year after enrolling about a thousand patients with non-small cell lung cancer. Once Novartis gets its hands on the IIb portion of the data, the pharma giant will have 90 days to decide whether it will exercise its option on the program. The data is scheduled to arrive in early 2012.
If Novartis decides to pull the trigger on the option--a deal structure that is growing increasingly common in drug development--Transgene will get a fee plus milestones along with co-promotion rights in a list of countries that includes France and China. Novartis will gain control of the program and take responsibility for further costs.
"We believe this agreement represents the best way to accelerate development and create long term value for our shareholders," says Transgene CEO Philippe Archinard. "It is also consistent with the company's goal of becoming a fully integrated biopharmaceutical company as under this agreement Transgene will maintain certain commercialization and manufacturing rights."
However, not everyone was impressed with the optional, uncertain terms of the agreement, andshares in the French biotechnology company went down 12 percent. "We view today's option announcement as slightly underwhelming, given that the ongoing burden of funding remains with Transgene for another two years," says Nomura Code analyst Gary Waanders.
Because Novartis wants to see the outcome of a mid-stage Phase IIb clinical trial before exercising its option, Waanders said he was reviewing his "neutral" rating and fair value estimate of 21.80 euros a share.
- check out the Transgene press release
- here's the Reuters story
Related Articles:
Is Transgene closing in on a major collaboration?
Transgene to partner after cancer vax passes trial
- Biotech VCs, Big Pharma stepping outside the comfort zone
BARCELONA - On Monday evening I moderated a panel on corporate venture financing at BIO-Europe Spring, joined by Roel Bulthuis, the head of Merck Serono Ventures, Anja (it's pronounced Anya) König, managing director of Novartis Venture Fund, Patrick Krol, a partner with Aescap and Malcolm Weir, the CEO at Heptares. I'd spoken with Weir before about his U.K. biotech company and knew that he and König went back. Novartis is an investor in Heptares, which we featured last year as a Fierce 15 company.
König's fund has a history of getting in early at a developer. And as she emphatically hammered home during the rather informal hour-long exchange about corporate VC goals and objectives, Novartis' venture arm is on the lookout for game-changing technologies. An incremental, short-yardage health gain isn't the objective.
Over the last year, König's longstanding interest in the cutting-edge has become an increasingly common feature in the drug development scene. As Big Pharma companies apply shock therapy to their R&D empires, it's clear that the top CEOs are focused on getting their organizations to think more like biotech organizations. If they can't become more efficient at development and shed some of the bureaucracy that has grown around their empires even as they grow bolder in their scientific objectives, then they won't be nimble enough to get out from under the avalanche of patent expirations that is tumbling their way. That process won't ever be pretty, but it is understandable.
That's a lesson, though, that more biotech execs need to take to heart as well. Safety is great. Low risk is great--if you can find it, and I'm not sure you can. But if you aren't trying to change the game of health, it's going to be very difficult to find a licensing partner when you need one. Getting backing from a venture group that thinks that way is the best kind of validation you can hope for as you're going into the clinic.
Thanks to everyone on the panel for a lively discussion. And we appreciated a big, receptive audience. Moving from the world of virtual, online news production to the world of face-to-face communication helps make simple truths come alive. - John Carroll twitter | email
More from BIO-Europe:
'Externalization' takes center stage at Bio-Europe Spring
The biotech spring arrives in Barcelona
- Abbott buys Facet Biotech for $450M
Abbott has succeeded where Biogen Idec once failed. The company announced late Tuesday that it's purchasing Facet Biotech for $450 million, or $27 a share. That's 67 percent premium over the biotech's closing price of $16.21 earlier today.
Abbott says the acquisition will boost its early- and mid-stage pharmaceutical pipeline. The developer has its eyes on two primary therapeutic areas--immunology and oncology. The highest-priority program is daclizumab, a Phase II biologic for multiple sclerosis that will move into Phase III trials in Q2 of 2010. Facet is already partnered with Biogen Idec on the compound. The biotech also has oncology compounds for multiple myeloma and chronic lymphocytic leukemia in early to mid-stage trials.
Last year Biogen attempted to purchase Facet, eventually making a "best and final offer" of $430 million after its initial $356 million bid was deemed hopelessly unrealistic based on the developer's cash position and pipeline. But with the support of two major investors, Facet was able to fend Biogen off, while at the same time noting that it would be open to more substantial bids from other companies. Biogen will owe Facet a big milestone on the launch of a late-stage study for daclizumab.
"This acquisition will further strengthen Abbott's biologics capabilities and pharmaceutical pipeline," says John Leonard, M.D., senior vice president, global pharmaceutical research and development, Abbott. "Daclizumab is a promising treatment for multiple sclerosis, a disease that has a significant unmet medical need, and has the potential to become an important treatment option for patients. We continue to explore multiple mechanisms to treat autoimmune diseases and cancer with both biologic and small molecule approaches."
Abbott has been on a buying spree as of late. It spent $10 billion on new acquisitions last year, paying $3 billion for Advanced Medical Optics and $6.6 billion for the prescription drug business of Solvay.
- here's Abbott's release
- read the BusinessWeek article for more
Related Articles:
Facet seeks new bids after Biogen offer flops
Biogen ups the ante for Facet
Biogen turns hostile in $356M bid to acquire Facet
Abbott CEO White still interested in fresh acquisitions
- AutoImmune calls it quits
After considering all of its options, Pasadena, CA-based AutoImmune has decided to liquidate its assets and to dissolve the company. The developer had been working on products to treat autoimmune and other cell-mediated inflammatory conditions. The company ran into trouble after the Phase III failure of multiple sclerosis drug dirucotide, a treatment it had been developing with BioMS. In October, AutoImmune retained Junewicz & Co. to explore its strategic options. Shuttering its operations proved to be the best course, and the company plans to distribute all available cash to stockholders.
"After evaluating the Company's strategic options, the Board of Directors reached the conclusion that it is in the best interest of stockholders to liquidate and dissolve the Company," says CEO Robert Bishop in a statement. "In connection with the Company's plans to liquidate, we have begun the orderly wind down of the Company's operations, including seeking purchasers for the Company's intellectual property and other tangible and intangible assets and providing for the Company's outstanding and potential liabilities."
- here's AutoImmune's release
Related Article:
The 2009 Biotech Graveyard
Lilly, BioMS shutter MS drug program
BioMS stocks plunge on failed trial
- Abbott Laboratories to Buy Facet Biotech for $722 Million
- Provides Promising Biologic Intended to Treat Multiple Sclerosis and Compounds that Complement Abbott's Existing Diverse Oncology Program
ABBOTT PARK, Ill. and REDWOOD CITY, Calif., March 9 /PRNewswire-FirstCall/ -- Abbott (NYSE:ABT - News) and Facet Biotech Corporation (Nasdaq:FACT - News) announced today a definitive agreement for Abbott to acquire Facet, enhancing Abbott's early- and mid...
- Novartis Corporation Takes Option on TRANSGENE Cancer Vaccine; Gets $10 Million, Milestones Could Reach $950 Million
- Reuters -- Novartis has taken an exclusive option to develop Transgene's (TRNG.PA) cancer vaccine TG4010, but the deal fell short of investors' hopes, pulling the shares in the French biotechnology company down 12 percent.
- Neuropharm Group plc to Mull Voluntary Liquidation to Return Cash
- Neuropharm Group plc (AIM: NPH), a speciality pharmaceutical company focused on neurodevelopmental disorders, today provides an update to shareholders on developments in relation to the proposed sale or merger of the Company.
Neuropharm has been in discussions with a number of parties since it entered an offer period on 3 November 2009 and announced that it was pursuing a proposed sale or...
- Affymax, Inc. Receives $5 Million Milestone Payment from Takeda Pharmaceutical Co. Ltd. on Initiation of Phase 3 Clinical Trials for Hematide in Japan
- PALO ALTO, Calif.--(BUSINESS WIRE)--Affymax, Inc. (Nasdaq: AFFY - News) today announced that it has received a $5 million development milestone payment from Takeda Pharmaceutical Company as part of the companies exclusive global agreement to develop and commercialize Hematide, Affymaxs investigational drug for the treatment of anemia in chronic renal failure patients. The milestone was achieved...
- University of California, San Diego (UCSD) Study Shows Potential for Using Algae to Produce Human Therapeutic Proteins
- UCSD -- Pharmaceutical companies could substantially reduce the expense of costly treatments for cancer and other diseases produced from mammalian or bacterial cells by growing these human therapeutic proteins in algaerapidly growing aquatic plant cells that have recently gained attention for their ability to produce biofuels.
- Watson Pharmaceuticals, Inc., Takeda Pharmaceutical Co. Ltd. Resolve Actos Patent Litigation
- MORRISTOWN, N.J., March 10 /PRNewswire-FirstCall/ -- Watson Pharmaceuticals, Inc. (NYSE:WPI - News), today announced that it has reached a settlement agreement with Takeda Pharmaceutical Company Limited and Takeda Pharmaceuticals North America resolving outstanding patent litigation related to Watson's generic equivalent version of Actos (Pioglitazone Hydrochloride) 15mg, 30mg and 45mg tablets. Under...
- Obesity And Type 2 Diabetes Market Closely Linked But Vastly Different In Outlook
- Melbourne, 10 March 2010. The independent business analyst forecasts that the antidiabetics market will be worth $37 billion by 2018 up from $20 billion in 2008. This rapid market expansion presents significant opportunities for pharmaceutical companies who are able to develop new therapies to address the unmet clinical needs in type 2 diabetes. In contrast, Datamonitor expects opportunities in the...
- OSI Pharmaceuticals, Inc. Bid Likely to Rise as Astellas Pharma Inc. Seeks Cancer Sales
- Bloomberg -- OSI Pharmaceuticals Inc.s status as one of the few U.S. biotechnology companies with income from an approved cancer drug likely will drive up the price Tokyo-based Astellas Pharma Inc. must pay to acquire it.
- EUSA Pharma Completes Establishment of Commercial Infrastructure With Appointment of President for Europe and International Region
- OXFORD, England and LANGHORNE, Pennsylvania, March 8, 2010 /PRNewswire/ -- EUSA Pharma ('EUSA'), a transatlantic specialty pharmaceutical company focused on oncology, pain control and critical care, today announced the appointment of Iain McGill to the role of President, Europe and International. The appointment marks the completion of the build of both EUSA's executive management team and the company...
- Omthera Pharmaceuticals, Inc. Closes a $6.5M Series A led by to Advance Epanova(TM), a Prescription Omega 3 Therapy
- NEW YORK--(BUSINESS WIRE)--Omthera Pharmaceuticals, Inc., an emerging specialty pharmaceutical company focusing on the clinical development of new dyslipidemia therapies, today announced commencement of operations in Bedminster, New Jersey. Omtheras lead product candidate, Epanova, an Omega 3 fatty acid containing a novel formulation of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)...
- Pharma Layoff Stats Show the Glory Days of Drugs Won't Be Coming Back
- BNET -- Pharmaceutical companies are currently cutting more jobs than any other business sector of the economy, and plan to hire the fewest workers back, according to a survey by recruitment firm Challenger, Gray & Christmas. The numbers are only a snapshot from the January-February period this year and last year, but they suggest that the glory days of Big Pharma are behind it and wont be coming...
- Dutch Government Wants To Sell Flu Vaccines Back To Novartis AG And GlaxoSmithKline
- AMSTERDAM (Reuters) - The Dutch government wants to sell 21 million unused H1N1 flu vaccine doses back to their manufacturers after they proved unnecessary and no other country wanted to buy them, the Health Ministry said on Saturday.
- Life Sciences Gets Push From Missouri Policymakers
- R&D Mag -- State and regional economies can benefit from Missouri's push into biotechnology and the life sciences, Gov. Jay Nixon said Monday.
- FDA to Increase Criminal Prosecutions of Execs
- IN VIVO -- The pharmaceutical industry spends plenty on lawyers for all sorts of things - patent challenges, product-liability litigation, employment matters. The list is long, but it may be time to add another reason - criminal defense of executives.
- The Pharmaceutical R&D Model is Broken. Here's How to Fix It
- Xconomy -- Research is the lifeblood of the biotech and pharmaceuticals business. The pharma and biotech industry spent some $65 billion dollars on R & D in 2008, according to the Pharmaceutical Research and Manufacturers Association. Thats a tremendous amount of money considering that the FDA only approved 24 new drugs (21 new molecular entities and 3 biologics) that same year. If the PhRMA numbers...
- Big Pharma Struggles To Benefit From Increased CVD Drug Usage
- New York, NY - Pharmaceutical companies will struggle to profit from the cardiovascular disease (CVD) market over the next decade despite growing drug usage, according to Datamonitor. New research* by the independent business analyst predicts that the CVD pharma market will grow from $99bn in 2008 to $107bn in 2018. Patent expiries and generic competition will have a major impact and Datamonitor expects...
- Experimental Vaccine Protects Monkeys Against Mosquito-Borne Chikungunya Virus, University of Texas Study
- ScienceDaily (Mar. 5, 2010) Imagine a mosquito-borne virus that has already infected millions of people in recent outbreaks in South and Southeast Asia, the islands of the Indian Ocean, Africa and northern Italy. Although seldom fatal, it causes highly painful arthritis-like symptoms that can linger for months or even years. It's capable of adapting to spread through a mosquito species common in...
- Merck & Co., Inc. Sues Teva Pharmaceutical Industries Limited to Block Generic Vytorin
- Bloomberg News -- Merck & Co. and its Schering unit is suing Teva Pharmaceutical Industries Ltd. to prevent it from selling a generic version of the cholesterol drug Vytorin in the United States until 2017.
- Biocitech SAS Appoints as CEO
- Paris, March 5, 2010-Biocitech SAS, the Paris life science technology park, today announced that its board has appointed Jean-Franois Boussard as CEO with effect from April 1st. Jean-Franois Boussard replaces Jacques Lhomel, who is taking retirement to pursue a number of personal projects.
Jean-Franois Boussard, 58, joins Biocitech after a long and successful biotechnology career in both...
- Adamis and La Jolla Pharmaceutical Company Kill Merger Deal
- SAN DIEGO, Mar 05, 2010 (BUSINESS WIRE) -- La Jolla Pharmaceutical Company (Pink Sheets: LJPC) today announced that La Jolla and Adamis Pharmaceuticals Corporation /quotes/comstock/11k!admp (ADMP 0.29, -0.01, -3.33%) have agreed to terminate their merger agreement relating to the proposed merger of the two companies. The termination follows La Jolla's announcement on March 3, 2010, that its common...
- How Should Georgia Boost Biotech?
- AJC -- How do we build up our biotech industry? It should be a more powerful job creator here, given all of our universities, medical operations and the CDC.
- Dow AgroSciences LLC Announces More Than $340 Million, Multi-Year Research and Development Expansion in Indianapolis; More Than 550 Jobs to Be Added
- INDIANAPOLIS--(BUSINESS WIRE)--Dow AgroSciences, a growing and thriving life sciences company, announces plans for a multi-year expansion of its global headquarters in northwest Indianapolis, with investment of more than $340 million and the addition of more than 550 scientific and commercial jobs over the next five years. Company executives were joined by Indiana Governor Mitch Daniels and Indianapolis...
- Possible Vaccine for Mesothelioma Proven Safe, Erasmus University Medical Center Study
- Newswise Researchers have demonstrated the safety of a potential vaccine against mesothelioma, a rare cancer associated primarily with asbestos exposure. The vaccine, which infuses uses a patients own dendritic cells (DC) with antigen from the patients tumor, was able to induce a T-cell response against mesothelioma tumors.
- Pfizer Inc. Reportedly to Offer $4.1 Billion for Ratiopharm
- Reuters -- Pfizer Inc (PFE.N) is set to make a near $4 billion offer for German generic drug maker Ratiopharm GmbH this week, competing with bids from Teva Pharmaceutical Industries Ltd (TEVA.TA) and Actavis, several sources familiar with the situation said.
- EKR Therapeutics, Inc. Appoints as Interim President & Chief Executive Officer
- BEDMINSTER, N.J.--(BUSINESS WIRE)--EKR Therapeutics, Inc., a specialty pharmaceutical company focused on commercializing acute-care hospital products, today announced that its Executive Chairman John Bailye has been appointed Interim President and Chief Executive Officer replacing Howard Weisman who is no longer with the Company. Mr. Weisman will also no longer serve on EKRs Board of Directors....
- Vaxart, Inc. Raises $12.5 Million Series B
- SAN FRANCISCO, March 4 /PRNewswire/ -- Vaxart, Inc., a San Francisco biotechnology company developing oral-delivery vaccines, has closed a $12.5 million Series B financing, led by Care Capital of Princeton NJ. The funding will be used to advance the Company's lead product, an oral vaccine for Avian influenza, through Phase I clinical trials."We are excited to be within a year of launching Phase...
- Merck KGaA to Move U.S. Chem. Unit to Bay State
- Xconomy.com -- The chairman of Germany-based Merck KGaA told the Boston Globe this week that the company plans to move the headquarters of its U.S. chemical business from New Jersey to Billerica, MA, following his firms deal to purchase Billerica-based life sciences firm Millipore for $7.2 billion. The Massachusetts-based division will be called EMD Millipore, Merck chairman Karl-Ludwig Kley told...
- AstraZeneca PLC Shuffles, Eliminates 550 Delaware R&D Jobs
- AP -- Pharmaceutical company AstraZeneca PLC is reorganizing its research and development and eliminating about 1,800 R&D jobs as part of a previously announced cost-cutting plan.