> Schering-Plough plans to shutter a veterinary products plant in Bray, Ireland, by 2011, eliminating 240 jobs in the process. Report
> Gilead Sciences said Wednesday that its acquisition of CV Therapeutics will proceed after regulators ended a mandatory antitrust review period. Report [1]
> Seeking to remove unapproved drugs from the marketplace, the FDA ordered nine companies to stop making narcotics whose therapeutic claims haven't been proved. FDA release [2]
> Glenmark Pharmaceuticals said it will cease distributing its morphine sulfate product in the U.S., as it is among the nine companies issued warning letters by the FDA. Report [3]
> GlaxoSmithKline asked the FDA and European regulators to approve the use of its Tyverb/Tykerb cancer treatment as a first-line therapy in combination with anti-hormonal remedies for patients with advanced, hormone-senstive breast cancer. Release [4]
> Wyeth is seeking U.S. approval to sell a new version of its blockbuster infant vaccine Prevnar, which protects against more strains of a germ that causes pneumonia. Report [5]
> Financially struggling Akorn, which has faced borrowing restrictions under its revolving-credit agreement, said a company linked to Chairman John N. Kapoor bought out the lending rights in a move that is expected to bolster the company's financial condition. Report [6]
> Retired Sanofi Pasteur Chairman and CEO David J. Williams has been named to the board of directors of Xcellerex. Release [7]
> Par Pharmaceutical agreed to buy MDRNA's manufacturing facilities n Hauppauge, New York, along with its generic drug candidate calctonin-salmon nasal spray. MDRNA's release [8]
> Genzyme has scooped up key worldwide rights to the leukemia drug Campath--which is being studied as a treatment for MS--and two cancer therapies from its development partner Bayer HealthCare in a deal with a potential $2.8 billion payout. Report [9]
> Facing an FDA delay on its lead therapy [10], Dyax got out the budget-cutting axe and chopped 60 jobs as it scrambled to conserve cash. Report [11]
> The FDA has approved Novartis' Afinitor (everolimus) to treat the most common kind of kidney cancer. And analysts predict that the drug is on track to become a blockbuster, with new approvals for other cancers down the road. Report [12]
And Finally... Scientists at Penn have built a protein from scratch that can carry oxygen, a big step toward creating artificial blood. Report [13]
Links:
[1] http://finance.yahoo.com/news/Gilead-Sciences-says-apf-14811624.html
[2] http://www.fiercebiotech.com/press-releases/fda-acts-halt-marketing-certain-unapproved-prescription-narcotic-drugs
[3] http://www.nasdaq.com/aspxcontent/NewsStory.aspx?cpath=20090401\ACQDJON200904010056DOWJONESDJONLINE000008.htm&selected=9999&selecteddisplaysymbol=9999&StoryTargetFrame=_top&mkt=WORLD&chk=unchecked&lang=&link=&headlinereturnpage=http://www.international.na
[4] http://www.fiercebiotech.com/press-releases/gsk-submits-tyverb-r-tykerb-r-lapatinib-first-line-treatment-metastatic-breast-cancer
[5] http://www.philly.com/philly/business/breaking/20090331_Wyeth_seeking_approval_for_advanced_Prevnar.html
[6] http://www.chicagotribune.com/business/chi-biz-akorn-financial-april1,0,7253051.story
[7] http://www.fiercebiotech.com/press-releases/xcellerex-appoints-david-j-williams-retired-chairman-ceo-sanofi-pasteur-its-board-dir
[8] http://www.fiercebiotech.com/press-releases/mdrna-inc-sells-contract-manufacturing-operation-company-eliminates-cash-burn-related
[9] http://www.fiercebiotech.com/story/genzyme-gains-ms-drug-rights-2-8b-deal/2009-03-31
[10] http://www.fiercebiotech.com/story/dyax-shares-sink-fda-rejects-drug/2009-03-27
[11] http://www.fiercebiotech.com/story/dyax-chops-60-jobs-after-fda-delay/2009-03-31
[12] http://www.fiercebiotech.com/story/novartis-wins-fda-approval-cancer-blockbuster/2009-03-31
[13] http://www.fiercebioresearcher.com/story/penn-protein-may-open-path-artificial-blood/2009-03-31