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 Pipeline Articles

Product news

March 18, 2008

Hawthorn Pharmaceuticals announced the FDA approval of the company's Granisol (granisetron HCl) oral solution. Granisol is an oral solution for the prevention of nausea and vomiting associated with cancer therapy.
 

Alkermes: Lilly to end inhaled insulin deal

Stephen McGuire March 07, 2008

Biotech firm Alkermes said today it expects Eli Lilly to soon back out of its inhaled insulin development deal between the companies.
 

Ambling toward patent cliff, flinty Pfizer boasts of pipeline

Matthew Arnold March 06, 2008

Pfizer delivered a low-key analyst day, offering no surprises as it advances toward a "cliff" of patent expirations on major products.
 

FDA delays Requip XL approval

Stephen McGuire February 06, 2008

The FDA has delayed approval of GlaxoSmithKline and SkyePharma's reformulated Requip XL (ropinirole) as a treatment for Parkinson's disease.
 

FDA approves fewest novel drugs in 24 years: reports

Stephen McGuire January 08, 2008

The FDA approved 19 novel drugs last year, the lowest number since 1983, according to published reports.
 

Takeda submits NDA for Actos replacement as DPP-IV pipeline heats up

Stephen McGuire January 07, 2008

Takeda Pharmaceutical has submitted a new DPP-IV diabetes drug candidate -- Alogliptin -- in hopes the drug will replace its major earner Actos which loses patent protection in 2011.
 

Sepracor in licensing pact for anti-epileptic compound

Stephen McGuire January 03, 2008

Sepracor has entered a licensing deal with Bial for the development and commercialization of Bial's anti-epileptic compound BIA 2-093 in the US and Canada.
 

Company news

January 03, 2008

Merck and Addex Pharmaceuticals entered a deal to develop a drug candidate for schizophrenia, under which Merck will pay Addex up to $702 million in cash plus royalties.
 

Wyeth sees generic threats, another delay on Viviant

Marc Iskowitz December 26, 2007

Competitors have stepped up efforts to market generic versions of some of Wyeth's biggest drugs, threatening to sap hundreds of millions of dollars in sales.
 

FDA seeks more info on Cervarix

Stephen McGuire December 17, 2007

GlaxoSmithKline said approval of Cervarix will be delayed in the US after FDA regulators requested more information on the vaccine in a "complete response letter" to the drugmaker.