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Product Articles
Medtronic enters stent fray with Endeavor
Matthew Arnold
February 01, 2008
Medtronic won approval for its Endeavor drug-eluting stent, making it the third player in a market likely to get much more competitive.
Nycomed finds a US partner for asthma drug
Marc Iskowitz
January 29, 2008
The decision by Sepracor to in-license the US marketing rights to inhaled corticosteroid Alvesco caps a four-year commercial and regulatory odyssey for the asthma drug.
Merck/Schering-Plough launch newspaper ads, take down Vytorin TV
Matthew Arnold
January 24, 2008
Merck/Schering-Plough launched patient education ads for Vytorin and Zetia in newspapers over the weekend while temporarily suspending broadcast advertising for the brands.
Account wins
January 24, 2008
Shire Pharmaceuticals tapped InVentiv's Palio to handle professional advertising and promotion for Fosrenol, which is indicated for hyperphosphatemia in patients with end stage renal disease.
Product news
January 15, 2008
Novo Nordisk discontinued its experimental AERx inhaler and took a charge of $260 million in 2007, saying the product offered little clinical benefit.
Vytorin study's a stinker
Matthew Arnold
January 14, 2008
Zetia doesn't even move the needle.
Product news
January 08, 2008
Eli Lilly said the FDA has approved Cialis (tadalafil) for once daily use in 2.5 mg and 5 mg doses to treat erectile dysfunction (ED).
Product news
January 03, 2008
Sciele Pharma said the FDA has approved all four dosage strengths of the new Sular formulation, which utilizes SkyePharma's patented Geomatrix technology and provides a lower dose of Sular for each of its current doses.
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.
Product news
December 20, 2007
Indevus Pharmaceuticals has received a non-approvable letter from FDA for Valstar related to its chemistry, manufacturing and controls NDA supplement submitted to the FDA in May 2007.
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