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Wyeth provides mid-year update

This estimate is pro forma as it excludes any potential restructuring charges resulting from the company’s ongoing review of business processes and systems. “Our expectations for 2006 reflect

Caraco gets FDA approval for Pfizer generic

Glucotrol is indicated as an adjunct to diet for the control of hyperglycemia and the associated symptomatology in patients with non-insulin-dependent diabetes mellitus type-2 diabetes. Caraco Pharma will

Kos seeks FDA OK for Niaspan caplets

Niaspan is the only FDA-approved once-daily prescription niacin formulation for the treatment of lipid disorders with the ability to elevate HDL, or ‘good,’ cholesterol by up to 26%.

Serenex begins phase II oral mucositis trial

Oral mucositis results in inflammation and ulceration of the mouth and throat tissue lining and is the most common debilitating toxicity induced by chemotherapy and radiation therapy regimens.

Genzyme reports strong Q2 financials

Revenue rose to $793.4 million, up from $668.1 million in the second quarter a year ago. A large contributor to this was the company’s end-stage renal disease drug

GSK adjuvant system boosts Cervarix response

Additionally, Olsen, who is the company’s current chief operating officer, will continue to serve in that capacity for both divisions while the board of directors engages in a

IQ achieves key anthrax milestone

IQ announced that it has successfully completed PER.C6 clone generation for the production of its two fully human monoclonal antibodies, or mAbs, against the anthrax lethal toxin components

UK researchers working on allergy prevention drugs

Professor David Garrod of Manchester’s Faculty of Life Sciences said the research, which was recently shortlisted for the Northwest Regional Development Agency’s Bionow project of the year, takes