Why Biodel Is Breathing Easy, Part 2 [View article]
lOOKS great TO ME As part of the normal course of the FDA’s review, Biodel has received and responded to the FDA’s 74-day letter regarding the NDA and recently submitted a 120-day safety update on patient experience with the drug, including data from the recently completed VIAject Phase 3 extension trials. The company will be presenting results from the VIAject program at the Deutsche Diabetes Gesellschaft meeting in Stuttgart, Germany, May 12-15, and will be presenting a number of abstracts on several of the company’s product candidates at the American Diabetes Association’s annual meeting in June. www.pharmacynews.eu/he...
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Why Biodel Is Breathing Easy, Part 2 [View article]
Why Biodel Is Breathing Easy, Part 2 [View article]
Why Biodel Is Breathing Easy, Part 2 [View article]
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