FDA delays review of Takeda's alogliptin
The FDA informed Takeda that it will miss the review deadline for alogliptin, a type 2 diabetes treatment. The NDA was supposed to be reivewed by October 7, 2008. The good news for Takeda, however, is that the delay is not due to problems with the drug's applications, but "internal resource constraints" at the agency. "[T]he FDA did not provide Takeda with any guidance on when a review might be completed nor did it raise any issues with the data in the alogliptin NDA," said Dean Sundberg, senior vice president, regulatory affairs at Takeda.
- here's Takeda's release
Related Articles:
Affymax, Takeda suspend ESA development
Takeda case could be sign of tougher FDA stance
September FDA news in review
FDA staffing push yields 1,300 hires
How the FDA will spend your fees
Comments
Post new comment
Paid Research Reports
- RNA therapy: the next big thing after monoclonal antibodies?
- Biotech M&A Strategies: Deal assessments, trends and future prospects
- The Dermatology Market Outlook to 2013: Competitive landscape, pipeline analysis and growth opportunities
- Pipeline Insight: Cancer Overview - Breast, Gynecological, Genitourinary - Diverse drugs approaching the market for many tumor t
- Sales Force Effectiveness


