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Avance Clinical has guided 710 emerging biotechs through critical clinical trial inflection points, accelerating timelines by up to nine months. The company's comprehensive approach to Phase I clinical development has helped clients secure follow-on funding, progress to Phase II trials, and initiate pivotal studies. Avance Clinical addresses common hurdles that stall early-stage biotechs by assessing early data, preparing regulatory submissions, and providing strategic planning to anticipate potential bottlenecks.
The U.S. Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) goal date for Axogen Inc.’s (NASDAQ:AXGN) Biologics License Application (BLA) for Avance Nerve Graft by three months, pushing the deadline to December 5, 2025. This decision follows a communication from the FDA indicating that the information submitted by Axogen in response to an FDA information request was deemed a Major Amendment to its BLA. This additional time allows the FDA to thoroughly review the submission, which includes substantial new manufacturing and facility data [1].
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