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Axcella Announces FDA IND Clearance Supporting Regulatory Path to Registration of AXA1125 for Long C

Phase 2b/3 study may proceed under U.S. Investigational New Drug applicationStudy design now accepted by U.S. and U.K. regulatory authoritiesAxcella to present at Long COVID forum co-sponsored by BIO and Solve M.E.Axcella to host a conference call February 16 at 8:00 a.m. ET; To register, click hereCAMBRIDGE, Mass.-.

Axcella Therapeutics (AXLA) Announces FDA IND Clearance Supporting Regulatory Path to Registration of AXA1125

Axcella Therapeutics (AXLA) Announces FDA IND Clearance Supporting Regulatory Path to Registration of AXA1125
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