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.-...