Omilancor shows efficacy and tolerability as a potential once-daily, oral, gut-restricted therapy for mild-to-moderate UC patients
Following the recent positive End-of-Phase 2 meeting with the FDA, Landos initiated clinical trial site feasibility studies for the planned global pivotal Phase 3 trial of omilancor in UC
https://finance.yahoo.com/news/landos-biopharma-phase-2-data-110000903.html
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.