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Find Clinical Drug Pipeline Developments & Deals for ME-401
Updated Phase 1b data on ME-401 for the treatment of follicular lymphoma and other B-cell malignancies, will be presented in a poster session at the Virtual Edition of the 25th European Hematology Association (EHA) Annual Congress.
MEI and Kyowa Kirin will co-develop and co-promote ME-401 in the U.S., with MEI booking all revenue from U.S. sales. Kyowa Kirin has exclusive commercialization rights outside of the U.S.
MEI is conducting TIDAL, a Phase 2 trial evaluating ME-401 in patients with relapsed or refractory follicular lymphoma. TIDAL is intended to boost an accelerated marketing application approval by FDA.