Johnson & Johnson announced the submission of a supplemental Biologics License Application to the U.S. FDA seeking approval of a subcutaneous induction regimen of Tremfya for the treatment of adults with moderately to severely active UC. The filing is supported by data from the Phase 3 ASTRO study of Tremfya SC induction therapy in adults with UC and builds upon the recent U.S. approval of Tremfya in this indication.
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