Johnson & Johnson Submits Application to U.S. FDA Seeking Approval of TREMFYA® (guselkumab) for the Treatment of Moderately to Severely Active Crohn’s Disease
Submission is supported by 48-week results from the Phase 3 GALAXI and GRAVITI programs TREMFYA® is the only IL-23 inhibitor to demonstrate strong endoscopic outcomes with subcutaneous (SC) induction, consistent… Read More




