Merck announced that new data highlighting the long-term efficacy and safety of tulisokibart (MK-7240), an investigational humanized monoclonal antibody directed to a novel target, tumor necrosis factor-like cytokine 1A, in ulcerative colitis and Crohn’s disease will be presented at the United European Gastroenterology Week 2024 Congress in Vienna, Austria. Long-term efficacy and safety data for tulisokibart from the open-label extension period of the Phase 2 ARTEMIS-UC and APOLLO-CD studies will be featured in two oral presentations. In both studies, at week 50, maintenance of treatment efficacy was generally observed in 12-week induction responders. The observed safety profile in the study extensions was consistent with previously reported data.
Elevate Your Investing Strategy:
- Take advantage of TipRanks Premium at 55% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on MRK:
- Merck reports Phase 3 KEYFORM-007 trial did not meet primary endpoint
- Merck announces approval of new indications for KEYTRUDA in Japan
- Merck Animal Health expands Nobivac NXT vaccine platform
- Morning Movers: Apellis slips following negative CHMP opinion
- Merck announces CHMP recommendation for two Keytruda indications