MSD's tulisokibart met Phase 3 UC trial endpoints
The anti-TL1A antibody achieved clinical remission at 12 weeks in patients with moderately to severely active ulcerative colitis, with no safety concerns identified.
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Research-intensive biopharmaceutical company
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In short: MSD achieved positive Phase III results for tulisokibart in ulcerative colitis and expanded its oncology pipeline through the acquisition of Terns.
The anti-TL1A antibody achieved clinical remission at 12 weeks in patients with moderately to severely active ulcerative colitis, with no safety concerns identified.
MSD remains confident in their ADC collaboration's multibillion-dollar opportunity. Daiichi Sankyo handles manufacturing for most ADCs; MSD for gocatamig.
The Science publication details a scalable enzyme-based method for producing the investigational oral PCSK9 inhibitor, offering sustainability and manufacturing efficiencies.
The deal adds TERN-701, an investigational BCR::ABL1 inhibitor for chronic myeloid leukemia, to MSD’s oncology pipeline. Transaction valued at $5.8 billion.
MSD’s investigational humanised monoclonal antibody targeting tumour necrosis factor-like cytokine 1...
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced positive topline results from the Phase 3 ATLAS-UC induction-only study...
RAHWAY, N.J.--(BUSINESS WIRE)--$MRK #MRK--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced that the U.S. Food and Drug Administration...
Belzutifan, a first-in-class drug that arose from scientific discoveries at UT Southwestern Medical Center, has been approved by the Food and Drug Administration to treat...
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