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A Phase 3, Randomized, Double-Blind, Placebo-Controlled Program to Evaluate the Efficacy and Safety of MK-7240 in Participants with Moderately to Severely Active Ulcerative Colitis

To evaluate the efficacy of MK-7240 compared to Placebo as assessed by the proportion of participants achieving clinical remission per Modified Mayo Score at Week 12


Why this Research Matters

A phase three study to evaluate the safety and tolerability of MK-7240 for patients who have moderate to severely active ulcerative colitis (UC).


Who can Participate

Adult

UC as defined by Modified May Score of 5-9, Endoscopic sub-score greater than or equal to 2 Has inadequate response or LOR to 1 more prior UC therapy.


Study ID

Protocol Number: 23-2563

Meet the Team

Image of Principal Investigator

Mark Gerich, MD

Principal Investigator


Locations