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A Study to Evaluate Efficacy and Safety of MK-8690 in Participants With Moderately to Severely Active Ulcerative Colitis (MK-8690-002) | MicrobiomeTrials
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A Study to Evaluate Efficacy and Safety of MK-8690 in Participants With Moderately to Severely Active Ulcerative Colitis (MK-8690-002) Recruiting PHASE2 INTERVENTIONAL
Read the full scientific description See full eligibility requirements Trial Details Start: 2026-03-24Est. Completion: 2027-10-28
Enrollment target: 100 participantsLocations Clinnova Research ( Site 1042), Anaheim, California, United States Peak Gastroenterology Associates ( Site 1052), Colorado Springs, Colorado, United States South Denver Gastroenterology, PC ( Site 1068), Englewood, Colorado, United States Nature Coast Clinical Research ( Site 1045), Inverness, Florida, United States Research Associates of South Florida - Miami - Southwest 8th Street ( Site 1072), Miami, Florida, United States Gastroenterology Associates of Central Georgia ( Site 1060), Macon, Georgia, United States University of Kansas Medical Center ( Site 1077), Kansas City, Kansas, United States Tulane University School of Medicine ( Site 1073), New Orleans, Louisiana, United States BVL Research - Kansas ( Site 1054), Liberty, Missouri, United States Radboudumc ( Site 1650), Nijmegen, Gelderland, Netherlands Wonju Severance Christian Hospital ( Site 1602), Wŏnju, Kang-won-do, South Korea Korea University Ansan Hospital ( Site 1603), Ansan-si, Kyonggi-do, South Korea Kangbuk Samsung Hospital ( Site 1601), Seoul, South Korea
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