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Recruiting Phase 2 Interventional

A Study to Evaluate Efficacy and Safety of MK-8690 in Participants With Moderately to Severely Active Ulcerative Colitis (MK-8690-002)

ClinicalTrials.gov ID: NCT07463183

Public ClinicalTrials.gov record NCT07463183. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:36 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2a Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of MK-8690 in Adult Participants With Moderately to Severely Active Ulcerative Colitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this protocol is to evaluate the efficacy of MK-8690 in participants with moderately to severely active ulcerative colitis. The primary hypothesis is that MK-8690 is superior to placebo with respect to the proportion of participants achieving clinical remission per Modified Mayo Score at Week 12.

Study identification

NCT ID
NCT07463183
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 23, 2026
Primary completion
Oct 27, 2027
Completion
Dec 20, 2028
Last update posted
Aug 30, 2026

2026 – 2028

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Clinnova Research ( Site 1042) Anaheim California 92805 Recruiting
Southern California Research Center ( Site 1044) Coronado California 92118 Recruiting
Peak Gastroenterology Associates ( Site 1052) Colorado Springs Colorado 80907 Recruiting
South Denver Gastroenterology, PC ( Site 1068) Englewood Colorado 80113 Recruiting
Nature Coast Clinical Research ( Site 1045) Inverness Florida 34452 Recruiting
Research Associates of South Florida - Miami - Southwest 8th Street ( Site 1072) Miami Florida 33134 Recruiting
Gastroenterology Associates of Central Georgia ( Site 1060) Macon Georgia 31201 Recruiting
University of Kansas Medical Center ( Site 1077) Kansas City Kansas 66160 Recruiting
Tulane University School of Medicine-Gastroenterology and Hepatology ( Site 1073) New Orleans Louisiana 70112 Recruiting
BVL Research - Kansas ( Site 1054) Liberty Missouri 64068 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07463183, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 30, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07463183 live on ClinicalTrials.gov.

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