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Tirzepatide

Mounjaro, Zepbound, LY3298176

Quick Stats
Studies 183
Trials 100
Recruiting PHASE3 INTERVENTIONAL NCT06937086

Mirikizumab Administered at the Same Time as Tirzepatide in Adult Participants With Moderately to Severely Active Ulcerative Colitis and Obesity or Overweight: Phase 3b Study

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The main purpose of this study is to show whether in these individuals, treatment with both mirikizumab and tirzepatide, compared with treatment with mirikizumab and placebo, leads to decrease or disappearance of UC symptoms, and loss of at least one-tenth of the overall body weight. Participation in this study will last up to 61 weeks, including 52 weeks of treatment.

Interventions

Name: Mirikizumab
Type: DRUG
Description: Administered IV
Name: Mirikizumab
Type: DRUG
Description: Administered SC
Name: Tirzepatide
Type: DRUG
Description: Administered SC
Name: Placebo
Type: DRUG
Description: Administered SC

Primary Outcomes

Measure: Percentage of Participants Who Simultaneously Achieve Clinical Remission and at Least 10% Weight Reduction
TimeFrame: Week 52
Description: Percentage of participants who simultaneously achieve clinical remission and at least 10% weight reduction.

Trial Information

NCT ID

NCT06937086

Status

Recruiting

Study Type

INTERVENTIONAL

Phases

PHASE3

Sponsor

Eli Lilly and Company

Last Updated

December 15, 2025