Mirikizumab
DrugAdministered IV
Other names: LY3074828
NCT Number: NCT06937086
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.
Interested in participating?
Request Info18 year–70 year
All sexes
Interventional
Phase 3
Medizinische Universität Graz, Graz, Austria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administered IV
Other names: LY3074828
Administered SC
Other names: LY3298176
Administered SC
Time frame: Week 52
Percentage of participants who simultaneously achieve clinical remission and at least 10% weight reduction.
Time frame: Week 24 and Week 52
Percentage of participants who achieve clinical remission.
Time frame: Week 24 and Week 52
Percentage of participants who achieve endoscopic response.
Time frame: Week 24 and Week 52
Percentage of participants who achieve histologic-endoscopic mucosal improvement plus absence of neutrophils
Time frame: Week 24 and Week 52
Percentage of participants who achieve clinical response.
Time frame: Week 24 and Week 52
Percentage of participants who achieve endoscopic remission.
Time frame: Week 24 and Week 52
The Urgency NRS is a patient-reported, single-item instrument that measures the severity for the urgency, sudden, or immediate need, to have a bowel movement in the past 24 hours using an 11 point NRS ranging from 0 "no urgency" to 10 "worst possible urgency"
Time frame: Week 24 and Week 52
Percentage of participants achieving histologic remission.
Contact information is provided by the study sponsor or research team.
Physicians interested in becoming principal investigators please contact
CONTACT
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
CONTACT
Eli Lilly and Company
Industry
A Phase 3b, Randomized, Multicenter, Controlled Study of Mirikizumab and Placebo or Mirikizumab Concomitantly Administered With Tirzepatide in Adult Participants With Moderately to Severely Active Ulcerative Colitis and Obesity or Overweight
Acronym: COMMIT-UC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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