Skip to content
Trial Eligibility
Menu

A Study of LY4395089 and Mirikizumab (LY3074828) Given Together and Mirikizumab (Alone) in Adults With Crohn's Disease

NCT07483099

This study is recruiting at 10 US sites in 8 states, according to its ClinicalTrials.gov record last updated .

Summary

The main purpose of this study is to see how the safety and efficacy of a farnesoid X receptor (FXR) agonist (LY4395089), given together with mirikizumab compares with mirikizumab (alone) in adults with moderately to severely active Crohn's disease (CD). This study is part of the IIBD master protocol and will last approximately 62 weeks.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Crohn Disease

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 to 80 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Eli Lilly and Company
Last updated on ClinicalTrials.gov
October 8, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 1

  • Om Research LLC · Oxnard, CA

Colorado · 1

  • South Denver Gastroenterology · Englewood, CO

Florida · 2

  • Gastro Health Research - Miami · Miami, FL
  • Ezy Medical Research · Miami Lakes, FL

Georgia · 1

  • Atlanta Gastroenterology Associates - Peachtree Dunwoody · Atlanta, GA

Kansas · 1

  • Cotton O'Neil Digestive Health Center · Topeka, KS

Missouri · 1

  • KAD Clinical Research · St Louis, MO

Nevada · 1

  • Vector Clinical Trials · Las Vegas, NV

Texas · 2

  • One of a Kind Clinical Research Center - Kingwood · Kingwood, TX
  • Southern Star Research Institute · San Antonio, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.