For Healthcare Professionals

A Study to Evaluate the Long-Term Efficacy and Safety of Mirikizumab in Participants With Moderately to Severely Active Ulcerative Colitis (LUCENT 3)

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About the study

This study is designed to evaluate the long-term efficacy and safety of mirikizumab in participants with moderately to severely active ulcerative colitis (UC).
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria

  1. Participants from Study AMAC (NCT02589665) or AMBG (NCT03524092) who have had at least one study drug administration and have not had early termination of study drug.
  2. Female participants must agree to contraception requirements.

EXCLUSION CRITERIA

Exclusion Criteria

  1. Participants must not have developed a new condition, including cancer in the originator study.
  2. Participants must not have any important infections including, but not limited to, hepatitis B, hepatitis C, HIV/AIDS, and active tuberculosis (TB) during either originator study
  3. Participants may not have received surgery for UC in the originator study or are likely to require surgery for treatment of UC during the study.
  4. Participants must not have developed adenomatous polyps during the originator study that have not been removed prior to the start of this study.
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 1-317-615-4559Email iconEmail Study Center

Study’s details


Contition

Ulcerative Colitis

Age (in years)

18 - 80

Phase

Phase 3

Participants needed

960

Est. Completion Date

Apr 25, 2029

Treatment type

Interventional


Sponsor

Eli Lilly and Company

ClinicalTrials.gov identifier

NCT03519945

Study number

I6T-MC-AMAP

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