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NCT02568423 · ClinicalTrials.gov registry record · Phase 1

A Study of Mirikizumab (LY3074828) in Healthy Participants

A Phase 1 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
51
Enrollment target

NCT02568423: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT02568423 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 51 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02568423, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
51 participants
Enrollment target

Study Summary

The main purpose of this study is to explore the safety and tolerability of mirikizumab in healthy Japanese and Caucasian participants. The study will also estimate how much mirikizumab gets into the blood stream and how long it takes the body to remove it. The study is expected to last about 16 weeks for each participant.

Primary Outcome

SAE is any adverse event (AE) from this study that results in one of the following outcomes: 1. death 2. initial or prolonged inpatient hospitalization 3. a life-threatening experience (that is, immediate risk of dying) 4. persistent or significant disability/incapacity 5. congenital anomaly/birth defect 6. considered significant by the investigator for any other reason

Interventions

  • DRUG Placebo - IV
  • DRUG Placebo - SC
  • DRUG Mirikizumab - IV
  • DRUG Mirikizumab - SC

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2015-12-02
Est. Completion 2018-10-24
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT02568423 record still lists

NCT02568423 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower).

The record links to 0 conditions, and to 4 interventions - of which Placebo - IV is the first listed.

NCT02568423 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02568423 about?

NCT02568423 is a clinical study titled "A Study of Mirikizumab (LY3074828) in Healthy Participants". The main purpose of this study is to explore the safety and tolerability of mirikizumab in healthy Japanese and Caucasian participants. The study will also estimate how much mirikizumab gets into the blood stream and how long it takes the body to remove it. The study is expected to last about 16 wee...

What is the current status of trial NCT02568423?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 51 participants. The study started on 2015-12-02. Estimated completion is 2018-10-24.

What interventions are being tested in trial NCT02568423?

The interventions under investigation include: Placebo - IV (DRUG), Placebo - SC (DRUG), Mirikizumab - IV (DRUG), Mirikizumab - SC (DRUG).

Who is sponsoring clinical trial NCT02568423?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02568423's enrollment target sits among peer trials

51 969th of 2000 higher than 1,028 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02568423, the US trial registry maintained by the National Library of Medicine. NCT02568423 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.