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NCT03083561 · ClinicalTrials.gov registry record · Phase 1
A Study of LY3337641 in Japanese and Caucasian Healthy Participants
A Phase 1 study, sponsored by Eli Lilly and Company.
- Completed
- Registry status
- Phase 1
- Development phase
- 36
- Enrollment target
NCT03083561: Completed Phase 1 study, sponsored by Eli Lilly and Company.
NCT03083561 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 36 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03083561, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 36 participants
- Enrollment target
Study Summary
The main purpose of this study is to evaluate the safety and tolerability of LY3337641 in healthy Japanese and Caucasian participants. The study will also investigate how the body processes LY3337641 and the effect of LY3337641 on the body. The study will last up to 4 weeks for each participant. Screening may occur within 28 days prior to first dose of study drug.
Primary Outcome
Clinically significant events were defined as serious adverse events (SAE). A summary of other nonserious AEs, and all SAE's, regardless of causality, is located in the Reported Adverse Events section.
Interventions
- DRUG Placebo
- DRUG LY3337641
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2017-03-15 |
| Est. Completion | 2017-05-25 |
| Phase | Phase 1 |
What the finished NCT03083561 record still lists
NCT03083561 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT03083561 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03083561 about?
NCT03083561 is a clinical study titled "A Study of LY3337641 in Japanese and Caucasian Healthy Participants". The main purpose of this study is to evaluate the safety and tolerability of LY3337641 in healthy Japanese and Caucasian participants. The study will also investigate how the body processes LY3337641 and the effect of LY3337641 on the body. The study will last up to 4 weeks for each participant. Scr...
What is the current status of trial NCT03083561?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2017-03-15. Estimated completion is 2017-05-25.
What interventions are being tested in trial NCT03083561?
The interventions under investigation include: Placebo (DRUG), LY3337641 (DRUG).
Who is sponsoring clinical trial NCT03083561?
This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03083561's enrollment target sits among peer trials
36 1210th of 2000 higher than 743 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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