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NCT03662100 · ClinicalTrials.gov registry record · Phase 1
A Study of Two Formulations of LY3074828 in Healthy Participants
A Phase 1 study, sponsored by Eli Lilly and Company.
- Completed
- Registry status
- Phase 1
- Development phase
- 66
- Enrollment target
NCT03662100: Completed Phase 1 study, sponsored by Eli Lilly and Company.
NCT03662100 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 66 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03662100, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 66 participants
- Enrollment target
Study Summary
The purpose of this study is to look at the amount of the study drug, LY3074828, that gets into the blood stream and how long it takes the body to get rid of LY3074828 when given as different formulations. The tolerability of LY3074828 will also be evaluated and information about any side effects experienced will be collected. Screening is required within 28 days prior to the start of the study. For each participant, the study will last about 12 weeks, not including screening.
Primary Outcome
Pharmacokinetics: Cmax of LY3074828
Interventions
- DRUG LY3074828
- BIOLOGICAL LY3074828
- DEVICE Auto-injector (AI)
- DEVICE Prefilled syringe (PFS)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2018-09-06 |
| Est. Completion | 2019-01-25 |
| Phase | Phase 1 |
What the finished NCT03662100 record still lists
NCT03662100 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% higher).
The record links to 0 conditions, and to 4 interventions - of which LY3074828 is the first listed.
NCT03662100 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03662100 about?
NCT03662100 is a clinical study titled "A Study of Two Formulations of LY3074828 in Healthy Participants". The purpose of this study is to look at the amount of the study drug, LY3074828, that gets into the blood stream and how long it takes the body to get rid of LY3074828 when given as different formulations. The tolerability of LY3074828 will also be evaluated and information about any side effects ex...
What is the current status of trial NCT03662100?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 66 participants. The study started on 2018-09-06. Estimated completion is 2019-01-25.
What interventions are being tested in trial NCT03662100?
The interventions under investigation include: LY3074828 (DRUG), LY3074828 (BIOLOGICAL), Auto-injector (AI) (DEVICE), Prefilled syringe (PFS) (DEVICE).
Who is sponsoring clinical trial NCT03662100?
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 NCT03662100's enrollment target sits among peer trials
66 786th of 2000 higher than 1,203 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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