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NCT03188510 · ClinicalTrials.gov registry record · Phase 1

A Study of Two Different Formulations of LY3074828 in Healthy Participants

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

Completed
Registry status
Phase 1
Development phase
54
Enrollment target

NCT03188510: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT03188510 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 54 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03188510, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
54 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 total duration of the clinical trial will be approximately 13 weeks, not including screening.

Primary Outcome

PK: Dose-normalized Area Under the Serum Concentration-Time Curve From Time Zero to Last Quantifiable Concentration (DN-AUC\[0-tlast\]) of LY3074828 was evaluated. Unit of measure expansion: microgram\*day per milliliter per milligram (µg\*day/mL/mg).

Interventions

  • BIOLOGICAL LY3074828

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2017-06-30
Est. Completion 2017-11-27
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT03188510 record still lists

NCT03188510 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% lower).

The record links to 0 conditions, and to 1 intervention - of which LY3074828 is the first listed.

NCT03188510 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03188510 about?

NCT03188510 is a clinical study titled "A Study of Two Different 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 NCT03188510?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2017-06-30. Estimated completion is 2017-11-27.

What interventions are being tested in trial NCT03188510?

The interventions under investigation include: LY3074828 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03188510?

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 NCT03188510's enrollment target sits among peer trials

54 931st of 2000 higher than 1,053 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 NCT03188510, the US trial registry maintained by the National Library of Medicine. NCT03188510 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.