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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 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 66 participants.

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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.

Interventions

  • DRUG LY3074828
  • BIOLOGICAL LY3074828
  • DEVICE Auto-injector (AI)
  • DEVICE Prefilled syringe (PFS)

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2018-09-06
Est. Completion 2019-01-25
Phase Phase 1

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT03662100

The ClinicalTrials.gov registry entry for NCT03662100 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which LY3074828 is the first listed.

NCT03662100 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.