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NCT03695198 · ClinicalTrials.gov registry record · Phase 1

A Study of LY3361237 in Healthy Participants

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

Completed
Registry status
Phase 1
Development phase
64
Enrollment target

NCT03695198: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT03695198 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 64 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03695198, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
64 participants
Enrollment target

Study Summary

The purposes of this study are to determine: * The safety of LY3361237 and any side effects that might be associated with it. * How much LY3361237 gets into the blood stream and how long it takes the body to remove it in healthy participants. Participants will be admitted to the clinical research unit (CRU) for 4 overnight stays. The study will last about 12 weeks for each participant, not including screening.

Primary Outcome

A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module

Interventions

  • DRUG Placebo - IV
  • DRUG Placebo - SC
  • DRUG LY3361237 - SC
  • DRUG LY3361237 - IV

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2018-10-26
Est. Completion 2019-08-29
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT03695198 record still lists

NCT03695198 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

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

NCT03695198 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03695198 about?

NCT03695198 is a clinical study titled "A Study of LY3361237 in Healthy Participants". The purposes of this study are to determine: * The safety of LY3361237 and any side effects that might be associated with it. * How much LY3361237 gets into the blood stream and how long it takes the body to remove it in healthy participants. Participants will be admitted to the clinical research ...

What is the current status of trial NCT03695198?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2018-10-26. Estimated completion is 2019-08-29.

What interventions are being tested in trial NCT03695198?

The interventions under investigation include: Placebo - IV (DRUG), Placebo - SC (DRUG), LY3361237 - SC (DRUG), LY3361237 - IV (DRUG).

Who is sponsoring clinical trial NCT03695198?

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 NCT03695198's enrollment target sits among peer trials

64 808th of 2000 higher than 1,181 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 NCT03695198, the US trial registry maintained by the National Library of Medicine. NCT03695198 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.