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NCT03765502 · ClinicalTrials.gov registry record · Phase 1

A Study Comparing User Experience of Different Delivery Devices for Glucagon

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

Completed
Registry status
Phase 1
Development phase
99
Enrollment target

NCT03765502: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT03765502 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 99 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03765502, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
99 participants
Enrollment target

Study Summary

The purpose of the study is to learn more about different devices for delivering glucagon during simulations of severe hypoglycemic (low blood sugar) emergencies. The study will be carried out using medical manikins to simulate real life scenarios. No drug will be administered to humans. Part A will last approximately 17 days for Trained Users and Participants with Diabetes (PWD). Part B will last approximately nine (9) days for Untrained Users. Each part will be separated by approximately 7 days.

Primary Outcome

Percentage of trained users who found both devices and performed a successful administration of both rescue devices for both simulations.

Interventions

  • DEVICE Nasal Glucagon Device (NG)
  • DEVICE GEK
  • DRUG IM Glucagon

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2018-11-19
Est. Completion 2019-01-03
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT03765502 record still lists

NCT03765502 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 99 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% higher).

The record links to 0 conditions, and to 3 interventions - of which Nasal Glucagon Device (NG) is the first listed.

NCT03765502 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03765502 about?

NCT03765502 is a clinical study titled "A Study Comparing User Experience of Different Delivery Devices for Glucagon". The purpose of the study is to learn more about different devices for delivering glucagon during simulations of severe hypoglycemic (low blood sugar) emergencies. The study will be carried out using medical manikins to simulate real life scenarios. No drug will be administered to humans. Part A will...

What is the current status of trial NCT03765502?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 99 participants. The study started on 2018-11-19. Estimated completion is 2019-01-03.

What interventions are being tested in trial NCT03765502?

The interventions under investigation include: Nasal Glucagon Device (NG) (DEVICE), GEK (DEVICE), IM Glucagon (DRUG).

Who is sponsoring clinical trial NCT03765502?

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 NCT03765502's enrollment target sits among peer trials

99 590th of 2000 higher than 1,409 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 NCT03765502, the US trial registry maintained by the National Library of Medicine. NCT03765502 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.