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NCT03091673 · ClinicalTrials.gov registry record · Phase 3

Glucose Response of G-Pen (Glucagon Injection) in Pediatric T1D Patients

A Phase 3 study, sponsored by Xeris Pharmaceuticals.

Completed
Registry status
Phase 3
Development phase
31
Enrollment target

NCT03091673: Completed Phase 3 study, sponsored by Xeris Pharmaceuticals.

NCT03091673 is a Phase 3 study that has completed, run by Xeris Pharmaceuticals. The registered enrollment target is 31 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03091673, a Phase 3 study, has completed, sponsored by Xeris Pharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
31 participants
Enrollment target

Study Summary

This is a sequential efficacy and safety study in pediatric patients with type 1 diabetes. Subjects will be administered insulin to induce a low normal glycemic state and will then receive an age-appropriate dose of G-Pen (glucagon injection) in a clinical research center (CRC) or comparable setting.

Primary Outcome

The primary endpoint for this study is an evaluation of change in plasma glucose following treatment with G-Pen, with an emphasis on the increase from baseline to 30 minutes post-dosing.

Interventions

  • DRUG Glucagon

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2017-03-27
Est. Completion 2017-09-27
Phase Phase 3
Xeris Pharmaceuticals

14 total trials

What the finished NCT03091673 record still lists

NCT03091673 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (96% lower).

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

NCT03091673 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03091673 about?

NCT03091673 is a clinical study titled "Glucose Response of G-Pen (Glucagon Injection) in Pediatric T1D Patients". This is a sequential efficacy and safety study in pediatric patients with type 1 diabetes. Subjects will be administered insulin to induce a low normal glycemic state and will then receive an age-appropriate dose of G-Pen (glucagon injection) in a clinical research center (CRC) or comparable setting...

What is the current status of trial NCT03091673?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 31 participants. The study started on 2017-03-27. Estimated completion is 2017-09-27.

What interventions are being tested in trial NCT03091673?

The interventions under investigation include: Glucagon (DRUG).

Who is sponsoring clinical trial NCT03091673?

This trial is sponsored by Xeris Pharmaceuticals, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03091673's enrollment target sits among peer trials

31 1914th of 2000 higher than 84 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT03091673, the US trial registry maintained by the National Library of Medicine. NCT03091673 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.