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NCT03770637 · ClinicalTrials.gov registry record · Phase 2

Glucagon Ready to Use (RTU) in Subjects With Hyperinsulinemic Hypoglycemia After Bariatric Surgery

A Phase 2 study of Hyperinsulinemic Hypoglycemia, sponsored by Xeris Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
14
Enrollment target
5
Study locations

NCT03770637: Completed Phase 2 study of Hyperinsulinemic Hypoglycemia, sponsored by Xeris Pharmaceuticals.

NCT03770637 is a Phase 2 study of Hyperinsulinemic Hypoglycemia that has completed, run by Xeris Pharmaceuticals. The registered enrollment target is 14 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower). The trial reports 5 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03770637, a Phase 2 study of Hyperinsulinemic Hypoglycemia, has completed, sponsored by Xeris Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
14 participants
Enrollment target
5
Study locations

Study Summary

This is a double-blind, placebo-controlled Phase 2 study to assess the efficacy, safety and tolerability of Glucagon RTU when administered to subjects with a history of bariatric surgery during episodes of post-postprandial hypoglycemia. Twelve eligible subjects will be randomly assigned to receive Glucagon RTU or placebo at the first of two clinical research center (CRC) visits, followed by the other treatment at the second CRC visit. Subjects will be randomly assigned to either Glucagon RTU or Placebo for the duration of a 12-week Outpatient Stage. A follow-up safety assessment visit will occur 14 to 28 days after a subject's last dose of study drug.

Primary Outcome

Number of subjects with blood glucose \> 70 mg/dL

Interventions

  • OTHER Placebo
  • DRUG Glucagon RTU

Study Locations (5)

Colorado

  • University of Colorado-Denver - Aurora

Maryland

  • Johns Hopkins Hospital - Baltimore

Massachusetts

  • Joslin Diabetes Center - Boston

Minnesota

  • Mayo Clinic- Rochester - Rochester

North Carolina

  • Duke Early Phase Clinical Research - Durham

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2019-05-10
Est. Completion 2020-02-26
Phase Phase 2
Xeris Pharmaceuticals

14 total trials

What the finished NCT03770637 record still lists

NCT03770637 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower).

The record links to 1 condition, with Hyperinsulinemic Hypoglycemia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT03770637 lists 5 locations in 5 states (Colorado, Maryland, Massachusetts).

Frequently Asked Questions

What is clinical trial NCT03770637 about?

NCT03770637 is a clinical study titled "Glucagon Ready to Use (RTU) in Subjects With Hyperinsulinemic Hypoglycemia After Bariatric Surgery". This is a double-blind, placebo-controlled Phase 2 study to assess the efficacy, safety and tolerability of Glucagon RTU when administered to subjects with a history of bariatric surgery during episodes of post-postprandial hypoglycemia. Twelve eligible subjects will be randomly assigned to receive ...

What is the current status of trial NCT03770637?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 14 participants. The study started on 2019-05-10. Estimated completion is 2020-02-26.

What conditions does trial NCT03770637 study?

This clinical trial studies the following conditions: Hyperinsulinemic Hypoglycemia.

What interventions are being tested in trial NCT03770637?

The interventions under investigation include: Placebo (OTHER), Glucagon RTU (DRUG).

Who is sponsoring clinical trial NCT03770637?

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

Where is trial NCT03770637 being conducted?

This trial has 5 study locations across Colorado, Maryland, Massachusetts, Minnesota, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT03770637's enrollment target sits among peer trials

14 1941st of 2000 higher than 54 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03770637, the US trial registry maintained by the National Library of Medicine. NCT03770637 (small enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.