Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01972152 · ClinicalTrials.gov registry record · Phase 2

Safety, Tolerability, Pharmacokinetic (PK) and Pharmacodynamic (PD) Study of G-Pen(TM) (Glucagon Injection) to Treat Severe Hypoglycemia

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

Completed
Registry status
Phase 2
Development phase
30
Enrollment target
1
Study location

NCT01972152 is a Phase 2 study of Hypoglycemia that has completed, run by Xeris Pharmaceuticals. The registered enrollment target is 30 participants, below the 506-participant average among 40 other Hypoglycemia trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01972152, a Phase 2 study of Hypoglycemia, has completed, sponsored by Xeris Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to demonstrate that G-Pen(TM) glucagon is comparable to Lilly Glucagon(TM) in terms of safety and efficacy, as a treatment for severe hypoglycemia, a complication of diabetes.

Conditions Studied

Interventions

  • DRUG G-Pen(TM) 1 mg
  • DRUG Lilly Glucagon(TM) 1 mg
  • DRUG G-Pen(TM) 0.5 mg

Study Locations (1)

Texas

  • Texas Diabetes Institute, University Health System - San Antonio

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2013-10
Est. Completion 2014-02
Phase Phase 2

Sponsor

Xeris Pharmaceuticals

14 total trials

What the Registry Record Tells You About NCT01972152

The ClinicalTrials.gov registry entry for NCT01972152 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 506-participant average among 40 other Hypoglycemia trials with a reported enrollment target (94% lower). The listed sponsor is Xeris Pharmaceuticals, which has 14 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hypoglycemia appearing as the primary indexed condition, and to 3 interventions - of which G-Pen(TM) 1 mg is the first listed.

NCT01972152 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT01972152 about?

NCT01972152 is a clinical study titled "Safety, Tolerability, Pharmacokinetic (PK) and Pharmacodynamic (PD) Study of G-Pen(TM) (Glucagon Injection) to Treat Severe Hypoglycemia". The purpose of this study is to demonstrate that G-Pen(TM) glucagon is comparable to Lilly Glucagon(TM) in terms of safety and efficacy, as a treatment for severe hypoglycemia, a complication of diabetes.

What is the current status of trial NCT01972152?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2013-10. Estimated completion is 2014-02.

What conditions does trial NCT01972152 study?

This clinical trial studies the following conditions: Hypoglycemia.

What interventions are being tested in trial NCT01972152?

The interventions under investigation include: G-Pen(TM) 1 mg (DRUG), Lilly Glucagon(TM) 1 mg (DRUG), G-Pen(TM) 0.5 mg (DRUG).

Who is sponsoring clinical trial NCT01972152?

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

Where is trial NCT01972152 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Hypoglycemia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

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.