A Trial to Evaluate the Immunogenicity of Dasiglucagon and GlucaGen in Patients With Type 1 Diabetes Mellitus

NCT ID: NCT03216226

Last Updated: 2021-05-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 112 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-06-28
• Study Completion Date: 2018-02-13

Brief Summary

The trial's objective is to evaluate the immunogenicity of repeated single doses of dasiglucagon* and GlucaGen following subcutaneous (SC) administration in patients with type 1 diabetes mellitus (T1DM) and further to evaluate the safety and tolerability of dasiglucagon and GlucaGen.

*dasiglucagon is the proposed International Nonproprietary Name (pINN) for ZP4207

Detailed Description

Patients with T1DM were randomly assigned in a 1:1 ratio to receive 3 SC injections of either dasiglucagon (0.6 mg) or GlucaGen (1 mg), with 1 week between doses. Patients were followed for 15 weeks from the day of the first dose to assess the immune response. Patients with previous exogenic glucagon exposure were not excluded from the trial, but the information on previous glucagon administration was recorded to enable subgroup analyses. It was expected that 112 patients in total would be randomly assigned to treatment groups and treated. A total of 90 patients were expected to complete the trial (45 in each treatment arm). To qualify as completed, the patient had to be dosed according to the procedure described in the protocol and to have blood drawn for the antidrug antibody analyses as scheduled.

Conditions

Hypoglycemia; Diabetes Mellitus, Type 1

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

dasiglucagon (ZP4207)

Repeated single fixed doses (s.c.injection) of dasiglucagon

Group Type: EXPERIMENTAL

dasiglucagon

Intervention Type: DRUG

Glucagon Analog

GlucaGen

Repeated single fixed doses (s.c.injection) of GlucaGen

Group Type: EXPERIMENTAL

GlucaGen

Intervention Type: DRUG

Native Glucagon

Interventions

dasiglucagon

Glucagon Analog

Intervention Type: DRUG

GlucaGen

Native Glucagon

Intervention Type: DRUG

Other Intervention Names

ZP4207; GlucaGen HypoKit

Eligibility Criteria

Inclusion Criteria

• Informed consent obtained before any trial-related activities (trial-related activities are any procedure that would not have been performed during normal management of the patient)
• Availability for the entire trial period
• Age between 18 and 70 years, both inclusive
• Male or female patients with T1DM for at least 1 year. Diagnostic criteria as defined by the American Diabetes Association
• Hemoglobin A1c (HbA1c) <10%
• Stable anti-diabetic treatment for at least 1 month (e.g. within 10% insulin dose adjustment)

Exclusion Criteria

• Previous administration of dasiglucagon (previously referred to as ZP4207)
• Known or suspected allergy to trial medication(s) or related products
• History of anaphylaxis or symptoms of severe systemic allergy (such as angioedema)
• Previous participation (randomization) in this trial
• Females who are pregnant according to a positive pregnancy test, actively attempting to get pregnant, or are lactating
• Patients on a closed loop artificial pancreas
• Receipt of any investigational drug within 3 months prior to screening
• Active malignancy within the last 5 years
• Congestive heart failure, New York Heart Association class II-IV
• Inadequately treated blood pressure as defined as systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥90 mmHg at screening
• Current bleeding disorder, including use of anticoagulant treatment
• Known presence or history of pheochromocytoma (i.e. adrenal gland tumor) or insulinoma (i.e. insulin-secreting pancreas tumor)
• Known or suspected HIV infection
• Use of a systemic beta-blocker drug, indomethacin, warfarin or anticholinergic drugs in the previous 28 days before Day 1 of this trial
• Use of systemic corticosteroids, anti-inflammatory biological agents, kinase inhibitors or other immune modulating agents within the last 3 months prior to screening
• Donation of blood or plasma in the past month, or in excess of 500 mL within 12 weeks prior to screening
• A positive result in the alcohol and/or urine drug screen at the screening visit. Significant history of alcoholism or drug abuse as judged by the investigator or consuming more than 24 g alcohol per day for men, or more than 12 g alcohol per day for women.
• Surgery or trauma with significant blood loss within the last 2 months prior to screening
• Use of prescription or non-prescription medications known to cause QT prolongation

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

SynteractHCR

INDUSTRY

Sponsor Role: collaborator

Zealand Pharma

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Christina Sylvest, MSc Pharm

Role: STUDY_DIRECTOR

Zealand Pharma A/S

Locations

Compass Research

Orlando, Florida, United States

Advanced Clinical Research

Meridian, Idaho, United States

CRC - Clinical Research Center, Medizinische Universität Graz

Graz, , Austria

LMC Manna Research

Barrie, , Canada

LMC Calgary

Calgary, , Canada

LMC Diabetes & Manna Research

Toronto, , Canada

Diabeteszentrum Hamburg West, Gemeinschaftspraxis für Innere Medizin

Hamburg, , Germany

Countries

United States; Austria; Canada; Germany

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

ZP4207-16136

Identifier Type: -

Identifier Source: org_study_id