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OpenTrials
Completed

NCT Number: NCT00034255

Single Dose and 34-Day Tolerance Study of INGAP Peptide in Insulin Deficient Patients

The purpose of this study is to evaluate the safety and tolerability of single and multiple doses of intramuscular INGAP Peptide given for the first time in humans as a potential treatment for diabetes.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

VASDHS Medical Center, San Diego, California, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients meeting all of the following inclusion criteria at screening can be considered for admission to the study.

Stage 1 and Stage 2:

  • Male and female patients with, type 1 diabetes mellitus that are 18 through 70 years of age, or type 2 diabetes mellitus that are 30 through 70 years of age.
  • Patients who are insulin deficient and are diagnosed with type 1 or type 2 diabetes mellitus, and are currently well managed with insulin, with or without metformin.
  • Patients who have been on stable doses of insulin treatment for 90 days prior to study randomization.

Exclusion criteria

Patients meeting any of the following exclusion criteria at screening will not be enrolled in the study:

  • Patients with a history of any clinically significant retinopathy, symptomatic autonomic neuropathy, unstable angina, or kidney problems.
  • Patients with an uncontrolled or untreated significant pulmonary, neurological condition, or cardiovascular disease, including hypertension, congestive heart failure, angina, or peripheral vascular disease.
  • Patients who have received any investigational product within 30 days of admission into the study.
  • Patients with a history or clinical evidence of multiple organ autoimmune disorders.
  • Patients with a medical condition, serious intercurrent illness, or extenuating circumstance that would significantly decrease study compliance, including all prescribed follow-up.
  • Patients who are lactating and breastfeeding.

Treatment and study plan

INGAP Peptide

Drug

Sponsors and collaborators

Lead sponsor

GMP Endotherapeutics

Industry

Registry information

Important dates

Study start
2001
First posted
Apr 25, 2002
Registry last updated
Jun 24, 2005

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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