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

Primary Purpose

Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
INGAP Peptide
Sponsored by
GMP Endotherapeutics
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • VASDHS Medical Center
  • MedStar Research Institute - Clinical Research Center
  • UNC Diabetes, Endocrinology, Metabolism Clinic
  • Texas Diabetes Institute

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
April 24, 2002
Last Updated
June 23, 2005
Sponsor
GMP Endotherapeutics
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1. Study Identification

Unique Protocol Identification Number
NCT00034255
Brief Title
Single Dose and 34-Day Tolerance Study of INGAP Peptide in Insulin Deficient Patients
Official Title
Single Dose and 34-Day Tolerance Study of INGAP Peptide in Insulin Deficient Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2003
Overall Recruitment Status
Completed
Study Start Date
December 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
GMP Endotherapeutics

4. Oversight

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
Double
Allocation
Randomized
Enrollment
62 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
INGAP Peptide

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Facility Information:
Facility Name
VASDHS Medical Center
City
San Diego
State/Province
California
ZIP/Postal Code
92161
Country
United States
Facility Name
MedStar Research Institute - Clinical Research Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20003
Country
United States
Facility Name
UNC Diabetes, Endocrinology, Metabolism Clinic
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27713
Country
United States
Facility Name
Texas Diabetes Institute
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78284
Country
United States

12. IPD Sharing Statement

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

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