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Completed Phase 2 Interventional

Safety and Efficacy of INGAP-Peptide in Patients With Type 2 Diabetes

ClinicalTrials.gov ID: NCT00071422

Public ClinicalTrials.gov record NCT00071422. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 9, 2026, 1:45 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled, Rising-dose, Multicenter Study to Evaluate the Efficacy and Safety of 90 Days of 300 or 600 mg Daily Subcutaneous Injections of INGAP Peptide in Insulin-using Type 2 Diabetes Mellitus Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Insulin is a chemical that the body needs in order to use or store sugar. It is made by a type of cell called a beta cell which resides in an organ known as the pancreas. Type 2 diabetes is a disease where the beta cells are unable to meet a person's insulin needs. Sugar levels rise in the blood as a result. INGAP-Peptide is being tested to attempt to create new beta cells in the pancreas, and to improve the ability to produce insulin in type 2 diabetic patients.

Study identification

NCT ID
NCT00071422
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Exsulin Corporation
Industry
Enrollment
126 participants

Conditions and interventions

Eligibility (public fields only)

Age range
35 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2003
Primary completion
May 31, 2004
Completion
May 31, 2004
Last update posted
Jul 10, 2014

2003 – 2004

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Diabetes and Endocrine Associates La Jolla California 92037
VA Hospital UCSD San Diego California 92161
Diablo Clinical Research Walnut Creek California 94598
Not listed Denver Colorado 80209
Longmont Medical Research Network Longmont Colorado 80501
MedStar Clinical Research Center Washington D.C. District of Columbia 20003
Future Care Studies Springfield Massachusetts 01107
Mercury Street Medical Butte Montana 59701
Diabetes-Endocrinology Center of WNY Buffalo New York 14209
UNC Diabetes Care Center Durham North Carolina 27713
Piedmont Medical Group Winston-Salem North Carolina 27103
Clinical Research Institute of Southern Oregon Medford Oregon 97504
Mountain View Clinical Research Greer South Carolina 29651
Dallas Diabetes and Endocrine Center Dallas Texas 75230
University of Texas Health Science Center - Texas Diabetes Institute San Antonio Texas 78207
DGD Research Associates San Antonio Texas 78229
Charlottesville Medical Research Charlottesville Virginia 22911

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00071422, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 10, 2014 · Synced Sep 9, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00071422 live on ClinicalTrials.gov.

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