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Terminated Phase 3 Interventional

A Phase III Study to Investigate the Impact of Diamyd in Patients Newly Diagnosed With Type 1 Diabetes (USA)- DIAPREVENT

ClinicalTrials.gov ID: NCT00751842

Public ClinicalTrials.gov record NCT00751842. 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 Oct 21, 2026, 2:55 PM 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 Phase III, 3-Arm, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Investigate the Impact of Diamyd on the Progression of Diabetes in Patients Newly Diagnosed With Type 1 Diabetes Mellitus (USA)

Brief summary

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

The intended purpose of this study was to determine whether Diamyd (rhGAD65 formulated in alum) is effective in preserving the body's own insulin producing capacity in patients recently diagnosed with type 1 diabetes. Based on results from other clinical trials with the study drug it was judged unlikely this study would meet the intended primary or secondary efficacy endpoints. Therefore the primary focus of this study was changed to ensure that safety data was available for at least 6 months following the last dose of active study drug. Thereafter the study was terminated.

Study identification

NCT ID
NCT00751842
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Diamyd Therapeutics AB
Industry
Enrollment
331 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
10 Years to 20 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 2008 (Type not available)
Primary completion
Mar 2012 (Actual)
Completion
Jul 2012 (Actual)
Last update posted
Oct 10, 2012

2008 – 2012

United States locations

U.S. sites
43
U.S. states
28
U.S. cities
43
Facility City State ZIP Site status
University of Arizona Tucson Arizona 85724 —
Arkansas Children's Hospital Research Institute Little Rock Arkansas 72202 —
Alex Endocrine Associates Rogers Arkansas 72758 —
Children's Hospital Orange County Orange California 92868 —
Rady Children's Hospital San Diego California 92123 —
Stanford University Medical Center Stanford California 94305 —
Barbara Davis Center for Childhood Diabetes Aurora Colorado 80045 —
Christina Care Research institute Newark Delaware 19713 —
University of Florida Gainsville Florida 32610 —
Nemours Children's Clinic Jacksonville Florida 32207 —
Miami Children's Hospital Research Institute Miami Florida 33155 —
University of South Florida Tampa Florida 33606 —
Atlanta Diabetes Associates Atlanta Georgia 30309 —
Rocky Mountain Diabetes and Osteoporosis Center Idaho Falls Idaho 83404 —
University of Iowa Hospitals and Clinicals Iowa City Iowa 52242 —
Mid America Diabetes Associates Wichita Kansas 67211 —
University of Kentucky College of Medicine Lexington Kentucky 40536 —
University of Louisville Research Foundation Louisville Kentucky 40202 —
Children's Hospital New Orleans Louisiana 70118 —
University of Maryland Medical Center Baltimore Maryland 21201 —
Tufts Medical Center Boston Massachusetts 02111 —
UMass Memorial Medical Center Worcester Massachusetts 01655 —
University of Michigan Health System Ann Arbor Michigan 48109 —
Alzohaili Medical Consultants Dearborn Michigan 48126 —
The Children's Mercy Hospital Kansas City Missouri 64108 —
St. Louis Children's Hospital St Louis Missouri 63110 —
Creighton Diabetes Center Omaha Nebraska 68131 —
Kathryn Eckert Reno Nevada 89502 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Morristown Memorial Hospital Morristown New Jersey 07962 —
Winthrop University Hospital Mineola New York 11501 —
Naomi Berrie Diabetes Center of Columbia University New York New York 10032 —
University of Rochester Rochester New York 14642 —
SUNY Institute for Human Performance Syracuse New York 13210 —
Children's Hospital Medical Center of Akron Akron Ohio 44308 —
University of Oklahoma, Schustermann Center Clinic Tulsa Oklahoma 74135 —
Children's Hospital of Pittsburgh of UPMC Pittsburgh Pennsylvania 15224 —
Regional Medical Clinic - Endocrinology Rapid City South Dakota 57701 —
LeBonheur Children's Medical Center Memphis Tennessee 38103 —
Cook Children's Medical Center Fort Worth Texas 76104 —
CHRISTUS Santa Rosa Children's Hospital San Antonio Texas 78207 —
Virginia Commonwealth University Richmond Virginia 23219 —
Benaroya Research Institute Seattle Washington 98101 —

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 NCT00751842, 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 Oct 10, 2012 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00751842 live on ClinicalTrials.gov.

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