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Terminated Phase 2 Interventional Results available

Inducing Remission in Type 1 Diabetes With Alefacept

ClinicalTrials.gov ID: NCT00965458

Public ClinicalTrials.gov record NCT00965458. 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 2, 2026, 7:18 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

Inducing Remission in New Onset Type 1 Diabetes Mellitus With Alefacept (Amevive®)

Brief summary

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

The purpose of this trial is to test whether a drug called alefacept will slow or halt destruction of the beta cells in the pancreas. If the destruction of the beta cells is stopped, the patients might be able to produce insulin on their own longer, which could stop or slow the progression of their type 1 diabetes. This is a multi-center prospective, placebo-controlled, double-blind and randomized trial to investigate the ability of alefacept to protect residual beta cells from ongoing autoimmune destruction in adolescents and young adults with newly diagnosed Type 1 Diabetes Mellitus (T1DM).

Study identification

NCT ID
NCT00965458
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
49 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
12 Years to 35 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
Feb 28, 2011
Primary completion
Feb 28, 2013
Completion
Mar 31, 2014
Last update posted
Jul 5, 2017

2011 – 2014

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
University of Arizona Tucson Arizona 85724
Children's Hospital of Los Angeles Los Angeles California 90027
University of California - San Francisco San Francisco California 94143
Barbara Davis Center for Childhood Diabetes - University of Colorado Aurora Colorado 80045
Emory University Atlanta Georgia 30322
Indiana University Indianapolis Indiana 46202
University of Iowa Hospital & Clinics Iowa City Iowa 52242
University of Maryland Baltimore Maryland 21201
Massachusetts General Hospital Boston Massachusetts 02114
Children's Mercy Hospitals and Clinics Kansas City Missouri 64108
Creighton University Omaha Nebraska 68131
University of North Carolina Durham North Carolina 27713
The Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104
University of Texas Southwestern Medical Center Dallas Texas 75390
Benaroya Research Institute at Virginia Mason 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 NCT00965458, 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 5, 2017 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00965458 live on ClinicalTrials.gov.

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