CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 212 enrolled
Drug / intervention
CTLA4-Ig (Abatacept) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01773707
NCT01773707Phase 2Completed

CTLA4-Ig (Abatacept)for Prevention of Abnormal Glucose Tolerance and Diabetes in Relatives At -Risk for Type 1 Diabetes

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)·interventional·Posted Jan 23, 2013·Updated Jun 6, 2024

In Brief

A Phase 2 clinical trial evaluating CTLA4-Ig (Abatacept) and Placebo for Abnormal Glucose Tolerance and Type 1 Diabetes. Completed, enrolled 212 participants across 17 sites in 2 countries.

Detailed Summary

The study is a 2-arm, multicenter, 1:1 randomized, placebo controlled clinical trial. All subjects will receive close monitoring for development of AGT or T1DM. Subjects will receive Abatacept or placebo and close monitoring for development of AGT or T1DM. To assess the safety, efficacy, and mode of action of Abatacept to prevent AGT and T1DM. The primary objective is to determine whether intervention with Abatacept will prevent or delay the development of AGT in at-risk autoantibody positive non-diabetic relatives of patients with T1DM. Secondary outcomes include: the effect of Abatacept on the incidence of T1DM; analyses of C-peptide and other measures from the OGTT; safety and tolerability; and mechanistic outcomes.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJan 23, 2013
Enrollment StartMar 1, 2013
Primary CompletionDec 14, 2021
Study CompletionDec 14, 2022
TodayJul 2, 2026
Enrollment to primary: 8.8 yearsPosted 13.4 years ago

Interventions

CTLA4-Ig (Abatacept)drug

Given as 30 minute IV infusion

Placebodrug

Saline given as 30 minute IV infusion