CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 23 enrolled
Drug / intervention
Abataceptdrug
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/NCT01835470
NCT01835470Phase 3Completed

A Phase III, Multicenter, Open-Label Study to Assess Efficacy, Safety, Pharmacokinetics and Immunogenicity of Abatacept Administered Intravenously in Japanese Children and Adolescents With Active Juvenile Idiopathic Arthritis Who Have a History of an Inadequate Response or Intolerance to Methotrexate or Biologics

Bristol-Myers Squibb·interventional·Posted Apr 19, 2013·Updated Feb 26, 2021

In Brief

A Phase 3 clinical trial evaluating Abatacept for Juvenile Idiopathic Arthritis. Completed, enrolled 23 participants across 13 sites.

Detailed Summary

The purpose of this study is to assess the efficacy of Abatacept after intravenous administration in Japanese children and adolescents with active juvenile idiopathic arthritis who have a history of an inadequate response or intolerance to Methotrexate or biologics

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesJapan

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedApr 19, 2013
Enrollment StartAug 9, 2013
Primary CompletionNov 24, 2015
Study CompletionJul 30, 2018
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 13.2 years ago

Interventions

Abataceptdrug