CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 119 enrolled
Drug / intervention
branebrutinib +2 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/NCT04186871
NCT04186871Phase 2Completed

A Randomized, Placebo-Controlled, Double-Blind, Multicenter Study to Assess the Efficacy and Safety of Branebrutinib Treatment in Subjects With Active Systemic Lupus Erythematosus or Primary Sjögren's Syndrome, or Branebrutinib Treatment Followed by Open-label Abatacept Treatment in Subjects With Active Rheumatoid Arthritis

Bristol-Myers Squibb·interventional·Posted Dec 5, 2019·Updated Jan 16, 2024

In Brief

A Phase 2 clinical trial evaluating branebrutinib, abatacept, and 1 other intervention for Autoimmune Disorder and 3 related conditions. Completed, enrolled 119 participants across 81 sites in 10 countries.

Detailed Summary

The purpose of this study is to evaluate the safety and effectiveness of treatment with branebrutinib treatment in participants with active systemic Lupus Erythematosus (SLE) or Primary Sjögren's Syndrome (pSS), or branebrutinib treatment followed by open-label abatacept treatment in study participants with active Rheumatoid Arthritis (RA).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Belgium, France, Germany, Mexico, Netherlands, Poland, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedDec 5, 2019
Enrollment StartJan 7, 2020
Primary CompletionDec 5, 2022
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 6.6 years ago

Interventions

branebrutinibdrug

Specified dose on specified days

abataceptdrug

Specified dose on specified days

branebrutinib placebodrug

Specified dose on specified days