Recruiting
Study to Assess Safety and Effectiveness of Branebrutinib Treatment in Participants With Active Systemic Lupus Erythematosus or Primary Sjögren's Syndrome, or Branebrutinib Treatment Followed by Open-label Abatacept Treatment in Study Participants With Active Rheumatoid Arthritis - IM014-029
Updated: 5 October, 2020 | ClinicalTrials.gov
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For more information regarding Bristol Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com. Inclusion Criteria: Sub-study for Systemic Lupus Erythematosus (SLE) - Active SLE as defined by the Systemic Lupus Erythematosus International Collaborating Clinics (SLICC) classification - Diagnosed with SLE more than 24 weeks before screening visit Sub-study for primary Sjögren's Syndrome (pSS) - Moderate to severe pSS, meeting ACR-EULAR classification criteria Sub-study for active Rheumatoid Arthritis (RA) - Moderate to severe adult-onset RA - ACR global functional status class I to III Women and men must agree to follow instructions for methods of contraception. Exclusion Criteria: Sub-study for Systemic Lupus Erythematosus - Certain other autoimmune diseases and overlap syndromes Sub-study for primary Sjögren's Syndrome - Certain other immune-mediated diseases, active fibromyalgia, or other medical conditions Sub-study for Rheumatoid Arthritis (RA) - Diagnosis with juvenile arthritis or idiopathic arthritis before age 16 For all sub-studies: - History of any significant drug allergy - Active infection, significant concurrent medical condition, or clinically significant abnormalities Other protocol defined inclusion/exclusion criteria could apply
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