A study of LY3871801 in adult patients with autoimmune disease
- Conditions
- Health Condition 1: M059- Rheumatoid arthritis with rheumatoid factor, unspecified
- Registration Number
- CTRI/2023/12/060508
- Lead Sponsor
- Eli Lilly and Company India Pvt Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Have a diagnosis of adult-onset RA for at least 3 months prior to screening as defined by the 2010 ACR/European League Against Rheumatism (EULAR) classification criteria.
2. Have moderately-to-severely active RA at screening and baseline, defined by the presence of
=6 swollen joints based on 66 joint count, and
=6 tender joints based on 68 joint count.
3. Have had a history of failure (an inadequate response, intolerance, or loss of response) to at least 1 conventional synthetic disease modifying anti rheumatic drug (csDMARD) and either 1 biologic (bDMARD), or targeted synthetic (tsDMARD) treatment.
1. Have Class IV RA according to ACR revised criteria
2. Have presence of 1 or more significant concurrent medical conditions per investigator judgment, including but not limited to poorly controlled diabetes or hypertension, chronic kidney disease stage IIIa or IIIb, IV, or V, symptomatic heart failure according to New York Heart Association class II, III, or IV, myocardial infarction, unstable angina pectoris, stroke, or transient ischemic attack within the past 12 months before randomization, severe chronic pulmonary disease, for example, requiring oxygen therapy, major chronic inflammatory disease or connective tissue disease other than RA, including but not limited to systemic lupus erythematosus, psoriatic arthritis, axial spondyloarthritis, including ankylosing spondylitis and non-radiographic axial spondyloarthritis, reactive arthritis, gout, scleroderma, polymyositis, dermatomyositis, active fibromyalgia, or multiple sclerosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Phase 2a: Change from Baseline in Disease Activity Score - high-sensitivity C-reactive protein (DAS28-hsCRP) <br/ ><br>2. Phase 2b: Percentage of Participants Achieving American College of Rheumatology (ACR)50Timepoint: 1. Baseline, Week 12 <br/ ><br>2. Baseline to Week 12
- Secondary Outcome Measures
Name Time Method