Efficacy and safety of SAR441344 in the treatment of Systemic Lupus Erythematosus

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 138

Inclusion Criteria

Diagnosis of SLE for at least 6 months prior to screening by fulfilling the Revised Criteria for Classification of SLE according to the 1997 Update of the 1982 ACR criteria, Positive ANA (titer =1:80) during screening, Positivity for at least one serological characteristic, Total hSELENA-SLEDAI score =6 (including points attributed from arthritis and rash) during screening and at least 4 points from clinical features at randomization as confirmed by a Sponsor-selected independent reviewer(s), At least 1 BILAG A score or 2 BILAG B scores during screening as confirmed by a Sponsor-selected independent reviewer(s), Receiving at least one of the SOC for SLE (combination is possible), Body weight within 45 kg to 120 kg (inclusive) at screening, Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.

Exclusion Criteria

Primary diagnosis of a rheumatic disease besides SLE or an inflammatory joint or skin disease other than SLE that could confound the disease activity assessments, High dose of steroids, or a change in dose within 4 weeks prior to randomization, High dose of antimalarial, or a change in dose within 12 weeks prior to randomization, High dose of immunosuppressants or a change in dose within 12 weeks prior to randomization, Use of cyclophosphamide within 3 months prior to screening, Previous parenteral (IV), intramuscular (IM), or intra-articular steroid administration within 4 weeks prior to randomization, Participants likely to require multiple courses of OCS during the study for chronic diseases other than SLE, Administration of any live (attenuated) vaccine within 3 months prior to randomization (eg, varicella zoster vaccine, oral polio, rabies), Administration of any non-live vaccine (eg, seasonal influenza, COVID-19) within 4 weeks prior to randomization, Active and severe lupus nephritis, Active severe or unstable neuropsychiatric SLE including but not limited to seizures, psychosis, acute confusional state, transverse myelitis, central nervous system vasculitis and optic neuritis, Known or suspected drug-induced lupus, History, clinical evidence, suspicion or significant risk, for thromboembolic events, as well as myocardial infarction, stroke, and/or antiphospholipid syndrome and any participants requiring antithrombotic treatment, History or current hypogammaglobulinemia, Serious systemic viral, bacterial or fungal infection, Participants with a history of invasive opportunistic infections, such as, but not limited to histoplasmosis, listeriosis, coccidioidomycosis, candidiasis, pneumocystis jirovecii, and aspergillosis, regardless of resolution, Evidence of active or untreated latent tuberculosis as documented by medical history (eg, chest X-rays) and examination, and tuberculosis testing

Study & Design

Study Type: Interventional clinical trial of medicinal product

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method

Secondary Outcome Measures

Name	Time	Method

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