Safety, Pharmacokinetics, and Efficacy of Subcutaneous Isatuximab in Adults With Warm Autoimmune Hemolytic Anemia (wAIHA)

Recruitment & Eligibility

Status: Terminated

Sex: All

Target Recruitment: Not specified

Inclusion Criteria

Inclusion criteria : - Participant must be =18 to years of age, inclusive, at the time of signing the informed consent. - Males and females with a confirmed diagnosis of primary w AIHA or systemic lupus erythematosus (SLE)-associated w AIHA (without other SLE-related manifestations apart from cutaneous and musculoskeletal manifestations) who meet the following criteria: 1. Hemoglobin level <10 g/dL at screening. 2. Hemolysis (haptoglobin =40 mg/dL and total or indirect/unconjugated bilirubin above the upper limit of normal). 3. Positive direct antiglobulin test (DAT) (IgG or IgG + complement C3d pattern or IgM warm autoantibodies (positive dual DAT)). - Participants who have previously failed to maintain a sustained response after treatment with corticosteroids (corticosteroid-refractory or corticosteroid-dependent primary wAIHA). - Part A only: Participants who have previously failed to maintain a sustained response after treatment with rituximab (or other anti-CD20 monoclonal antibodies). The last dose of the anti-CD20 antibody must have been administered at least 12 weeks before enrollment. - Part B: Participants who have had an insufficient response to at least 1 prior therapy in addition to corticosteroids (splenectomy is regarded as a prior therapy). - Contraceptive use by men and women Exclusion criteria: - Clinically significant medical history or ongoing chronic illness that would jeopardize the safety of the participant or compromise the quality of the data derived from his or her participation in the study as determined by the Investigator. - Serious infection that required hospitalization within 3 months prior to enrollment. - Secondary wAIHA from any cause including drugs, lymphoproliferative disorders, infectious or autoimmune disease (SLE without other SLE-related manifestations apart from cutaneous and musculoskeletal manifestations is allowed), or active hematologic malignancies. Participants with positive antinuclear antibodies but without a definitive diagnosis of an autoimmune disease are allowed. - History of coagulation or bleeding disorders (Evans Syndrome is allowed). - Uncontrolled or active HBV or HCV infection - HIV infection. - Serum gammaglobulin levels <3 g/L. - Females who are pregnant, lactating, or considered unreliable with respect to contraceptive practice. - Concurrent treatment with corticosteroids, unless the participant has been on a stable daily dose for = 15 days prior to enrollment. - Treatment with cyclophosphamide within 4 weeks prior to enrollment. - Treatment with cytotoxic drugs (other than cyclophosphamide) within 12 weeks prior to enrollment. - Treatment with non-cytotoxic, immunomodulatory drugs (including but not limited to Cyclosporine, Sirolimus, Tacrolimus, Idelalisib, Ibrutinib), excluding biologic agents, within 4 weeks prior to enrollment. - Treatment with any biologic agent within 12 weeks prior to enrollment. The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Exclusion Criteria

Not provided

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Part A: Number of Participants With Treatment Emergent Adverse Events (TEAEs) And Treatment Emergent Serious Adverse Events (TESAEs);Part A: Number of Participants With Potentially Clinically Significant Abnormality (PCSA): Hematology;Part A: Number of Participants With PCSA: Clinical Chemistry And Electrolyte Parameters;Part A: Number of Participants With Potentially Clinically Significant Abnormality: Urinalysis;Part A: Number of Participants With Potentially Clinically Significant Abnormality: Vital Signs;Part B: Overall Response Rate (Response [R] Or Complete Response [CR]) At Day 85

Secondary Outcome Measures

Name	Time	Method

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