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Not Yet Recruiting

Study of Zola-cel (BMS-986353), in Participants With Autoimmune Cytopenia (Breakfree-AiCE) - CA061-1040

Mis à jour: 8 juillet, 2026   |   ClinicalTrials.gov

Résumé imprimable

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Imprimer cette page et le guide d’essai pour vous aider à parler avec votre médecin.
Utiliser le Guide du participant à l’étude pour découvrir comment participer à un essai clinique. Comprendre les principaux facteurs à envisager avant de prendre une décision et poser des questions à votre équipe soignante.

Détails de l’essai

  • Phase 2

    Phase

  • Sexe(s)

  • 18+

    Tranche d’âge

  • 6

    Site(s)

  • Not Yet Recruiting

Options de traitement

Bras de l’étude
INTERVENTION ASSIGNÉE
Experimental: Cohort 1 Part A AIHA
Biological: BMS-986353 Drug: Fludarabine Phosphate, Cyclophosphamide
Experimental: Cohort 1 Part A ITP
Biological: BMS-986353 Drug: Fludarabine Phosphate, Cyclophosphamide
Experimental: Cohort 1 Part B
Biological: BMS-986353 Drug: Fludarabine Phosphate, Cyclophosphamide
Experimental: Cohort 2
Biological: BMS-986353 Drug: Fludarabine Phosphate, Cyclophosphamide

Principaux critères d’éligibilité

Inclusion Criteria Inclusion Criteria for ITP - Documented clinical diagnosis of chronic ITP (cITP) without other clinical manifestations of systemic autoimmune disease. - Has relapsed after or is intolerant to corticosteroids (with or without intravenous immunoglobulin (IVIG) or anti-Rh0(D) Ig) AND has failed, relapsed after, or is intolerant to therapies with ≥ 2 mechanisms of action, with at least one being immunosuppressive or immunomodulatory. Platelet count < 30 × 109/L. For participants on thrombopoietin receptor agonist (TPO-RA): platelet count < 50 × 109/L. Inclusion Criteria for AIHA - Documented clinical diagnosis of AIHA (including warm autoimmune hemolytic anemia (wAIHA), cold agglutinin disease (CAD), or mixed AIHA) without other clinical manifestations of systemic autoimmune disease. o wAIHA and mixed warm and cold AIHA: Failed, relapsed after, or is intolerant to at least 2 prior lines of treatment with 2 mechanisms of action (not including corticosteroids or IVIG), one of which is an anti-CD20 monoclonal antibody unless there is a documented contraindication. o CAD (all of the following must apply): Failed, relapsed after, or is intolerant to at least 2 prior lines of treatment with 2 mechanisms of action, one of which is an anti-CD20 monoclonal antibody with or without chemotherapy unless there is a documented contraindication. - Hb <10 g/dL without red blood cell transfusion, or transfusion dependent - Documented hemolysis Exclusion Criteria Medical Conditions - ITP or AIHA associated with: Evans syndrome, other systemic autoimmune disease or single organ autoimmune disease requiring systemic immunosuppressive therapy, hepatitis C virus, HIV, drug induced (eg, non-steroidal anti-inflammatory drug (NSAIDS), trimethoprim/sulfamethoxazole (TMP-SMX), anticonvulsants), surgical procedures, or hematologic malignancies. - COVID-19 Vaccine-induced immune thrombotic thrombocytopenia - Prior history of solid organ malignancies, unless the participant has been free of the disease for ≥ 2 years. Laboratory Test Findings - Peripheral blood ANC < 1.5 × 109/L or requiring G-CSF or GM-CSF support o ALT/AST: ITP: ALT/AST: > 3 × ULN AIHA: ALT > 3 ULN. AST up to 5 × ULN may be permitted. o Bilirubin: ITP: total bilirubin > 1.5 × ULN AIHA: direct bilirubin > 1.5 × ULN o International normalized ratio (INR) > 1.5 × ULN Other protocol-defined inclusion/exclusion criteria may apply.