BMS-986353
BiologicalSpecified dose of specified days
Other names: Zolacabtagene autoleucel, Zola-cel, CC-97540
NCT Number: NCT07603557
The purpose of this study is to evaluate the safety and efficacy of Zola-cel (BMS-986353), in participants with chronic immune thrombocytopenia (cITP) and autoimmune hemolytic anemia (AIHA).
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 2
Local Institution - 201, Odense, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Inclusion criteria
for ITP
Platelet count < 30 × 109/L. For participants on thrombopoietin receptor agonist (TPO-RA): platelet count < 50 × 109/L.
Inclusion criteria
for AIHA
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.
Exclusion criteria
Medical Conditions
Laboratory Test Findings
Other protocol-defined inclusion/exclusion criteria may apply.
Specified dose of specified days
Other names: Zolacabtagene autoleucel, Zola-cel, CC-97540
Specified dose of specified days
Specified dose on specified days
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 6
Time frame: Up to approximately Month 6
Time frame: Up to approximately Month 6
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 6
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately 12 months from Zola-cel infusion
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Time frame: Up to approximately Month 36
Contact information is provided by the study sponsor or research team.
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
CONTACT
First line of the email MUST contain NCT # and Site #.
CONTACT
Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
Industry
A Phase 2, Multicenter, Open-Label Study of Zolacabtagene Autoleucel (BMS-986353), CD19-Targeted NEX-T CAR T Cells, in Participants With Chronic Immune Thrombocytopenia (cITP) and Autoimmune Hemolytic Anemia (AIHA)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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