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NCT06297226
Study of Arlocabtagene Autoleucel (BMS-986393) a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma
The purpose of this study is to evaluate the effectiveness and safety of Arlocabtagene Autoleucel (BMS-986393) in participants with relapsed or refractory multiple myeloma.
Trial Details
NCT ID NCT06297226
Phase PHASE2
Sponsor Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
Status RECRUITING
Cancer Type Relapsed/Refractory Multiple Myeloma
Interventions
Locations (sample) Birmingham, Alabama, United States|33.52066,-86.80249 Gilbert, Arizona, United States|33.35283,-111.78903 Little Rock, Arkansas, United States|34.74648,-92.28959 Los Angeles, California, United States|34.05223,-118.24368 San Francisco, California, United States|37.77493,-122.41942
Key Eligibility Criteria
Documented diagnosis of multiple myeloma (MM) as per International Myeloma Working Group (IMWG) criteria. Received at least 4 classes of MM treatment \[including immunomodulatory drug (IMiD), proteasome inhibitor (PI), anti CD38 mAb, anti-BCMA therapy, … Documented disease progression during or after their last anti-myeloma regimen as per IMWG 2016 criteria. Participants must have measurable disease during screening.
For full eligibility, visit ClinicalTrials.gov .