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arlocabtagene autoleucel

Generic: Arlocabtagene Autoleucel

arlocabtagene autoleucel: 4 clinical trials tracked.

arlocabtagene autoleucel evidence translation

What we can confirm

4 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about arlocabtagene autoleucel, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 3 study sponsors
Clinical Trials (4)

A Phase 3, Randomized, Open-Label, Multicenter Study to Compare the Efficacy and Safety of Arlocabtagene Autoleucel (BMS-986393), a GPRC5D-directed CAR-T Cell Therapy, Versus Standard Regimens in Adult Participants With Relapsed or Refractory and Lenalidomide-exposed Multiple Myeloma

NCT06615479·Phase 3·BMY
Recruiting

Primary endpoint: Progression Free Survival (PFS)

InterventionalRandomizedopen440 targetStarted 2025-03Completion 2032-0650 sites · Argentina, Australia, Austria, Belgium…Juno Therapeutics, Inc., a Bristol-Myers Squibb Company

A Phase 2, Open-Label, Multicenter Study of Arlocabtagene Autoleucel (BMS-986393), a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma (QUINTESSENTIAL)

NCT06297226·Phase 2·JUNO
Recruiting

Primary endpoint: Cohort 1: Best overall response (BOR) of partial response (PR) or better

Interventionalopen230 targetStarted 2024-03Completion 2032-0650 sites · Australia, Canada, Japan, United StatesJuno Therapeutics, Inc., a Bristol-Myers Squibb Company

A Phase 1, Multicenter, Open-label Study to Evaluate the Safety and Preliminary Efficacy of Arlocabtagene Autoleucel (BMS-986393) in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma and Determine the Recommended Dose for Each Add-on Investigational Component

NCT06121843·Phase 1·BMY
Recruiting

Primary endpoint: Incidence of adverse events (AEs)

Interventionalopen187 targetStarted 2024-02Completion 2028-0819 sites · Canada, United StatesJuno Therapeutics, Inc., a Bristol-Myers Squibb Company

A Phase 1, Multicenter, Open-Label Study of CC-95266 in Subjects With Relapsed and/or Refractory Multiple Myeloma

NCT04674813·Phase 1·FLNA
Completed

Primary endpoint: Number of participants with Adverse Events (AEs)

Interventionalopen130 enrolledStarted 2021-02Completion 2025-1210 sites · United StatesJuno Therapeutics, a Subsidiary of Celgene