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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 company relationship

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 · 0 study sponsors

Related indications

Study sponsors

No additional listed-company sponsor is linked.

Clinical Trial Registry Records (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

NCT06615479Registry updated 2026-09-15·Phase 3
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)

NCT06297226Registry updated 2026-10-06·Phase 2
Recruiting

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

Interventionalopen230 targetStarted 2024-03Completion 2032-0652 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

NCT06121843Registry updated 2026-07-16·Phase 1
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

NCT04674813Registry updated 2026-02-09·Phase 1
Completed

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

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