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idecabtagene vicleucel

Generic: idecabtagene vicleucel·Brand: Abecma

idecabtagene vicleucel: 3 clinical trials tracked.

idecabtagene vicleucel evidence translation

What we can confirm

3 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 idecabtagene vicleucel, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Clinical Trial Registry Records (3)

Long-Term Safety Follow-Up Surveillance for Phase 3 Trial (KarMMA-9/CA089-1043) to Compare the Efficacy and Safety of Idecabtagene Vicleucel With Lenalidomide Maintenance Therapy Versus Lenalidomide Maintenance Therapy Alone in Adult Participants With Newly Diagnosed Multiple Myeloma Who Have Suboptimal Response After Autologous Stem Cell Transplantation

NCT06698887Registry updated 2026-10-01·BMY
Recruiting

Primary endpoint: Participant adverse events

Observational15 targetStarted 2024-09Completion 2031-035 sites · South KoreaBristol-Myers Squibb

A Randomized, Open-Label, Phase 3 Trial to Compare the Efficacy and Safety of Idecabtagene Vicleucel With Lenalidomide Maintenance Versus Lenalidomide Maintenance Therapy Alone in Adult Participants With Newly Diagnosed Multiple Myeloma Who Have Suboptimal Response After Autologous Stem Cell Transplantation (KarMMa-9)

NCT06045806Registry updated 2026-03-05·Phase 3

Primary endpoint: Progression Free Survival (PFS)

InterventionalRandomizedopen79 targetStarted 2023-10Completion 2029-1150 sites · Australia, Austria, Belgium, Canada…Celgene

Feasibility Trial of Autologous Anti-B Cell Maturation Antigen Chimeric Antigen Receptor T Cell Therapy Using Ide-Cel for Multiple Myeloma Patients Status Post Hematopoietic Cell Transplantation

NCT05393804Registry updated 2026-02-17·Phase 2
Recruiting

Primary endpoint: feasibility of manufacturing Ide-Cel (to dose of at least 300 million cells)

Interventionalopen32 targetStarted 2022-05Completion 2027-057 sites · United StatesMemorial Sloan Kettering Cancer Center