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cemacabtagene ansegedleucel

Generic: Cemacabtagene Ansegedleucel

cemacabtagene ansegedleucel: 3 clinical trials tracked.

cemacabtagene ansegedleucel 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 cemacabtagene ansegedleucel, 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)

A Randomized, Open-label Study Evaluating the Efficacy and Safety of Cemacabtagene Ansegedleucel in Participants With Minimal Residual Disease After Response to First Line Therapy for Large B-cell Lymphoma

NCT06500273Registry updated 2026-10-02·Phase 2·ALLO
Recruiting

Primary endpoint: Event-free survival per independent review committee assessment

InterventionalRandomizedopen250 targetStarted 2024-06Completion 2032-1285 sites · Australia, Canada, South Korea, United StatesAllogene Therapeutics

A Randomized, Open-Label, Phase 2 Study Evaluating Lymphodepletion With ALLO-647, Fludarabine, and Cyclophosphamide, vs. Fludarabine and Cyclophosphamide Alone, in Subjects With Relapsed/Refractory Large B-Cell Lymphoma Receiving ALLO-501A Allogeneic CAR T Cell Therapy

NCT05714345Registry updated 2026-03-02·Phase 2·ALLO
Terminated

Primary endpoint: Progression-Free Survival (PFS) of a Lymphodepletion Regimen Containing FCA vs FC Alone Per Independent Review Committee

InterventionalRandomizedopen2 targetStarted 2023-11Completion 2024-102 sites · Belgium, United StatesAllogene Therapeutics

A Single-Arm, Open-Label, Phase 1/2 Study Evaluating the Safety, Efficacy, and Cellular Kinetics/Pharmacodynamics of ALLO-501A, an Anti-CD19 Allogeneic CAR T Cell Therapy, and ALLO-647, an Anti-CD52 Monoclonal Antibody, in Subjects With Relapsed/Refractory Large B-Cell Lymphoma (LBCL)

NCT04416984Registry updated 2026-03-04·Phase 1/Phase 2·ALLO
Active, not recruiting

Primary endpoint: Phase 1a: Proportion of subjects experiencing Dose Limiting Toxicities (DLT) at increasing doses of ALLO-501A

Interventionalopen160 targetStarted 2020-05Completion 2029-0529 sites · Australia, Canada, United StatesAllogene Therapeutics