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obecabtagene autoleucel

Generic: obecabtagene autoleucel·Brand: Aucatzyl

obecabtagene autoleucel: 5 clinical trials tracked.

obecabtagene autoleucel evidence translation

What we can confirm

5 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 obecabtagene autoleucel, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence3 indications · 0 study sponsors

Study sponsors

No additional listed-company sponsor is linked.

Clinical Trial Registry Records (5)

A Phase II Trial of Obecabtagene Autoleucel Consolidation in Adult Patients With Acute Lymphoblastic Leukemia in First Complete Remission Without Measurable Residual Disease

NCT07400029Registry updated 2026-08-20·Phase 2
Recruiting

Primary endpoint: relapse free survival (RFS) (Cohort A)

Interventionalopen40 targetStarted 2026-02Completion 2029-029 sites · United StatesMemorial Sloan Kettering Cancer Center

A Single-Arm, Open-Label, Phase II Study to Determine the Safety and Efficacy of Obecabtagene Autoleucel (Obe-cel) in Participants With Severe, Refractory Systemic Lupus Erythematosus With Active Lupus Nephritis

NCT07053800Registry updated 2026-08-24·Phase 2
Recruiting

Primary endpoint: Proportion of participants who achieve complete renal response (CRR)

Interventionalopen35 targetStarted 2026-01Completion 2029-1015 sites · Brazil, Greece, United Kingdom, United States…Autolus Limited

Phase 2 Study Assessing the Clinical Activity and Safety of Obecabtagene Autoleucel as a Consolidation in Patients With Newly Diagnosed High-risk B-cell Acute Lymphocytic Leukemia (ALL)

NCT07053059Registry updated 2026-08-12·Phase 2
Recruiting

Primary endpoint: Safety and Adverse Events (AEs)

Interventionalopen30 targetStarted 2025-08Completion 2030-051 site · United StatesM.D. Anderson Cancer Center

A Single-arm, Open-label, Phase I Study to Determine the Safety, Tolerability, and Preliminary Efficacy of Obe-cel in Participants With Refractory Progressive Forms of Multiple Sclerosis

NCT07139743Registry updated 2026-03-23·Phase 1
Recruiting

Primary endpoint: Percentage of participants receiving obe-cel who experience dose-limiting toxicities (DLTs))

Interventionalopen18 targetStarted 2025-08Completion 2029-087 sites · Spain, United Kingdom, United StatesAutolus Limited

A Single-Arm, Open-Label, Phase I Study to Determine the Safety, Tolerability and Preliminary Efficacy of Obecabtagene Autoleucel in Patients With Severe, Refractory Systemic Lupus Erythematosus

NCT06333483Registry updated 2026-07-31·Phase 1
Active, not recruiting

Primary endpoint: Dose-limiting toxicities

Interventionalopen16 enrolledStarted 2024-02Completion 2027-096 sites · Spain, United KingdomAutolus Limited