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ciltacabtagene autoleucel

Generic: ciltacabtagene autoleucel·Brand: Carvykti

ciltacabtagene autoleucel: 6 clinical trials tracked.

ciltacabtagene autoleucel evidence translation

What we can confirm

6 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 ciltacabtagene autoleucel, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Clinical Trials (6)

A Phase 2 Multicohort Trial to Further Characterize the Efficacy and Safety of Ciltacabtagene Autoleucel

NCT07149857·Phase 2·GHRS
Recruiting

Primary endpoint: Minimal Residual Disease (MRD)-negative Complete Response (CR) After Cilta-cel Infusion

Interventionalopen60 targetStarted 2025-10Completion 2029-0417 sites · Australia, Spain, United StatesJanssen Research & Development, LLC

A Phase 2, Open-Label, Multicenter Study of Ciltacabtagene Autoleucel and Talquetamab for the Treatment of Participants With High-Risk Multiple Myeloma

NCT06550895·Phase 2
Active, not recruiting

Primary endpoint: Number of Participants With Adverse Events (AE) by Severity According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0

Interventionalopen11 targetStarted 2024-09Completion 2027-089 sites · Australia, United StatesJanssen Research & Development, LLC

A Phase 2, Open-label Study to Evaluate the Efficacy and Safety of Different Sequences of Ciltacabtagene Autoleucel (Cilta-cel), Talquetamab SC in Combination With Daratumumab SC (Tal-D) and Teclistamab SC in Combination With Daratumumab SC (Tec-D) Following Induction With Daratumumab, Bortezomib, Lenalidomide and Dexamethasone (DVRd) in Participants With Standard-risk Newly Diagnosed Multiple Myeloma

NCT06577025·Phase 2·GHRS
Active, not recruiting

Primary endpoint: Rate of Response with Curative Potential

InterventionalRandomizedopen43 targetStarted 2024-08Completion 2030-0916 sites · Australia, Brazil, Germany, Spain…Janssen Research & Development, LLC

Long-term Follow-up Study for Participants Previously Treated With Ciltacabtagene Autoleucel

NCT05201781·Phase 4·GHRS
Recruiting

Primary endpoint: Number of Participants with New Malignancies and Recurrence of Pre-existing Malignancy

Interventionalopen295 targetStarted 2022-03Completion 2042-0650 sites · Belgium, China, France, Israel…Janssen Research & Development, LLC

A Phase 3 Randomized Study Comparing Bortezomib, Lenalidomide and Dexamethasone (VRd) Followed by Ciltacabtagene Autoleucel, a Chimeric Antigen Receptor T Cell (CAR-T) Therapy Directed Against BCMA Versus Bortezomib, Lenalidomide, and Dexamethasone (VRd) Followed by Lenalidomide and Dexamethasone (Rd) Therapy in Participants With Newly Diagnosed Multiple Myeloma for Whom Hematopoietic Stem Cell Transplant is Not Planned as Initial Therapy

NCT04923893·Phase 3·GHRS
Active, not recruiting

Primary endpoint: Progression Free Survival (PFS)

InterventionalRandomizedopen743 targetStarted 2021-08Completion 2036-0950 sites · Argentina, Australia, Austria, Belgium…Janssen Research & Development, LLC

A Phase 3 Randomized Study Comparing JNJ-68284528, a Chimeric Antigen Receptor T Cell (CAR-T) Therapy Directed Against BCMA, Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) or Daratumumab, Pomalidomide and Dexamethasone (DPd) in Subjects With Relapsed and Lenalidomide-Refractory Multiple Myeloma

NCT04181827·Phase 3·GHRS
Active, not recruiting

Primary endpoint: Progression Free Survival (PFS)

InterventionalRandomizedopen419 targetStarted 2020-06Completion 2027-0350 sites · Australia, Belgium, Denmark, France…Janssen Research & Development, LLC