Idecabtagene vicleucel
Idecabtagene vicleucel is an intervention with 15 clinical trials. Currently 10 active trials ongoing.
Registry-listed formulations
idecabtagene vicleucel · mesh:C000715380
Each study is counted once in the molecule profile. Registry products remain separate. Naming an ingredient does not establish that products are interchangeable or what participants received.
11 source entries across 11 studies. This list may not include all unresolved or historical entries.
- idecabtagene vicleucelRegistry product
Named ingredient; product remains distinct
Formulation reported by source: CELL SUSPENSION FOR INJECTION
View study and source - idecabtagene vicleucelRegistry product
Named ingredient; product remains distinct
Formulation reported by source: CELL SUSPENSION FOR INJECTION
View study and source - Abecma, Intravenous SuspensionRegistry intervention
Linked study entry; product equivalence not established
View study and source - idecabtagene vicleucelRegistry product
Named ingredient; product remains distinct
Formulation reported by source: CELL SUSPENSION FOR INJECTION
View study and source - bb2121Registry intervention
Linked study entry; product equivalence not established
View study and source - BB2121Registry intervention
Linked study entry; product equivalence not established
View study and source - bb2121Registry intervention
Linked study entry; product equivalence not established
View study and source - Ide-cel (bb2121)Registry intervention
Linked study entry; product equivalence not established
View study and source - idecabtagene vicleucelRegistry product
Named ingredient; product remains distinct
Formulation reported by source: CELL SUSPENSION FOR INJECTION
View study and source - Abecma 260 - 500 x 10^6 cells dispersion for infusionRegistry product
Named ingredient; product remains distinct
Formulation reported by source: DISPERSION FOR INFUSION
View study and source - Abecma 260 - 500 x 10^6 cells dispersion for infusionRegistry product
Named ingredient; product remains distinct
Formulation reported by source: DISPERSION FOR INFUSION
View study and source
Success Metrics
Phase Distribution
Phase Distribution
2
Early Stage
6
Mid Stage
3
Late Stage
Highest Phase Reached
Phase 4Trial Status & Enrollment
80.0%
4 of 5 finished
20.0%
1 ended early
10
trials recruiting
15
all time
Detailed Status
Development Timeline
Analytics
Development Status
Trials by Phase
Trials by Status
Recent Activity
A Study to Evaluate the Long-Term Safety of Idecabtagene Vicleucel Treatment in Adults With Newly Diagnosed Multiple Myeloma in Korea
Temporal Characterization of Extracellular Vesicles During Cellular Therapy Using CAR-T Cells and During the Occurrence of Immune Effector Cell-Associated Neurotoxicity Syndrome
Long-Term Follow-up Protocol for Participants Treated With Gene-Modified T Cells
The Norwegian Immunotherapy in Multiple Myeloma Study
Safety and Efficacy of bb2121 (Ide-cel) Combinations in Multiple Myeloma
Clinical Trials (15)
A Study to Evaluate the Long-Term Safety of Idecabtagene Vicleucel Treatment in Adults With Newly Diagnosed Multiple Myeloma in Korea
Temporal Characterization of Extracellular Vesicles During Cellular Therapy Using CAR-T Cells and During the Occurrence of Immune Effector Cell-Associated Neurotoxicity Syndrome
Long-Term Follow-up Protocol for Participants Treated With Gene-Modified T Cells
The Norwegian Immunotherapy in Multiple Myeloma Study
Safety and Efficacy of bb2121 (Ide-cel) Combinations in Multiple Myeloma
Efficacy and Safety Study of bb2121 Versus Standard Regimens in Subjects With Relapsed and Refractory Multiple Myeloma (RRMM)
Upfront Chimeric Antigen Receptor T-Cell to Upgrade Response in Multiple Myeloma
A Study of Whether Ide-cel (bb2121) Can Be Made From People With Multiple Myeloma Who Have Had a Hematopoietic Cell Transplant
A Study 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
An Efficacy and Safety Study of bb2121 in Subjects With Relapsed and Refractory Multiple Myeloma and in Subjects With High-Risk Multiple Myeloma
MT2017-45: CAR-T Cell Therapy for Heme Malignancies
Transgene Assay Testing Service of Tumor Samples From Patients Who Received a Bristol-Myers Squibb Manufactured Gene Modified Cell Therapy and Have a Qualifying Second Primary Malignancy
Real-World Outcomes in Relapsed/Refractory Multiple Myeloma Patients Treated, or Eligible for Treatment, With Idecabtagene Vicleucel
A Study to Evaluate the Safety of bb2121 in Subjects With High Risk, Newly Diagnosed Multiple Myeloma (NDMM)
A phase I/II study of CAR-T cells in AutoiMmune disease resistant to B cell Abrogation - CARAMBA
All 15 trials loaded
Drug Details
- Intervention Type
- Varies by study
- Total Trials
- 15