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

Completion Rate
80%(4/5)
Active Trials
10(67%)
Results Posted
50%(2 trials)
Terminated
1(7%)

Phase Distribution

Phase 2
4
27%
Phase 2/3
1
7%
Phase 3
2
13%
Phase 4
1
7%
Phase 1
2
13%
Phase 1/2
1
7%

Phase Distribution

2

Early Stage

6

Mid Stage

3

Late Stage

Phase Distribution11 total trials
Phase 1Safety & dosage
2(18.2%)
Phase 1/2Combined phases
1(9.1%)
Phase 2Efficacy & side effects
4(36.4%)
Phase 2/3Combined phases
1(9.1%)
Phase 3Large-scale testing
2(18.2%)
Phase 4Post-market surveillance
1(9.1%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

80.0%

4 of 5 finished

Non-Completion Rate

20.0%

1 ended early

Currently Active

10

trials recruiting

Total Trials

15

all time

Status Distribution
Active(10)
Completed(4)
Terminated(1)

Detailed Status

Recruiting6
Active, not recruiting4
Completed4
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
15
Active
10
Success Rate
N/A
Most Advanced
Phase 3

Trials by Phase

Phase 12 (18.2%)
Phase 1/21 (9.1%)
Phase 24 (36.4%)
Phase 2/31 (9.1%)
Phase 32 (18.2%)
Phase 41 (9.1%)

Trials by Status

active_not_recruiting427%
completed427%
recruiting640%
terminated17%

Recent Activity

Clinical Trials (15)

Showing 15 of 15 trials
NCT06698887

A Study to Evaluate the Long-Term Safety of Idecabtagene Vicleucel Treatment in Adults With Newly Diagnosed Multiple Myeloma in Korea

Recruiting
NCT06706102Phase 4

Temporal Characterization of Extracellular Vesicles During Cellular Therapy Using CAR-T Cells and During the Occurrence of Immune Effector Cell-Associated Neurotoxicity Syndrome

Recruiting
NCT03435796Phase 2/3

Long-Term Follow-up Protocol for Participants Treated With Gene-Modified T Cells

Recruiting
NCT06855121

The Norwegian Immunotherapy in Multiple Myeloma Study

Recruiting
NCT04855136Phase 1

Safety and Efficacy of bb2121 (Ide-cel) Combinations in Multiple Myeloma

Terminated
NCT03651128Phase 3

Efficacy and Safety Study of bb2121 Versus Standard Regimens in Subjects With Relapsed and Refractory Multiple Myeloma (RRMM)

Completed
NCT05032820Phase 2

Upfront Chimeric Antigen Receptor T-Cell to Upgrade Response in Multiple Myeloma

Completed
NCT05393804Phase 2

A Study of Whether Ide-cel (bb2121) Can Be Made From People With Multiple Myeloma Who Have Had a Hematopoietic Cell Transplant

Active Not Recruiting
NCT06045806Phase 3

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

Active Not Recruiting
NCT03601078Phase 2

An Efficacy and Safety Study of bb2121 in Subjects With Relapsed and Refractory Multiple Myeloma and in Subjects With High-Risk Multiple Myeloma

Completed
NCT03642626Phase 2

MT2017-45: CAR-T Cell Therapy for Heme Malignancies

Active Not Recruiting
NCT06357754

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

Recruiting
NCT06154902

Real-World Outcomes in Relapsed/Refractory Multiple Myeloma Patients Treated, or Eligible for Treatment, With Idecabtagene Vicleucel

Active Not Recruiting
NCT04196491Phase 1

A Study to Evaluate the Safety of bb2121 in Subjects With High Risk, Newly Diagnosed Multiple Myeloma (NDMM)

Completed
SYFd2c362a43b7c4d6dae5f1ca07a420dfdPhase 1/2

A phase I/II study of CAR-T cells in AutoiMmune disease resistant to B cell Abrogation - CARAMBA

Recruiting

All 15 trials loaded

Drug Details

Intervention Type
Varies by study
Total Trials
15

Names & Codes

Trade Names

abecma

Research Codes

bb2121