drugset / Trial / NCT04776018
A Study Of TAK-981 Given With Monoclonal Antibodies (mAbs) In Adults With Relapsed or Refractory Multiple Myeloma (RRMM)
Non-randomizedSequentialOpen-labelTreatment
Summary
TAK-981 is being tested in combination with anti-CD38 monoclonal antibodies (mAbs) to treat participants who have relapsed or refractory multiple myeloma (RRMM). The main aims of the study are to evaluate the safety and efficacy of TAK-981 in combination with anti-CD38 (mAbs) and to determine the recommended Phase 2 dose (RP2D). Participants will be on this combination treatment for 28-day cycles. They will continue with this treatment until disease progression or unacceptable toxicity.
Timeline
- Start
- 2021-04-20
- Primary completion
- 2023-08-02
- Completion
- 2023-11-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Daratumumab and Hyaluronidase-fihj | Unknown | 1800 mg | Subcutaneous |
| Subject | Mezagitamab | Monoclonal antibody | 600 mg | Subcutaneous |
| Subject | TAK-981 | Small molecule | — | Intravenous |