drugset / Trial / NCT04776018

A Study Of TAK-981 Given With Monoclonal Antibodies (mAbs) In Adults With Relapsed or Refractory Multiple Myeloma (RRMM)

NCT04776018

Phase 1/2 Terminated 27 enrolled Takeda
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

EvaluationDrugModalityDoseRoute
Subject Daratumumab and Hyaluronidase-fihj Unknown 1800 mg Subcutaneous
Subject Mezagitamab Monoclonal antibody 600 mg Subcutaneous
Subject TAK-981 Small molecule Intravenous