drugset / Trial / NCT04272775

A Study of MLN9708 in Japanese Participants With Relapsed and/or Refractory Multiple Myeloma (RRMM)

NCT04272775 ↗

Phase 1 Terminated 14 enrolled Takeda
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to evaluate the tolerability, safety, pharmacokinetics (PK) of ixazomib alone or in combination with lenalidomide and dexamethasone (Rd), and antitumor activity of ixazomib in participants with RRMM.

Timeline

Start
2012-06-05
Primary completion
2019-02-15
Completion
2019-02-15

Outcome

Outcome not reported

Stopped (Business): “Business Decision; No Safety Or Efficacy Concerns”

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexamethasone Small molecule 40 mg Oral
Subject Ixazomib Unknown 4 mg Oral
Subject Ixazomib Unknown 5.5 mg Oral
Subject Lenalidomide Other / unclassified 25 mg Oral