drugset / Trial / NCT01698801

A Phase 2 Study of Lenalidomide to Evaluate the Efficacy in Japanese Patients With Newly Diagnosed Multiple Myeloma

NCT01698801 ↗

Phase 2 Completed 26 enrolled Celgene Corporation
NaSingle-groupOpen-labelTreatment

Summary

To determine the efficacy of lenalidomide in combination with low-dose dexamethasone in Japanese subjects with previously untreated multiple myeloma.

Timeline

Start
2012-10-01
Primary completion
2013-11-26
Completion
2018-06-26

Outcome

Met primary endpoint

registry p <0.0001; Overall dichotomized response rate 87.5 (95% CI 74.269 to 100) NCT01698801 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 25 mg Oral
Background Dexamethasone Small molecule 40 mg Oral

Indications