drugset / Trial / NCT02336815

Selinexor Treatment of Refractory Myeloma

NCT02336815 ↗

Phase 2 Completed 202 enrolled Karyopharm Therapeutics Inc
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 2b, single-arm, open-label, multicenter study of selinexor 80 mg plus dexamethasone 20 mg (Sd) dosed twice weekly in four-week cycles, in patients with penta-refractory MM (Parts 1 and 2) or quad refractory MM (Part 1 only).

Timeline

Start
2015-05-26
Primary completion
2019-07-26
Completion
2019-07-26

Outcome

Met primary endpoint

paper that met its primary endpoint, with overall response of 26% (95% confidence interval [CI], 19 to 35%). reads as met primary endpoint PMID 34488662 ↗

release “In STORM, XPOVIO achieved a 26% overall response rate” reads as unknown karyopharm.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexamethasone Small molecule 20 mg Oral
Subject Selinexor Other / unclassified 80 mg Oral

Indications