drugset / Trial / NCT02400242

Study of ACY-241 Alone and in Combination With Pomalidomide and Dexamethasone in Multiple Myeloma

NCT02400242

Phase 1 Terminated 85 enrolled Celgene Corporation
NaSingle-groupOpen-labelTreatment

Summary

This is a phase 1a/1b, multicenter, single-arm, open-label, dose escalation study to determine the maximum tolerated dose (MTD) and evaluate the safety and preliminary antitumor activity of ACY-241 for oral administration as monotherapy and in combination therapy with orally administered pomalidomide and low-dose dexamethasone in eligible patients with relapsed or relapsed-and-refractory multiple myeloma (MM).

Timeline

Start
2015-05-07
Primary completion
2024-06-03
Completion
2024-06-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Citarinostat Small molecule 180 mg Oral
Subject Citarinostat Small molecule 480 mg Oral
Background Dexamethasone Small molecule 40 mg Oral
Background Pomalidomide Other / unclassified 4 mg Oral

Indications