Clinical Trials Directory

Trials / Terminated

TerminatedNCT01979276

Study of Pomalidomide, Dexamethasone, and Romidepsin for Rel/Ref Myeloma

A Phase I/II Study of Pomalidomide (CC-4047®), Dexamethasone and Romidepsin in Patients With Relapsed or Refractory Multiple Myeloma (Romi Poma)

Status
Terminated
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
4 (actual)
Sponsor
Weill Medical College of Cornell University · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

Summary

This clinical trial is for subjects with multiple myeloma that has returned after treatment (relapsed) or did not respond to prior treatment (refractory). The study is in two parts, Phase I and Phase II. Phase I will determine the maximum tolerated dose of romidepsin in combination with pomalidomide and dexamethasone. The purpose of Phase II is to evaluate the effectiveness of combining romidepsin with pomalidomide and dexamethasone. The hypothesis is that overall response in a cohort of patients treated with romidepsin + pomalidomide + dexamethasone will be 60 percent.

Detailed description

This phase I/II study is a treatment program for patients with relapsed or refractory multiple myeloma. Up to 48 patients will be enrolled. Phase I will follow a 3+3 dose escalation design to find the maximum tolerated dose of romidepsin in combination with pomalidomide and dexamethasone. In Phase I, subjects will receive: * Pomalidomide 4mg daily by mouth on days 1-21 of a 28-day cycle * Dexamethasone 40mg by mouth on days 1, 8, 15 and 22 of a 28-day cycle * Romidepsin intravenously (9 mg/m2, 12 mg/m2, 15 mg/m2 or 18 mg/m2) on days 1 and 15 of a 28-day cycle. Phase II will expand the number of subjects in the MTD arm of the trial until 48 subjects are enrolled. In Phase II, subjects subjects will receive: * Pomalidomide 4mg daily by mouth on days 1-21 of a 28-day cycle * Dexamethasone 40mg by mouth on days 1, 8, 15 and 22 of a 28-day cycle * Romidepsin intravenously on days 1 and 15 of a 28-day cycle at the Maximum Tolerated Dose determined by Phase I

Conditions

Interventions

TypeNameDescription
DRUGRomidepsinRomidepsin intravenously on days 1 and 15 of a 28-day cycle
DRUGpomalidomidePomalidomide 4mg daily by mouth on days 1-21 of a 28-day cycle
DRUGDexamethasoneDexamethasone 40mg by mouth on days 1, 8, 15 and 22 of a 28-day cycle

Timeline

Start date
2013-11-01
Primary completion
2016-10-01
Completion
2016-10-01
First posted
2013-11-08
Last updated
2018-06-06
Results posted
2018-01-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01979276. Inclusion in this directory is not an endorsement.