CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 57 enrolled
Drug / intervention
Revlimid (Lenalidomide)drug
Likely dose
Revlimid (Lenalidomide) 10 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01178814
NCT01178814Phase 2Completed

A Prospective Trial of Revlimid® in Transfusion Dependent Patients With Non-del (5q) Low/Intermediate-1 Risk Myelodysplastic Syndrome

Columbia University·interventional·Posted Aug 10, 2010·Updated Jun 24, 2024

In Brief

A Phase 2 clinical trial evaluating Revlimid (Lenalidomide) for Myelodysplastic Syndrome. Completed, enrolled 57 participants across 1 site.

Detailed Summary

This is a prospective trial of Revlimid for subjects who have a blood cell cancer called myelodysplastic syndrome (MDS). Cells in their marrow make proteins through messages that are carried from the genes. The amount of the message tells researchers if the protein it is going to make is high or low. This is known as expression of genes. The purpose of this study is to conduct a prospective trial testing the idea that expression of specific genes can help to predict which patients will respond to study drug administration with Revlimid (lenalidomide).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsCelgene Corporation

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedAug 10, 2010
Enrollment StartJun 1, 2009
Primary CompletionSep 1, 2022
Study CompletionDec 7, 2022
TodayJul 2, 2026
Enrollment to primary: 13.3 yearsPosted 15.9 years ago

Interventions

Revlimid (Lenalidomide)drug

The starting dose will be 10 mg days 1-28 with the first dose reduction going to 5 mg days 1-28 of a 28 day cycle. Therapy will cease if there is no response after 12 weeks.