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Immunomodulatory Agent
Revlimid (Lenalidomide) for Myelodysplastic Syndrome
Phase 2
Waitlist Available
Led By Mark Heaney, MD
Research Sponsored by Columbia University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 12 weeks from baseline
Awards & highlights
Study Summary
This trial will test if a gene's expression can predict if a patient with myelodysplastic syndrome will respond to the study drug Revlimid.
Eligible Conditions
- Myelodysplastic Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 12 weeks from baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 12 weeks from baseline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Response Signature in Transfusion Dependent MDS Patients
Trial Design
1Treatment groups
Experimental Treatment
Group I: RevlimidExperimental Treatment1 Intervention
Revlimid (Lenalidomide) capsule taken orally once a day
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Revlimid (Lenalidomide)
2009
Completed Phase 2
~30
Find a Location
Who is running the clinical trial?
Columbia UniversityLead Sponsor
1,433 Previous Clinical Trials
2,460,958 Total Patients Enrolled
Celgene CorporationIndustry Sponsor
444 Previous Clinical Trials
58,179 Total Patients Enrolled
Mark Heaney, MDPrincipal InvestigatorColumbia University
1 Previous Clinical Trials
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