Efficacy Study of Revlimid® and Low Dose Continuously Administered Melphalan to Treat High Risk MDS

PHASE2CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

January 31, 2008

Primary Completion Date

January 31, 2012

Study Completion Date

December 31, 2012

Conditions
Myelodysplastic SyndromesLeukemia, Myelomonocytic, ChronicAngiogenesis
Interventions
DRUG

Lenalidomide and melphalan

Lenalidomide (Revlimid) 10 mg po daily for 21d/28 Melphalan (Melphalan) 2 mg po daily for 21d/28

Trial Locations (1)

M4N3M5

Sunnybrook Health Sciences Centre, Odette Cancer Center, Toronto

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Celgene

INDUSTRY

lead

Sunnybrook Health Sciences Centre

OTHER

NCT00744536 - Efficacy Study of Revlimid® and Low Dose Continuously Administered Melphalan to Treat High Risk MDS | Biotech Hunter | Biotech Hunter