MORE - Monitoring Revlimid - Collecting of Patient Information From Myelodysplastic Syndrome (MDS) Italian National Registry

• Status: Completed
• Trial end date: 2013-06-30
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to collect clinical and laboratory data for patients affected by intermediate 1 and low risk Myelodysplastic Syndrome (MDS) associated by deletion 5q who were prescribed Revlimid from 31October 2008 to present. Revlimid is available in Italy for these patients since October 2008 based on a local disposition of the Italian Drug Agency (AIFA) issued according to a National law named 648/96.

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Celgene; Celgene Corporation
• Treatments: Lenalidomide; Thalidomide

Criteria

Inclusion Criteria:

• intermediate 1 and low risk MDS patients associated with:

1. transfusion dependency anemia (at least 2 units per 8 weeks before starting of Revlimid treatment )

2. 5q31-33 deletion isolated or associated to other chromosomal abnormalities.

Exclusion Criteria:

• patients with serum creatinine > 2.5mg/dl

• child bearing potential females who do not use adequate contraceptive methods