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

Myelodysplastic Syndrome Clinical Trial

Official title:
Observational, Non-interventional, Multicenter Study Aimed at Collecting Retrospective/Prospective 648/96 Italian Registry Data Related to Lenalidomide (Revlimid®) Prescription to Patients With Myelodysplastic Syndromes

Clinical Trial 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.

Clinical Trial Description

There will be retrospective collection and integration of clinical laboratory data as well as prospective data collection on the same patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01347944
Study type Observational
Source Celgene
Contact
Status Completed
Phase
Start date January 1, 2011
Completion date June 30, 2013
View Details
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