An Extension to Study AZA PH GL 2003 CL 001 Allowing for Continuation of Azacitidine Treatment in Patients With Myelodysplastic Syndromes (MDS)

PHASE3CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

April 1, 2007

Primary Completion Date

September 1, 2009

Study Completion Date

September 1, 2009

Conditions
Myelodysplastic Syndromes
Interventions
DRUG

Azacitidine

Azacitidine was injected subcutaneously (SC) for 7 days. The 7-day dosing was repeated every 28 days with dose adjustments allowed. The initial dose during the primary study was 75mg/m\^2/day.

Trial Locations (22)

Unknown

East Melbourne

Herston

Perth

Woolloongabba

Plovdiv

Aulnay-sous-Bois

Berlin

Düsseldorf

Essen

Kiel

Heraklio

Haidari

Budapest

Bologna

Florence

Genova

Rome

Nijmegen

Lodz

Avda Campanar

León

London

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celgene

INDUSTRY