CompletedPhase 3NCT01074047
Study of Vidaza Versus Conventional Care Regimens for the Treatment of Acute Myeloid Leukemia (AML)
Studying Acute promyelocytic leukemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Celgene
- Principal Investigator
- C L Beach, PharmDCelgene Corporation
- Intervention
- Azacitidine(drug)
- Enrollment
- 488 enrolled
- Eligibility
- 65 years · All sexes
- Timeline
- 2010 – 2016
Study locations (30)
- Massachusetts General Hospital, Boston, Massachusetts, United States
- MD Anderson Cancer Center, Houston, Texas, United States
- Prince of Wales Hospital, Randwick, New South Wales, Australia
- Royal Adelaide Hospital, Adelaide, South Australia, Australia
- Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
- Western Hospital, Footscray, Victoria, Australia
- Royal Melbourne Hospital, Melbourne, Victoria, Australia
- St Vincent's Hospital, Fitzroy, Australia
- Klinikum Wels-Grieskirchen GmbH, Wels, Upper Austria, Austria
- Wilhelminenspital, I Medizinische Abt., Vienna, Vienna, Austria
- Landeskliniken Salzburg Saint Johanns-Spital, III Medizinische Abteilung, Salzburg, Austria
- Grand Hôpital de Charleroi, Charleroi, Hainaut, Belgium
- Cliniques Universitaires UCL de Mont-Godinne, Yvoir, Namur, Belgium
- Universitair Ziekenhuis Gent, Ghent, Oost-vlaanderen, Belgium
- Algemeen Ziekenhuis Sint-Jan, Bruges, West-vlaanderen, Belgium
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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