A 2 -Year, Multi-Center, Phase II, Open-Label, Fixed-Dose, Randomized Comparative Trial of Azacitidine, with or without Deferasirox in Patients with Higher Risk Myelodysplasic Syndromes
Principal Investigator(s)
Email for information
Funded by
Henry Jackson Foundation
Research Start Date
Status
Active
The primary objective of the study is to compare the overall response rate (inclusive of complete response, partial response and hematologic improvement) per IWG 2006 criteria in patients with higher risk MDS treated with azacitidine with or without deferasirox achieved over the course of one year. Hematologic improvement must be maintained for at least 8 weeks.
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