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Phase 3
18 Years
80 Years
Not Enrolling
Myelodysplastic Syndromes

Thank you

Trial Information

Inclusion Criteria

- Eligible patients must have a diagnosis of myelodysplastic syndrome

- Life expectancy of at least 6 months.

- Patients must be able to adhere to the study visit schedule and other protocol

- Patients must understand and voluntarily sign an informed consent document.

- Women of childbearing potential (WCBP) must agree to practice abstinence or to use
TWO methods of contraception beginning 4 weeks prior to the start of study medication
and throughout the course of treatment.

- Males must use barrier contraception when engaging in reproductive sexual activity
with women of childbearing potential.

Type of Study:


Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


United States: Food and Drug Administration

Study ID:




Start Date:

August 2001

Completion Date:

February 2004

Related Keywords:

  • Myelodysplastic Syndromes
  • Myelodysplastic Syndromes
  • Preleukemia



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