Phase II Decitabine (DAC) Versus Azacitidine (AZA) in Myelodysplastic Syndrome (MDS) | Aplastic Anemia & MDS International Foundation
Phase II Decitabine (DAC) Versus Azacitidine (AZA) in Myelodysplastic Syndrome (MDS)

Clinical Trial: NCT02269280

Instructions

If you are interested in learning more about your possible participation in this clinical trial, please complete the form. Your information will be forwarded directly to the sponsoring company.

Status: 
Recruiting
Associated Drug(s): 
Phase: 
Phase 2
Gender: 
Female
Male
Age Group: 
18 years and older
Accepts Healthy Volunteers: 
No
Inclusion Criteria: 
  1. Sign an IRB-approved informed consent document.
  2. Age ≥18 years.
  3. IPSS low- or intermediate-1 –risk MDS, including CMML-1.
  4. ECOG performance status of
  5. Organ function defined as: Serum creatinine
  6. Women of childbearing potential must have a negative serum or urine pregnancy test within 7 days and will also need to use contraceptives. Men must agree not to father a child and agree to use a condom if his partner is of child bearing potential.
Exclusion Criteria: 
  1. Breast feeding females.
  2. Prior therapy with decitabine or azacitidine.

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