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Terminated Phase 4 Interventional Results available

To Demonstrate Superiority of Decitabine Over Azacitidine in Subjects With Intermediate- or High-risk MDS.

ClinicalTrials.gov ID: NCT01011283

Public ClinicalTrials.gov record NCT01011283. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 29, 2026, 12:18 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-label, Parallel-Group Study Comparing the Efficacy and Safety of DACOGEN (Decitabine) for Injection and VIDAZA (Azacitidine) for Injection In Subjects With Intermediate or High Risk Myelodysplastic Syndromes (MDS)

Study identification

NCT ID
NCT01011283
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Eisai Inc.
Industry
Enrollment
26 participants

Conditions and interventions

Interventions

  • azacitidine Drug
  • decitabine Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2009
Primary completion
Dec 31, 2010
Completion
Not listed
Last update posted
Oct 28, 2014

Started 2009

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Birmingham Hematology and Oncology Associates Birmingham Alabama 35205
Stanford University Cancer Center Stanford California 94305
Stockton Hematology Oncology Stockton California 95204
Florida Cancer Specialists Fort Myers Florida 33619
Pasco Pinellas Cancer Center New Port Richey Florida 34652
Gulf Coast Oncology St. Petersburg Florida 33705
University of Chicago Chicago Illinois 60637
Siouxland Haeatology - Oncology Associates Sioux City Iowa 51101
Center for Cancer and Blood Disorders Bethesda Maryland 20817
Sletten Cancer Institute Great Falls Montana 59405
Cornell Medical Center New York New York 10021
Carolinas Medical Center NorthEast NorthEast Oncology Associates Concord North Carolina 28025
Gabrail Cancer Center Canton Ohio 44718
Oncology and Hematology Care Cincinnati Ohio 45242
University of Pittsburgh School of Medicine Pittsburgh Pennsylvania 15232
Charleston Hematology Oncology Associates Charleston South Carolina 29403
Sarah Cannon Cancer Center Nashville Tennessee 37203
Utah Cancer Specialists Salt Lake City Utah 84106
Gunderson Clinic Ltd. La Crosse Wisconsin 54601

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01011283, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 28, 2014 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01011283 live on ClinicalTrials.gov.

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