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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 Oct 29, 2026, 11:48 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)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to compare the response of patients with Intermediate or High Risk myelodysplastic syndromes (MDS) following treatment with decitabine or azacitidine.

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

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
Nov 2009 (Type not available)
Primary completion
Jan 2011 (Actual)
Completion
Not listed
Last update posted
Oct 29, 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 29, 2014 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01011283 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →