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Completed Phase 2 Interventional

Phase 2 Study of Pracinostat With Azacitidine in Patients With Previously Untreated Myelodysplastic Syndrome

ClinicalTrials.gov ID: NCT01873703

Public ClinicalTrials.gov record NCT01873703. 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 Jun 25, 2026, 10:41 AM 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 Phase 2 Randomized Double-Blind Placebo-Controlled Study of Pracinostat in Combination With Azacitidine in Patients With Previously Untreated International Prognostic Scoring System (IPSS) Intermediate Risk-2 or High-Risk Myelodysplastic Syndrome (MDS)

Study identification

NCT ID
NCT01873703
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Helsinn Healthcare SA
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

  • pracinostat Drug
  • Placebo Drug
  • Azacitidine 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
May 31, 2013
Primary completion
Oct 31, 2015
Completion
Oct 31, 2016
Last update posted
Sep 12, 2018

2013 – 2016

United States locations

U.S. sites
24
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
Southern Cancer Center Mobile Alabama 36608
Scripps Cancer Center La Jolla California 92037
Colorado Blood Cancer Institute Denver Colorado 80218
Florida Cancer Specialists South Fort Myers Florida 33916
Woodlands Medical Specialists Pensacola Florida 32503
Florida Cancer Specialists North St. Petersburg Florida 33705
Florida Cancer Specialist and Research Institute Tallahassee Florida 32308
H. Lee Moffitt Cancer Center Tampa Florida 33612
Fort Wayne Medical Oncology and Hematology Fort Wayne Indiana 46804
Indiana University Simon Cancer Ctr Indianapolis Indiana 46202
Sidney Kimmel Comprehensive Cancer at Johns Hopkins Baltimore Maryland 21287
Center for Cancer and Blood Disorders Bethesda Maryland 20817
Henry Ford Hospital Detroit Michigan 48202
Michigan State University Lansing Michigan 48910
Nebraska Methodist Omaha Nebraska 68114
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89148
Weill Cornell Medical Center New York New York 10065
Oncology Hematology Care Cincinnati Ohio 45242
Cleveland Clinic Foundation Cleveland Ohio 44195
Tennessee Oncology - Chattanooga Chattanooga Tennessee 37404
Sarah Cannon Cancer Center, Tennessee Oncology Nashville Tennessee 37203
MD Anderson Cancer Center Houston Texas 77030
Cancer Care Centers of South Texas San Antonio Texas 78229
Swedish Cancer Institute Seattle Washington 98104

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 NCT01873703, 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 Sep 12, 2018 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01873703 live on ClinicalTrials.gov.

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