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Completed Phase 2 Interventional

Safety and Efficacy of Obatoclax Mesylate (GX15-070MS)for the Treatment of Myelodysplastic Syndromes (MDS)

ClinicalTrials.gov ID: NCT00413114

Public ClinicalTrials.gov record NCT00413114. 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 Sep 22, 2026, 9:43 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 II Study of Obatoclax Mesylate (GX15-070MS) in Patients With Previously-Untreated Myelodysplastic Syndromes (MDS) With Anemia and/or Thrombocytopenia

Brief summary

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

Defects in the apoptotic process can lead to the onset of cancer by allowing cells to grow unchecked when an oncogeneic signal is present. Obatoclax is designed to restore apoptosis through inhibition of the Bcl-2 family of proteins, thereby reinstating the natural process of cell death that is often inhibited in cancer cells. This is a multi-center, open-label, Phase II study of obatoclax administered in 2-week cycles to patients with previously-untreated Myelodysplastic Syndromes with anemia and/or thrombocytopenia. Treatment may be administered on an outpatient basis. No investigational or commercial agents or therapies other than those described herein may be administered with the intent to treat the patient's malignancy. Supportive care measures including those directed at controlling symptoms resulting from Myelodysplastic Syndromes are allowed

Study identification

NCT ID
NCT00413114
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gemin X
Industry
Enrollment
24 participants

Conditions and interventions

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 30, 2006
Primary completion
Jan 31, 2009
Completion
Oct 31, 2009
Last update posted
Aug 25, 2013

2006 – 2009

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Stanford University Stanford California 00000
Georgetown University Medical Center Washington D.C. District of Columbia 20007
James A. Haley Veterans Hospital Tampa Florida 33612
Emory University School of Medicine/ Winship Cancer Center Atlanta Georgia 30322
Northwest Georgia Oncology Centers Marietta Georgia 30060
University of Chicago Chicago Illinois 60637
University of Massachusetts Medical Center Worcester Massachusetts 01605
Michigan State University, Breslin Cancer Center CTO Lansing Michigan 48910
Hematology-Oncology Centers of the Northern Rockies Billings Montana 59101
St. Vincent's Comprehensive Cancer Center New York New York 01605
Pacific Oncology Portland Oregon 97210
The West Clinic Memphis Tennessee 38120
Sarah Cannon Cancer Research Institute Nashville Tennessee 37203
Arlington Cancer Center Arlington Texas 76012
Texax Oncology, P.A., Presbyterian/ Mary Crowley Clinical Research Centers Dallas Texas 75231
Mary Crowley Medical Research Center Dallas Texas 75246
MD Anderson Cancer Center (Protocol 2006-0688) Houston Texas 77030

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00413114, 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 Aug 25, 2013 · Synced Sep 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00413114 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →