Myelodysplastic Syndrome Clinical Trial

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

Summary

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

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Pathological confirmation of Myelodysplastic Syndromes (MDS)
Patients must have had no prior systemic therapy
Must have normal organ functions
Must have the ability to understand and willingness to sign a written informed consent form

Exclusion Criteria:

Must not be a result of prior chemotherapy and/or radiotherapy for another malignancy
No other agents or therapies administered in the intent to treat
Uncontrolled, intercurrent illness
Pregnant women and women who are breast feeding

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

24

Study ID:

NCT00413114

Recruitment Status:

Completed

Sponsor:

Gemin X

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There are 19 Locations for this study

See Locations Near You

Stanford University
Stanford California, 00000, United States
Georgetown University Medical Center
Washington District of Columbia, 20007, United States
James A. Haley Veterans Hospital
Tampa Florida, 33612, United States
Emory University School of Medicine/ Winship Cancer Center
Atlanta Georgia, 30322, United States
Northwest Georgia Oncology Centers
Marietta Georgia, 30060, United States
University of Chicago
Chicago Illinois, 60637, United States
University of Massachusetts Medical Center
Worcester Massachusetts, 01605, United States
Michigan State University, Breslin Cancer Center CTO
Lansing Michigan, 48910, United States
Hematology-Oncology Centers of the Northern Rockies
Billings Montana, 59101, United States
St. Vincent's Comprehensive Cancer Center
New York New York, 01605, United States
Pacific Oncology
Portland Oregon, 97210, United States
The West Clinic
Memphis Tennessee, 38120, United States
Sarah Cannon Cancer Research Institute
Nashville Tennessee, 37203, United States
Arlington Cancer Center
Arlington Texas, 76012, United States
Texax Oncology, P.A., Presbyterian/ Mary Crowley Clinical Research Centers
Dallas Texas, 75231, United States
Mary Crowley Medical Research Center
Dallas Texas, 75246, United States
MD Anderson Cancer Center (Protocol 2006-0688)
Houston Texas, 77030, United States
Tom Baker Cancer Centre
Calgary Alberta, , Canada
QEII HSC
Halifax Nova Scotia, B3H 2, Canada
Princess Margaret Hospital
Toronto Ontario, M5G 2, Canada
Hospital Notre-Dame du Chum
Montreal Quebec, H2L4M, Canada
Maisonneuve-Rosemont Hospital
Montreal Quebec, , Canada

How clear is this clinincal trial information?

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

24

Study ID:

NCT00413114

Recruitment Status:

Completed

Sponsor:


Gemin X

How clear is this clinincal trial information?

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