Status:
COMPLETED
Vosaroxin and Azacitidine in Treating Patients With Myelodysplastic Syndromes
Lead Sponsor:
Washington University School of Medicine
Collaborating Sponsors:
Sunesis Pharmaceuticals
Conditions:
Myelodysplastic Syndromes
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
This phase I trial studies the side effects and the best dose of vosaroxin when given together with azacitidine in treating patients with myelodysplastic syndromes. Drugs used in chemotherapy, such as...
Eligibility Criteria
Inclusion
- Diagnosis of myelodysplastic syndrome and one of the following:
- Cytopenias requiring red blood cell and/or platelet transfusions or neutropenia (ANC \<1 X109/L)
- IPSS score of INT-1 or higher at screening
- MDS with excess blasts in transformation as defined by FAB criteria (20-29% bone marrow blasts) or
- Chronic myelomonocytic leukemia
- Age ≥18 years old
- Adequate renal and hepatic function defined as all of the following:
- total bilirubin ≤ 2.0 mg/dl, except in cases of Gilbert's disease;
- AST and ALT ≤2.5 institutional ULN;
- serum creatinine within normal institutional limits or estimated creatinine clearance ≥60 mL/min/1.73 m2 by the Cockcroft-Gault equation
- ECOG performance status ≤2
- Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).
- Females must be surgically or biologically sterile or postmenopausal or if of childbearing potential, must agree to use an adequate method of contraception during the study until 30 days after the last treatment. Males must be surgically or biologically sterile or agree to use an adequate method of contraception during the study until 30 days after the last treatment. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.
- Patients may have received up to 3 prior cycles of hypomethylator therapy (i.e. decitabine or azacitidine) prior to enrollment and may have received supportive care measures (growth factors, erythropoietin stimulating agents, transfusion, etc.
- Either enrolled in HRPO# 201011766 ("Tissue Acquisition for Analysis of Genetic Progression Factors in Hematologic Diseases"), which facilitates collection of blood, bone marrow, and skin for correlative studies, or consents to collection of blood, bone marrow, and skin as part of this protocol.
Exclusion
- Prior treatment with four or more cycles of hypomethylator therapy.
- Receiving concomitant chemotherapy, radiation therapy, or immunotherapy during the duration of treatment on protocol.
- Known seropositivity for or active viral infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV). Patients who are seropositive because of hepatitis B virus vaccine are eligible. Patients who are seropositive for HCV, but have a negative viral load are also eligible. Documentation that the patients have completed a course of therapy for HCV is required and will be obtained.
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- Pregnant and/or breastfeeding.
Key Trial Info
Start Date :
November 22 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 29 2024
Estimated Enrollment :
35 Patients enrolled
Trial Details
Trial ID
NCT01913951
Start Date
November 22 2013
End Date
April 29 2024
Last Update
May 2 2024
Active Locations (1)
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1
Washington University School of Medicine
St Louis, Missouri, United States, 63110