Status:
TERMINATED
A Study of Oral Clofarabine in Adult Patients With Myelodysplastic Syndromes (MDS)
Lead Sponsor:
Genzyme, a Sanofi Company
Conditions:
Myelodysplastic Syndromes
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
This study will be used to determine the maximum tolerated dose of oral clofarabine when administered daily for 14 consecutive days repeated every 21 days.
Eligibility Criteria
Inclusion
- Provide signed, written informed consent.
- Be at least 18 years old.
- Have a pathologically confirmed MDS and score according to the IPSS at study entry. Pathologic confirmation is the responsibility of the investigator.
- Have been treated previously for MDS as follow: a.Patients must have had at least 1, but no more than 2, prior treatment regimens; b.Patients must not have refractory (i.e., disease progression or no evidence of response while on treatment) to more than 1 prior treatment regimen.
- Have Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- Be able to comply with study procedures and follow-up examinations.
- Have adequate hepatic and renal function.
- Be non-fertile or agree to use birth control during the study through the end of the last treatment visit and at least 90 days after.
Exclusion
- Have had a readjustment of dose and/or schedule of erythropoietin, granulocyte colony stimulating factor(G-CSF) or other growth factors within 8 weeks prior to the first dose of oral clofarabine.
- Have had any other chemotherapy or any investigational therapy for MDS within 4 weeks of the first dose of oral clofarabine.
- Have not recovered to ≤ Grade 2 in severity of any drug-related non-hematologic toxicity prior to the first dose of oral clofarabine.
- Have an uncontrolled systemic fungal, bacterial, viral or other infection. Have a history of serious disease involving the heart.
- Have a clinically significant cardiac assessment at screening or a known family history QT prolongation.
- Currently uses a medication known to prolong the QT interval.
- Have had any prior treatment with clofarabine (IV or oral).
- Have had a diagnosis of another malignancy, unless the patient has been disease free for at least 3 years after completing curative intent therapy except for the following: a. Patients with treated non-melanoma skin cancer, in situ carcinoma, or cervical intraepithelial neoplasia, regardless of the disease-free duration, are eligible for this study if definitive treatment or the condition has been completed. b. Patients with organ-confined prostate cancer with no evidence of recurrent or progressive disease based on prostate specific antigen (PSA) values are also eligible for this study if hormonal therapy has been initiated or a radical prostatectomy has been performed.
- Have prior positive test for the human immunodeficiency virus (HIV).
- Have gastrointestinal disease or prior surgery, which may affect the ability of the patient to absorb oral clofarabine.
- Is currently participating in another concurrent investigational protocol that is not restricted to data and/or sample collection for patient demographic and/or disease purposes.
Key Trial Info
Start Date :
September 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2008
Estimated Enrollment :
2 Patients enrolled
Trial Details
Trial ID
NCT00750334
Start Date
September 1 2008
End Date
October 1 2008
Last Update
May 21 2015
Active Locations (3)
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1
Malignant Hematology Administration, H. Lee Moffitt Cancer Center
Tampa, Florida, United States
2
Division of Hematology Mayo Clinic
Rochester, Minnesota, United States
3
Cancer Care Centers of South Texas
San Antonio, Texas, United States