Expired Study
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Little Rock, Arkansas 72205


Purpose:

The purpose of this study is to evaluate the efficacy and safety of Thalidomide in patients with leukemia.


Study summary:

Patients will take Thalidomide tablets at bedtime daily until remission. The dose will be increased gradually and modified according to side-effects. The drug will be given daily up to the time of complete remission then as long as it is beneficial.


Criteria:

Inclusion Criteria: - Diagnosis of refractory or relapsed leukemia: acute leukemia, CML, CLLm and MDS. - Signed informed consent, including patient agreeing to use safe contraceptive methods during the treatment and for at least 4 months after the treatment is completed - Serum creatinine < or = 2.5mg/dL - Serum bilirubin< or = 2.5mg/dL - Negative pregnancy test - Age 18 years or older - Performance status < or = 3 Exclusion Criteria: - Pregnant or lactating women - Concurrent treatment with cytotoxic chemotherapy, or radiation - History of seizures, neurotoxicity, or active CNS disease - Serious infections not controlled by antibiotics


NCT ID:

NCT00083694


Primary Contact:

Principal Investigator
Barthel Barlogie, M.D., Ph.D.
UAMS


Backup Contact:

N/A


Location Contact:

Little Rock, Arkansas 72205
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 16, 2017

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