Thalidomide Anti-Angiogenesis Therapy of Relapsed or Refractory Leukemia
Completed · Phase 2
Conditions studied: Leukemia
In brief
The purpose of this study is to evaluate the efficacy and safety of Thalidomide in patients with leukemia.
Key facts
- Study ID
- NCT00083694
- Run by
- University of Arkansas
- People needed
- 25
- Starts
- 1998-08-01
- Expected to finish
- 2005-05-01
- Last updated by the study team
- 2010-07-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- University of Arkansas for Medical Sciences/MIRT — Little Rock, Arkansas, United States
Full record on ClinicalTrials.gov
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