Oral Valganciclovir Versus Valacyclovir
Completed · Phase 2
Conditions studied: Chronic Lymphocytic Leukemia, Leukemia
In brief
To determine if the rate of cytomegalovirus reactivation during treatment with alemtuzumab (Campath) is reduced by the use of valganciclovir prophylaxis.
Key facts
- Study ID
- NCT00562770
- Run by
- M.D. Anderson Cancer Center
- People needed
- 46
- Starts
- 2003-09-01
- Expected to finish
- 2006-07-01
- Last updated by the study team
- 2012-07-31
Who can join
Age: 16 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients receiving alemtuzumab
- Age > 15
- Signed informed consent form
You may not qualify if…
- Active cytomegalovirus disease or infection. Asymptomatic patients with positive CMV pp65 antigenemia will not be excluded.
- Patients with a creatinine clearance of < 10 ml/min as calculated via the Cockcroft-Gault equation.
Where it is running
- The University of Texas M.D. Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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