A Pilot Study of the Effect of Cidofovir for the Treatment of Progressive Multifocal Leukoencephalopathy (PML) in Subjects With Acquired Immunodeficiency Syndrome (AIDS)
Cidofovir
+ Probenecid
Infectious Encephalitis+27
+ Blood-Borne Infections
+ Neuroinflammatory Diseases
Treatment Study
Summary
PML is a demyelinating disease of the brain's white matter, occurring when the JC virus infects the brain of patients infected with HIV-1. Cidofovir is known to be an effective treatment for cytomegalovirus of the eye and, in laboratory and animal testing, has also been shown to be effective against several other viruses. However, cidofovir is considered investigational as a treatment for PML. In this multicenter, open-label study 24 patients receive cidofovir iv over 1 hr on days 0, 7, then every 2 wk for a total of 13 doses. Oral probenecid is given 3h prior to and 2h and 8h following cidofovir administration. Nucleoside and non-nucleoside reverse transcriptors are withheld on days of probenecid administration. Protease inhibitors are continued during probenecid administration.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.24 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria You may be eligible for this study if you: Are HIV-positive. Have had symptoms of PML for no more than 90 days before study entry, or have had abnormal neurological exams related to PML. Have negative tests for bacterial or fungal infections. Agree to practice abstinence or use effective methods of birth control during the study. Are at least 18 years old. Have a life expectancy of at least 6 months. Exclusion Criteria You will not be eligible for this study if you: Have a history of uveitis. Are allergic to sulfa drugs or probenecid. Have had active opportunistic infections other than Kaposi's sarcoma within 30 days before study entry. Have sickle cell anemia or trait. Are pregnant or breast-feeding.
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 19 locations
Univ of Alabama at Birmingham
Birmingham, United StatesOpen Univ of Alabama at Birmingham in Google MapsSan Francisco AIDS Clinic / San Francisco Gen Hosp
San Francisco, United StatesSan Francisco Gen Hosp
San Francisco, United StatesUniv of Colorado Health Sciences Ctr
Denver, United States