To evaluate the anti-HIV activity, safety, and tolerance of adefovir dipivoxil ( bis-POM PMEA ) in combination with standard antiretroviral therapy for 48 weeks.
Patients are randomized to receive either adefovir dipivoxil or placebo daily for 24 weeks, after which all patients will receive open-label drug for an additional 24 weeks. Study drug is administered in combination with a current antiretroviral regimen for the entire 48 weeks. Patients are followed every 4 weeks during the first 24 weeks of study, then every 8 weeks during the last 24 weeks.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
400
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Univ of Alabama at Birmingham
Birmingham, Alabama, United States
East Bay AIDS Ctr
Berkeley, California, United States
Kraus Med Partners
Los Angeles, California, United States
San Francisco Gen Hosp
San Francisco, California, United States
Santa Clara Valley Med Ctr
San Jose, California, United States
San Mateo County Med Ctr / San Mateo County AIDS Prog
San Mateo, California, United States
Pacific Oaks Research
Sherman Oaks, California, United States
Harbor UCLA Med Ctr
Torrance, California, United States
Georgetown Univ Med Ctr
Washington D.C., District of Columbia, United States
Institute for Clinical Research
Washington D.C., District of Columbia, United States
...and 17 more locations