A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA during reverse tran...
Used in combination with other antiretroviral agents for the treatment of human immunovirus (HIV) infections.
National Pediatric Hosp., Cambodia CIPRA CRS, Phnom Penh, Cambodia
Social Health Clinic, Cambodia CIPRA CRS, Phnom Penh, Cambodia
Prapokklao Hosp. CIPRA CRS, Chantaburi, Thailand
Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office, Bethesda, Maryland, United States
St. Vincent's Hospital, Sydney, New South Wales, Australia
Boehringer Ingelheim Investigational Site, Soweto, South Africa
Academic Medical Center, Amsterdam, NH, Netherlands
College of Medicine, Blantyre, Malawi
Siriraj Hospital Mahidol University CRS, Bangkok, Bangkoknoi, Thailand
Bhumibol Adulyadej Hosp. CRS, Saimai, Bangkok, Thailand
Chiangrai Prachanukroh Hospital CRS, Chiangrai, Thailand
Columbia IMPAACT CRS, New York, New York, United States
Chicago Children's CRS, Chicago, Illinois, United States
SUNY Stony Brook NICHD CRS, Stony Brook, New York, United States
Miller Children's Hospital, Long Beach, California, United States
Hospital Fêmina S.A. Unidade Perinatal de Transmissão Vertical, Porto Alegre, Rio Grande do Sul, Brazil
University of FL, Gainesville, Florida, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.