A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group.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 transcription. It improves immunologic function, partially reverses the HIV-induced neurological dysfunction, and improves certain other clinical abnormalities associated with AIDS. Its principal toxic effect is dose-dependent suppression of bone marrow, resulting in anemia and leukopenia. [PubChem]
Used in combination with other antiretroviral agents for the treatment of human immunovirus (HIV) infections.
George Clinic CRS (30273), Lusaka, Zambia
Makerere University - JHU Research Collaboration (30293), Kampala, Uganda
University of North Carolina Lilongwe (12001), Lilongwe, Malawi
Prapokklao Hosp. CRS, Muang District, Chantaburi, Thailand
Siriraj Hospital Mahidol University CRS, Bangkok, Ratchathewi, Thailand
Chonburi Hosp. CRS, Chonburi, Thailand
JCRC CRS, Kampala, Uganda
Les Centres GHESKIO CRS, Bicentenaire, Port-au-Prince, Haiti
Barranco CRS, Lima, Peru
CEDRA Clinical Research, Austin, Texas, United States
CEDRA Clinical Research, LLC, Austin, Texas, United States
Hospital del Nino, Panama City, Panama
St. Jude Children's Research Hospital, Memphis, Tennessee, United States
Children's Diagnostic and Treatment Center, Inc, Fort Lauderdale, Florida, United States
Hospital Privado Modelo, Buenos Aires, Argentina
Bhumibol Adulyadej Hospital, Saimai, Bangkok, Thailand
Nopparat Rajathanee Hospital, Kannayao, Bangkok, Thailand
Banglamung Hospital, Banglamung, Chonburi, Thailand
Mtubatuba SIckbay, Kwazulu-Natal, South Africa
Umtata Sickbay, Eastaern Cape, South Africa
South African Military Health Services (SAMHS), Centurion, South Africa
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