A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group.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.
CNPS Hospital, Yaoundé, Cameroon
National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
National Institutes of Health Clinical Center, Bethesda, Maryland, United States
Instituto de Pesquisa Clinica Evandro Chagas (12101), Rio de Janeiro, Brazil
University of North Carolina Lilongwe CRS (12001), Lilongwe, Malawi
Soweto ACTG CRS (12301), Johannesburg, South Africa
Tororo District Hospital, Tororo, Uganda
University of Miami Sylvester Comprehensive Cancer Center - Miami, Miami, Florida, United States
George Clinic CRS (30273), Lusaka, Zambia
Makerere University - JHU Research Collaboration (30293), Kampala, Uganda
University of North Carolina Lilongwe (12001), Lilongwe, Malawi
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