发明名称 Inhibition of HIV infection through chemoprophyalxis
摘要 A process is provided for protecting a primate host from a self-replicating infection by an immunodeficiency retrovirus. Protection is achieved by administering to the primate host a combination of a pharmaceutically effective amount of a nucleoside reverse transcriptase inhibitor and a pharmaceutically effective amount of a nucleotide reverse transcriptase inhibitor prior to exposure to the immunodeficiency retrovirus. The administration is effective if provided in a single dose within 24 hours of the exposure. A regime of regular daily doses is also effective in providing protection against an immunodeficiency retrovirus becoming self-replicating after infecting a primate host. A process for controlling retrovirus transmission within a population includes the administration to a subpopulation at high risk for contracting an immunodeficiency retroviral infection the detailed combination prior to sexual exposure to a source of immunodeficiency retrovirus so as to preclude the immunodeficiency retrovirus from becoming self-replicating in a member of the subpopulation.
申请公布号 US9579333(B2) 申请公布日期 2017.02.28
申请号 US201514679887 申请日期 2015.04.06
申请人 THE UNITED STATES OF AMERICA, as represented by the Secretary, Department of Health and Human Services 发明人 Heneine Walid;Folks Thomas M.;Janssen Robert;Otten Ronald A.;Garcia Lerma Jose Gerardo
分类号 A61K31/675;A61K31/505;A61F6/06;A61K9/00;A61K31/683;A61K31/513;A61K31/7072;A61K45/06 主分类号 A61K31/675
代理机构 Klarquist Sparkman, LLP 代理人 Klarquist Sparkman, LLP
主权项 1. A process of protecting a primate host from a self-replicating infection by an immunodeficiency retrovirus comprising: (a) selecting a primate host not infected with the immunodeficiency retrovirus, and (b) administering directly to an uninfected primate host a combination comprising: i. a pharmaceutically effective amount of emtricitabine, wherein the pharmaceutically effective amount of the emtricitabine is administered orally, subcutaneously or vaginally; andii. a pharmaceutically effective amount of tenofovir or tenofovir disoproxil fumarate, wherein the pharmaceutically effective amount of the tenofovir or tenofovir disoproxil fumarate is administered orally, subcutaneously or vaginally, and wherein the combination is administered prior to the exposure of the primate host to the immunodeficiency retrovirus, thereby protecting the primate host from infection with the immunodeficiency retrovirus.
地址 Washington DC US