Assuntos
Infecções por Coronavirus/tratamento farmacológico , Infecções por Coronavirus/prevenção & controle , Colaboração Intersetorial , Pandemias/prevenção & controle , Pneumonia Viral/tratamento farmacológico , Pneumonia Viral/prevenção & controle , Vacinas Virais , Betacoronavirus , COVID-19 , Vacinas contra COVID-19 , Indústria Farmacêutica , Humanos , National Institutes of Health (U.S.) , SARS-CoV-2 , Fatores de Tempo , Estados Unidos , United States Food and Drug Administration , Tratamento Farmacológico da COVID-19RESUMO
Investment, collaboration, and coordination have been key.
Assuntos
Pesquisa Biomédica , COVID-19 , Humanos , Pesquisa Biomédica/economia , Pesquisa Biomédica/tendências , COVID-19/prevenção & controle , COVID-19/terapia , National Institutes of Health (U.S.) , Investimentos em Saúde , Cooperação Internacional , Vacinas contra COVID-19 , Ensaios Clínicos como AssuntoRESUMO
Ideally, an anti-HIV drug should (1) be highly active against wild-type and mutant HIV without allowing breakthrough; (2) have high oral bioavailability and long elimination half-life, allowing once-daily oral treatment at low doses; (3) have minimal adverse effects; and (4) be easy to synthesize and formulate. R278474, a new diarylpyrimidine (DAPY) non-nucleoside reverse transcriptase inhibitor (NNRTI), appears to meet these criteria and to be suitable for high compliance oral treatment of HIV-1 infection. The discovery of R278474 was the result of a coordinated multidisciplinary effort involving medicinal chemists, virologists, crystallographers, molecular modelers, toxicologists, analytical chemists, pharmacists, and many others.