Resum
BENCHMRK-1 and -2 are ongoing double-blind phase III studies of raltegravir in patients experiencing failure of antiretroviral therapy with triple-class drug-resistant human immunodeficiency virus infection. At week 96 (combined data), raltegravir (400 mg twice daily) plus optimized background therapy was generally well tolerated, with superior and durable antiretroviral and immunological efficacy, compared with optimized background therapy alone. © 2010 by the Infectious Diseases Society of America. All rights reserved.
| Idioma original | Anglès |
|---|---|
| Pàgines (de-a) | 605-612 |
| Revista | Clinical Infectious Diseases |
| Volum | 50 |
| Número | 4 |
| DOIs | |
| Estat de la publicació | Publicada - 15 de febr. 2010 |
SDG de les Nacions Unides
Aquest resultat contribueix als següents objectius de desenvolupament sostenible.
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ODG 3 – Bona salut i benestar
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