Efficacy and Safety Profile of Fostemsavir for the Treatment of People with Human Immunodeficiency Virus-1 (HIV-1): Current Evidence and Place in Therapy

Autor: Muccini C, Canetti D, Castagna A, Spagnuolo V
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Drug Design, Development and Therapy, Vol Volume 16, Pp 297-304 (2022)
Druh dokumentu: article
ISSN: 1177-8881
Popis: Camilla Muccini,1,2,* Diana Canetti,2,* Antonella Castagna,1,2 Vincenzo Spagnuolo2 1School of Medicine, Vita-Salute San Raffaele University, Milan, Italy; 2Unit of Infectious Diseases, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) San Raffaele Hospital, Milan, Italy*These authors contributed equally to this workCorrespondence: Vincenzo SpagnuoloUnit of Infectious Diseases, IRCCS Ospedale San Raffaele, Via Stamira d’Ancona 20, Milan, Italy, Tel +390226437907, Fax +390226437903, Email spagnuolo.vincenzo@hsr.itAbstract: Heavily-treatment-experienced people living with human immunodeficiency virus (HTE-PLWH) represent a population with limited therapeutic options and at high-risk of clinical progression, morbidity, and mortality. The development of new drugs and new drug classes for the treatment of HIV-1 infection in HTE-PLWH is critical to successfully suppress HIV-1 replication, restore the immune system, and improve quality of life. Fostemsavir is the first attachment inhibitor approved by Food and Drug Administration and European Medicines Agency for the treatment of HIV-1 infection. It is approved in combination with other antiretrovirals, for HTE-PLWH with multi-drug resistant HIV-1 after failing their current antiretroviral regimen due to resistance, intolerance, or safety considerations. In this review, we present and discuss the mechanism of action, the pharmacodynamic and pharmacokinetic properties, and the efficacy and safety of fostemsavir as an antiretroviral agent for the treatment of HIV-1 infection.Keywords: fostemsavir, attachment inhibitor, human immunodeficiency virus, heavily treatment experienced, drug resistance
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