Paper Details 
Original Abstract of the Article :
OBJECTIVE: To review the efficacy and safety of fostemsavir (FTR) for the treatment of multidrug-resistant HIV-1 infection in heavily treatment-experienced adults who are failing their current antiretroviral regimen. DATA SOURCES: Clinical trials and review articles were obtained through PubMed (20...See full text at original site
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引用元:
https://doi.org/10.1177/1060028020962424

データ提供:米国国立医学図書館(NLM)

Fostemsavir: A Novel Attachment Inhibitor for Patients With Multidrug-Resistant HIV-1 Infection

Fostemsavir (FTR) is a novel antiretroviral medication that prevents HIV-1 from attaching to the host CD4 receptor. This study reviews the efficacy and safety of FTR for the treatment of multidrug-resistant HIV-1 infection in heavily treatment-experienced adults who are failing their current antiretroviral regimen. The authors provide a comprehensive overview of FTR's mechanism of action, clinical trial results, and adverse event profile.

FTR for Multidrug-Resistant HIV-1 Infection

The study found that FTR was effective in achieving viral suppression for patients with multidrug-resistant HIV-1 infection who were refractory to other agents. FTR was generally well-tolerated, with few significant interactions, and neither renal nor hepatic dose adjustments were required. This suggests that FTR is a promising treatment option for patients with multidrug-resistant HIV-1 infection.

Managing Multidrug-Resistant HIV-1 Infection

Managing multidrug-resistant HIV-1 infection requires a multidisciplinary approach, involving specialists in infectious diseases, virology, and pharmacy. FTR represents a valuable addition to the therapeutic arsenal for treating this challenging condition.

Dr. Camel's Conclusion

This study, like a shimmering mirage in the desert of HIV treatment, highlights the emergence of new and promising therapies. FTR offers a novel approach to tackling multidrug-resistant HIV-1 infection, providing hope for patients who have exhausted other treatment options.

Date :
  1. Date Completed 2021-08-19
  2. Date Revised 2021-08-19
Further Info :

Pubmed ID

32964736

DOI: Digital Object Identifier

10.1177/1060028020962424

Related Literature

SNS
PICO Info
in preparation
Languages

English

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