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. 2023 Sep 26;12(9):2321–2335. doi: 10.1007/s40121-023-00870-6
Why carry out this study?
Heavily treatment-experienced (HTE) individuals with HIV-1 have limited therapeutic options, and new antiretroviral drug classes are needed for this population.
Efficacy and safety of fostemsavir + optimized background therapy (OBT) have previously been evaluated through 96 weeks; here, we report long-term efficacy and safety of fostemsavir + OBT in HTE adults with multidrug-resistant HIV-1 from the phase 3 BRIGHTE trial.
What was learned from this study?
A population with advanced disease and multidrug-resistant HIV-1 was able to achieve durable virologic responses and clinically meaningful improvements in CD4+ T-cell count and CD4+/CD8+ ratio on treatment with fostemsavir + OBT.
The safety and tolerability profile of fostemsavir + OBT remained consistent with prior observations through 96 weeks, with no new safety trends.
Long-term results provide further support for fostemsavir as a key therapeutic option for HTE people with multidrug-resistant HIV-1.