| 英文摘要 |
As a first-in-class HIV-1 capsid inhibitor, lenacapavir is characterized by a unique antiviral mechanism, which entails interference with multiple stages of the viral life cycle. On the basis of data obtained from two Phase 3 clinical trials (PURPOSE 1 and 2), it was established that compared with daily oral PrEP, long-acting injectable lenacapavir PrEP demonstrated superior efficacy in preventing HIV infection, with no new safety concerns identified. A twice-yearly PrEP option contributes to addressing the challenges associated with adherence to and persistence with daily oral regimens. However, despite its promise in bringing an end to the HIV epidemic, widespread adoption must be accompanied by close surveillance of resistance-associated mutations (RAMs) and their impact on future therapeutic options. |