Gilead Sciences stock gains fresh support from HIV prevention data
π Gilead Sciences reported that 85.6% of participants in the PURPOSE 5 study remained persistent on twice-yearly lenacapavir at Week 52, significantly outperforming the 46.3% persistence rate of daily oral F/TDF.
π‘οΈ The Phase 2 trial showed zero HIV acquisitions among patients receiving lenacapavir, compared to one acquisition in the F/TDF group where drug levels were low.
π Gilead's data supports its long-acting HIV prevention strategy by demonstrating that a six-month dosing schedule improves continuity over daily oral regimens.
π The study enrolled patients in the UK and France who needed pre-exposure prophylaxis but were not taking PrEP at enrollment.
π₯ Gilead is presenting additional evidence for Biktarvy and investigational once-weekly or twice-yearly injectable treatments at the HIV Glasgow 2026 congress.
π° Gilead Sciences stock traded at 151.69 euros on November 10, 2026, following the release of the positive clinical data.
- Gilead Sciences demonstrated superior persistence in its Phase 2 PURPOSE 5 study, with 85.6% of patients remaining adherent to twice-yearly lenacapavir versus 46.3% for daily oral F/TDF at Week 52.
- The company reported zero HIV acquisitions in the lenacapavir group compared to one in the control group, validating the efficacy of its long-acting injectable prevention strategy.
- Fresh clinical evidence strengthens Gilead's long-acting HIV portfolio by addressing adherence constraints that limit real-world effectiveness of daily oral regimens.