!AS 2025: Once-monthly oral PrEP using MK-8527: the drug that will stop HIV
17 July 2025. Related: Conference reports, Treatment strategies, IAS 13th Kigali 2025.
Simon Collins, HIV i-Base
Another conference highlight included results from a large pharmacokinetic study of MK-8527 which is a follow-on NRTTI to islatravir that is being studied in a once-monthly oral formulation as PrEP. [1]
This was a phase 2 double-blind, multicentre study that randomised 350 adults (2:2:2:1) at low risk of HIV to one of three doses of MK-8527 (3, 6, or 12 mg) or matched placebo, given monthly for six months. This was an international study with sites in Israel, South Africa and the US. Safety follow-up continued for a further 8 weeks.
Baseline characteristics included median age 28 years, 58% women, and 51% white, 41% Black/African American, 2.3% Asian.
Results
Overall, 328/360 (93%) received all six doses and pharmacokinetics were generally dose-proportional.
Tolerability was good with generally mild side effects that were broadly similar in the active and placebo arms. Importantly, given the earlier history with islatravir, there were also no significant differences between arms in changes in total lymphocyte and CD4 counts. One participant in the 6 mg arm, however, discontinued due to grade 1 reductions, including a 36% drop in CD4 count, although they started with a nadir of 313 cells/mm3 and this resolved over several months after discontinuation.
PK results (Tmax and AUC) were dose-proportional with no evidence of the intracellular accumulation of the active triphosphate that led to the discontinuation of islatravir for monthly PrEP. Both the 6 mg and 12 mg doses produced drug exposure above the predicted levels needed for protection, including in PBMCs that persist for a further week, indicating window for dosing. Predicted protective levels were also achieved quickly, perhaps within an hour of dosing.
No HIV acquisitions occurred during the study.
Importantly, these data support further development and two large international phase 3 studies using – apparently using an 11 mg dose – in people at higher risk of HIV are planned to open later in 2025. [2]
EXPRESSIVE 10 will enrol 4580 adolescent girls and young women in Kenya, South Africa and Uganda and EXPRESSIVE 11 will enrol 4390 gay and bisexual men, transgender and non-binary people in Argentina, Brazil, Chile, Columbia, Dominican Republic, France, Guatemala, Kenya, Malaysia, Peru, The Philippines, South Africa, Switzerland, Thailand, USA and Vietnam. [2]
comment
Predictions are always uncertain, but this is the drug that will stop HIV – even if efficacy in phase 3 studies is lower than injectable PrEP.
These preliminary results are very promising, as previous preclinical and early studies with islatravir indicated similar pharmacokinetics that would suggest monthly oral PrEP might also work as PEP.
If effective in phase 3 studies, once-monthly oral PrEP could easily be as highly acceptable as six-monthly injections, and could have greater impact on a population level.
Oral NRTTIs are much easier to manufacture and distribute than injectable drugs, which would also help with generic formulations and global access. A foil strip with 12 small tablets would be innocuous and would cover a year of treatment, perhaps with a 7-day window for the monthly doses.
Single tablets, especially if effective as PEP, could easily broaden to over-the-counter access, with minimal safety risks in ways that would be much more difficult with injections.
Tolerability is so far good based on tiny numbers and date to informa the risk of drug resistance will be important.
References
- Mayer K et al. Safety and pharmacokinetics of MK-8527 oral once-monthly: a phase 2 study in adults at low risk of HIV-1 exposure. IAS 2025, 13-16 July 2025, Kigali, Rwanda. Oral late-breaker abstract OAS0106LB.
https://programme.ias2025.org/Abstract/Abstract/?abstractid=6515 - EXPRESSIVE 10 and EXPRESSIVE 11.