Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Pritelivir** is an orally administered, direct-acting antiviral small molecule and first-in-class herpes simplex virus helicase-primase inhibitor. It inhibits the HSV helicase-primase complex required for viral DNA replication, with activity against HSV-1 and HSV-2, including strains resistant to nucleoside analogues such as acyclovir and strains with reduced susceptibility to foscarnet. Originally discovered at Bayer and subsequently developed by AiCuris, pritelivir was approved by the FDA in October 2026 as Hovilpri for immunocompromised adults with mucocutaneous HSV lesions refractory, with or without documented resistance, to acyclovir, valacyclovir, or famciclovir. The approved oral regimen is a 400 mg loading dose on day 1 followed by 100 mg once daily until lesions heal.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on pritelivir.