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Trial on Efficacy and Safety of Pritelivir Tablets for Treatment of Acyclovir-resistant Mucocutaneous HSV (Herpes Simplex Virus) Infections in Immunocompromised Subjects

Testing Pritelivir for Acyclovir-resistant Herpes in Immunocompromised Patients.

Recruiting
16 years and older
All
Phase 3
This study is testing a medicine called **pritelivir** for people with a type of **Herpes Simplex Virus (HSV)** infection that doesn't respond well to a common treatment called **acyclovir**. HSV causes sores on the skin, and this study is for people who have trouble fighting infections, such as those with conditions like **HIV** or who have had organ transplants. Participants will take pritelivir tablets once a day, starting with a larger dose to quickly reach the right level in their blood. The study aims to see if pritelivir works better than other treatments like **foscarnet** or **cidofovir**. It will continue until the sores heal or up to 28 days, with a possible extension to 42 days based on progress. To join, participants must be 16 or older, have a type of HSV that doesn't respond to acyclovir, and meet other health criteria. **Key Points:** - Participants need to take daily medicine for up to 28-42 days. - The study includes regular health checks and specific entry requirements. - This trial is for people who have not responded to traditional HSV treatments. **Eligibility and exclusion criteria should be reviewed thoroughly with the study team to ensure fit.**
Study details
    HSV Infection

NCT03073967

AiCuris Anti-infective Cures AG

5 July 2025

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