Efficacy and safety results from the Phase 2 clinical trial of pritelivir versus foscarnet for treatment of acyclovir-refractory and/or resistant mucocutaneous HSV infections in immunocompromised subjects

Document Type

Conference Proceeding

Publication Date

1-11-2026

Publication Title

Open Forum Infect Dis

Keywords

aciclovir, foscarnet, pritelivir, valaciclovir, adult, adverse device effect, adverse drug reaction, conference abstract, controlled study, drug combination, drug resistance, drug therapy, drug withdrawal, electrolyte disturbance, epithelization, female, Food and Drug Administration, graft recipient, healing rate, herpes simplex, Herpes simplex virus, Herpes simplex virus 2, hospitalization, human, Human alphaherpesvirus 1, Human immunodeficiency virus infection, loading drug dose, male, multicenter study, nephrotoxicity, oral drug administration, phase 2 clinical trial, phase 3 clinical trial, randomized controlled trial, side effect, therapy, virus shedding

Abstract

Background: Treatment of herpes simplex viruses (HSV-1 or HSV-2) mucocutaneous infections in the immunocompromised (IC) host can be difficult due to refractory and/or acyclovir-resistant (ACV R/R) infection. Drug-resistant HSV infection occurs in up to 14% of hematopoietic cell transplant recipients and up to 7% in persons with HIV infection. Foscarnet is the only FDA-approved agent for ACV R/R HSV infection. While effective, foscarnet is associated with significant toxicity including nephrotoxicity and electrolyte disturbances necessitating hospitalization for treatment. Pritelivir is an investigational novel viral helicase primase inhibitor active against ACV and foscarnet-resistant HSV. Pritelivir showed a statistically significant reduction in viral shedding and clinical lesions in healthy persons with genital HSV-2 infection, compared to valacyclovir. We report the efficacy and safety of oral pritelivir versus foscarnet in a Phase 2 randomized, open label, multi-center comparative trial for the treatment of ACV R/R HSV in IC host; additional subjects received open label pritelivir for foscarnet resistant /intolerance (R/I) infection. Methods: In Part A, immunocompromised adult subjects with ACV-R/R HSV infection were randomized (2:1) to oral pritelivir (100 mg orally once daily, following a loading dose of 400 mg on Day 1) or IV foscarnet (120mg/kg/day divided every 8 or 12 hrs) for up to 28 days. In Part B, subjects with foscarnet R/I infection received open label pritelivir. Healing rate defined as complete epithelization of lesions, and safety were assessed up to Day 28. Results: In Part A, 22 subjects were randomized, n=15 to pritelivir and n=7 to foscarnet. Part B enrolled 8 subjects. 40% of patients were immunocompromised due HIV and 47% due to transplant. In Part A, 14 of 15 (93%) in the pritelivir arm and 4 of 7 (57%) in the foscarnet arm healed (95% CI -10,74), (p=0.0766). In Part B, 5 of 8 (62.6%) with foscarnet R/I HSV infection healed. Treatment emergent adverse events leading to drug discontinuation were more common for foscarnet (43%) versus pritelivir (4%). Conclusion: Pritelivir represents a promising oral anti-HSV agent for the treatment of refractory or resistant HSV infection in immunocompromised patients and is currently in a Phase 3 trial (NCT03073967).

Volume

13

First Page

S57

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