Drug intelligence / Profile preview

pritelivir

Development stage
Phase 3
Lead developer
AiCuris
Modality
Allosteric Modulators → Classical Binding Small Molecules → Small Molecules, Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

Pritelivir is a direct-acting antiviral small molecule in the thiazolylamide class that inhibits the helicase-primase enzyme complex of herpes simplex virus (HSV), specifically targeting both HSV-1 and HSV-2. By binding to and inhibiting the viral helicase–primase complex (composed of UL5 and UL52 proteins), pritelivir blocks viral DNA replication at an early stage, preventing further expression of early and late viral genes. This mechanism is distinct from nucleoside analogues like acyclovir, as it does not require activation by viral thymidine kinase and remains effective against acyclovir-resistant strains. Pritelivir is being developed primarily for immunocompromised patients with mucocutaneous HSV infections resistant to standard therapies such as acyclovir or foscarnet. The drug is currently in Phase III clinical development by AiCuris Anti-infective Cures AG[1][4][5][7][8].

Other names
pritelivir mesylate
02

Targets

Herpes simplex virus type 2 helicase-primase complex (UL5/UL52/UL8)

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