Drug intelligence / Profile preview

esomeprazole + pritelivir

Development stage
Unknown
Lead developer
AiCuris
Modality
Small Molecules
Administration
Oral
01

Overview

The combination of esomeprazole and pritelivir is primarily investigated in clinical pharmacology studies to evaluate drug-drug interactions, specifically the impact of gastric acid suppression on the pharmacokinetics of pritelivir. **Pritelivir** (formerly AIC316) is a first-in-class, potent small molecule inhibitor of the viral helicase-primase enzyme complex, developed by **AiCuris** for the treatment of herpes simplex virus (HSV) infections, including acyclovir-resistant strains. **Esomeprazole** is a proton pump inhibitor (PPI) and the S-isomer of omeprazole, which reduces gastric acid secretion by inhibiting the H+/K+-ATPase pump in parietal cells. Phase 1 trials (e.g., NCT02846311) have utilized this combination to determine if the increased gastric pH induced by esomeprazole affects the absorption and systemic exposure of pritelivir, which is critical for optimizing dosing in patients who may be co-prescribed acid-reducing therapies.

Other names
esomeprazole and pritelivirpritelivir and esomeprazole
02

Targets

ABCG2 (Breast cancer resistance protein)SLCO2B1 (Organic anion transporting polypeptide 2B1)Herpes simplex virus type 2 helicase-primase complex (UL5/UL52/UL8)CYP3A4 (Cytochrome P450 3A4)CYP2B6 (Cytochrome P450 2B6)CYP2C9 (Cytochrome P450 family 2 subfamily C member 9)CYP2C8 (Cytochrome P450 2C8)

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