Drug intelligence / Profile preview

adavosertib + omeprazole

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

Overview

Adavosertib + omeprazole is a drug combination primarily utilized in clinical pharmacology studies to evaluate the impact of gastric acid suppression on the pharmacokinetics of adavosertib. Adavosertib (formerly AZD1775 or MK-1775) is a first-in-class, small-molecule inhibitor of the WEE1 kinase, which regulates the G2/M checkpoint in the cell cycle. Because adavosertib exhibits pH-dependent solubility, co-administration with the proton pump inhibitor omeprazole is studied to determine if elevated gastric pH significantly alters the drug's absorption and systemic exposure. These studies are critical for defining dosing recommendations in cancer patients who may require acid-reducing agents.

Other names
AZD1775 + omeprazoleMK-1775 + omeprazole
02

Targets

ATP4A (Potassium–transporting ATPase alpha chain 1)WEE2 (Wee1-like protein kinase 2)WEE1 (WEE1 G2 checkpoint kinase)

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