Last reviewed · How we verify

Intravenous Esomeprazole

Chinese University of Hong Kong · Phase 3 active Small molecule

Intravenous esomeprazole inhibits gastric acid secretion by blocking the proton pump in parietal cells of the stomach.

Intravenous esomeprazole inhibits gastric acid secretion by blocking the proton pump in parietal cells of the stomach. Used for Acute gastroesophageal reflux disease (GERD), Peptic ulcer disease, Stress ulcer prophylaxis in critically ill patients.

At a glance

Generic nameIntravenous Esomeprazole
Also known asIV, nexium
SponsorChinese University of Hong Kong
Drug classProton pump inhibitor (PPI)
TargetH+/K+-ATPase (proton pump)
ModalitySmall molecule
Therapeutic areaGastroenterology
PhasePhase 3

Mechanism of action

Esomeprazole is the active S-enantiomer of omeprazole, a proton pump inhibitor (PPI). It irreversibly binds to and inhibits the H+/K+-ATPase enzyme on the secretory surface of gastric parietal cells, thereby suppressing both basal and stimulated gastric acid production. The intravenous formulation provides rapid onset of action for acute acid-related conditions.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: