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terlipressin (vasoconstrictor)

National Science and Technology Council, Taiwan · FDA-approved active Small molecule

Terlipressin is a vasopressin analog that selectively activates V1 receptors on vascular smooth muscle to cause vasoconstriction and reduce portal pressure.

Terlipressin is a vasopressin analog that selectively activates V1 receptors on vascular smooth muscle to cause vasoconstriction and reduce portal pressure. Used for Acute variceal bleeding in patients with portal hypertension, Prevention of rebleeding from esophageal varices, Hepatorenal syndrome.

At a glance

Generic nameterlipressin (vasoconstrictor)
Also known asvasoconstrictor
SponsorNational Science and Technology Council, Taiwan
Drug classVasopressin analog
TargetVasopressin V1 receptor
ModalitySmall molecule
Therapeutic areaGastroenterology / Hepatology
PhaseFDA-approved

Mechanism of action

Terlipressin binds to vasopressin V1 receptors on blood vessels, triggering vasoconstriction that reduces splanchnic blood flow and portal venous pressure. This mechanism is particularly useful in portal hypertension-related conditions where elevated portal pressure drives complications such as variceal bleeding. The drug has greater V1 selectivity and longer duration of action compared to native vasopressin.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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