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somatostatin or terlipressin

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

Somatostatin and terlipressin are vasoactive peptides that bind to somatostatin receptors and vasopressin receptors respectively, reducing splanchnic blood flow and portal pressure.

Somatostatin and terlipressin are vasoactive peptides that bind to somatostatin receptors and vasopressin receptors respectively, reducing splanchnic blood flow and portal pressure. Used for Acute variceal bleeding in portal hypertension, Prevention of variceal rebleeding.

At a glance

Generic namesomatostatin or terlipressin
Also known assomatostatin and terlipressin are vasoconstrictors.
SponsorNational Science and Technology Council, Taiwan
Drug classVasoactive peptide
TargetSomatostatin receptors (SSTR) / Vasopressin V1 receptor
ModalitySmall molecule
Therapeutic areaGastroenterology / Hepatology
PhaseFDA-approved

Mechanism of action

Somatostatin is a naturally occurring inhibitory peptide that binds to somatostatin receptors (SSTR1-5) on vascular smooth muscle and endothelial cells, causing vasoconstriction of splanchnic vessels and reducing portal venous inflow. Terlipressin is a selective vasopressin V1 receptor agonist that causes systemic and splanchnic vasoconstriction, increasing systemic vascular resistance and reducing portal pressure. Both agents are used acutely to control variceal bleeding by decreasing portal hypertension.

Approved indications

Common side effects

Key clinical trials

Primary sources

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