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Terlipressin & then Dummy

Aga Khan University · FDA-approved active Small molecule Quality 2/100

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

Terlipressin, marketed by Aga Khan University, holds a position in the pharmaceutical market with a key composition patent expiring in 2028. The drug's primary strength lies in its established market presence and ongoing revenue generation. The primary risk is the potential increase in competition following the patent expiry in 2028.

At a glance

Generic nameTerlipressin & then Dummy
Also known asNovapressin
SponsorAga Khan University
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, causing splanchnic vasoconstriction and reducing portal venous pressure. This mechanism is particularly useful in portal hypertension-related bleeding and hepatorenal syndrome, where it improves renal perfusion and reduces variceal bleeding risk. The drug has greater V1 selectivity compared to native vasopressin, resulting in fewer systemic side effects.

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

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