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Desmopressin Injectable Solution

Hamilton Health Sciences Corporation · Phase 3 active Small molecule

Desmopressin is a synthetic vasopressin analog that binds to V2 receptors on kidney collecting duct cells to increase water reabsorption and reduce urine output.

Desmopressin is a synthetic vasopressin analog that binds to V2 receptors on kidney collecting duct cells to increase water reabsorption and reduce urine output. Used for Central diabetes insipidus, Nocturnal enuresis, Von Willebrand disease.

At a glance

Generic nameDesmopressin Injectable Solution
Also known asDDAVP
SponsorHamilton Health Sciences Corporation
Drug classVasopressin analog
TargetV2 receptor (vasopressin receptor 2)
ModalitySmall molecule
Therapeutic areaEndocrinology
PhasePhase 3

Mechanism of action

Desmopressin mimics the action of endogenous antidiuretic hormone (ADH/vasopressin) by selectively activating V2 receptors in the renal collecting ducts, promoting aquaporin-2 water channel insertion and increasing water reabsorption. This mechanism reduces polyuria and increases urine osmolality, making it effective for conditions characterized by insufficient endogenous ADH or impaired renal response to ADH.

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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