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desmopressin tablet

University Hospital, Ghent · FDA-approved 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 (bedwetting), Polycystic kidney disease (adjunctive).

At a glance

Generic namedesmopressin tablet
Also known asDDAVP
SponsorUniversity Hospital, Ghent
Drug classVasopressin analog; antidiuretic agent
TargetV2 vasopressin receptor
ModalitySmall molecule
Therapeutic areaEndocrinology; Urology
PhaseFDA-approved

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 reduces urine volume and increases urine osmolality. It has minimal vasopressor activity compared to native vasopressin due to its selectivity for V2 over V1 receptors.

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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