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RenalFDA Approved

Desmopressin (DDAVP)

Overview

A synthetic analog of vasopressin with enhanced V2 receptor selectivity and minimal V1a vasopressor activity. Desmopressin has a deaminated cysteine at position 1 and D-arginine at position 8, increasing its antidiuretic potency 10-fold while largely eliminating the hypertensive effects of native vasopressin. Its prolonged half-life of 2-4 hours (vs. 10-20 minutes for vasopressin) allows convenient dosing for chronic conditions.

Key Research Findings

FDA-approved for central diabetes insipidus, primary nocturnal enuresis, hemophilia A, and von Willebrand disease (type 1). Releases stored von Willebrand factor and factor VIII from endothelial Weibel-Palade bodies. DDAVP challenge test used to assess coagulation factor response pre-procedurally. Risk of hyponatremia with fluid overloading requires careful monitoring, especially in elderly patients.

Route of Administration

Intranasal, Oral, Subcutaneous injection, Intravenous

Regulatory Status

FDA Approved

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