Drug intelligence / Profile preview

conivaptan + furosemide + nesiritide

Development stage
Discontinued
Lead developer
Astellas Pharma
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous
01

Overview

This combination therapy was evaluated in a clinical trial (NCT00806910) sponsored by the Albert Einstein Healthcare Network for the treatment of acute decompensated heart failure (ADHF) and hyponatremia. The regimen consists of **conivaptan**, a dual vasopressin V1A and V2 receptor antagonist; **furosemide**, a loop diuretic; and **nesiritide**, a recombinant human B-type natriuretic peptide (BNP). Conivaptan promotes aquaresis by blocking the V2 receptors in the renal collecting ducts, while furosemide induces natriuresis by inhibiting the Na-K-2Cl symporter in the loop of Henle. Nesiritide acts as a vasodilator and further promotes natriuresis by binding to natriuretic peptide receptor-A. The study aimed to determine if the addition of conivaptan to standard-of-care diuretics and vasodilators would enhance diuresis and improve renal function in patients with significant fluid overload and low sodium levels.

Brand names
VaprisolLasixNatrecor
Other names
o-Albert Einstein Healthcare Network-heart failure
02

Targets

NKCC2 (Sodium-potassium-chloride cotransporter 2)AVPR1A (Arginine vasopressin receptor 1A)NPR1 (Natriuretic peptide receptor 1)AVPR2 (Arginine vasopressin V2 receptor)

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