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IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Nesiritide

FDA approved · Rx

Recombinant natriuretic peptide

Also known as: Natrecor, BNP, nesiritida, nesiritidum, Nesiritide Recombinant, Human Brain Natriuretic Factor-32

Evidence score
92/ 100
Strong evidence

Strong, human-grade evidence

  • Regulatory standing. FDA-approved prescription medicine
  • Human trials. Backed by controlled human studies
  • Registered human trials. 289 registered studies on ClinicalTrials.gov, most advanced Phase 4
  • 1 cited source. Includes primary / regulatory sources

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

Nesiritide is a recombinant form of human B-type natriuretic peptide (BNP), a hormone normally released by the heart's ventricles. It binds natriuretic peptide receptors, raising cyclic GMP, which relaxes blood vessels and promotes sodium and water excretion. It was marketed under the brand name Natrecor as an intravenous hospital medicine.

What the evidence shows

Automatic summaryHuman trials

Nesiritide was approved for the treatment of acutely decompensated heart failure with shortness of breath, and it has been studied in hundreds of registered trials, including Phase 4. Large trials such as ASCEND-HF found it modestly eased breathlessness but did not improve survival or rehospitalization. The facts provided here did not confirm a current FDA listing, and the product has reportedly been discontinued in the US, so its present availability is unclear.

Key facts

Molecular formula
C143H244N50O42S4
Molecular weight
3464 g/mol

Registered human trials

Published literature

Sources

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