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Clinical Peptide Medicines

Nesiritide

Also referenced as: Natrecor

A recombinant B-type natriuretic peptide with historical heart-failure approval and subsequent withdrawal of approval.

Evidence grade
CEarly Human Research

Early Human Research

Regulatory status
Not FDA Approved

Natrecor was historically FDA-approved for a defined acute heart-failure indication; its approval was withdrawn effective June 15, 2020 and the product was discontinued.

Human data
Yes

Registered clinical trials exist

Last reviewed
October 27, 2026

Overview

A recombinant B-type natriuretic peptide with historical heart-failure approval and subsequent withdrawal of approval.

Natrecor was historically FDA-approved for a defined acute heart-failure indication; its approval was withdrawn effective June 15, 2020 and the product was discontinued.

Natrecor was approved, then discontinued; approval was withdrawn at the sponsor’s request in 2020. That history does not itself prove a safety-based withdrawal.

Why It's Being Studied

  • Acute decompensated heart failure
  • Natriuretic peptide signalling

Mechanism of Action

In plain language

Natriuretic peptide receptor activation increases cyclic GMP, producing vascular and renal physiological effects.

Technical detail

Natriuretic peptide receptor activation increases cyclic GMP, producing vascular and renal physiological effects. Natrecor was approved, then discontinued; approval was withdrawn at the sponsor’s request in 2020. That history does not itself prove a safety-based withdrawal.

Interactive diagram

From molecular target to clinical evidence

Tap each stage to see what happens.

Molecular target: Identify the receptor, enzyme, microbial membrane or binding site for the particular compound.

Background: Clinical Peptide Medicines

Clinical peptide medicines include endocrine treatments, antimicrobial drugs, receptor blockers and targeted diagnostic or cancer agents. They do not share one mechanism or one set of indications.

An approval belongs to a specific medicine and indication. A diagnostic tracer, an antibiotic and a hormone are not interchangeable wellness products; read each profile's own mechanism and prescribing source.

Research Areas & Routes Studied

Areas studied
  • Acute decompensated heart failure
  • Natriuretic peptide signalling
Routes used in research
  • Historical intravenous medicine

Evidence Summary

ASCEND-HF did not reduce death or readmission and did not meet its prespecified dyspnea-benefit criterion.

Evidence pyramid

Higher tiers carry more weight. Filled tiers have evidence for Nesiritide; tap to read it.

Human clinical trials
  • ASCEND-HF did not reduce death or readmission and did not meet its prespecified dyspnea-benefit criterion.
Source breakdown

2 cited sources.

  • Regulatory document1
  • Randomised controlled trial1

Human clinical evidence

  • ASCEND-HF did not reduce death or readmission and did not meet its prespecified dyspnea-benefit criterion.

Reported Adverse Events in Research

  • Hypotension increased in clinical research and may be clinically significant.

Limitations of Current Evidence

  • Natrecor was approved, then discontinued; approval was withdrawn at the sponsor’s request in 2020. That history does not itself prove a safety-based withdrawal.
  • Findings apply to the product, route and population studied; they do not establish benefits or safety for unrelated wellness uses or research-vial products.

How to Read This Research

Questions to ask
  • Is this a single molecule or a family of medicines?
  • Is the use diagnostic, therapeutic or investigational?
  • Does the quoted outcome match the exact product, formulation and population?
Reading tips
  • Use the compound-specific mechanism above; this diagram describes drug development, not a shared biological pathway.
  • Historical approval, present availability and off-label use are distinct questions.
  • For radiopharmaceuticals and hospital medicines, specialist handling is part of the treatment context.
Indication
The condition and population for which a medicine is approved.
Antagonist
A compound that blocks activity at a receptor.
Radiopharmaceutical
A medicine containing a radioactive isotope for imaging or treatment.

Compare With Other Compounds

Compare side by side
NesiritideTrofinetide
Evidence gradeC — Early Human ResearchB — Moderate Human Evidence
Regulatory statusNot FDA ApprovedFDA Approved for Specific Indication
Human dataYesYes
Clinical trialsRegistered trials existRegistered trials exist
Research routesHistorical intravenous medicineOral approved medicine
Cited sources22
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Frequently Asked Questions

Research References

  • Regulatory document

    Nesiritide — regulatory document

    View Source
  • Randomised controlled trial

    ASCEND-HF randomized trial

    View Source
This page is an educational research summary. It is not medical advice, does not recommend human use, and does not provide individualised dosing. Many compounds discussed here are research use only and are not approved medicines.