Regulatory status

Status at a glance

503A compounding status

Not nominated

We found no pending nomination for the 503A bulks list. Unless the substance has another legal pathway (for example, a USP monograph or use in an FDA-approved drug), 503A pharmacies generally may not compound with it.

Status recorded · FDA source document

FDA approval
An FDA-approved product contains this peptide
503B outsourcing
Not determined
Anti-doping (WADA)
Not on the WADA Prohibited List
DEA schedule
Not a controlled substance

About peptide status

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Status as of

Key takeaway

Terlipressin (sold as Terlivaz) is a long-acting vasopressin analog used to improve kidney function in adults with hepatorenal syndrome, a dangerous form of kidney failure that develops in advanced liver disease. It constricts the splanchnic circulation to redirect blood flow toward the kidneys. It has been FDA-approved in the U.S. since 2022, after long use abroad, and carries a boxed warning about serious respiratory failure.

At a glance

What it is
A long-acting vasopressin analog and prodrug, a V1 receptor agonist
Approved for
Improving kidney function in adults with hepatorenal syndrome and rapid decline in kidney function
Key fact
In the CONFIRM trial it reversed hepatorenal syndrome in about 32 percent of patients versus 17 percent on placebo
Route
Intravenous
Evidence strength
FDA approved

Summary

Terlipressin (Terlivaz) is an FDA-approved vasopressin analog that improves kidney function in hepatorenal syndrome. Learn how it works and its boxed warning.

What is terlipressin?

Terlipressin, sold under the brand Terlivaz, is a synthetic vasopressin analog that the body slowly converts into its active form, giving a longer and steadier effect than vasopressin itself. It is used for hepatorenal syndrome, a type of acute kidney failure that occurs in people with advanced liver disease and carries a poor prognosis. It was used in Europe and elsewhere for years before being approved in the United States in 2022.

How does terlipressin work?

Terlipressin is a prodrug: after injection, enzymes slowly cleave it to release lysine-vasopressin, which acts mainly at V1a receptors. In hepatorenal syndrome, the arteries supplying the gut (the splanchnic circulation) are abnormally dilated, which lowers the effective blood volume reaching the kidneys and shuts down kidney function. By constricting those splanchnic vessels, terlipressin reduces the pooling of blood in the gut circulation and redistributes it toward the systemic and kidney circulation, raising kidney perfusion.

The goal is to reverse the kidney failure while the underlying liver disease is addressed, often as a bridge to liver transplantation. The CONFIRM trial compared terlipressin with placebo:

Study findings for Terlipressin
Outcome Terlipressin Placebo
Hepatorenal syndrome reversedAbout 32% of patients17% of patients
Respiratory complicationsMore patients affectedFewer patients affected

Is it FDA-approved?

Editor’s note

Status: Yes. Terlipressin (Terlivaz) was approved by the FDA in 2022 to improve kidney function in adults with hepatorenal syndrome with rapid reduction in kidney function. It carries a boxed warning for serious or fatal respiratory failure and is avoided in patients who are already hypoxic.

Category: FDA-approved · Primary body area: Digestive & weight

Yes. Terlipressin (Terlivaz) was approved by the FDA in 2022 to improve kidney function in adults with hepatorenal syndrome with rapid reduction in kidney function. It carries a boxed warning for serious or fatal respiratory failure and is avoided in patients who are already hypoxic.

What is terlipressin prescribed for?

Terlipressin is prescribed for adults with hepatorenal syndrome (the type with rapidly worsening kidney function) to improve kidney function. It is used in a hospital setting with careful monitoring, including of oxygen levels, and the labeling advises against use in those with high baseline risk of respiratory or ischemic complications.

What are the side effects?

According to the prescribing information, common side effects include:

  • Abdominal pain
  • Nausea and diarrhea
  • Shortness of breath

More serious considerations include:

  • A boxed warning for serious or fatal respiratory failure, with higher risk in patients with fluid overload, so oxygenation is monitored and it is avoided in hypoxic patients
  • Reduced blood flow causing ischemia in the heart, brain, gut, fingers, or skin
  • Respiratory failure or ischemia that can make a patient ineligible for a liver transplant

Sources: FDA prescribing information for Terlivaz; the CONFIRM trial (Wong et al., The New England Journal of Medicine, 2021, DOI: 10.1056/NEJMoa2008290), indexed on PubMed. This document is educational and does not constitute medical advice.

Registered human trials

0 registered human trials on ClinicalTrials.gov that we reviewed

Sources

  1. [1]
  2. [2]

    approved

    Primary drugs.com

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