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Investigational and not approved by the FDA. This page is educational information only. It is not medical advice and not a recommendation to use anything.
IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Selepressin

Investigational

Vasopressin V1a receptor agonist

Also known as: Fe202158, Fe 202158, selepresina, selepressine, FE-202158, selepressinum

Evidence score
54/ 100
Moderate evidence

A real evidence base, with gaps

  • Regulatory standing. In clinical trials, not yet approved
  • Limited human data. Some human data exists, not conclusive
  • Registered human trials. 1 registered study on ClinicalTrials.gov, most advanced Phase 3
  • 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

Selepressin is a synthetic peptide analog of vasopressin designed to selectively activate the V1a receptor, which constricts blood vessels and raises blood pressure. It was developed by Ferring Pharmaceuticals as a potential treatment for low blood pressure in septic shock, with the aim of avoiding effects linked to other vasopressin receptors.

What the evidence shows

Automatic summaryLimited human data

Selepressin is not FDA-approved. It reached a registered Phase 3 trial in septic shock (the SEPSIS-ACT trial), which was stopped for futility after it did not improve the main outcome compared with placebo, so no clinical benefit has been established in humans.

Key facts

Molecular formula
C46H73N13O11S2
Molecular weight
1048.3 g/mol

Registered human trials

Live from ClinicalTrials.gov, refreshed daily.

1registered studies
Phase 3most advanced phase
0completed (sample)
0recruiting (sample)

Published literature

Sources

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