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Vasopressin administration

Assistance Publique Hopitaux De Marseille · Phase 3 active Small molecule Under review

Vasopressin administration is a Vasopressin receptor agonist Small molecule drug developed by Assistance Publique Hopitaux De Marseille. It is currently in Phase 3 development for Hemorrhagic shock, Cardiogenic shock, Severe burns.

Vasopressin acts as a potent vasoconstrictor by stimulating V1A receptors on vascular smooth muscle cells, causing blood vessels to constrict.

Vasopressin, a vasopressin V2 receptor agonist, is administered to treat conditions such as nephrogenic diabetes insipidus and lithium-induced nephropathy, as well as to improve concentration ability impaired by lithium treatment. It is also studied as a potential treatment for bipolar disorder and lithium toxicities.

Likelihood of approval
56.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
  • Cardiovascular Phase 3 risk -2.0pp
    Modern cardiovascular outcome trials are large + long; many fail to beat aggressive standard-of-care.
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameVasopressin administration
SponsorAssistance Publique Hopitaux De Marseille
Drug classVasopressin receptor agonist
TargetV1A and V2 receptors
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 3

Mechanism of action

This leads to increased blood pressure and improved perfusion of vital organs. Vasopressin also has antidiuretic effects by stimulating V2 receptors in the kidneys, reducing water loss in the urine.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Vasopressin administration

What is Vasopressin administration?

Vasopressin administration is a Vasopressin receptor agonist drug developed by Assistance Publique Hopitaux De Marseille, indicated for Hemorrhagic shock, Cardiogenic shock, Severe burns.

How does Vasopressin administration work?

Vasopressin acts as a potent vasoconstrictor by stimulating V1A receptors on vascular smooth muscle cells, causing blood vessels to constrict.

What is Vasopressin administration used for?

Vasopressin administration is indicated for Hemorrhagic shock, Cardiogenic shock, Severe burns.

Who makes Vasopressin administration?

Vasopressin administration is developed by Assistance Publique Hopitaux De Marseille (see full Assistance Publique Hopitaux De Marseille pipeline at /company/assistance-publique-hopitaux-de-marseille).

What drug class is Vasopressin administration in?

Vasopressin administration belongs to the Vasopressin receptor agonist class. See all Vasopressin receptor agonist drugs at /class/vasopressin-receptor-agonist.

What development phase is Vasopressin administration in?

Vasopressin administration is in Phase 3.

What are the side effects of Vasopressin administration?

Common side effects of Vasopressin administration include Hypertension, Nausea, Headache.

What does Vasopressin administration target?

Vasopressin administration targets V1A and V2 receptors and is a Vasopressin receptor agonist.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing