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Deucrictibant high dose

Pharvaris Netherlands B.V. · Phase 2 active Small molecule Under review

Deucrictibant high dose is a Bradykinin receptor antagonist Small molecule drug developed by Pharvaris Netherlands B.V.. It is currently in Phase 2 development for Hypertension.

Deucrictibant is a bradykinin receptor 2 antagonist.

Deucrictibant is a small molecule used to treat Hereditary Angioedema, specifically in the acute treatment of angioedema attacks in patients with Hereditary Angioedema. It is administered orally as part of a Phase II/III extension study.

Likelihood of approval
13.3% vs 15.3% industry baseline
If approved by FDA: likely 2031–2034
Steps remaining: Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 2 → approval rate +15.3pp
    Industry-wide phase 2 drugs reach approval ~15.3% 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 2031–2034
EMA EU 2032–2035 +0.7 yr
MHRA GB 2032–2035 +0.7 yr
Health Canada CA 2032–2036 +0.9 yr
TGA AU 2032–2036 +1.2 yr
PMDA JP 2032–2036 +1.5 yr
NMPA CN 2033–2037 +2.3 yr
MFDS KR 2032–2036 +1.4 yr
CDSCO IN 2032–2037 +1.8 yr
ANVISA BR 2033–2037 +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 nameDeucrictibant high dose
SponsorPharvaris Netherlands B.V.
Drug classBradykinin receptor antagonist
TargetB2 receptor
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 2

Mechanism of action

Deucrictibant works by blocking the action of bradykinin at its receptor, which is involved in blood pressure regulation. This leads to vasodilation and a decrease in blood pressure. Deucrictibant is being investigated for its potential to treat hypertension.

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 Deucrictibant high dose

What is Deucrictibant high dose?

Deucrictibant high dose is a Bradykinin receptor antagonist drug developed by Pharvaris Netherlands B.V., indicated for Hypertension.

How does Deucrictibant high dose work?

Deucrictibant is a bradykinin receptor 2 antagonist.

What is Deucrictibant high dose used for?

Deucrictibant high dose is indicated for Hypertension.

Who makes Deucrictibant high dose?

Deucrictibant high dose is developed by Pharvaris Netherlands B.V. (see full Pharvaris Netherlands B.V. pipeline at /company/pharvaris-netherlands-b-v).

What drug class is Deucrictibant high dose in?

Deucrictibant high dose belongs to the Bradykinin receptor antagonist class. See all Bradykinin receptor antagonist drugs at /class/bradykinin-receptor-antagonist.

What development phase is Deucrictibant high dose in?

Deucrictibant high dose is in Phase 2.

What are the side effects of Deucrictibant high dose?

Common side effects of Deucrictibant high dose include Hypotension.

What does Deucrictibant high dose target?

Deucrictibant high dose targets B2 receptor and is a Bradykinin receptor antagonist.

Related

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