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Deucrictibant high dose
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.
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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.
| 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 name | Deucrictibant high dose |
|---|---|
| Sponsor | Pharvaris Netherlands B.V. |
| Drug class | Bradykinin receptor antagonist |
| Target | B2 receptor |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | Phase 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
- Hypertension
Common side effects
- Hypotension
Key clinical trials
- Extension Study of Oral PHA-022121 for Acute Treatment of Angioedema Attacks in Patients With Hereditary Angioedema (PHASE2, PHASE3)
- Dose-ranging Study of Oral PHA-022121 for Acute Treatment of Angioedema Attacks in Patients With Hereditary Angioedema (PHASE2)
- Dose-ranging Study of Oral PHA-022121 for Prophylaxis Against Angioedema Attacks in Patients With Hereditary Angioedema Type I or Type II (PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial 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:
- Deucrictibant high dose CI brief — competitive landscape report
- Deucrictibant high dose updates RSS · CI watch RSS
- Pharvaris Netherlands B.V. portfolio CI
Frequently asked questions about Deucrictibant high dose
What is Deucrictibant high dose?
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Related
- Drug class: All Bradykinin receptor antagonist drugs
- Target: All drugs targeting B2 receptor
- Manufacturer: Pharvaris Netherlands B.V. — full pipeline
- Therapeutic area: All drugs in Cardiovascular
- Indication: Drugs for Hypertension
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing