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Vasexten (BARNIDIPINE)

Phase 2 active Small molecule

Vasexten (generic name: BARNIDIPINE) is a barnidipine drug. It is currently in Phase 2 development.

Vasexten works by blocking calcium channels in the heart and blood vessels, which helps to relax and widen blood vessels, reducing blood pressure.

Vasexten, also known as BARNIDIPINE, is a small molecule drug that targets voltage-gated L-type calcium channels. It is classified as a barnidipine drug class and is used to treat certain cardiovascular conditions. The commercial status of Vasexten is unclear, as it is not FDA-approved and its patent status is unknown. Key safety considerations include its low bioavailability of 1%. Vasexten is developed by an unknown original developer and is currently owned by an unknown entity.

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 nameBARNIDIPINE
Drug classbarnidipine
TargetVoltage-gated L-type calcium channel
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 2

Mechanism of action

Imagine your blood vessels are like roads in your body. When you have high blood pressure, the roads get congested and narrow. Vasexten helps to relax the muscles around the roads, making them wider and allowing blood to flow more easily. This helps to lower blood pressure and reduce the risk of heart disease.

Approved indications

No approved indications tracked.

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 Vasexten

What is Vasexten?

Vasexten (BARNIDIPINE) is a barnidipine drug.

How does Vasexten work?

Vasexten works by blocking calcium channels in the heart and blood vessels, which helps to relax and widen blood vessels, reducing blood pressure.

What is the generic name of Vasexten?

BARNIDIPINE is the generic (nonproprietary) name of Vasexten.

What drug class is Vasexten in?

Vasexten belongs to the barnidipine class. See all barnidipine drugs at /class/barnidipine.

What development phase is Vasexten in?

Vasexten is in Phase 2.

What are the side effects of Vasexten?

Common side effects of Vasexten include Drug interaction, Hypertensive crisis.

What does Vasexten target?

Vasexten targets Voltage-gated L-type calcium channel and is a barnidipine.

Related

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