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Zeria (EFONIDIPINE)

Phase 2 active Small molecule

Zeria (generic name: EFONIDIPINE) is a drug. It is currently in Phase 2 development for Hypertensive disorder.

Zeria works by blocking the T-type calcium channel, which helps to relax blood vessels and lower blood pressure.

Zeria (Efondipine) is a small molecule modality targeting the voltage-dependent T-type calcium channel subunit alpha-1H. It is used to treat hypertensive disorders. The commercial status of Zeria is currently unknown, and it is not clear if it is patented or available as a generic. Key safety considerations are not well-documented. Further research is needed to fully understand its pharmacological profile.

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 nameEFONIDIPINE
TargetVoltage-dependent T-type calcium channel subunit alpha-1H
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 2

Mechanism of action

Think of your blood vessels like a garden hose. When the T-type calcium channel is active, it's like someone is squeezing the hose, making it harder for blood to flow. By blocking this channel, Zeria helps to relax the blood vessels, making it easier for blood to flow and lowering blood pressure.

Approved indications

Common side effects

No common side effects on file.

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 Zeria

What is Zeria?

Zeria (EFONIDIPINE) is a Small molecule drug, indicated for Hypertensive disorder.

How does Zeria work?

Zeria works by blocking the T-type calcium channel, which helps to relax blood vessels and lower blood pressure.

What is Zeria used for?

Zeria is indicated for Hypertensive disorder.

What is the generic name of Zeria?

EFONIDIPINE is the generic (nonproprietary) name of Zeria.

What development phase is Zeria in?

Zeria is in Phase 2.

What does Zeria target?

Zeria targets Voltage-dependent T-type calcium channel subunit alpha-1H.

Related

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