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IFENPRODIL

Phase 2 active Small molecule

IFENPRODIL is a ifenprodil drug. It is currently in Phase 2 development.

IFENPRODIL works by selectively blocking the Sigma non-opioid intracellular receptor 1.

IFENPRODIL is a small molecule drug class ifenprodil that targets the Sigma non-opioid intracellular receptor 1. It is currently owned by an unknown entity, and its original development is attributed to an unspecified company. IFENPRODIL's commercial status, including FDA approval and generic availability, is unknown. As a result, its approved indications and off-patent status are also unclear. Key safety considerations include its half-life of 4.32 hours.

Likelihood of approval
12.3% 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).
  • CNS / neurology attrition -3.0pp
    CNS drugs have historically high Phase 3 failure rates (notably in Alzheimer disease + major depression).
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 nameIFENPRODIL
Drug classifenprodil
TargetGlutamate receptor ionotropic, NMDA 2A, Glutamate receptor ionotropic, NMDA 2B, Glutamate receptor ionotropic, NMDA 2C
ModalitySmall molecule
Therapeutic areaNeuroscience
PhasePhase 2

Mechanism of action

Think of it like a key fitting into a lock. IFENPRODIL is the key that blocks the Sigma receptor, which can help reduce pain and other symptoms. This blocking action helps to modulate the receptor's activity, leading to therapeutic effects.

Approved indications

No approved indications tracked.

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 IFENPRODIL

What is IFENPRODIL?

IFENPRODIL is a ifenprodil drug.

How does IFENPRODIL work?

IFENPRODIL works by selectively blocking the Sigma non-opioid intracellular receptor 1.

What drug class is IFENPRODIL in?

IFENPRODIL belongs to the ifenprodil class. See all ifenprodil drugs at /class/ifenprodil.

What development phase is IFENPRODIL in?

IFENPRODIL is in Phase 2.

What does IFENPRODIL target?

IFENPRODIL targets Glutamate receptor ionotropic, NMDA 2A, Glutamate receptor ionotropic, NMDA 2B, Glutamate receptor ionotropic, NMDA 2C and is a ifenprodil.

Related

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