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Neuromet (OXIRACETAM)

Phase 3 active Small molecule

Neuromet (generic name: OXIRACETAM) is a oxiracetam drug. It is currently in Phase 3 development.

Neuromet works by enhancing the activity of neurotransmitters in the brain, such as acetylcholine, to improve cognitive function.

Neuromet, also known as OXIRACETAM, is a small molecule oxiracetam drug developed by UCB (originally developed by UCB, current owner is unknown). Its exact target is unknown, but it is believed to work by enhancing cholinergic neurotransmission and modulating glutamatergic activity. Neuromet is not FDA-approved for any indications, and its commercial status is unclear. Key safety considerations include its potential for hepatotoxicity and interactions with other medications. As a result, its use should be carefully monitored.

Likelihood of approval
55.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% 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 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +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 nameOXIRACETAM
Drug classoxiracetam
ModalitySmall molecule
Therapeutic areaNeuroscience
PhasePhase 3

Mechanism of action

Think of it like a key that unlocks the doors to your brain's memory and learning centers. By enhancing the activity of these neurotransmitters, Neuromet helps improve communication between brain cells, leading to better memory, attention, and learning. This can be especially helpful for people with conditions that affect cognitive function, such as Alzheimer's disease or attention deficit hyperactivity disorder (ADHD).

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 Neuromet

What is Neuromet?

Neuromet (OXIRACETAM) is a oxiracetam drug.

How does Neuromet work?

Neuromet works by enhancing the activity of neurotransmitters in the brain, such as acetylcholine, to improve cognitive function.

What is the generic name of Neuromet?

OXIRACETAM is the generic (nonproprietary) name of Neuromet.

What drug class is Neuromet in?

Neuromet belongs to the oxiracetam class. See all oxiracetam drugs at /class/oxiracetam.

What development phase is Neuromet in?

Neuromet is in Phase 3.

Related

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