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AVP-786-28

Otsuka Pharmaceutical Development & Commercialization, Inc. · Phase 3 active Small molecule ✓ Verified Jun 2026

AVP-786-28 is a Sigma-1 receptor agonist Small molecule drug developed by Otsuka Pharmaceutical Development & Commercialization, Inc.. It is currently in Phase 3 development for Agitation associated with Alzheimer's disease dementia, Agitation in other neurodegenerative diseases.

AVP-786 is a combination of deuterated dextromethorphan and quinidine that enhances sigma-1 receptor signaling to reduce agitation and behavioral symptoms in neurodegenerative diseases.

AVP-786-28 is an intervention in a clinical trial studying the efficacy, safety, and tolerability of AVP-786 for the treatment of agitation in participants with dementia of the Alzheimer's type. The conditions studied in this trial include agitation in participants with dementia of the Alzheimer's type, among others such as neurobehavioral disinhibition and intermittent explosive disorder.

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 nameAVP-786-28
SponsorOtsuka Pharmaceutical Development & Commercialization, Inc.
Drug classSigma-1 receptor agonist
TargetSigma-1 receptor
ModalitySmall molecule
Therapeutic areaNeurology
PhasePhase 3

Mechanism of action

The drug combines dextromethorphan (a sigma-1 receptor agonist) with quinidine, which inhibits the metabolism of dextromethorphan and increases its bioavailability. Sigma-1 receptor activation is thought to modulate neuroprotective pathways and reduce neuroinflammation. The deuteration of dextromethorphan improves its pharmacokinetic profile and duration of action.

Approved indications

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 AVP-786-28

What is AVP-786-28?

AVP-786-28 is a Sigma-1 receptor agonist drug developed by Otsuka Pharmaceutical Development & Commercialization, Inc., indicated for Agitation associated with Alzheimer's disease dementia, Agitation in other neurodegenerative diseases.

How does AVP-786-28 work?

AVP-786 is a combination of deuterated dextromethorphan and quinidine that enhances sigma-1 receptor signaling to reduce agitation and behavioral symptoms in neurodegenerative diseases.

What is AVP-786-28 used for?

AVP-786-28 is indicated for Agitation associated with Alzheimer's disease dementia, Agitation in other neurodegenerative diseases.

Who makes AVP-786-28?

AVP-786-28 is developed by Otsuka Pharmaceutical Development & Commercialization, Inc. (see full Otsuka Pharmaceutical Development & Commercialization, Inc. pipeline at /company/otsuka-pharmaceutical-development-commercialization-inc).

What drug class is AVP-786-28 in?

AVP-786-28 belongs to the Sigma-1 receptor agonist class. See all Sigma-1 receptor agonist drugs at /class/sigma-1-receptor-agonist.

What development phase is AVP-786-28 in?

AVP-786-28 is in Phase 3.

What are the side effects of AVP-786-28?

Common side effects of AVP-786-28 include Dizziness, Somnolence, Headache, Nausea.

What does AVP-786-28 target?

AVP-786-28 targets Sigma-1 receptor and is a Sigma-1 receptor agonist.

Related

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