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A 52-Week, Phase 3, Open-Label Extension Study of ACP-204 in Adults With Lewy Body Dementia Psychosis (LBDP)

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521711-39-00
Acronym
ACP-204-013
Enrollment
49
Registered
2025-11-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lewy body Dementia psychosis (LBDP)

Brief summary

Treatment-emergent adverse events (TEAEs)

Interventions

None listed

Sponsors

Acadia Pharmaceuticals Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Treatment-emergent adverse events (TEAEs)

Countries

Bulgaria, Czechia, France, Italy

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026