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A Double-Blind, Placebo-Controlled, Phase 2, Efficacy and Safety Study of ACP-204 in Adults with Lewy Body Dementia Psychosis (LBDP)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521710-25-00
Acronym
ACP-204
Enrollment
77
Registered
2025-10-29
Start date
2025-12-04
Completion date
Unknown
Last updated
2025-11-20

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

Change from Baseline in SAPS-LBDP total score at Week 6

Interventions

DRUGPlacebo for ACP-204 capsules

Sponsors

Acadia Pharmaceuticals Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Change from Baseline in SAPS-LBDP total score at Week 6

Countries

Bulgaria, Czechia, France, Italy

Outcome results

None listed

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