Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 2

Phase 2, Efficacy and Safety Study of ACP-204 in Lewy Body Dementia Psychosis

NCT07029581 · View on ClinicalTrials.gov ↗

Study Summary

Multicenter, randomized, 6-week, double-blind, placebo-controlled, parallel-group, Phase 2 study in subjects with LBDP.

Interventions

  • DRUG Placebo
  • DRUG ACP-204

Study Locations (20)

Florida

  • Humanity Clinical Research, Corp — Aventura
  • Parkinson's Disease and Movement Disorders Center of Boca Raton — Boca Raton
  • K2 Medical Research Winter Garden LLC — Clermont
  • K2 Summit Research — Lady Lake
  • Neurology Associates, P. A. — Maitland
  • Homestead Associates in Research Inc — Miami
  • Premier Clinical Research Institute, Inc. — Miami
  • Advanced Clinical Research Network, Corp — Miami
  • MediClear Medical & Research Center, Inc. — Miami
  • Health Synergy Clinical Research, LLC — West Palm Beach

Texas

  • Horizon Clinical Research Group — Cypress
  • The University of Texas Health Science Center San Antonio — San Antonio

California

  • ATP Clinical Research Inc. — Irvine

Hawaii

  • Hawaii Pacific Neuroscience — Honolulu

Kansas

  • University of Kansas Medical Center Research Institute Inc. — Kansas City

New York

  • Parkinson's Disease and Movement Disorders Center of Boca Raton d/b/a Parkinson's Research Center of America-Long Island — Commack

North Carolina

  • UNC Hospitals — Chapel Hill

Ohio

  • The Ohio State University, Energy Advancement and Innovation Center — Columbus

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2025-08-06
Est. Completion 2028-03
Phase Phase 2

Sponsor

ACADIA Pharmaceuticals

10 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07029581

The ClinicalTrials.gov registry entry for NCT07029581 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 180 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ACADIA Pharmaceuticals, which has 10 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Lewy Body Dementia Psychosis appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07029581 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Florida, Texas, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07029581 about?

NCT07029581 is a clinical study titled "Phase 2, Efficacy and Safety Study of ACP-204 in Lewy Body Dementia Psychosis". Multicenter, randomized, 6-week, double-blind, placebo-controlled, parallel-group, Phase 2 study in subjects with LBDP.

What is the current status of trial NCT07029581?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 180 participants. The study started on 2025-08-06. Estimated completion is 2028-03.

What conditions does trial NCT07029581 study?

This clinical trial studies the following conditions: Lewy Body Dementia Psychosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07029581?

The interventions under investigation include: Placebo (DRUG), ACP-204 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07029581?

This trial is sponsored by ACADIA Pharmaceuticals, which has 10 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07029581 being conducted?

This trial has 20 study locations across California, Florida, Hawaii, Kansas, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial