Skip to main content
OpenTrials
Completed

NCT Number: NCT00490516

ACP-104 in Acutely Psychotic Subjects With Schizophrenia

This is a randomized, double-blind, placebo-controlled parallel-group, 6-week study, evaluating two dose levels of ACP-104 or Placebo twice a day in patients with schizophrenia who are experiencing an acute psychotic episode.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Anaheim, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female; 18-60 years of age
  • The subject is physically healthy and medically stable.
  • The subject is able to provide informed consent
  • The subject has been diagnosed with schizophrenia for at least 1 year
  • Currently experiencing an acute episode of psychosis
  • The subject is willing to comply with all study-related events including in-patient hospitalization for at least 3 weeks.
  • The subject has a caregiver who is willing and able to support the subject to ensure compliance with treatment and outpatient visits.
  • If the subject is female, subject must be of non-childbearing potential - OR- if she is capable of becoming pregnant, agrees to commit to use one of the approved methods of contraception, as defined by the protocol.

Exclusion criteria

  • If the subject is a pregnant or lactating (breast-feeding) female.
  • The subject has a significant risk of suicide, homicide, and/or harm to self or others.
  • Subject's psychotic symptoms have not improved with a therapeutic dose of antipsychotic treatment over the last 2 years.
  • The subject is experiencing his/her first episode of schizophrenia.
  • The subject has another psychotic disorder or has a history of autistic disorder or other pervasive developmental disorder (for example, mental retardation).
  • The subject has been prescribed or exposed to clozapine before.
  • The subject has donated blood or plasma within 56 days prior to the Screening Visit.
  • The subject has participated in any clinical study within 30 days prior to the Screening Visit.

In addition to the criteria described above, subjects will be evaluated at screening to ensure that all criteria for study participation are met. These evaluations will include specific measures of the subject's health, including psychosis (mental health -the extent to which subject is unable to think clearly), heart condition, and pregnancy status. Patients may be excluded from the study based on these assessments (and specifically if it is determined that their baseline condition does not meet all protocol-specified entry criteria).

Treatment and study plan

ACP-104

Drug

200 mg, tablet, BID, 6 weeks

Placebo

Drug

placebo, tablet BID, 6 weeks

Primary outcomes

  1. PANSS

    Time frame: 6 weeks

Sponsors and collaborators

Lead sponsor

ACADIA Pharmaceuticals Inc.

Industry

Registry information

Official study title

A Six-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Phase II Study of the Efficacy and Safety of ACP-104 in Acutely Psychotic Subjects With Schizophrenia

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Jun 22, 2007
Registry last updated
Jan 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.