Antipsychotic and Motor Effects of ACP-103 When Administered in Combination With Haloperidol and Risperidone
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Purpose
The primary purpose of this study is to determine whether a combination of ACP-103 (the study medication) with either haloperidol or risperidone will show antipsychotic efficacy and that it is safe and well tolerated. Further purposes of this study are to determine whether ACP-103, in combination with either haloperidol or risperidone, will enhance their antipsychotic effectiveness, demonstrate effectiveness against the negative symptoms, improve motoric tolerability, and is safe and well tolerated.
This is a seven-week study (one week screening and six weeks of study medication) where a total of 400 patients who meet entrance criteria will randomly be assigned to receive one of five groups of study treatments of either low dose haloperidol plus ACP-103, low dose haloperidol plus placebo (a substance similar to a sugar pill), low dose risperidone plus ACP-103, low dose risperidone plus placebo, or high dose risperidone plus placebo. The study will begin with with a three to seven day drug-free period followed by six weeks of a stable daily dosage of study medication. Study subjects will be treated as hospital in-patients during screening and for the first 14 days of the study. Study subjects will be closely monitored throughout the study.
| Condition | Intervention | Phase |
|---|---|---|
|
Schizophrenia |
Drug: ACP-103 |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A Randomized, Double Blind, Multi-Center Study to Assess the Antipsychotic and Motor Effects of ACP-103 When Administered in Combination With Haloperidol or Risperidone to Schizophrenic Subjects |
- Total score on the Positive and Negative Symptom Scale (PANSS).
- Clinical Global Impression-Severity (CGI-S), Simpson Angus Scale (SAS), Barnes Akathisia Scale (BAS), Calgary Depression Scale for Schizophrenia (CDSS)
| Estimated Enrollment: | 400 |
| Study Start Date: | August 2005 |
| Study Completion Date: | March 2007 |
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- male or female subjects ages 18-65 diagnosed with schizophrenia
- experiencing an acute exacerbation of psychosis
- has had prior response to antipsychotic therapy within the previous 3 years
- female subjects must be of non-childbearing potential or must comply with double-barrier protection methods against conception
- ability of subject or caregiver or legally authorized representative to provide informed consent
- subjects must be hospitalized at screening and must be willing to remain in the hospital at least 14 days after baseline and must comply with all study events through completion of the study
Exclusion Criteria:
- inability of the subject or caregiver or legally authorized representative to provide consent
- any female subject who is pregnant or breast feeding
- any subject with concurrent mental illness or disability
- any subject considered to be a danger to themselves or others
- recent use of certain antipsychotics or other medications that might interfere with this study's medication
- abnormal clinical laboratory values
- presence, or recent history, of serious medical conditions or drug abuse
- likely allergy or sensitivity to ACP-103, haloperidol, or risperidone, based on known allergies to drugs of the same class
- any subject who has participated in a prior clinical trial of ACP-103
- any subject judged by the Principal Investigator to be inappropriate for the study
Contacts and Locations| United States, California | |
| Cerritos, California, United States, 90703 | |
| Garden Grove, California, United States, 92845 | |
| Glendale, California, United States, 91206 | |
| Paramount, California, United States, 90723 | |
| Pico Rivera, California, United States, 90660 | |
| San Diego, California, United States, 92126 | |
| San Diego, California, United States, 92123 | |
| United States, District of Columbia | |
| Washington, District of Columbia, United States, 20016 | |
| United States, Missouri | |
| St. Louis, Missouri, United States, 63118 | |
| United States, Texas | |
| Austin, Texas, United States, 78756 | |
| Irving, Texas, United States, 75062 | |
| Brazil | |
| Salvador, BA, Brazil, 40325-090 | |
| Aparecida de Goiânia, GO, Brazil, 74922-810 | |
| Curitiba, PR, Brazil, 80520-000 | |
| Curitiba, PR, Brazil, 80430-050 | |
| Rio de Janeiro, RJ, Brazil, 21020-130 | |
| São Paulo, SP, Brazil, 05403-010 | |
| Study Chair: | Daniel van Kammen, MD, PhD | ACADIA Pharmaceuticals Inc. |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00361166 History of Changes |
| Other Study ID Numbers: | ACP-103-008 |
| Study First Received: | August 3, 2006 |
| Last Updated: | March 20, 2007 |
| Health Authority: | United States: Food and Drug Administration Brazil: Ministry of Health Brazil: National Committee of Ethics in Research |
Keywords provided by ACADIA Pharmaceuticals Inc.:
|
Schizophrenia psychosis delusions hallucination |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders Haloperidol Antipsychotic Agents Risperidone Antiemetics Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions Central Nervous System Agents |
Therapeutic Uses Gastrointestinal Agents Tranquilizing Agents Central Nervous System Depressants Psychotropic Drugs Dopamine Antagonists Dopamine Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Anti-Dyskinesia Agents Serotonin Antagonists Serotonin Agents |
ClinicalTrials.gov processed this record on June 17, 2013