Efficacy and Safety Study for Cognitive Deficits in Adult Subjects With Schizophrenia
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Purpose
This is an efficacy and safety study evaluating an experimental treatment for cognitive deficits in adults with schizophrenia.
| Condition | Intervention | Phase |
|---|---|---|
|
Cognitive Deficits in Schizophrenia |
Drug: ABT-288 Low Dose Drug: Placebo Drug: ABT-288 High Dose |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Study of the Safety and Efficacy of ABT-288 in the Treatment of Cognitive Deficits in Schizophrenia (CDS) |
- Cognition: MCCB [ Time Frame: Measurements from screening period through 12-week treatment period ] [ Designated as safety issue: No ]
- Functioning: UPSA-2 [ Time Frame: Measurements from screening period through 12-week treatment period ] [ Designated as safety issue: No ]
- Cognition: CANTAB [ Time Frame: Measurements from screening period through 12-week treatment period ] [ Designated as safety issue: No ]
- Symptom Severity: PANSS, NSA-16, CGI-S [ Time Frame: Measurements from screening period through 12-week treatment period ] [ Designated as safety issue: No ]
| Enrollment: | 214 |
| Study Start Date: | March 2010 |
| Study Completion Date: | July 2011 |
| Primary Completion Date: | July 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: ABT-288 Dose 1
low dose of ABT-288
|
Drug: ABT-288 Low Dose |
|
Experimental: ABT-288 Dose 2
high dose of ABT-288
|
Drug: ABT-288 High Dose |
|
Placebo Comparator: Sugar Pill
inactive substance
|
Drug: Placebo
inactive substance
|
Detailed Description:
This is a Phase 2 study designed to evaluate the efficacy and safety of ABT-288 in approximately 210 adults with schizophrenia. Subjects will be randomized to one of three treatment groups (ABT-288 Dose 1, ABT-288 Dose 2 or placebo) for a 12-week Treatment Period. The purpose of this research study is to find out whether ABT-288 compared to placebo can improve cognition and what side effects ABT 288 may cause. Cognition is the way a person thinks, and it includes abilities like paying attention, focusing, remembering things, and solving problems. Acronyms listed in the Outcomes and/or Eligibility sections for this study are defined below:
- MCCB: Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery
- UPSA-2: University of California at San Diego (UCSD) Performance-Based Skills Assessment-2
- CANTAB: Cambridge Neuropsychological Test Automated Battery
- PANSS: Positive and Negative Syndrome Scale
- NSA-16: Negative Symptom Assessment-16
- CGI-S: Clinical Global Impression - Severity
Eligibility| Ages Eligible for Study: | 20 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Has current DSM-IV-TR diagnosis of schizophrenia confirmed by the Mini-International Neuropsychiatric Interview.
- Is clinically stable while receiving antipsychotic therapy with one or two atypical antipsychotic medications: lack of hospitalizations from 4 months of Initial Screening Visit; taking same antipsychotic medication(s) for at least 8 weeks prior to the Day -1 visit; core positive symptoms of PANSS no worse than moderate in severity throughout Screening Period of at least 4 weeks.
- Has been diagnosed with or treated for schizophrenia for at least 2 years prior to Initial Screening Visit.
- Has had continuity in psychiatric care (e.g., mental health system, clinic or physician) for at least 6 months prior to Initial Screening Visit.
- Has an identified responsible contact person (e.g., family member, social worker, case worker, or nurse) that can provide support to the subject and ensure compliance with protocol requirements.
Exclusion Criteria:
- Has valid current or past diagnosis of schizoaffective disorder, bipolar disorder, manic episode, dementia, posttraumatic stress disorder, obsessive compulsive disorder, or a current major depressive episode.
- Has history of substance abuse (excluding nicotine or tobacco products) or alcohol abuse within 6 months prior to Screening Visit; has a substance dependence disorder (excluding nicotine or tobacco products) that has not been remitted for at least 1 year prior to Initial Screening Visit.
- Is taking any medication for extrapyramidal symptoms at any time from the Initial Screening Visit until the Day -1 Visit.
- Is taking any antidepressant that is excluded, including tricyclic antidepressants and monoamine oxidase inhibitors, at any time from 8 weeks prior to the Day -1 Visit.
- Has significant suicidal ideation at Initial Screening Visit.
- Has had a suicide attempt within 1 year prior to the Day -1 Visit.
- Has participated in another trial utilizing the MATRICS Consensus Cognitive Battery (MCCB) or UCSD Performance-Based Skills Assessment (UPSA) (any version) within 6 months prior to Initial Screening Visit.
- Is currently enrolled in any form of cognitive remediation training.
Contacts and Locations| United States, California | |
| Site Reference ID/Investigator# 21662 | |
| Anaheim, California, United States, 92804 | |
| Site Reference ID/Investigator# 21683 | |
| Garden Grove, California, United States, 92845 | |
| Site Reference ID/Investigator# 21581 | |
| National City, California, United States, 91950 | |
| Site Reference ID/Investigator# 45310 | |
| Norwalk, California, United States, 90650 | |
| Site Reference ID/Investigator# 26400 | |
| Pasadena, California, United States, 91106 | |
| Site Reference ID/Investigator# 21584 | |
| Pico Rivera, California, United States, 90660 | |
| Site Reference ID/Investigator# 45312 | |
| Riverside, California, United States, 92506 | |
| Site Reference ID/Investigator# 45309 | |
| San Diego, California, United States, 92128 | |
| United States, Florida | |
| Site Reference ID/Investigator# 46603 | |
| Plantation, Florida, United States, 33317 | |
| United States, Illinois | |
| Site Reference ID/Investigator# 21681 | |
| Chicago, Illinois, United States, 60640 | |
| United States, Louisiana | |
| Site Reference ID/Investigator# 26397 | |
| Shreveport, Louisiana, United States, 71104-2136 | |
| United States, Massachusetts | |
| Site Reference ID/Investigator# 21761 | |
| Pittsfield, Massachusetts, United States, 01201 | |
| United States, Missouri | |
| Site Reference ID/Investigator# 21591 | |
| St. Louis, Missouri, United States, 63139 | |
| United States, New York | |
| Site Reference ID/Investigator# 26409 | |
| Brooklyn, New York, United States, 11235 | |
| Site Reference ID/Investigator# 21588 | |
| Cedarhurst, New York, United States, 11516 | |
| United States, Ohio | |
| Site Reference ID/Investigator# 21589 | |
| Dayton, Ohio, United States, 45417 | |
| United States, Oklahoma | |
| Site Reference ID/Investigator# 26407 | |
| Oklahoma City, Oklahoma, United States, 73103 | |
| United States, Pennsylvania | |
| Site Reference ID/Investigator# 21601 | |
| Philadelphia, Pennsylvania, United States, 19131 | |
| United States, South Carolina | |
| Site Reference ID/Investigator# 26399 | |
| Charleston, South Carolina, United States, 29407 | |
| United States, Texas | |
| Site Reference ID/Investigator# 21582 | |
| Austin, Texas, United States, 78754 | |
| Site Reference ID/Investigator# 21590 | |
| Austin, Texas, United States, 78731 | |
| Site Reference ID/Investigator# 26406 | |
| DeSoto, Texas, United States, 75115 | |
| Site Reference ID/Investigator# 26402 | |
| Houston, Texas, United States, 77008 | |
| United States, Washington | |
| Site Reference ID/Investigator# 27502 | |
| Bellevue, Washington, United States, 98007 | |
| Study Director: | George Haig, PharmD | AbbVie |
More Information
No publications provided
| Responsible Party: | AbbVie ( AbbVie (prior sponsor, Abbott) ) |
| ClinicalTrials.gov Identifier: | NCT01077700 History of Changes |
| Other Study ID Numbers: | M10-503 |
| Study First Received: | February 26, 2010 |
| Last Updated: | March 29, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders |
ClinicalTrials.gov processed this record on May 23, 2013