Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizophrenia
Primary Purpose
Cognitive Deficits in Schizophrenia
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
ABT-126
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Cognitive Deficits in Schizophrenia
Eligibility Criteria
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.
Sites / Locations
- Site Reference ID/Investigator# 26267
- Site Reference ID/Investigator# 45320
- Site Reference ID/Investigator# 27068
- Site Reference ID/Investigator# 52568
- Site Reference ID/Investigator# 26266
- Site Reference ID/Investigator# 26388
- Site Reference ID/Investigator# 45315
- Site Reference ID/Investigator# 26271
- Site Reference ID/Investigator# 27045
- Site Reference ID/Investigator# 45314
- Site Reference ID/Investigator# 26264
- Site Reference ID/Investigator# 27072
- Site Reference ID/Investigator# 27043
- Site Reference ID/Investigator# 26395
- Site Reference ID/Investigator# 26268
- Site Reference ID/Investigator# 26392
- Site Reference ID/Investigator# 27073
- Site Reference ID/Investigator# 26262
- Site Reference ID/Investigator# 27071
- Site Reference ID/Investigator# 36020
- Site Reference ID/Investigator# 28063
- Site Reference ID/Investigator# 27070
- Site Reference ID/Investigator# 27069
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
ABT-126 Dose 1
ABT-126 Dose 2
Sugar Pill
Arm Description
Outcomes
Primary Outcome Measures
Cognition: MCCB
Secondary Outcome Measures
Functioning: UPSA-2
Cognition: CANTAB
Symptom Severity: PANSS, NSA-16, CGI-S
Full Information
NCT ID
NCT01095562
First Posted
March 26, 2010
Last Updated
June 1, 2018
Sponsor
AbbVie (prior sponsor, Abbott)
1. Study Identification
Unique Protocol Identification Number
NCT01095562
Brief Title
Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizophrenia
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Study of the Safety and Efficacy of ABT-126 in the Treatment of Cognitive Deficits in Schizophrenia (CDS)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
March 2010 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
September 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AbbVie (prior sponsor, Abbott)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is an efficacy and safety study evaluating an experimental treatment for cognitive deficits in adults with schizophrenia.
Detailed Description
This is a Phase 2 study designed to evaluate the efficacy and safety of ABT-126 in approximately 210 adults with schizophrenia. Subjects will be randomized to one of three treatment groups (ABT-126 Dose 1, ABT-126 Dose 2 or placebo) for a 12-week Treatment Period. The purpose of this research study is to find out whether ABT-126 compared to placebo can improve cognition and what side effects ABT-126 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
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Deficits in Schizophrenia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
207 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ABT-126 Dose 1
Arm Type
Experimental
Arm Title
ABT-126 Dose 2
Arm Type
Experimental
Arm Title
Sugar Pill
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
ABT-126
Intervention Description
ABT-126 Dose 1, ABT-126 Dose 2
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Cognition: MCCB
Time Frame
Measurements from screening period through 12-week treatment period
Secondary Outcome Measure Information:
Title
Functioning: UPSA-2
Time Frame
Measurements from screening period through 12-week treatment period
Title
Cognition: CANTAB
Time Frame
Measurements from screening period through 12-week treatment period
Title
Symptom Severity: PANSS, NSA-16, CGI-S
Time Frame
Measurements from screening period through 12-week treatment period
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
George Haig, PharmD
Organizational Affiliation
AbbVie
Official's Role
Study Director
Facility Information:
Facility Name
Site Reference ID/Investigator# 26267
City
Cerritos
State/Province
California
ZIP/Postal Code
90703
Country
United States
Facility Name
Site Reference ID/Investigator# 45320
City
Costa Mesa
State/Province
California
ZIP/Postal Code
92626
Country
United States
Facility Name
Site Reference ID/Investigator# 27068
City
Escondido
State/Province
California
ZIP/Postal Code
92025
Country
United States
Facility Name
Site Reference ID/Investigator# 52568
City
Garden Grove
State/Province
California
ZIP/Postal Code
92845
Country
United States
Facility Name
Site Reference ID/Investigator# 26266
City
Granada Hills
State/Province
California
ZIP/Postal Code
91344
Country
United States
Facility Name
Site Reference ID/Investigator# 26388
City
Oceanside
State/Province
California
ZIP/Postal Code
92056
Country
United States
Facility Name
Site Reference ID/Investigator# 45315
City
San Bernardino
State/Province
California
ZIP/Postal Code
92408
Country
United States
Facility Name
Site Reference ID/Investigator# 26271
City
San Diego
State/Province
California
ZIP/Postal Code
92102
Country
United States
Facility Name
Site Reference ID/Investigator# 27045
City
Santa Ana
State/Province
California
ZIP/Postal Code
92701
Country
United States
Facility Name
Site Reference ID/Investigator# 45314
City
Santa Ana
State/Province
California
ZIP/Postal Code
92705
Country
United States
Facility Name
Site Reference ID/Investigator# 26264
City
Torrance
State/Province
California
ZIP/Postal Code
90502
Country
United States
Facility Name
Site Reference ID/Investigator# 27072
City
Tampa
State/Province
Florida
ZIP/Postal Code
33613
Country
United States
Facility Name
Site Reference ID/Investigator# 27043
City
Wichita
State/Province
Kansas
ZIP/Postal Code
67214
Country
United States
Facility Name
Site Reference ID/Investigator# 26395
City
Lake Charles
State/Province
Louisiana
ZIP/Postal Code
70629
Country
United States
Facility Name
Site Reference ID/Investigator# 26268
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63118
Country
United States
Facility Name
Site Reference ID/Investigator# 26392
City
Fresh Meadows
State/Province
New York
ZIP/Postal Code
11366
Country
United States
Facility Name
Site Reference ID/Investigator# 27073
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Facility Name
Site Reference ID/Investigator# 26262
City
Rochester
State/Province
New York
ZIP/Postal Code
14618
Country
United States
Facility Name
Site Reference ID/Investigator# 27071
City
Beachwood
State/Province
Ohio
ZIP/Postal Code
44122
Country
United States
Facility Name
Site Reference ID/Investigator# 36020
City
Media
State/Province
Pennsylvania
ZIP/Postal Code
19063
Country
United States
Facility Name
Site Reference ID/Investigator# 28063
City
Norristown
State/Province
Pennsylvania
ZIP/Postal Code
19401
Country
United States
Facility Name
Site Reference ID/Investigator# 27070
City
Sellersville
State/Province
Pennsylvania
ZIP/Postal Code
18960
Country
United States
Facility Name
Site Reference ID/Investigator# 27069
City
Dallas
State/Province
Texas
ZIP/Postal Code
75243
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26044974
Citation
Hashimoto K. Targeting of alpha7 Nicotinic Acetylcholine Receptors in the Treatment of Schizophrenia and the Use of Auditory Sensory Gating as a Translational Biomarker. Curr Pharm Des. 2015;21(26):3797-806. doi: 10.2174/1381612821666150605111345.
Results Reference
background
PubMed Identifier
28433500
Citation
Georgiades A, Davis VG, Atkins AS, Khan A, Walker TW, Loebel A, Haig G, Hilt DC, Dunayevich E, Umbricht D, Sand M, Keefe RSE. Psychometric characteristics of the MATRICS Consensus Cognitive Battery in a large pooled cohort of stable schizophrenia patients. Schizophr Res. 2017 Dec;190:172-179. doi: 10.1016/j.schres.2017.03.040. Epub 2017 Apr 20.
Results Reference
derived
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Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizophrenia
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