Safety and Efficacy of Cariprazine (RGH-188) in the Acute... | NCT00694707 | Trialant
NCT00694707
Sponsor
Forest Laboratories
Status
Completed
Last Update Posted
Jun 12, 2019Actual
Enrollment
732Actual
Phase
Phase 2
Conditions
Schizophrenia
Interventions
Placebo
Cariprazine
Risperidone
Countries
United States
India
Malaysia
Russia
Ukraine
Protocol Section
Identification Module
NCT ID
NCT00694707
Obsolete or Duplicate NCT IDs
NCT00892528
Organization Study
RGH-MD-16
Secondary IDs
Not provided
Brief Title
Safety and Efficacy of Cariprazine (RGH-188) in the Acute Exacerbation of Schizophrenia
Official Title
Evaluation of the Safety and Efficacy of RGH-188 in the Acute Exacerbation of Schizophrenia
Acronym
Not provided
Organization
Forest LaboratoriesINDUSTRY
Status Module
Record Verification Date
May 2019
Overall Recruitment Status or Expanded Access Status
Completed
Last Known Status
Not provided
Delayed Posting
Not provided
Why Stopped
Not provided
Expanded Access Info
No
Start Date
Jun 30, 2008Actual
Primary Completion Date
Aug 31, 2009Actual
Completion Date
Aug 31, 2009Actual
First Submitted Date
Jun 6, 2008
First Submission Date that Met QC Criteria
Jun 9, 2008
First Posted Date
Jun 10, 2008Estimated
Results Waived
Not provided
Results First Submitted Date
May 17, 2019
Results First Submitted that Met QC Criteria
May 17, 2019
Results First Posted Date
Jun 12, 2019Actual
Certification/Extension (aka Delayed Results) First Submitted Date
Mar 2, 2012
Certification/Extension First Submitted that Passed QC Review
Mar 2, 2012
Certification/Extension First Posted Date
Mar 6, 2012Estimated
Last Update Submitted Date
May 17, 2019
Last Update Posted Date
Jun 12, 2019Actual
Sponsor/Collaborators Module
Responsible Party, by Official Title
Sponsor
Lead Sponsor
Forest LaboratoriesINDUSTRY
Collaborators
Name
Class
Gedeon Richter Ltd.
INDUSTRY
Oversight Module
Has Data Monitoring Committee (DMC)
No
Is FDA Regulated Drug
Not provided
Is FDA Regulated Device
Not provided
Is Unapproved Device
Not provided
Pediatric Postmarket Surveillance of a Device Product
Not provided
Product Exported from US
Not provided
FDAAA801 Violation
Not provided
Description Module
Brief Summary
This is a study to evaluate the safety, efficacy, and tolerability of cariprazine (RGH-188) relative to placebo in adult patients (18-60 years of age) with acute exacerbation of schizophrenia.
Detailed Description
Not provided
Conditions Module
Conditions
Schizophrenia
Keywords
Not provided
Design Module
Study Type
Interventional
Number of References to an Expanded Access Study
Not provided
Expanded Access Types
Not provided
Patient Registry
Not provided
Target Follow-Up Duration
Not provided
Phases
Phase 2
Interventional Study Design
Allocation
Biospecimen
No data available
No data is available for this block.
Enrollment
732Actual
Arms/Interventions Module
Arm Groups
Label
Type
Description
Intervention Names
Placebo
Placebo Comparator
Participants received placebo orally once a day for 6 weeks.
Drug: Placebo
Cariprazine 1.5 mg
Experimental
Participants received cariprazine 1.5 mg orally once a day for 6 weeks.
Drug: Cariprazine
Cariprazine 3.0 mg
Experimental
Participants received cariprazine 3.0 mg orally once a day for 6 weeks.
Drug: Cariprazine
Cariprazine 4.5 mg
Experimental
Participants received cariprazine 4.5 mg orally once a day for 6 weeks.
Drug: Cariprazine
Risperidone 4.0 mg
Active Comparator
Participants received risperidone 4.0 mg orally once a day for 6 weeks.
Drug: Risperidone
Interventions
Name
Type
Description
Arm Group Labels
Other Names
Placebo
Drug
Placebo was supplied in capsules.
Placebo
Cariprazine
Outcomes Module
Primary Outcomes
Measure
Description
Time Frame
Change From Baseline to Week 6 in the PANSS Total Score
The Positive and Negative Syndrome Scale (PANSS) is a 30-item rating scale that assesses the positive and negative symptoms of individuals with schizophrenia. Responses to the 30 items are based on a structured clinical interview with the patient and on supporting clinical information obtained from family, hospital staff, or other reliable informants. Of the 30 psychiatric parameters measured by the scale, 7 assess positive symptoms (eg, delusions, grandiosity); 7 assess negative symptoms (eg, blunted affect, emotional withdrawal); and 16 assess general psychopathology (eg, poor attention, active social avoidance). Each item is scored on a 7-point scale (1 = absent, 2 = minimal, 3 = mild, 4 = moderate, 5 = moderately severe, 6 = severe, and 7 = extreme). The PANSS total score can range from 30 to 210. A higher score indicates worse symptoms. A negative change score indicates improvement.
Baseline to Week 6
Secondary Outcomes
Measure
Description
Time Frame
Change From Baseline to Week 6 in the CGI-S Score
The Clinical Global Impressions-Severity (CGI-S) scale is a 7-point scale that measures the overall severity of the illness compared with the severity of illness in other patients the Investigator has observed. The Investigator assesses the severity of the patient's illness as one of the following: 1 = Normal, not at all ill; 2 = Borderline ill; 3 = Mildly ill; 4 = Moderately ill; 5 = Markedly ill; 6 = Severely ill; 7 = Among the most extremely ill patients. The CGI-S score can range from 1 to 7. A higher score indicates more severe illness. A negative change score indicates improvement.
Other Outcomes
Not provided
Eligibility Module
Eligibility Criteria
Inclusion Criteria:
Male or female, 18 to 60 years of age.
Meets Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) criteria for schizophrenia (paranoid type, disorganized type, catatonic type, or undifferentiated type) based on a Structured Clinical Interview for DSM-IV (SCID).
Total Positive and Negative Syndrome Scale (PANSS) score ≥ 80 and ≤ 120.
Diagnosis of schizophrenia for at least 1 year.
Exclusion Criteria:
Abnormalities on physical examination or abnormal vital signs, electrocardiogram, or clinical laboratory values.
Laszlovszky I, Barabassy A, Nemeth G. Cariprazine, A Broad-Spectrum Antipsychotic for the Treatment of Schizophrenia: Pharmacology, Efficacy, and Safety. Adv Ther. 2021 Jul;38(7):3652-3673. doi: 10.1007/s12325-021-01797-5. Epub 2021 Jun 6.
Barabassy A, Sebe B, Acsai K, Laszlovszky I, Szatmari B, Earley WR, Nemeth G. Safety and Tolerability of Cariprazine in Patients with Schizophrenia: A Pooled Analysis of Eight Phase II/III Studies. Neuropsychiatr Dis Treat. 2021 Apr 7;17:957-970. doi: 10.2147/NDT.S301225. eCollection 2021.
See Also Links
Not provided
Available IPD Information
Not provided
IPD Sharing Statement Module
No data available
No data is available for this block.
Results Section
Participant Flow Module
Pre-assignment Details
Not provided
Recruitment Details
Not provided
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
FG000
Placebo
Participants received placebo orally once a day for 6 weeks.
FG001
Cariprazine 1.5 mg
Participants received cariprazine 1.5 mg orally once a day for 6 weeks.
Marder S, Fleischhacker WW, Earley W, Lu K, Zhong Y, Nemeth G, Laszlovszky I, Szalai E, Durgam S. Efficacy of cariprazine across symptom domains in patients with acute exacerbation of schizophrenia: Pooled analyses from 3 phase II/III studies. Eur Neuropsychopharmacol. 2019 Jan;29(1):127-136. doi: 10.1016/j.euroneuro.2018.10.008. Epub 2018 Nov 20.
Earley W, Durgam S, Lu K, Laszlovszky I, Debelle M, Kane JM. Safety and tolerability of cariprazine in patients with acute exacerbation of schizophrenia: a pooled analysis of four phase II/III randomized, double-blind, placebo-controlled studies. Int Clin Psychopharmacol. 2017 Nov;32(6):319-328. doi: 10.1097/YIC.0000000000000187.
Citrome L, Durgam S, Lu K, Ferguson P, Laszlovszky I. The effect of cariprazine on hostility associated with schizophrenia: post hoc analyses from 3 randomized controlled trials. J Clin Psychiatry. 2016 Jan;77(1):109-15. doi: 10.4088/JCP.15m10192.
Durgam S, Starace A, Li D, Migliore R, Ruth A, Nemeth G, Laszlovszky I. An evaluation of the safety and efficacy of cariprazine in patients with acute exacerbation of schizophrenia: a phase II, randomized clinical trial. Schizophr Res. 2014 Feb;152(2-3):450-7. doi: 10.1016/j.schres.2013.11.041. Epub 2014 Jan 10.
FG002
Cariprazine 3.0 mg
Participants received cariprazine 3.0 mg orally once a day for 6 weeks.
FG003
Cariprazine 4.5 mg
Participants received cariprazine 4.5 mg orally once a day for 6 weeks.
FG004
Risperidone 4.0 mg
Participants received risperidone 4.0 mg orally once a day for 6 weeks.
FG000151 subjects
FG001145 subjects
FG002147 subjects
FG003148 subjects
FG004141 subjects
COMPLETED
FG00079 subjects
FG00190 subjects
FG00296 subjects
FG00398 subjects
FG004101 subjects
NOT COMPLETED
FG00072 subjects
FG00155 subjects
FG00251 subjects
FG00350 subjects
FG00440 subjects
Type
Comment
Reasons
Did Not Receive Treatment
FG0000 subjects
FG0010 subjects
FG0021 subjects
FG0031 subjects
FG0041 subjects
Adverse Event
FG00022 subjects
FG00114 subjects
FG0028 subjects
FG00312 subjects
FG004
Insufficient Therapeutic Response
FG00033 subjects
FG00118 subjects
FG00217 subjects
FG00315 subjects
FG004
Protocol Violation
FG0001 subjects
FG0012 subjects
FG0021 subjects
FG0033 subjects
FG004
Withdrawal of Consent
FG00014 subjects
FG00118 subjects
FG00222 subjects
FG00316 subjects
FG004
Lost to Follow-up
FG0000 subjects
FG0011 subjects
FG0022 subjects
FG0030 subjects
FG004
Jeopardizing Parole Status
FG0001 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Death in the Family
FG0001 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Arrest by Police
FG0000 subjects
FG0011 subjects
FG0020 subjects
FG0030 subjects
FG004
Administrative Reasons
FG0000 subjects
FG0011 subjects
FG0020 subjects
FG0032 subjects
FG004
Notification of Past Head Injury
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0031 subjects
FG004
Safety population: All randomized participants who took at least 1 dose of double-blind investigational product.
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
BG000
Placebo
Participants received placebo orally once a day for 6 weeks.
BG001
Cariprazine 1.5 mg
Participants received cariprazine 1.5 mg orally once a day for 6 weeks.
BG002
Cariprazine 3.0 mg
Participants received cariprazine 3.0 mg orally once a day for 6 weeks.
BG003
Cariprazine 4.5 mg
Participants received cariprazine 4.5 mg orally once a day for 6 weeks.
BG004
Risperidone 4.0 mg
Participants received risperidone 4.0 mg orally once a day for 6 weeks.
BG005
Total
Total of all reporting groups
Denominators
Units
Counts
Participants
BG000151
BG001145
BG002146
BG003147
BG004140
BG005729
Baseline Measures
Title
Description
Population Description
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Denominator Units Selected
Denominators
Classes
Age, Continuous
Mean
Standard Deviation
years
Title
Denominators
Categories
Title
Measurements
BG00036.0± 10.8
BG00136.8± 9.6
BG00237.1± 10.4
BG003
Sex: Female, Male
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Female
BG00050
BG00152
BG002
Ethnicity (NIH/OMB)
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Hispanic or Latino
BG0006
BG0017
BG002
Race (NIH/OMB)
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
American Indian or Alaska Native
BG0001
BG0012
BG002
Weight
Mean
Standard Deviation
kg
Title
Denominators
Categories
Title
Measurements
BG00074.4± 18.6
BG00171.7± 17.7
BG002
Height
Mean
Standard Deviation
cm
Title
Denominators
Categories
Title
Measurements
BG000170.8± 11.2
BG001169.0± 10.5
BG002
Body Mass Index (BMI)
Mean
Standard Deviation
kg/m^2
Title
Denominators
Categories
Title
Measurements
BG00025.2± 4.5
BG00124.9± 4.9
BG002
Waist circumference
Mean
Standard Deviation
cm
Title
Denominators
Categories
Title
Measurements
BG00086.7± 12.9
BG00185.2± 13.1
BG002
Type
Title
Description
Population Description
Reporting Status
Anticipated Posting Date
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Time Frame
Units Analyzed
Denominator Units Selected
Arm/Group Information
Denominators
Classes
Analyses
Primary
Change From Baseline to Week 6 in the PANSS Total Score
The Positive and Negative Syndrome Scale (PANSS) is a 30-item rating scale that assesses the positive and negative symptoms of individuals with schizophrenia. Responses to the 30 items are based on a structured clinical interview with the patient and on supporting clinical information obtained from family, hospital staff, or other reliable informants. Of the 30 psychiatric parameters measured by the scale, 7 assess positive symptoms (eg, delusions, grandiosity); 7 assess negative symptoms (eg, blunted affect, emotional withdrawal); and 16 assess general psychopathology (eg, poor attention, active social avoidance). Each item is scored on a 7-point scale (1 = absent, 2 = minimal, 3 = mild, 4 = moderate, 5 = moderately severe, 6 = severe, and 7 = extreme). The PANSS total score can range from 30 to 210. A higher score indicates worse symptoms. A negative change score indicates improvement.
Intent-to-treat population: All participants who took at least 1 dose of double-blind investigational product and who had at least 1 post-baseline assessment of the primary efficacy parameter, the PANSS total score.
Posted
Mean
Standard Error
Units on a scale
Baseline to Week 6
ID
Title
Description
OG000
Placebo
Participants received placebo orally once a day for 6 weeks.
OG001
Cariprazine 1.5 mg
Participants received cariprazine 1.5 mg orally once a day for 6 weeks.
OG002
Cariprazine 3.0 mg
Participants received cariprazine 3.0 mg orally once a day for 6 weeks.
OG003
Cariprazine 4.5 mg
Participants received cariprazine 4.5 mg orally once a day for 6 weeks.
OG004
Risperidone 4.0 mg
Participants received risperidone 4.0 mg orally once a day for 6 weeks.
Units
Counts
Participants
OG000148
OG001140
OG002140
OG003
Title
Denominators
Categories
Baseline
Title
Measurements
OG00097.3± 0.8
OG00197.1± 0.8
OG00297.2± 0.7
OG003
Group IDs
Group Description
Statistical Method
Statistical Comment
P-Value
P-Value Comment
Parameter Type
Parameter Value
Dispersion Type
Dispersion Value
Confidence Interval Sides
Confidence Interval %
CI Lower Limit
CI Upper Limit
CI Lower Limit Comment
CI Upper Limit Comment
Estimate Comment
Tested Non-Inferiority
Non-Inferiority Type
Non-Inferiority Comment
Other Analysis Description
OG000
OG001
ANCOVA
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline PANSS total score as the covariate.
0.0005
Least squares mean difference
-7.5
2-Sided
95
-11.8
-3.3
Superiority or Other
OG000
OG002
ANCOVA
Secondary
Change From Baseline to Week 6 in the CGI-S Score
The Clinical Global Impressions-Severity (CGI-S) scale is a 7-point scale that measures the overall severity of the illness compared with the severity of illness in other patients the Investigator has observed. The Investigator assesses the severity of the patient's illness as one of the following: 1 = Normal, not at all ill; 2 = Borderline ill; 3 = Mildly ill; 4 = Moderately ill; 5 = Markedly ill; 6 = Severely ill; 7 = Among the most extremely ill patients. The CGI-S score can range from 1 to 7. A higher score indicates more severe illness. A negative change score indicates improvement.
Intent-to-treat population: All participants who took at least 1 dose of double-blind investigational product and who had at least 1 post-baseline assessment of the primary efficacy parameter, the PANSS total score.
Posted
Mean
Standard Error
Units on a scale
Baseline to Week 6
ID
Title
Description
OG000
Placebo
Participants received placebo orally once a day for 6 weeks.
OG001
Cariprazine 1.5 mg
Participants received cariprazine 1.5 mg orally once a day for 6 weeks.
OG002
Cariprazine 3.0 mg
Participants received cariprazine 3.0 mg orally once a day for 6 weeks.
Time Frame
Not provided
Description
Safety population: All randomized participants who took at least 1 dose of double-blind investigational product.
All-Cause Mortality Comment
Not provided
Arm/Groups
ID
Title
Description
Deaths (Affected)
Deaths (At Risk)
Serious Events (Affected)
Serious Events (At Risk)
Other Events (Affected)
Other Events (At Risk)
EG000
Placebo
Participants received placebo orally once a day for 6 weeks.
0
151
7
151
67
151
EG001
Cariprazine 1.5 mg
Participants received cariprazine 1.5 mg orally once a day for 6 weeks.
0
145
5
145
73
145
EG002
Cariprazine 3.0 mg
Participants received cariprazine 3.0 mg orally once a day for 6 weeks.
0
146
0
146
74
146
EG003
Cariprazine 4.5 mg
Participants received cariprazine 4.5 mg orally once a day for 6 weeks.
0
147
4
147
87
147
EG004
Risperidone 4.0 mg
Participants received risperidone 4.0 mg orally once a day for 6 weeks.
0
140
3
140
80
140
Serious Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Schizophrenia
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG0001 affected151 at risk
EG0011 affected145 at risk
EG0020 affected146 at risk
EG0031 affected147 at risk
EG0040 affected140 at risk
Aggression
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0010 affected145 at risk
EG0020 affected146 at risk
EG003
Agitation
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0010 affected145 at risk
EG0020 affected146 at risk
EG003
HIV test positive
Investigations
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0010 affected145 at risk
EG0020 affected146 at risk
EG003
Atrioventricular block second degree
Cardiac disorders
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0011 affected145 at risk
EG0020 affected146 at risk
EG003
Fear of needles
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0011 affected145 at risk
EG0020 affected146 at risk
EG003
Femoral neck fracture
Injury, poisoning and procedural complications
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0011 affected145 at risk
EG0020 affected146 at risk
EG003
Foot fracture
Injury, poisoning and procedural complications
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0011 affected145 at risk
EG0020 affected146 at risk
EG003
Psychotic behaviour
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG0003 affected151 at risk
EG0011 affected145 at risk
EG0020 affected146 at risk
EG003
Spinal compression fracture
Metabolism and nutrition disorders
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0011 affected145 at risk
EG0020 affected146 at risk
EG003
Blood creatine phosphokinase increased
Investigations
MedDRA (12.0)
Systematic Assessment
EG0001 affected151 at risk
EG0010 affected145 at risk
EG0020 affected146 at risk
EG003
Chest pain
Cardiac disorders
MedDRA (12.0)
Systematic Assessment
EG0000 affected151 at risk
EG0010 affected145 at risk
EG0020 affected146 at risk
EG003
Grand mal convulsion
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG0001 affected151 at risk
EG0010 affected145 at risk
EG0020 affected146 at risk
EG003
Psychotic disorder
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG0001 affected151 at risk
EG0010 affected145 at risk
EG0020 affected146 at risk
EG003
Other Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Nausea
Gastrointestinal disorders
MedDRA (12.0)
Systematic Assessment
EG0005 affected151 at risk
EG0017 affected145 at risk
EG00211 affected146 at risk
EG00311 affected147 at risk
EG0049 affected140 at risk
Constipation
Gastrointestinal disorders
MedDRA (12.0)
Systematic Assessment
EG0006 affected151 at risk
EG00114 affected145 at risk
EG0029 affected146 at risk
EG003
Vomiting
Gastrointestinal disorders
MedDRA (12.0)
Systematic Assessment
EG0005 affected151 at risk
EG0014 affected145 at risk
EG0029 affected146 at risk
EG003
Weight increased
Investigations
MedDRA (12.0)
Systematic Assessment
EG0001 affected151 at risk
EG0013 affected145 at risk
EG0025 affected146 at risk
EG003
Extrapyramidal disorder
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG0009 affected151 at risk
EG00117 affected145 at risk
EG00214 affected146 at risk
EG003
Akathisia
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG0008 affected151 at risk
EG00113 affected145 at risk
EG00214 affected146 at risk
EG003
Headache
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG00017 affected151 at risk
EG00117 affected145 at risk
EG00211 affected146 at risk
EG003
Sedation
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG0006 affected151 at risk
EG0018 affected145 at risk
EG0027 affected146 at risk
EG003
Dizziness
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG0003 affected151 at risk
EG0015 affected145 at risk
EG0023 affected146 at risk
EG003
Tremor
Nervous system disorders
MedDRA (12.0)
Systematic Assessment
EG0006 affected151 at risk
EG0015 affected145 at risk
EG0027 affected146 at risk
EG003
Insomnia
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG00011 affected151 at risk
EG00115 affected145 at risk
EG00224 affected146 at risk
EG003
Schizophrenia
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG00012 affected151 at risk
EG0016 affected145 at risk
EG0027 affected146 at risk
EG003
Anxiety
Psychiatric disorders
MedDRA (12.0)
Systematic Assessment
EG0005 affected151 at risk
EG0016 affected145 at risk
EG0028 affected146 at risk
EG003
Certain Agreements
Are all PI(s) employees of the sponsor?
No
Restriction Type
OTHER
Results Disclosure Restriction on PI(s)?
Yes
Other Details
All data generated in this study will be the property of Forest Research Institute, Inc. An integrated clinical and statistical report will be prepared at the completion of the study. Publication of the results by the Investigator will be subject to mutual agreement between the Investigator and Forest Research Institute, Inc.
Point of Contact
Title
Organization
Phone
Extension
Email
Willie R. Earley, MD Associate Vice President Clinical Development-CNS
Allergan
714-246-4500
IR-CTRegistration@allergan.com
ID
Term
D012559
Schizophrenia
Ancestor Terms
ID
Term
D019967
Schizophrenia Spectrum and Other Psychotic Disorders
D001523
Mental Disorders
Browse Leaves
Not provided
Browse Branches
Not provided
ID
Term
C533287
cariprazine
D018967
Risperidone
Ancestor Terms
ID
Term
D011744
Pyrimidinones
D011743
Pyrimidines
D006573
Heterocyclic Compounds, 1-Ring
D006571
Heterocyclic Compounds
Browse Leaves
Not provided
Browse Branches
Not provided
13 subjects
10 subjects
1 subjects
15 subjects
0 subjects
0 subjects
0 subjects
0 subjects
0 subjects
0 subjects
35.8
± 10.8
BG00436.5± 11.1
BG00536.4± 10.5
39
BG00344
BG00442
BG005227
Male
BG000101
BG00193
BG002107
BG003103
BG00498
BG005502
2
BG0034
BG0045
BG00524
Not Hispanic or Latino
BG000145
BG001138
BG002144
BG003143
BG004135
BG005705
Unknown or Not Reported
BG0000
BG0010
BG0020
BG0030
BG0040
BG0050
0
BG0030
BG0040
BG0053
Asian
BG00036
BG00134
BG00237
BG00339
BG00437
BG005183
Native Hawaiian or Other Pacific Islander
BG0000
BG0010
BG0020
BG0030
BG0040
BG0050
Black or African American
BG00034
BG00132
BG00238
BG00332
BG00435
BG005171
White
BG00080
BG00177
BG00271
BG00375
BG00467
BG005370
More than one race
BG0000
BG0010
BG0020
BG0031
BG0041
BG0052
Unknown or Not Reported
BG0000
BG0010
BG0020
BG0030
BG0040
BG0050
74.8
± 16.3
BG00372.4± 16.6
BG00475.1± 18.2
BG00573.7± 17.5
170.7
± 10.3
BG003170.3± 10.4
BG004170.0± 10.5
BG005170.2± 10.6
25.6
± 4.6
BG00324.8± 4.2
BG00425.8± 4.8
BG00525.2± 4.6
87.6
± 12.6
BG00385.8± 12.7
BG00488.0± 13.0
BG00586.7± 12.9
145
OG004138
96.7
± 0.8
OG00498.1± 0.8
Change at Week 6
Title
Measurements
OG000-9.5± 1.6
OG001-17.3± 1.7
OG002-18.7± 1.8
OG003-20.2± 1.6
OG004-25.3± 1.7
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline PANSS total score as the covariate.
<0.0001
Least squares mean difference
-8.8
2-Sided
95
-13.1
-4.6
Superiority or Other
OG000
OG003
ANCOVA
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline PANSS total score as the covariate.
<0.0001
Least squares mean difference
-10.4
2-Sided
95
-14.6
-6.2
Superiority or Other
OG000
OG004
ANCOVA
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline PANSS total score as the covariate.
<0.0001
Least squares mean difference
-15.0
2-Sided
95
-19.4
-10.8
Superiority or Other
OG003
Cariprazine 4.5 mg
Participants received cariprazine 4.5 mg orally once a day for 6 weeks.
OG004
Risperidone 4.0 mg
Participants received risperidone 4.0 mg orally once a day for 6 weeks.
Units
Counts
Participants
OG000148
OG001140
OG002140
OG003145
OG004138
Title
Denominators
Categories
Baseline
Title
Measurements
OG0004.9± 0.1
OG0014.7± 0.1
OG0024.9± 0.1
OG0034.8± 0.1
OG0044.8± 0.1
Change at Week 6
Title
Measurements
OG000-0.6± 0.1
OG001-0.9± 0.1
OG002-1.1± 0.1
OG003
Group IDs
Group Description
Statistical Method
Statistical Comment
P-Value
P-Value Comment
Parameter Type
Parameter Value
Dispersion Type
Dispersion Value
Confidence Interval Sides
Confidence Interval %
CI Lower Limit
CI Upper Limit
CI Lower Limit Comment
CI Upper Limit Comment
Estimate Comment
Tested Non-Inferiority
Non-Inferiority Type
Non-Inferiority Comment
Other Analysis Description
OG000
OG001
ANCOVA
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline CGI-S score as the covariate.
0.0040
Least squares mean difference
-0.4
2-Sided
95
-0.6
-0.1
Superiority or Other
OG000
OG002
ANCOVA
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline CGI-S score as the covariate.
0.0003
Least squares mean difference
-0.5
2-Sided
95
-0.7
-0.2
Superiority or Other
OG000
OG003
ANCOVA
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline CGI-S score as the covariate.
<0.0001
Least squares mean difference
-0.6
2-Sided
95
-0.9
-0.4
Superiority or Other
OG000
OG004
ANCOVA
The analysis of covariance (ANCOVA) included treatment group and study center as factors and the Baseline CGI-S score as the covariate.