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Brexpiprazole in Borderline Personality Disorder

A Double-Blind, Placebo-Controlled Study of Brexpiprazole in the Treatment of Borderline Personality Disorder.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03418675
Enrollment
80
Registered
2018-02-01
Start date
2018-11-26
Completion date
2021-04-14
Last updated
2022-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Borderline Personality Disorder

Brief summary

The primary objective of the proposed study is to evaluate the safety and efficacy of Brexpiprazole in adults with borderline personality disorder (BPD). The hypothesis to be tested is that brexpiprazole will be more effective and well tolerated in adults with BPD compared to placebo. The proposed study will provide needed data on the treatment of a disabling disorder.

Detailed description

Borderline personality disorder is characterized by mood instability, cognitive symptoms, impulsive behavior, and disturbed relationships (1-3). A variety of psychotherapies have been developed (4-6) and, while research on the use of medication is ongoing, no drug has been approved in the United States or elsewhere for its treatment (7). Second generation antipsychotics have been the most intensively studied (8-11). Current treatments for BPD are often inadequate. Dialectical behavioral therapy has been shown to reduce BPD but finding trained psychologists is difficult. Dysfunctions in the serotoninergic and dopaminergic systems have been demonstrated in-and considered as possible causes for-symptoms associated with the disorder (25-28). Several studies on the use of traditional (29) and atypical antipsychotic agents in patients with borderline personality disorder (30-31) have shown a positive effect on individual symptoms (29, 32-36). However, we are not aware of any study evaluating Brexpiprazole in the treatment of patients with borderline personality disorder. In the proposed double-blind, placebo-controlled study, the influence of Brexpiprazole on the multifaceted psychopathological symptoms and aggression of patients with borderline personality disorder will be investigated. Brexpiprazole therefore has distinctive properties that make it a promising option for patients with BPD. Brexpiprazole is a novel D2 partial agonist, has affinity for 5-HT1A, acts as an antagonist of the noradrenergic α1/2 receptor, partial agonist for D3, and antagonist for 5-HT2A (37-39). In addition, because of low rates of side effects, Brexpiprazole should be a well-tolerated and in fact desired medication approach to BPD.

Interventions

DRUGRexulti

Atypical antipsychotic

DRUGPlacebo

Pill that contains no medicine

Sponsors

Otsuka America Pharmaceutical
CollaboratorINDUSTRY
University of Chicago
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Men and women age 18-65; 2. Primary diagnosis of BPD 3. Zanarini scale score of at least 9 at baseline 4. Ability to understand and sign the consent form.

Exclusion criteria

1. Unstable medical illness based on history or clinically significant abnormalities on baseline physical examination 2. Subjects with schizophrenia or bipolar I disorder 3. Subjects with an active substance use disorder 4. Current pregnancy or lactation, or inadequate contraception in women of childbearing potential 5. Subjects considered an immediate suicide risk based on the Columbia Suicide Severity rating Scale (C-SSRS) (www.cssrs.columbia.edu/docs) 6. Illegal substance use based on urine toxicology screening 7. Initiation of psychological interventions within 3 months of screening 8. Use of any other psychotropic medication 9. Previous treatment with Brexpiprazole 10. Cognitive impairment that interferes with the capacity to understand and self-administer medication or provide written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Zanarini Rating Scale for Borderline Personality DisorderBaseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)A clinician-administered scale assessing Borderline Personality Scale severity at all study visits. Scores range from 0-36. Higher scores represent worse Borderline Personality Disorder severity, and lower scores represent milder Borderline Personality Disorder severity.

Secondary

MeasureTime frameDescription
Young Mania Rating ScaleBaseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)A clinician-administered, 11 item scale that assesses manic symptoms at baseline and over time. Higher total scores indicate higher severity of manic symptoms. This scale is used to rate the severity of manic abnormality in the patient. Subsets of the scale range from 0-4 with 0 indicating no severity. This scale will be assessed at all visits.
Self Report Version of Zanarini ScaleBaseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)A self-report scale assessing Borderline Personality severity that will be assessed at all visits.This scale is assessing severity and change in BPD symptoms. This is a 9-item scale measuring severity of different aspects of Borderline Personality Disorder, with each item rated on a 0-4 scale, 0=no symptoms, 4=severe symptoms. Total scores range from 0-36.
Borderline Evaluation of Severity Over Time (BEST)Assessed at Visits 1 to 8, change in scores from Visit 1 to Visit 8 (baseline to week 12) is reportedA self rated scale used to measure severity and change. The first 12 items of the scale are on a scale from 1-5, with 5 meaning that the item caused extreme distress, severe difficulties in relationships, and/or kept them from getting things done. The lowest rating (1) means it caused little or no problems. Items 13-15 (positive behaviors) are rated according to frequency. Completed at every visit.
Barratt Impulsiveness Scale (BIS)Baseline (Visit 1), Week 12 (Visit 8)A self-report assessment of impulsivity that will be assessed at baseline and visit 8. The BIS is composed of 30 items describing common impulsive or non-impulsive (for reverse scored items) behaviors and preferences. Items are scored on a 4-point scale: (Rarely/Never = 1, Occasionally = 2, Often = 3, Almost Always/Always = 4). These scores are summed to produce an overall impulsivity score ranging from 30 (not impulsive) to 120 (extremely impulsive).
Symptom Checklist-90 RevisedBaseline, Visit 8 (Week 12)An instrument that helps evaluate a broad range of psychological problems and symptoms of Borderline Personality Disorder psychopathology. This will be assessed at baseline and visit 8.The 115 items are rated by using a 5-step Likert scale (0=not at all, 4=very strong) and provide a global picture of borderline psychopathology. Global scores of borderline psychopathology are calculated by summing 12 items and range from 0-48. Higher scores indicate more severe symptoms of Borderline Personality Disorder.
Modified Overt Aggression Scale (MOAS)Baseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)A clinician-administered behavior rating scale measuring four types of aggressive behavior that will be assessed at all 9 visits. The subsets range on a scale from 0-4 with 0 indicating no aggression present. This scale tracks changes in level of aggression over time. The total weighted sum of the sections of the scale is recorded. Higher total scores indicate higher aggression levels.
Hamilton Depression Rating Scale (HAM-D)Assessed at Visits 1 to 8, change in scores from Visit 1 to Visit 8 (baseline to week 12) is reportedA clinician-administered assessment of depression that will be assessed at all study visits (Visits 1-8). Higher total scores indicate higher levels of depression (up to 52), while a score of 0 would indicate no depressive symptoms.
MINI International Neuropsychiatric InterviewBaseline (Week 1)A short-structured interview that assesses comorbid psychiatric disorders according to the DSM 5 criteria. This assessment will be done during the baseline visit.
Sheehan Disability Scale (SDS)Baseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)Subjects will complete the SDS at all visits. The change in scores from baseline to study completion will be assessed. The scale itself assesses the level of disability from borderline personality disorder (or target disorder) with higher scores indicating a more debilitating disorder. Scores range from 0-30.
Quality of Life Inventory (QOLI)Baseline (Week 1), Week 12 (Visit 8)A self-report assessment of patient perceived quality of life that will be assessed at baseline and visit 8. Higher scores indicate a higher quality of life, whereas lower scores indicate a lower quality of life. Participants are asked to rate the importance of each domain on a 3-point scale ranging from 1=not important to 3=very important, and to rate how satisfied they are with that domain on a 6-point scale, ranging from -3=very dissatisfied to +3=very satisfied. In scoring, importance ratings are multiplied by satisfaction ratings to produce weighted satisfaction scores for each of the 16 domains. Weighted satisfaction scores are summed and divided by the number of domains that were rated as important or very important to produce a raw score, which is then converted to a t-score, which provides a proxy measurement for perceived quality of life. T-scores range from very low perceived quality of life (0-36) to high perceived quality of life (58-77).
Columbia Suicide Severity Rating Scale (CSSRS)Baseline (Visit 1), Week 12 (Visit 8)A self-report scale measuring suicidality. Subjects will complete the scale at all visits. Subjects are asked about suicidal thoughts. If answers are no, rater can proceed to suicidal behavior section where subject is asked about any non-suicidal self injurious behavior. If yes, subject is asked about intensity of ideations. In the event of serious threat to themselves, the subject will be escorted to the emergency room. Total score indicates severity of suicidal ideation and behavior, with lower scores representing lower levels of suicidality and higher scores representing higher levels of suicidality. A score of 0 would reflect no suicidality present, whereas a maximum score of 5 would reflect active suicidal ideation with intent to act.
Hamilton Anxiety Rating Scale (HAM-A)assessed at Visits 1 to 8, change in scores from Visit 1 to Visit 8 (baseline to Week 12) is reportedA clinician-administered assessment of anxiety that will be assessed at all study visits (Visit 1-Visit 8). Changes in scores from baseline to final visit will be assessed. Higher scores (up to 56) indicate higher levels of anxiety, with 0 being no symptoms of anxiety.

Countries

United States

Participant flow

Participants by arm

ArmCount
Placebo
1 milligram per day for the first week and 1 milligram per day for the final taper week 2 milligrams per day for 10 weeks between taper periods. Placebo: Pill that contains no medicine
37
Rexulti
1 milligram per day day for the first week and 1 milligram per day for the final taper week 2 milligrams per day for 10 weeks between taper periods. Rexulti: Atypical antipsychotic
40
Total77

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event20
Overall StudyLost to Follow-up1310

Baseline characteristics

CharacteristicPlaceboRexultiTotal
Age, Continuous28.9 years30.9 years29.9 years
Education
Bachelors
11 Participants9 Participants20 Participants
Education
HS diploma/GED
5 Participants7 Participants12 Participants
Education
Less than HS diploma/GED
0 Participants0 Participants0 Participants
Education
Masters+
0 Participants3 Participants3 Participants
Education
Some college/Associates
20 Participants18 Participants38 Participants
Education
Unknown/ Not Reported
1 Participants3 Participants4 Participants
Employment Status
Full-time
11 Participants12 Participants23 Participants
Employment Status
Other
1 Participants1 Participants2 Participants
Employment Status
Part-time
2 Participants3 Participants5 Participants
Employment Status
Retired
0 Participants0 Participants0 Participants
Employment Status
Student
8 Participants8 Participants16 Participants
Employment Status
Unemployed
15 Participants11 Participants26 Participants
Employment Status
Unknown/Not Reported
0 Participants5 Participants5 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
8 Participants7 Participants15 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
13 Participants19 Participants32 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
16 Participants14 Participants30 Participants
Marital Status
Divorced/separated
3 Participants6 Participants9 Participants
Marital Status
Living together/engaged
1 Participants1 Participants2 Participants
Marital Status
Married
2 Participants3 Participants5 Participants
Marital Status
Single
31 Participants27 Participants58 Participants
Marital Status
Unknown/Not reported
0 Participants3 Participants3 Participants
Marital Status
Widowed
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
2 Participants1 Participants3 Participants
Race (NIH/OMB)
Black or African American
6 Participants7 Participants13 Participants
Race (NIH/OMB)
More than one race
1 Participants2 Participants3 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants1 Participants1 Participants
Race (NIH/OMB)
Unknown or Not Reported
6 Participants9 Participants15 Participants
Race (NIH/OMB)
White
22 Participants20 Participants42 Participants
Sex/Gender, Customized
Female
21 Participants24 Participants45 Participants
Sex/Gender, Customized
Male
12 Participants9 Participants21 Participants
Sex/Gender, Customized
Other
4 Participants2 Participants6 Participants
Sex/Gender, Customized
Unknown/Not reported
0 Participants5 Participants5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 400 / 40
other
Total, other adverse events
19 / 4011 / 40
serious
Total, serious adverse events
1 / 400 / 40

Outcome results

Primary

Zanarini Rating Scale for Borderline Personality Disorder

A clinician-administered scale assessing Borderline Personality Scale severity at all study visits. Scores range from 0-36. Higher scores represent worse Borderline Personality Disorder severity, and lower scores represent milder Borderline Personality Disorder severity.

Time frame: Baseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)

Population: Subjects assigned to Placebo or Rexulti who completed one-post randomization visit.

ArmMeasureGroupValue (MEAN)
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 46 score on a scale
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 114.9 score on a scale
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 27.6 score on a scale
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 34.7 score on a scale
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 54.2 score on a scale
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 65.7 score on a scale
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 75 score on a scale
PlaceboZanarini Rating Scale for Borderline Personality DisorderVisit 88.4 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 83.1 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 44.4 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 54.5 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 114.9 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 74 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 26.7 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 64.9 score on a scale
RexultiZanarini Rating Scale for Borderline Personality DisorderVisit 35.3 score on a scale
Secondary

Barratt Impulsiveness Scale (BIS)

A self-report assessment of impulsivity that will be assessed at baseline and visit 8. The BIS is composed of 30 items describing common impulsive or non-impulsive (for reverse scored items) behaviors and preferences. Items are scored on a 4-point scale: (Rarely/Never = 1, Occasionally = 2, Often = 3, Almost Always/Always = 4). These scores are summed to produce an overall impulsivity score ranging from 30 (not impulsive) to 120 (extremely impulsive).

Time frame: Baseline (Visit 1), Week 12 (Visit 8)

Population: Subjects who completed the study.

ArmMeasureGroupValue (MEAN)Dispersion
PlaceboBarratt Impulsiveness Scale (BIS)Visit 176.53 score on a scaleStandard Deviation 15.33
PlaceboBarratt Impulsiveness Scale (BIS)Visit 868.13 score on a scaleStandard Deviation 13.89
RexultiBarratt Impulsiveness Scale (BIS)Visit 172.27 score on a scaleStandard Deviation 15.5
RexultiBarratt Impulsiveness Scale (BIS)Visit 870.5 score on a scaleStandard Deviation 17.86
Secondary

Borderline Evaluation of Severity Over Time (BEST)

A self rated scale used to measure severity and change. The first 12 items of the scale are on a scale from 1-5, with 5 meaning that the item caused extreme distress, severe difficulties in relationships, and/or kept them from getting things done. The lowest rating (1) means it caused little or no problems. Items 13-15 (positive behaviors) are rated according to frequency. Completed at every visit.

Time frame: Assessed at Visits 1 to 8, change in scores from Visit 1 to Visit 8 (baseline to week 12) is reported

Population: Subjects assigned to Placebo or Rexulti who completed the study.

ArmMeasureGroupValue (MEAN)Dispersion
PlaceboBorderline Evaluation of Severity Over Time (BEST)Visit 140.90 score on a scaleStandard Deviation 10.91
PlaceboBorderline Evaluation of Severity Over Time (BEST)Visit 829.15 score on a scaleStandard Deviation 8.37
RexultiBorderline Evaluation of Severity Over Time (BEST)Visit 140.54 score on a scaleStandard Deviation 8.25
RexultiBorderline Evaluation of Severity Over Time (BEST)Visit 823.15 score on a scaleStandard Deviation 9.06
Secondary

Columbia Suicide Severity Rating Scale (CSSRS)

A self-report scale measuring suicidality. Subjects will complete the scale at all visits. Subjects are asked about suicidal thoughts. If answers are no, rater can proceed to suicidal behavior section where subject is asked about any non-suicidal self injurious behavior. If yes, subject is asked about intensity of ideations. In the event of serious threat to themselves, the subject will be escorted to the emergency room. Total score indicates severity of suicidal ideation and behavior, with lower scores representing lower levels of suicidality and higher scores representing higher levels of suicidality. A score of 0 would reflect no suicidality present, whereas a maximum score of 5 would reflect active suicidal ideation with intent to act.

Time frame: Baseline (Visit 1), Week 12 (Visit 8)

Population: Subjects who completed all baseline data

ArmMeasureGroupValue (MEAN)Dispersion
PlaceboColumbia Suicide Severity Rating Scale (CSSRS)Visit 11.15 score on a scaleStandard Deviation 1.72
PlaceboColumbia Suicide Severity Rating Scale (CSSRS)Visit 80.23 score on a scaleStandard Deviation 0.66
RexultiColumbia Suicide Severity Rating Scale (CSSRS)Visit 10.73 score on a scaleStandard Deviation 0.99
RexultiColumbia Suicide Severity Rating Scale (CSSRS)Visit 80.08 score on a scaleStandard Deviation 0.35
Secondary

Hamilton Anxiety Rating Scale (HAM-A)

A clinician-administered assessment of anxiety that will be assessed at all study visits (Visit 1-Visit 8). Changes in scores from baseline to final visit will be assessed. Higher scores (up to 56) indicate higher levels of anxiety, with 0 being no symptoms of anxiety.

Time frame: assessed at Visits 1 to 8, change in scores from Visit 1 to Visit 8 (baseline to Week 12) is reported

Population: Subjects assigned to Placebo or Rexulti who completed the study.

ArmMeasureValue (MEAN)Dispersion
PlaceboHamilton Anxiety Rating Scale (HAM-A)-2.41 change in score on a scaleStandard Deviation 8.43
RexultiHamilton Anxiety Rating Scale (HAM-A)-4.88 change in score on a scaleStandard Deviation 7.46
Secondary

Hamilton Depression Rating Scale (HAM-D)

A clinician-administered assessment of depression that will be assessed at all study visits (Visits 1-8). Higher total scores indicate higher levels of depression (up to 52), while a score of 0 would indicate no depressive symptoms.

Time frame: Assessed at Visits 1 to 8, change in scores from Visit 1 to Visit 8 (baseline to week 12) is reported

Population: Subjects assigned to placebo or Rexulti who completed the study

ArmMeasureValue (MEAN)Dispersion
PlaceboHamilton Depression Rating Scale (HAM-D)-2.09 change in score on a scaleStandard Deviation 6.91
RexultiHamilton Depression Rating Scale (HAM-D)-3.81 change in score on a scaleStandard Deviation 7.41
Secondary

MINI International Neuropsychiatric Interview

A short-structured interview that assesses comorbid psychiatric disorders according to the DSM 5 criteria. This assessment will be done during the baseline visit.

Time frame: Baseline (Week 1)

Population: Subjects who completed all baseline measures.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
PlaceboMINI International Neuropsychiatric InterviewPanic Disorder (Lifetime)11 Participants
PlaceboMINI International Neuropsychiatric InterviewSubstance Use Disorder (Past 12 months)11 Participants
PlaceboMINI International Neuropsychiatric InterviewAgoraphobia (Current)7 Participants
PlaceboMINI International Neuropsychiatric InterviewManic Episode (Current)2 Participants
PlaceboMINI International Neuropsychiatric InterviewAny Psychotic Disorder (Lifetime)0 Participants
PlaceboMINI International Neuropsychiatric InterviewMajor Depressive Disorder with Psychotic Features (Past)0 Participants
PlaceboMINI International Neuropsychiatric InterviewPost Traumatic Stress Disorder (Current)9 Participants
PlaceboMINI International Neuropsychiatric InterviewAnorexia Nervosa (current)0 Participants
PlaceboMINI International Neuropsychiatric InterviewManic Episode (Past)1 Participants
PlaceboMINI International Neuropsychiatric InterviewBulimia Nervosa (Current)4 Participants
PlaceboMINI International Neuropsychiatric InterviewAny Psychotic Disorder (Current)0 Participants
PlaceboMINI International Neuropsychiatric InterviewBinge Eating Disorder (Current)2 Participants
PlaceboMINI International Neuropsychiatric InterviewHypomanic Episode (Current)1 Participants
PlaceboMINI International Neuropsychiatric InterviewGeneralized Anxiety Disorder (Current)10 Participants
PlaceboMINI International Neuropsychiatric InterviewObsessive Compulsive Disorder (Current)3 Participants
PlaceboMINI International Neuropsychiatric InterviewAntisocial Personality Disorder (Lifetime)8 Participants
PlaceboMINI International Neuropsychiatric InterviewBipolar I Disorder (Current)0 Participants
PlaceboMINI International Neuropsychiatric InterviewADHD Combined Type (Current)2 Participants
PlaceboMINI International Neuropsychiatric InterviewMajor Depressive Disorder with Psychotic Features (Current)0 Participants
PlaceboMINI International Neuropsychiatric InterviewADHD Inattentive Type (Current)0 Participants
PlaceboMINI International Neuropsychiatric InterviewBipolar I Disorder (Past)0 Participants
PlaceboMINI International Neuropsychiatric InterviewADHD Hyperactive Type (Current)1 Participants
PlaceboMINI International Neuropsychiatric InterviewAlcohol Use Disorder (Past 12 months)13 Participants
PlaceboMINI International Neuropsychiatric InterviewTourette's Syndrome (Lifetime)0 Participants
PlaceboMINI International Neuropsychiatric InterviewBipolar II Disorder (Current)0 Participants
PlaceboMINI International Neuropsychiatric InterviewPersistent Motor Tic Disorder (Lifetime)1 Participants
PlaceboMINI International Neuropsychiatric InterviewMajor Depressive Episode (Current)16 Participants
PlaceboMINI International Neuropsychiatric InterviewProvisional Vocal Tic Disorder (Lifetime)0 Participants
PlaceboMINI International Neuropsychiatric InterviewBipolar II Disorder (Past)0 Participants
PlaceboMINI International Neuropsychiatric InterviewProvisional Tic Disorder (Lifetime)0 Participants
PlaceboMINI International Neuropsychiatric InterviewSocial Anxiety Disorder (Current)6 Participants
PlaceboMINI International Neuropsychiatric InterviewSpecific Phobia4 Participants
PlaceboMINI International Neuropsychiatric InterviewPanic Disorder (Current)6 Participants
PlaceboMINI International Neuropsychiatric InterviewBody Dysmorphic Disorder (Current)3 Participants
PlaceboMINI International Neuropsychiatric InterviewMajor Depressive Episode (Past)12 Participants
RexultiMINI International Neuropsychiatric InterviewBody Dysmorphic Disorder (Current)2 Participants
RexultiMINI International Neuropsychiatric InterviewSocial Anxiety Disorder (Current)9 Participants
RexultiMINI International Neuropsychiatric InterviewObsessive Compulsive Disorder (Current)3 Participants
RexultiMINI International Neuropsychiatric InterviewPost Traumatic Stress Disorder (Current)12 Participants
RexultiMINI International Neuropsychiatric InterviewAlcohol Use Disorder (Past 12 months)8 Participants
RexultiMINI International Neuropsychiatric InterviewSubstance Use Disorder (Past 12 months)8 Participants
RexultiMINI International Neuropsychiatric InterviewAny Psychotic Disorder (Lifetime)1 Participants
RexultiMINI International Neuropsychiatric InterviewMajor Depressive Disorder with Psychotic Features (Current)0 Participants
RexultiMINI International Neuropsychiatric InterviewMajor Depressive Episode (Current)18 Participants
RexultiMINI International Neuropsychiatric InterviewMajor Depressive Episode (Past)18 Participants
RexultiMINI International Neuropsychiatric InterviewManic Episode (Current)2 Participants
RexultiMINI International Neuropsychiatric InterviewManic Episode (Past)3 Participants
RexultiMINI International Neuropsychiatric InterviewHypomanic Episode (Current)0 Participants
RexultiMINI International Neuropsychiatric InterviewBipolar I Disorder (Current)0 Participants
RexultiMINI International Neuropsychiatric InterviewBipolar I Disorder (Past)0 Participants
RexultiMINI International Neuropsychiatric InterviewBipolar II Disorder (Current)0 Participants
RexultiMINI International Neuropsychiatric InterviewBipolar II Disorder (Past)1 Participants
RexultiMINI International Neuropsychiatric InterviewPanic Disorder (Current)6 Participants
RexultiMINI International Neuropsychiatric InterviewPanic Disorder (Lifetime)10 Participants
RexultiMINI International Neuropsychiatric InterviewAny Psychotic Disorder (Current)0 Participants
RexultiMINI International Neuropsychiatric InterviewMajor Depressive Disorder with Psychotic Features (Past)0 Participants
RexultiMINI International Neuropsychiatric InterviewAnorexia Nervosa (current)1 Participants
RexultiMINI International Neuropsychiatric InterviewBulimia Nervosa (Current)4 Participants
RexultiMINI International Neuropsychiatric InterviewBinge Eating Disorder (Current)4 Participants
RexultiMINI International Neuropsychiatric InterviewGeneralized Anxiety Disorder (Current)15 Participants
RexultiMINI International Neuropsychiatric InterviewAntisocial Personality Disorder (Lifetime)4 Participants
RexultiMINI International Neuropsychiatric InterviewADHD Combined Type (Current)4 Participants
RexultiMINI International Neuropsychiatric InterviewADHD Inattentive Type (Current)1 Participants
RexultiMINI International Neuropsychiatric InterviewADHD Hyperactive Type (Current)1 Participants
RexultiMINI International Neuropsychiatric InterviewTourette's Syndrome (Lifetime)1 Participants
RexultiMINI International Neuropsychiatric InterviewPersistent Motor Tic Disorder (Lifetime)1 Participants
RexultiMINI International Neuropsychiatric InterviewProvisional Vocal Tic Disorder (Lifetime)0 Participants
RexultiMINI International Neuropsychiatric InterviewProvisional Tic Disorder (Lifetime)0 Participants
RexultiMINI International Neuropsychiatric InterviewSpecific Phobia1 Participants
RexultiMINI International Neuropsychiatric InterviewAgoraphobia (Current)9 Participants
Secondary

Modified Overt Aggression Scale (MOAS)

A clinician-administered behavior rating scale measuring four types of aggressive behavior that will be assessed at all 9 visits. The subsets range on a scale from 0-4 with 0 indicating no aggression present. This scale tracks changes in level of aggression over time. The total weighted sum of the sections of the scale is recorded. Higher total scores indicate higher aggression levels.

Time frame: Baseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)

Population: No data displayed because data were not collected. Due to the outbreak of the COVID-19 pandemic and following restrictions, all study visits were moved to teleheath and only essential scales were completed.

Secondary

Quality of Life Inventory (QOLI)

A self-report assessment of patient perceived quality of life that will be assessed at baseline and visit 8. Higher scores indicate a higher quality of life, whereas lower scores indicate a lower quality of life. Participants are asked to rate the importance of each domain on a 3-point scale ranging from 1=not important to 3=very important, and to rate how satisfied they are with that domain on a 6-point scale, ranging from -3=very dissatisfied to +3=very satisfied. In scoring, importance ratings are multiplied by satisfaction ratings to produce weighted satisfaction scores for each of the 16 domains. Weighted satisfaction scores are summed and divided by the number of domains that were rated as important or very important to produce a raw score, which is then converted to a t-score, which provides a proxy measurement for perceived quality of life. T-scores range from very low perceived quality of life (0-36) to high perceived quality of life (58-77).

Time frame: Baseline (Week 1), Week 12 (Visit 8)

Population: Subjects who completed all visits.

ArmMeasureGroupValue (MEAN)Dispersion
PlaceboQuality of Life Inventory (QOLI)Visit 128.89 score on a scaleStandard Deviation 9.11
PlaceboQuality of Life Inventory (QOLI)Visit 830.75 score on a scaleStandard Deviation 10.62
RexultiQuality of Life Inventory (QOLI)Visit 835.71 score on a scaleStandard Deviation 6.43
RexultiQuality of Life Inventory (QOLI)Visit 128.70 score on a scaleStandard Deviation 11.18
Secondary

Self Report Version of Zanarini Scale

A self-report scale assessing Borderline Personality severity that will be assessed at all visits.This scale is assessing severity and change in BPD symptoms. This is a 9-item scale measuring severity of different aspects of Borderline Personality Disorder, with each item rated on a 0-4 scale, 0=no symptoms, 4=severe symptoms. Total scores range from 0-36.

Time frame: Baseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)

Population: Subjects assigned to Placebo or Rexulti who completed one-post randomization visit.

ArmMeasureGroupValue (MEAN)
PlaceboSelf Report Version of Zanarini ScaleVisit 410.7 score on a scale
PlaceboSelf Report Version of Zanarini ScaleVisit 212.8 score on a scale
PlaceboSelf Report Version of Zanarini ScaleVisit 59.7 score on a scale
PlaceboSelf Report Version of Zanarini ScaleVisit 118.2 score on a scale
PlaceboSelf Report Version of Zanarini ScaleVisit 78.7 score on a scale
PlaceboSelf Report Version of Zanarini ScaleVisit 310.7 score on a scale
PlaceboSelf Report Version of Zanarini ScaleVisit 89.3 score on a scale
PlaceboSelf Report Version of Zanarini ScaleVisit 69.6 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 85.8 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 117.6 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 210.9 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 37.9 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 48.0 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 66.6 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 76.0 score on a scale
RexultiSelf Report Version of Zanarini ScaleVisit 57.0 score on a scale
Secondary

Sheehan Disability Scale (SDS)

Subjects will complete the SDS at all visits. The change in scores from baseline to study completion will be assessed. The scale itself assesses the level of disability from borderline personality disorder (or target disorder) with higher scores indicating a more debilitating disorder. Scores range from 0-30.

Time frame: Baseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)

Population: Subjects who completed at least one post-randomization visit

ArmMeasureGroupValue (MEAN)
PlaceboSheehan Disability Scale (SDS)Visit 213.3 score on a scale
PlaceboSheehan Disability Scale (SDS)Visit 511.7 score on a scale
PlaceboSheehan Disability Scale (SDS)Visit 117.3 score on a scale
PlaceboSheehan Disability Scale (SDS)Visit 611.2 score on a scale
PlaceboSheehan Disability Scale (SDS)Visit 311.5 score on a scale
PlaceboSheehan Disability Scale (SDS)Visit 712.0 score on a scale
PlaceboSheehan Disability Scale (SDS)Visit 412.4 score on a scale
PlaceboSheehan Disability Scale (SDS)Visit 812.7 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 47.8 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 210.7 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 37.8 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 115.8 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 87.7 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 57.0 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 67.9 score on a scale
RexultiSheehan Disability Scale (SDS)Visit 76.9 score on a scale
Secondary

Symptom Checklist-90 Revised

An instrument that helps evaluate a broad range of psychological problems and symptoms of Borderline Personality Disorder psychopathology. This will be assessed at baseline and visit 8.The 115 items are rated by using a 5-step Likert scale (0=not at all, 4=very strong) and provide a global picture of borderline psychopathology. Global scores of borderline psychopathology are calculated by summing 12 items and range from 0-48. Higher scores indicate more severe symptoms of Borderline Personality Disorder.

Time frame: Baseline, Visit 8 (Week 12)

Population: Subjects who completed the study.

ArmMeasureGroupValue (MEAN)Dispersion
PlaceboSymptom Checklist-90 RevisedVisit 126.17 score on a scaleStandard Deviation 10.44
PlaceboSymptom Checklist-90 RevisedVisit 820.25 score on a scaleStandard Deviation 7.99
RexultiSymptom Checklist-90 RevisedVisit 125.42 score on a scaleStandard Deviation 11.58
RexultiSymptom Checklist-90 RevisedVisit 814.21 score on a scaleStandard Deviation 10.88
Secondary

Young Mania Rating Scale

A clinician-administered, 11 item scale that assesses manic symptoms at baseline and over time. Higher total scores indicate higher severity of manic symptoms. This scale is used to rate the severity of manic abnormality in the patient. Subsets of the scale range from 0-4 with 0 indicating no severity. This scale will be assessed at all visits.

Time frame: Baseline (Visit 1), Week 1 (Visit 2), Week 2 (Visit 3), Week 4 (Visit 4), Week 6 (Visit 5), Week 8 (Visit 6), Week 10 (Visit 7), Week 12 (Visit 8)

Population: No data displayed because data were not collected. Due to the outbreak of the COVID-19 pandemic and following restrictions, all study visits were moved to teleheath and only essential scales were completed.

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026