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Completed

NCT Number: NCT02953639

A Study to Evaluate the Effects of Basmisanil in Participants With Cognitive Impairment Associated With Schizophrenia (CIAS) Treated With Antipsychotics

This multicenter study assessed the effects of 24 weeks of basmisanil treatment on cognition and functioning of stable schizophrenia participants treated with antipsychotics.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Woodland International Research Group Inc., Little Rock, Arkansas, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of schizophrenia of any type utilizing the Mini International Neuropsychiatric Interview and diagnostic and statistical manual of mental disorders, fifth edition (DSM-5) direct clinical assessments, family informants and past medical records
  • Evidence of stability of symptoms for 3 months at screening, that is, without hospitalizations for schizophrenia or increase in level of psychiatric care due to worsening of symptoms of schizophrenia
  • Participants with schizophrenia clinical symptom severity defined by the following: hallucinatory behavior item score less than or equal to (</=) 5 and a delusion item score </= 5 of the PANSS
  • Participants on a stable regimen of antipsychotic therapy for at least 3 months at screening and receiving no more than two antipsychotics

Exclusion criteria

  • Participants with current DSM-5 diagnosis other than schizophrenia including bipolar disorder, schizoaffective disorder and major depressive disorder
  • Clinically significant neurological illness or significant head trauma that affects cognitive function, in the judgment of the principal investigator
  • Full scale intelligence quotient </=65 on the Wechsler Abbreviated Scale of Intelligence at screening
  • Positive result at screening for hepatitis B, hepatitis C, or human immunodeficiency virus-1 and 2
  • Moderate to severe substance use disorder (other than nicotine or caffeine), as defined by the DSM-5, within the last 12 months
  • Suicide attempt within 1 year or currently at risk of suicide in the opinion of the Investigator

Treatment and study plan

Basmisanil

Drug

Participants received either 80 milligrams (mg) or 240 mg of Basmisanil, as per the dosing schedules described above.

Placebo

Drug

Participants received matching Placebo to Basmisanil, as per the dosing schedules described above.

Primary outcomes

  1. Change From Baseline to Week 24 in MATRICS Consensus Cognitive Battery (MCCB) Neurocognitive Composite Score

    Time frame: Baseline up to Week 24

    The MCCB is a cognitive battery to assess 7 domains recommended by the MATRICS initiative (i.e., working memory, verbal learning, speed of processing, attention/vigilance, visual learning, social cognition, reasoning and problem solving). The MCCB neurocognitive composite T-score is a standardized mean of the six domain scores (excluding social cognition). Raw scores are converted to age and sex adjusted t-scores which are standardized to normative data, and have a mean of 50 and standard deviation of 10 in the general healthy population. A higher composite T-score represents lower impairment.

Secondary outcomes

  1. Change From Baseline to Week 24 in MCCB Cognitive Domain Scores

    Time frame: Baseline up to Week 24

    The MCCB is a cognitive battery to assess 7 domains recommended by the MATRICS initiative (i.e., working memory, verbal learning, speed of processing, attention/vigilance, visual learning, social cognition, reasoning and problem solving). Raw scores are converted to age and sex adjusted t-scores which are standardized to normative data, and have a mean of 50 and standard deviation of 10 in the general healthy population. A higher T-score represents lower impairment.

  2. Change From Baseline to Week 24 in Wechsler Memory Scale Fourth Edition, Verbal Paired Associates (WMS IV-PAL) Score

    Time frame: Baseline up to Week 24

    The Paired Associates Learning (PAL I and II) of the WMS-IV (Wechsler Memory Scale Fourth edition) is a test of verbal learning and memory that requires the participant to learn novel word pairs. The participant learns the word pairs across learning trials and is asked to recall them immediately (PAL I) or after a 30-minute delay (PAL II). Data is presented here for 3 Scores: VPA I total raw score, VPA II total raw score and VPA II Recognition total raw score. The total raw score ranges for these 3 Scores are 0 to 56, 0 to 14 and 0 to 40 respectively, with larger total raw scores indicating better performance.

  3. Change From Baseline to Week 24 in Wechsler Memory Scale Fourth Edition, Logical Memory Test (WMS IV-LM) Score

    Time frame: Baseline up to Week 24

    Logical memory (LM) assesses narrative memory under free-recall conditions. Two short stories are presented orally. The examinee is asked to retell each story from memory immediately after hearing it (LM I). In the delayed condition (LM II), the examinee is asked to retell both stories from the immediate condition (delayed free recall). Data is presented here for 2 Scores: LM I total raw score and LM II total raw score. The total raw score range is from 0 to 50 with larger total raw scores indicating better performance.

  4. Change From Baseline to Week 24 in Ratio Between Trail Making Test (TMT)- Part B and TMT- Part A Scores

    Time frame: Baseline up to Week 24

    The TMT consists of two parts: Trail Making Part A, which is a part of the standard MCCB and Trail Making Part B additionally included in this study. Circles containing numbers (Part A) or both numbers and letters (Part B) must be sequentially connected. The difference (ratio) in performance between Part A and Part B reflects executive processes and will be used to assess executive functioning including cognitive set shifting abilities and data for this ratio is presented here. Smaller ratio values, hence decreases from baseline (TMT-B/TMT-A ratio values below 1) indicate higher executive functioning capabilities.

  5. Change From Baseline to Week 24 in Personal and Social Performance (PSP) Total Score

    Time frame: Baseline up to Week 24

    The PSP Total Score is an integer result in the range of 0 to 100. Larger values, hence increases from baseline in the PSP total score, indicate higher social and personal functioning.

  6. Change From Baseline to Week 24 in Schizophrenia Cognition Rating Scale (SCoRS) Total Score

    Time frame: Baseline up to Week 24

    The main parameter of interest for the Schizophrenia Cognition Rating Scale (SCoRS) is the SCoRS 'Total Score'. The total score range is from 0 to 80 with lower scores indicating better day-to-day functioning.

  7. Change From Baseline to Week 24 in Clinical Global Impression Severity (CGI-S) Rating

    Time frame: Baseline up to Week 24

    Values for the CGI-S Scale are encoded by the numerical values from 1 to 7 respectively. Higher numerical values represent greater impairment.

  8. Change From Baseline to Week 24 in Clinical Global Impression Improvement (CGI-I) Rating

    Time frame: Baseline up to Week 24

    Values for the CGI-I Scale are encoded by the numerical values from 1 to 7 respectively. Higher numerical values represent greater impairment.

  9. Change From Baseline to Week 24 in Schizophrenia Quality of Life Scale (SQLS)

    Time frame: Baseline up to Week 24

    The SQLS is a patient reported scale consisting of 33 items: 2 domain scores (Cognition & Vitality Score [SQLS-CV] and Psycho-social Score [SQLS-P]) as well as a Total score (SQLS-T) are derived. The overall score range is from 0 to 100. On all scales, higher scores represent a lower quality of life.

  10. Percentage of Participants With Adverse Events (AEs)

    Time frame: Baseline up to 4 weeks after the last dose of study drug (up to 28 weeks)

    An Adverse Event (AE) is any untoward medical occurrence in a participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with the treatment. An Adverse Event can therefore be any unfavorable and unintended sign (including abnormal laboratory values or abnormal clinical test results), symptom, or disease temporally associated with the use of a pharmaceutical product, whether or not considered related to the pharmaceutical product. Preexisting conditions which worsen during a study are also considered as Adverse Events.

  11. Apparent Clearance of Basmisanil at Steady State (CL/F,ss)

    Time frame: Pre-dose (hour 0) in Days 7, 14, 42, 84, 168

    Population PK model estimated apparent oral clearance of Basmisanil at steady-state.

  12. Apparent Volume of Distribution of Basmisanil at Steady State (Vz/F,ss)

    Time frame: Pre-dose (hour 0) in Days 7, 14, 42, 84, 168

    Population PK model estimated apparent volume of distribution of Basmisanil at steady-state.

  13. Area Under the Curve of Basmisanil at Steady State (AUC,ss)

    Time frame: Pre-dose (hour 0) in Days 7, 14, 42, 84, 168

    Population PK model estimated AUC of Basmisanil at steady-state.

  14. Maximum Plasma Concentration of Basmisanil at Steady State (Cmax,ss)

    Time frame: Pre-dose (hour 0) in Days 7, 14, 42, 84, 168

    Population PK model estimated maximum plasma concentration of Basmisanil at steady-state (ss).

Sponsors and collaborators

Lead sponsor

Hoffmann-La Roche

Industry

Registry information

Official study title

A Phase IIb, Multicenter, Randomized, Double-Blind, Parallel Group, Placebo Controlled Study to Evaluate the Efficacy, Safety and Tolerability of Basmisanil (RO5186582) as Adjunctive Treatment in Patients With Cognitive Impairment Associated With Schizophrenia Treated With Antipsychotics

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Nov 3, 2016
Registry last updated
Feb 9, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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