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Trial · NCT01760993

Outcomes14

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline in Positive and Negative Syndrome Scale (PANSS) Scores at 52 WeeksBasline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYChange From Baseline in Cognitive Test Battery (CogState Battery) Score at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYColumbia-Suicide Severity Rating Scale (C-SSRS)Up to 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYChange From Baseline in Calgary Depression Scale for Schizophrenia (CDSS) at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYChange From Baseline in Simpson Angus Scale (SAS) Total Score at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYChange From Baseline in Barnes Akathisia Scale (BAS) Total Score at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYChange From Baseline in the Abnormal Involuntary Movement Scale (AIMS) at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYChange From Baseline in Clinical Evaluation of Harmful Behavior (CEHB) Scale at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
PRIMARYChange From Baseline in Amphetamine Cessation Symptom Assessment (ACSA) Total Score at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
SECONDARYChange From Baseline in Negative Symptom Assessment (NSA-16) Total Score at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
SECONDARYChange From Baseline in the Personal and Social Performance (PSP) Scale Score at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
SECONDARYClinical Global Impression-Schizophrenia Severity of Illness (CGI-SCH-S) ScaleBaseline and week 52Study was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
SECONDARYClinical Global Impression-Schizophrenia Degree of Change (CGI-SCH-C) ScaleUp to 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized
SECONDARYChange From Baseline in Social Functioning Scale (SFS) at 52 WeeksBaseline and 52 weeksStudy was discontinued due to non-safety related business prioritization decisions. No subjects were randomized

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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