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Efficacy and Safety of Asenapine With Placebo and Olanzapine (41022)(P05947)

A Multicenter, Randomized, Double-Blind, Flexible-Dose, 6-Week Trial of the Efficacy and Safety of Asenapine Compared With Placebo Using Olanzapine Positive Control in Subjects With an Acute Exacerbation of Schizophrenia

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00151424
Enrollment
277
Registered
2005-09-09
Start date
2005-02-15
Completion date
2006-02-06
Last updated
2024-08-15

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

Conditions

Schizophrenia

Brief summary

Schizophrenia is a brain disease. The primary features of schizophrenia are characterized by Positive symptoms (symptoms that should not be there, inability to think clearly, to distinguish reality from fantasy i.e., hearing voices) and Negative symptoms (a reduction or absence of normal behaviors or emotions, i.e., unable to manage emotions, make decisions and relate to others). Other symptoms include reduced ability to recall and learn new information, difficulty with problem solving, or maintaining productive employment. The symptoms of schizophrenia may be due to an imbalance in chemicals in the brain, primarily dopamine and serotonin, which enables brain cells to communicate with each other. Asenapine is an investigational drug that may help to correct the imbalance in dopamine and serotonin. This is a 6 week study to test the efficacy and safety of asenapine and a comparator agent (olanzapine) in the treatment of patients with schizophrenia. Patients that complete this trial will have the option of continuing in an additional one year extension trial.

Interventions

DRUGasenapine

Asenapine 5-10mgBID

DRUGPlacebo

Matched against asenapine and olanzapine

DRUGOlanzapine

10-20 mg QD

Sponsors

Organon and Co
Lead SponsorINDUSTRY

Study design

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

Eligibility

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

Inclusion criteria

* Currently suffering from an acute exacerbation of schizophrenia.

Exclusion criteria

* Have an uncontrolled, unstable medical condition. Have any other psychiatric disorder other than schizophrenia as a primary diagnosis.

Design outcomes

Primary

MeasureTime frameDescription
Change in total Positive and Negative Syndrome Scale (PANSS) score at endpoint (6-week double-blind or last assessment after baseline) from baselineScreen, baseline, days 4, 7, 14, 21, 28, 35, 42A 30-item, clinician rated instrument for assessing the symptoms of schizophrenia. Ratings for each item could range from 1 (absent) to 7 (extreme).

Secondary

MeasureTime frameDescription
Clinical Global Impression Improvement (CGI-I) scoresDays 4,7,14,21,28,35,42This was not a prespecified key secondary outcome
Neurocognition and cognitive functioningBaseline , day 42This was not a prespecified key secondary outcome
AnxietyBaseline, day 42This was not a prespecified key secondary outcome
Suicidal thinkingBaseline, day 42This was not a prespecified key secondary outcome
Quality of life and patient functionalityBaseline, day 42This was not a prespecified key secondary outcome
Readiness to discharge, at scheduled assessments and endpoint from baselineBaseline up to day 14This was not a prespecified key secondary outcome
Changes in PANSS subscale and Marder factor score Clinical Global Impression-Severity of Illness (CGI-S) scoresScreen, baseline, Days 4,7,14,21,28,35,42This was not a prespecified key secondary outcome
Laboratory parametersBaseline, Days 14,,28,,42This was not a prespecified key secondary outcome
Vital signsBaseline, Days ,14,21,28,42This was not a prespecified key secondary outcome
WeightBaseline, Days 14,,28,,42This was not a prespecified key secondary outcome
Electrocardiograms (ECGs)Baseline, Days ,14, 28, 42This was not a prespecified key secondary outcome
Adverse events (including serious adverse events)Screen, baseline, Days 4,7,14,21,28,35,42 and recorded continuously for AEs up to 7 days after endpointThis was not a prespecified key secondary outcome
Serious adverse events (SAEs) up to 30 days after endpointScreen, baseline, Days 4,7,14,21,28,35,42 and recorded continuously for AEs up to 30 days after endpointThis was not a prespecified key secondary outcome
Extrapyramidal symptomsBaseline, Days 4,7,14,21,28,35,42This was not a prespecified key secondary outcome

Outcome results

None listed

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