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Long-Term Efficacy and Safety of Asenapine Using Olanzapine as a Positive Control (41512)(COMPLETED)(P05784)

A Multicenter, Randomized, Double-Blind, Flexible-Dose, Long-Term Extension Trial of the Safety and Maintenance of Effect of Asenapine Using Olanzapine Positive Control in Subjects Who Complete Protocols 041021 or 041022.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00156091
Enrollment
260
Registered
2005-09-12
Start date
2005-04-30
Completion date
2007-06-30
Last updated
2022-02-16

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. The clinical development of asenapine, as described in the 2007 IDB appears to have antipsychotic activity with superior symptomatic control compared to placebo and an improved safety profile compared to currently available neuroleptics. Its fast dissolving formulation may further add to treatment compliance. While various titration schedules have been used in previous studies, dose increases at 5 mg BID up to 10 mg BID have been well tolerated. Therefore, further exploration in a larger group of subjects with acute exacerbation of schizophrenia using an asenapine flexible dosing design ( 5 or 10 mg BID) will mimic actual clinical practice in a long-term 52-week extension trial.

Interventions

DRUGOlanzapine

5- 20 mg QD

DRUGAsenapine

5 or 10 mg BID

OTHERPlacebo

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

* Completed the short-term trial ( 041021 or 021022) * Continued to meet all demographic and procedural inclusion criteria of the short-term trial upon entry into this long-term extension trial * Sign a written informed consent for the 041512 trial. * Demonstrated an acceptable degree of compliance with trial medication in the short-term trials in the opinion of the investigator

Exclusion criteria

* CGI-S score of greater or equal to 6 ( severely psychotic) * Occurrence(s) of AE or other clinically significant findings that would prohibit their continuation * Met any of

Design outcomes

Primary

MeasureTime frame
To assess long-term safety including overall symptoms (AEs; SAEs); Vital signs; ISST; EPS; and maintenance of effect; for asenapine with haloperidol control.Weeks 1;2; 4; 8; 12; 16; 24; 32; 40; 52 (Endpoint)
Quality of Life and Patient Functionality (QLS; Q-LES-Q and PETIT)Weeks 16; 32; 52(Endpoint)

Secondary

MeasureTime frame
Neurocognition and cognitive functioningWeeks 24 and 52 (Endpoint)
Weight and abdominal girthWeeks 4;8;12; 16; 24; 32;40;52(Endpoint)
Pregnancy tests; Lab testsWeeks 8; 16; 32; 52 (Endpoint)
Depression (CDSS)Weeks 12; 24; 52 (Endpoint)
ECGsWeeks 2;4;8;24;52(Endpoint)
Physical examsWeek 12; 24; 52 (Endpoint)

Outcome results

None listed

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