Not provided
Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| Hera; | |||
| 41512 |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Active Comparator | Olanzapine 20 mg QD |
|
| 2 | Experimental | Asenapine 5 or 10 mg BID |
|
| 3 | Other | Double-Blind subjects randomized to only placebo medication for 6 weeks in the short-term 041021 or 041022 asenapine trials, were randomized (double-blind) Into the long-term 041512 asenapine extension trial and received asenapine 5 mg BID for Week 1. After Week 1, subjects received asenapine (either 5 mg BID or 10 mg BID) for the remainder of the 52 week trial. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Olanzapine | Drug | 5- 20 mg QD |
| |
| Asenapine |
| Measure | Description | Time 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) |
| Measure | Description | Time Frame |
|---|---|---|
| Pregnancy tests; Lab tests | Weeks 8; 16; 32; 52 (Endpoint) | |
| Physical exams | Week 12; 24; 52 (Endpoint) | |
| Neurocognition and cognitive functioning |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D012559 | Schizophrenia |
| ID | Term |
|---|---|
| D019967 | Schizophrenia Spectrum and Other Psychotic Disorders |
| D001523 | Mental Disorders |
Not provided
Not provided
| ID | Term |
|---|---|
| D000077152 | Olanzapine |
| C522667 | asenapine |
| ID | Term |
|---|---|
| D001569 | Benzodiazepines |
| D001552 | Benzazepines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Drug |
5 or 10 mg BID |
|
| Placebo | Other |
|
| Weeks 24 and 52 (Endpoint) |
| Weight and abdominal girth | Weeks 4;8;12; 16; 24; 32;40;52(Endpoint) |
| ECGs | Weeks 2;4;8;24;52(Endpoint) |
| Depression (CDSS) | Weeks 12; 24; 52 (Endpoint) |
| D006571 | Heterocyclic Compounds |