A Study of the Efficacy and Safety of Asenapine in Participants With an Acute Exacerbation of Schizophrenia (P05688)

Organon

Status and phase: Completed; Phase 3

Conditions: Schizophrenia

Treatments: Drug: Olanzapine; Drug: Placebo Asenapine; Drug: Placebo Olanzapine; Drug: Asenapine

Study type: Interventional

Funder types: Industry

Identifiers

NCT01617187

P05688

2010-018407-28 (EudraCT Number)

Details and patient eligibility

About

The purpose of this trial is to assess the effect of asenapine 2.5 and 5 mg sublingually twice daily (BID) compared with placebo in the treatment of schizophrenia (overall symptoms) as measured by the Positive and Negative Syndrome Scale (PANSS). Olanzapine administered 15 mg orally once daily (QD) was used as an active control. The primary hypothesis is that at least one of the asenapine doses is superior to placebo in improving schizophrenia symptoms as measured by the change from Baseline in the PANSS total score at Day 42. The first key secondary hypothesis is that at least one of the asenapine doses is superior to placebo in improving schizophrenia symptoms as measured by the change from Baseline in Clinical Global Impression Scale-Severity (CGI-S) score at Day 42. The second key secondary hypothesis is that at least one of the asenapine doses is superior to placebo in improving schizophrenia symptoms as measured by the rate of PANSS responders (≥30% Reduction From Baseline in PANSS Total Score) at Day 42.

Full description

The trial consists of a screening/tapering period, treatment period, and follow-up period. The 6-week active treatment period includes an inpatient phase and outpatient phase. Participants who complete the trial may continue treatment under a long-term extension protocol (P05689). Participants who do not continue in the treatment continuation trial (whether they complete the 6-week trial or discontinue prematurely) will have a follow-up visit 7 days after their last dose of trial medication.

Enrollment: 360 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Current diagnosis of schizophrenia of paranoid, disorganized, or undifferentiated subtype
• Minimum PANSS total score of 70 at Screening and Baseline
• Score of at least 4 (moderate) in two or more of the five items in the positive subscale of the PANSS
• Confirmed to be experiencing an acute exacerbation of schizophrenia
• CGI-S scale score of at least 4 (moderately ill) at Baseline
• Has responded positively to an antipsychotic medication other than clozapine (Clozaril®) in a prior episode

Exclusion criteria

• Body mass index (BMI) <18.5 or >40.0 kg/m^2
• Laboratory and/or clinical evidence of clinically significant hepatic conditions
• Known history of, or undergoing treatment for, narrow angle glaucoma
• Diagnosed with epilepsy or has had any seizure disorder beyond childhood febrile seizures
• Known serological evidence of human immunodeficiency virus (HIV) antibody
• History of neuroleptic malignant syndrome or tardive dyskinesias
• Past or current diagnosis of schizoaffective disorder, schizophrenia of residual subtype, schizophrenia of catatonic subtype, current diagnosis of schizophrenia with course specifiers continuous, single episode in partial remission, or single episode in full remission, or borderline personality disorder

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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360 participants in 4 patient groups, including a placebo group

Asenapine 2.5 mg BID

Experimental group

Treatment:

Drug: Asenapine

Drug: Placebo Olanzapine

Asenapine 5 mg BID

Experimental group

Treatment:

Drug: Asenapine

Drug: Placebo Olanzapine

Olanzapine 15 mg QD

Active Comparator group

Treatment:

Drug: Placebo Olanzapine

Drug: Olanzapine

Drug: Placebo Asenapine

Placebo BID

Placebo Comparator group

Treatment:

Drug: Placebo Olanzapine

Drug: Placebo Asenapine