Staccato Loxapine in Agitation (Proof of Concept)
Summary
The purpose of this study is to assess efficacy and safety of Staccato Loxapine in the treatment of acute agitation in schizophrenic patients. The study will be conducted in 120 agitated schizophrenic patients - either newly admitted to a hospital setting or a research unit for acute agitation or already in hospital for chronic underlying conditions. Patients meeting entry criteria will be randomized to one of two doses of Staccato Loxapine or to Staccato Placebo. Following administration of study drug, assessment of agitation state will be conducted at serial time points using standard agitation scales over a 24 hour period.
Timeline
- Start
- 2006-08
- Primary completion
- 2007-01
- Completion
- 2007-01
Outcome
Met primary endpoint
registry analysis (superiority test); Inhaled Placebo vs Inhaled Loxapine 10 mg; p = 0.0002; ANCOVA NCT00369577 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | loxapine | Small molecule | 5 mg | Inhaled |
| Subject | loxapine | Small molecule | 10 mg | Inhaled |