drugset / Trial / NCT01307800
A Study of LY2140023 in Patients With Schizophrenia
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to determine whether at least 1 dose level of LY2140023 given to acutely ill patients with schizophrenia will demonstrate significantly greater efficacy as compared to placebo.
Timeline
- Start
- 2011-03
- Primary completion
- 2012-09
- Completion
- 2012-09
Outcome
Missed primary endpoint
Stopped: “The decision to stop the trial was based on efficacy results in the overall schizophrenia participant population.”
registry 80 mg LY2140023, BID vs Placebo; p = 0.994; LS mean difference 4.1 (95% CI -0.5 to 8.8) NCT01307800 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | LY2140023 | Unknown | 10 mg | Oral |
| Subject | LY2140023 | Unknown | 40 mg | Oral |
| Subject | LY2140023 | Unknown | 80 mg | Oral |