The Safety and Effectiveness of Latuda Post-marketing Surveillance in the Treatment of Chinese Schizophrenia Patients
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- STATUS
- Recruiting
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- End date
- Jan 27, 2023
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- participants needed
- 3000
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- sponsor
- Sumitomo Pharmaceutical (Suzhou) Co., Ltd.
Summary
It's a prospective, non-interventional, observational Post-marketing Surveillance..
Description
It's a prospective, non-interventional, observational Post-marketing Surveillance, the aim of the surveillance is to observe the safety and overall effectiveness of Latuda in the treatment of Chinese patients with schizophrenia for 12 weeks in real clinical practice, as well as the dose of Latuda for monotherapy or combination therapy.
Details
| Condition | Schizophrenia, Schizophrenia and Schizoaffective Disorders, Schizophrenia and Schizoaffective Disorders (Pediatric), Schizophrenia and Schizoaffective Disorders, Schizophrenia and Schizoaffective Disorders (Pediatric), schizophrenia disorders |
|---|---|
| Treatment | Lurasidone HCl |
| Clinical Study Identifier | NCT04432688 |
| Sponsor | Sumitomo Pharmaceutical (Suzhou) Co., Ltd. |
| Last Modified on | 27 January 2021 |
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