The Safety and Effectiveness of Latuda Post-marketing Surveillance in the Treatment of Chinese Schizophrenia Patients

  • STATUS
    Recruiting
  • End date
    Jan 27, 2023
  • participants needed
    3000
  • sponsor
    Sumitomo Pharmaceutical (Suzhou) Co., Ltd.
Updated on 27 January 2021

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 IdentifierNCT04432688
SponsorSumitomo Pharmaceutical (Suzhou) Co., Ltd.
Last Modified on27 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Schizophrenia Patients who begin to receive Latuda

Exclusion Criteria

No exclusion criteria
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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