A Phase IIIb Multi-Center, Open-Label, Mirror-Image, Trial in Adult Subjects with Schizophrenia Treated Prospectively for 6-months with Abilify MyCite®

  • STATUS
    Recruiting
Updated on 23 November 2020

Summary

To compare inpatient psychiatric hospitalization rates (proportion of subjects with ≥ 1 inpatient psychiatric hospitalizations) between the retrospective period (Months 1 to 3) while subjects are on oral standard-of-care antipsychotic treatment and the prospective period (Months 1 to 3) after the subjects switch to Abilify MyCite®.

 

Description

Details
Condition Schizophrenia and Schizoaffective Disorders
Clinical Study IdentifierTX229387
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Subject possesses the capacity to utilize the technology interfaces (eg, open and navigate software apps using the touch screen) and telephone features of a smartphone (Android or iOS)
The subject has satisfactory mobile phone reception (preferably 3 bars or more or have wireless fidelity [Wi-Fi]) at home and/or at work for wireless carrier
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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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