Clinical Trial of BI 425809 Effect on Cognition and Functional Capacity in Schizophrenia.

  • STATUS
    Recruiting
Updated on 23 November 2020

Summary

The objective of the study is to investigate the efficacy, safety and pharmacokinetics of four different doses of BI 425809 once daily compared to placebo given for 12 weeks in patients with schizophrenia on stable antipsychotic treatment.

 

Description

Qualified participants receive study-related medical care and study medication or placebo at no cost and may be compensated for time and travel.

Details
Condition Depression (Major/Severe)
Clinical Study IdentifierTX220939
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Participant is diagnosed with Schizophrenia
Patient must be located within 60 miles of CNS study location
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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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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