Add-On Treatment for Schizophrenia Symptom Management

Updated on 23 November 2020


The primary objective of this study is to evaluate the effectiveness of NaBen® (sodium benzoate) (1000 mg/day) compared to Placebo (0 mg/day), in improving symptoms associated with schizophrenia in adults, when added to your current schizophrenia treatment.



  • All study-related visits, exams, and study drugs will be provided at no cost.
  • In addition, reimbursement for study-related travel may be provided.
  • Details
    Condition Schizophrenia and Schizoaffective Disorders
    Clinical Study IdentifierTX218252
    Last Modified on23 November 2020


    Yes No Not Sure

    Inclusion Criteria

    Is your age between 18 yrs and 45 yrs?
    Gender: Male or Female
    Do you have Schizophrenia and Schizoaffective Disorders?
    Male or female
    Age 18 to 45 years
    Have a diagnosis of schizophrenia
    Be clinically stable with residual symptoms of schizophrenia
    Clear my responses

    How to participate?

    Step 1 Connect with a site
    What happens next?
    • You can expect the study team to contact you via email or phone in the next few days.
    • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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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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