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Schizophrenia 
Trial Solutions

Enhancing study success with advanced clinical research technologies and expert solutions for schizophrenia trials.

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Effective solutions for advancing Schizophrenia research

Schizophrenia is a leading cause of patient suffering and disability around the world. Despite the compelling, unmet need for new and more effective treatments, the development process remains challenging. At Signant, we offer study sponsors a team with the scientific expertise and global experience, as well as innovative technology, to help run successful schizophrenia trials. Leverage our Signant SmartSignals suite to help your adult or pediatric trial succeed.

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Why Signant Health

  • Monitor COA Data in Real-Time
  • Manage Rater Quality to Improve Data Reliability
  • Simplify Assessments and Adherence for Participants
  • Simplify Study Medication Management
  • Maximize Signal Detection Opportunities
  • Digitize Studies for End-to-end Accuracy and Visibility
  • Monitor COA Data in Real-Time

    Monitor COA Data in Real-Time

    Built on our unparalleled experience and largest data sets in Schizophrenia research, PureSignal Analytics, our leading blinded data analytics solution, safeguards the accuracy and reliability of endpoint data from inception to closeout. Our clinicians and data scientists analyze COA data at all relevant levels (rater, site, country, region, and study) to detect trends, anomalies and statistically significant discrepancies.  In close collaboration with your study team, we review potential quality concerns that could impact signal detection and deliver timely and targeted interventions.

  • Manage Rater Quality to Improve Data Reliability

    Manage Rater Quality to Improve Data Reliability

    Our solutions provide site independent assessment of key eligibility criteria, ensuring that appropriate patients are enrolled, and that raters adhere to scoring and administrative conventions for efficacy outcomes.

  • Simplify Assessments and Adherence for Participants

    Simplify Assessments and Adherence for Participants

    Patient-reported and clinician-reported outcome assessments are vital to fully evaluate schizophrenia treatment efficacy and impact. Our eCOA solution can be tailored to sites' and patient's needs – guided assessments and built-in edit checks reduce COA errors, while alerts and reminders help improve adherence to medication dosing schedules.

  • Simplify Study Medication Management

    Simplify Study Medication Management

    Handle the medication management and patient randomization requirements in your protocol with ease. Our RTSM system and powerful algorithms handle complex dosing schedules, patient cohort schemes, and adaptive designs. Plus, our agile implementation model allows for rapid deployment including mid-study amendments.

  • Maximize Signal Detection Opportunities

    Maximize Signal Detection Opportunities

    Talk through your schizophrenia protocol with our science and medicine experts, who serve as an extension of your study team. We guide the selection and acquisition of endpoints and assessments, advise on inclusion/exclusion criteria, and recommend methods to decrease site and participant burdens. Our end goal is to optimize the reliability of your study's endpoint data.

  • Digitize Studies for End-to-end Accuracy and Visibility

    Digitize Studies for End-to-end Accuracy and Visibility

    While all of our solutions can be applied individually, when combined they enhance the data accuracy and operational efficiency of your schizophrenia study. Gain immediate access to electronic data to streamline and accelerate product approval.

Comprehensive Schizophrenia experience

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Schizophrenia Trial Solutions Overview


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Schizophrenia Trial Solutions



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CASE STUDY

Signant’s RTSM Manages Clinical IP Dispensation in Schizophrenia Study

 
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eClinical solutions for Schizophrenia trials

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