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Drug Abuse Liability

Discover the Abuse Potential of Investigational Drugs

Accurately assessing and evaluating the human abuse potential of investigational compounds can make trials complex and resource-heavy when using traditional paper and pencil methods.

Cambridge Cognition offers a computerised patient-report system enabling quick, accurate and paperless measurement of the abuse potential for investigational drugs in clinical trials. As a trusted system of choice with leading organisations conducting abuse liability studies, the regulatory approved Clinical Trial Information System for Abuse Liability (CTIS-AL) is a cost-effective digital solution to paper and pencil questionnaires and scales, reducing staff workloads and trial costs.
 

Benefits of  CTIS-AL

  • Minimises the risk of late stage failure
  • Regulatory approved to support label claims
  • Enhances decision making in drug development
  • Clinically relevant outcomes measured
  • Reduces trial costs

Features

World leading cognitive assessment tool

Rapid abuse potential profiling

Sensitive to acute pharmacologically-induced cognitive effects

Suitable for use in Phases I-IV

Reduces trial workloads & costs

Simple, scalable touchscreen testing

Automated & standardised test administration

Electronic data capture

Secure, cloud-based data storage

Real-time access to data

Secure HTTPS data encryption & HIPAA/GDPR and SOC II certified data storage

24/7 customer service

 

Confidently assess abuse potential

CTIS-AL enables configuration of questionnaires and visual analogue scales ensuring the outcome measures meets the exact objectives of the trial. Scales have exact selection capabilities on uni- and bi-polar scales for high precision and sensitive detection of changes in subjective measurements over time.

Common Measures:

Drug effects

Overall drug liking

Drug similarity

Subjective drug value

Likelihood to take drug again

Access comprehensive support for a successful study

Our dedicated support teams are on hand to help you every step of the way to ensure your clinical trial runs successfully.


Experienced study management

Our dedicated Project Managers have a 100% customer satisfaction rating and are on hand to co-ordinate all study activities from study initiation, all the way through to completion of your trial, on time and on budget.

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Secure data management

All test data are captured electronically, encrypted at source and processed using our study-specific data management service. Our Data Management team perform ongoing review and query resolution to guarantee the most accurate data possible.

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Technical support

Support is available globally through our 24/7 helpline, providing assistance with all technical questions.

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