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