ConcertAI has introduced its next-generation CTO 2.0 solution for supporting design and execution of clinical trials.
The new solution, released for clinical trial optimisation, now has three new features.
It has expanded data assets through sources that are publicly available for including site and physician level trial information on existing and previous trials.
In partnership with data partners, working operational trial metrics and site profile information it helps highlight trial performance and capabilities of study centres.
The solution also includes social determinants of health information at the physical site as well as the physician/patient levels.
Using the latest information, CTO 2.0 will be able to provide recommendations that automate the selection process of trial sites through a data-driven approach.
Additionally, the SaaS technology will help clinicians and researchers select suitable sites for clinical trials.
This balances potential participants available and previous trial performances at the trial sites to provide the highest likelihood of a study success.
Trial operators will also be able to comply with the FDA mandate that trials should provide meaningful information for the subject outcomes.
CTO 2.0 also ensures research can be conducted at scale using the latest clinical informatics integrations and data standards.
ConcertAI COO Ronan Brown said: “There is a practical and moral imperative to make clinical trials available to all patients, which naturally means expansion of trials into community settings, where over 75% of patients receive their care.
“This aligns with the FDA mandate, and also with the urgent necessity to increase trial diversity. CTO 2.0 is a direct response to these needs.”