According to
Taconic Biosciences, only 12% of drug candidates that enter the clinical trial stage are approved by regulatory bodies. The longest and most-expensive stage of the drug creation process, clinical trials involve multiple phases of human testing, and each phase involves hundreds or thousands of participants.
The traditional linear process of randomized controlled trials (RCTs) hasn’t changed in decades. It lacks the flexibility, speed, and analytical power necessary for the precision medicine model to thrive. Companies struggle to find the right participants, not to mention recruit, retain, and manage them effectively. This process inefficiency greatly contributes to the rising costs of drug discovery and development, as well as low approval rates. It also thwarts innovation.
Pharma companies can use predictive AI models throughout the clinical trial stage of drug development, from design all the way to data analysis, to help:
- Identify suitable patients by mining publicly available content.
- Assess trial site performance in real time.
- Automate data sharing across platforms.
- Provide data for final reports.
Coupling algorithms with effective tech infrastructure ensures that the constant stream of clinical data is cleaned, aggregated, stored, and managed effectively. Thus, researchers can better understand the safety and efficacy of the drug without having to manually collate and analyze the huge datasets generated by trials.