Predictive analytics refers to using statistical algorithms, machine learning techniques, and historical data to forecast future events. In clinical trials, this means integrating diverse data sources – such as, past clinical trials, patient records, and real-world evidence (RWE) – to provide more accurate predictions about trial outcomes, patient responses, and potential risks3. By analyzing patterns from this data, predictive analytics offers a powerful tool for improving the efficiency, accuracy, and safety of clinical trials1.
Traditionally, clinical trials have been labor-intensive and costly, often taking years to yield results4. Researchers had to rely on historical outcomes, guesswork, and incomplete data to design trials and predict success. Predictive analytics changes this paradigm by enabling data-driven decision-making5. By analyzing data from clinical trials, and real-world data (RWD) – including but not limited to patient demographics, electronic health records (EHRs), and claims data-, predictive models can help physicians and researchers make informed decisions about trial design, patient selection, and potential treatment outcomes.
Predictive analytics is particularly valuable because it can integrate multiple data modalities, such as clinical, biological, genomic, biomarker, and imaging data. The ability to combine and analyze this wealth of information is central to predictive analytics’ potential to revolutionize the clinical trial process.
As the healthcare landscape continues to evolve, predictive analytics will play an increasingly central role in the clinical trial process, driving innovation and improving patient outcomes6.
As with any emerging technology, the adoption of predictive analytics in clinical trials requires collaboration between pharmaceutical companies, regulatory agencies, and healthcare providers. However, the potential benefits are too great to ignore. With predictive analytics at the helm, the future of clinical trials looks promising, offering a path to faster, safer, and more effective drug development.
By leveraging on machine learning, SOPHiA DDM™ facilitates the integration and standardization of diverse data modalities – including but not limited to clinical, biological, radiomics, genomics, and digital pathology data – generating powerful insights to support you in accelerating drug development.
Our multimodal AI data analytics helps you optimize your clinical trial and enhance your post-launch access strategy, by predicting patient response to treatment, disease progression, risk of developing adverse events, and supporting treatment decision-making.
A great example of how SOPHiA GENETICS is spearheading innovation in cancer research by applying predictive analytics is the collaboration with UroCCR, the French Kidney Cancer Research Network, to develop a multimodal machine-learning model for predicting post-operative outcomes for individuals facing renal cell carcinoma (RCC). Using real-world prospective data from the UroCCR network, one of the world’s largest collaborative kidney cancer databases, this study showed that the AI model co-constructed by SOPHiA GENETICS and UroCCR provided a strong prediction for postoperative outcomes, outperforming the predictive performance of most usual risk scores. The results of this study have recently been published in npj Precision Oncology.
With a global network of 780+ institutions, across 70+ countries, and over 1.8 million genomics profiles analyzed to date, the SOPHiA DDM™ Platform accelerates the advances in the field of precision medicine. To learn more about SOPHiA DDM™ Multimodal Healthcare Analytics and our flagship programs visit our page.
SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise.
SOPHiA DDM™ Dx Hereditary Cancer Solution, SOPHiA DDM™ Dx RNAtarget Oncology Solution and SOPHiA DDM™ Dx Homologous Recombination Deficiency Solution are available as CE-IVD products for In Vitro Diagnostic Use in the European Economic Area (EEA), the United Kingdom and Switzerland. SOPHiA DDM™ Dx Myeloid Solution and SOPHiA DDM™ Dx Solid Tumor Solution are available as CE-IVD products for In Vitro Diagnostic Use in the EEA, the United Kingdom, Switzerland, and Israel. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us at [email protected] to obtain the appropriate product information for your country of residence.
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