The pharmaceutical industry as a whole is projected to reach a negative ROI in 2020, due to a 95% failure in drug trials and a cost of $2bn+ to bring a successful drug to market. This productivity decline is causing a major burden on society, in terms of the increasing cost of approved drugs, and lack of new medicines for rare and complex diseases, including cancer, metabolic disease, and neurological disorders. More than 50% of clinical trials fail due to safety and efficacy and due to starting with the wrong drug target. Yet, today, no single tool, platform or database prioritizes drug targets based on safety and efficacy, and no solution exists for the systematic identification of multiple drug targets and the selection of optimal therapeutic strategies for complex diseases.
BioXplor is building a next-gen AI-powered platform, combining emerging CRISPR and DECL screening technologies to solve this problem through better early prediction of efficacy and safety to reduce downstream failure, reduce time to clinic, and improve ROI. By this approach, we encourage drug discovery programs to target more of the 7000 rare and complex diseases at lower cost and risk, with an estimated 70% cost saving per target and a 25x-100x acceleration through data-driven discovery. The impact of this technology can help usher in a new era of drug discovery for complex diseases with unmet medical needs, including cancer, metabolic disease, and neurological disorders, which affect ~80mil people in the EU alone.