Abstract The high attrition rate of oncology drug candidates is frequently driven by an insufficient understanding of a compound's therapeutic index early in development. Many promising molecules advance based on potent efficacy, only to fail later due to unanticipated safety concerns. To address this, there is a critical need for a comprehensive in vitro strategy that can simultaneously and systematically evaluate anti-cancer activity and organ-specific toxicity risks in the preclinical phase, enabling more informed and de-risked candidate selection. To address this gap, we developed an integrated in vitro profiling platform that synergizes a robust Efficacy Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3153.
Tu et al. (Fri,) studied this question.
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