Oncology drug development is especially risky with only 5% of new compounds reaching market approval. The lack of patient-relevant, early-stage preclinical models that can be rapidly expanded for drug screening is contributing to this poor success rate.

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  • The key patient-derived organoids (PDO or HUB Organoids) features which makes them best-in-class models for drug development
  • How HUB Organoids are revolutionizing drug development by providing translatable and predictive in vitro pharmacology data
  • How to predict patient response in the clinic by setting up prospective studies using HUB Organoids as patient avatars
  • The evolution from genomic-led drug development to an integrated genomic and organoid screening-based approach

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