Hartwig Medical Foundation

We're a foundation that has been developing a diagnostic whole genome sequencing test for tumors, to speed-up the uptake of personalized cancer treatments for patients in the Netherlands. While the developed diagnostic test results in a complete and high quality list of applicable biomarkers per patient, we see that it is still difficult for the patients to get a personalized (experimental) treatment due to the very large number of options and frequently changing treatment options in a still very manual hospital set-up. We're trying to solve this by building an algorithm that not only takes into account the molecular data that we generate for a patient, but also the clinical data. We use this data to create a report that contains a comprehensive overview of standard of care treatments and trials that are available for the patient, as well as a patient-like-me approach that helps clinicians in their decision making.