Every patient’s cancer is unique, and their treatment should reflect that.

VitroScan offers predictive assays that enable clinicians and patients to individualize treatment strategies, thereby improving efficacy, reducing adverse events, and enhancing patient outcomes.

Our robust and validated platform delivers high‑quality, reproducible data that mitigate risk throughout the drug development pipeline. By delivering actionable insights early, VitroScan informs rational therapy selection, accelerates development timelines and supports the successful translation of innovative therapies from lab to patient.

VitroScans precision oncology assays bring reliable data to support confident decision making. 

Functional response profiling

Cancer treatment decisions are increasingly informed by clinical characteristics, pathology and molecular profiling. Ex vivo tumor testing adds another perspective: functional response.

Instead of looking only at what the tumor is, our assays measures how patient-derived tumor tissue responds when exposed to treatment. This provides additional information that can complement existing clinical and molecular evidence.

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Translational insights to de-risk drug development

VitroScan integrates ex vivo micro‑tumor testing into a comprehensive solution that de‑risks drug development and accelerates the translation of new therapies into clinically relevant treatment options.

Near-clinical testing for impactful decision‑making

VitroScan’s ex vivo platform supports the development and clinical translation of innovative therapeutics through near clinical testing. By preserving tumor heterogeneity and the tumor microenvironment (TME), the platform enables modeling of patient-specific treatment responses. As a new approach methodology (NAM), it delivers insights that capture the real-world patient population. The platform’s predictive value helps to de-risk drug development, inform patient stratification for clinical trials, and helps to prevent late-stage failure of promising new therapies.

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Clinical trial program

VitroScan’s clinical trial program brings our ex vivo micro‑tumor platform directly into the clinic. The trials integrate patient‑derived micro‑tumor assays alongside traditional clinical endpoints. Eligible participants undergo minimally invasive tissue collection, enabling the generation of individualized micro‑tumors that are screened against investigational therapeutics, standard‑of‑care therapies, and rational combination regimens.

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VitroScan Team

Development driven by scientific experts

The VitroScan team, collaborating clinicians, and our investors are convinced that accurate prediction of true responders and non-responders to cancer drugs can substantially improve the care of cancer patients. Our team consists of highly motivated experts in oncology, cell biology, immunology, bioinformatics, and clinical trials. We collaborate with experts in the field to maximize the benefits of our technology platform, advance VitroScan’s development, and build a resilient, forward-looking organization.

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Connect with VitroScan

Contact us for more information on how our testing solutions can help you reduce risk and maximize success in your drug development process or for any other inquiries!

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Quality Management

VitroScan's laboratories are operating under an ISO-15189 compliant quality management system. This internationally recognized standard sets the benchmark for excellence in medical laboratories, ensuring that every clinical sample analysis meets the highest levels of quality, reliability, and regulatory compliance.