Strategic Approaches to Developing and Commercializing Companion Diagnostics

April 22, 2020 12:00 PM - 1:00 PM

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Add to Calendar 4/22/2020 12:00:00 PM 4/22/2020 1:00:00 PM Strategic Approaches to Developing and Commercializing Companion Diagnostics The COVID-19 pandemic has proven the importance of diagnostic tests in overcoming healthcare crises and saving lives; but it has required rapid scale up and deployment of point of care and lab based tests hopefully with lessons learned for the future. Join us to learn more about the journey of developing a companion diagnostic from discovery through commercialization.

Precision medicine is an emerging method that factors in an individual’s molecular profile, environment, and lifestyle in order to prevent, diagnose, and treat diseases more effectively. It’s about considering individual differences in the course of prevention, diagnosis, and treatment.

Patients can be classified into subgroups based on how susceptible they are to certain diseases, how those diseases will develop, or how they’ll respond to particular treatments. This information can then be used to predict what the most effective course of action will be. Companion Diagnostics are tools employed to identify those patients who are most likely to benefit from a particular therapeutic product, highlight those at increased risk for serious side effects, and monitor treatment response.

But what about those tasked with bringing precision medicine tests and treatments to the market? What are they doing, what challenges do they face, and how are they working with stakeholders within the wider healthcare ecosystem? We’ll follow the journey of developing a companion diagnostic from discovery through commercialization and answer those questions in this informative forum. Please come prepared with your questions.

Sponsored by the Medtech/Digital Health working group.

NOTE: As MassBio transitions to virtual events, we are striving to make them as inclusive as possible given the challenges and restrictions inherent in virtual events. Thank you for your understanding.

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Senior Director, Oncology Companion Diagnostics Commercialization, Thermo Fisher Scientific
Jane Li is the global lead for NGS companion diagnostics commercialization at Thermo Fisher Scientific. Over the past five years, she was a key member of NGS CDx program, and led effort to launch Oncomine Dx Target Test, 1st NGS CDx with multiple therapies in NSCLC, in several countries, including US, EU, Japan, and Korea. She oversees all aspects of CDx commercial launch, including obtaining favorable reimbursement coverage and pricing in launched countries. She also leads commercial collaborations with pharma partners globally.