abstract
Future of Health Summit 2023

Can Cell and Gene Therapies Be Made Cheaper?

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Cell and gene therapies were set to take the market by storm and transform the treatment landscape. But more than five years out from the first approval in 2017, fewer cell and gene therapies have been approved in the US than expected. The cost of developing and manufacturing these transformative therapies remains astronomical and has brought into question their commercial viability. Why have advances in science and technology not translated into efficiencies in this area? What are the opportunities and challenges to lowering the costs to develop cell and gene therapies, and how low can it really go?

    Moderator

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    Kevin Davies

    Executive Editor, The CRISPR Journal; Author, Editing Humanity

    Speakers

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    Mike Lehmicke

    Senior Vice President, Science and Industry Affairs, Alliance for Regenerative Medicine
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    Peter Marks

    Director, Center for Biologics Evaluation and Research, US Food and Drug Administration
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    Nabiha Saklayen

    Co-Founder and CEO, Cellino
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    Ran Zheng

    CEO, Landmark Bio