Innovation Forum Events

Healthcare 2.0 – Cell & Gene Therapy

Monday, October 14th 2024

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18:00 – 22:00 (GMT)

The Cavendish, 22 Duchess Mews, London W1G 9DT

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Description

Monday, October 14th 2024

18:00 – 22:00 (GMT)
Location: The Cavendish, 22 Duchess Mews, London W1G 9DT

Join us at our latest Healthcare 2.0 conference for a collaborative exploration of the latest advancements in Cell and Gene Therapy. This event, uniting experts from the UK, Europe, and beyond, focuses on practical strategies, upcoming challenges, and innovative solutions in healthcare.

  • Discover how Cell and Gene Therapy is setting new standards in medical treatments and what future developments lie beyond current genome editing techniques like CRISPR.
  • Connect with the top healthcare professionals, industrial and academic researchers, start-ups, and investors who are shaping the future of medicine.
  • Engage with experts as we discuss the enormous potential and challenges of effective Cell and Gene Therapy treatments reaching the market.

Keynote

Keynote speaker and content to be announced

Panel Discussions

Panel I - Future Directions in Cell and Gene Therapy: Allogeneic, Autologous, and In-Vivo

  • Carlo Rinaldi, Clinical Academic, University of Oxford
  • Professor Simon Waddington, University College London and Founder, Bloomsbury Genetic Therapies

Panel II - The Business Case: From the Lab to Clinical Trials

  • Michael Anstey, Partner, Cambridge Innovation Capital
  • Kathryn Golden, SVP Tech Ops / Manufacturing, bit.bio
  • Lee Dunham, Director of Business Development, Cell and Gene Therapy Catapult
  • Jesus Zurdo, Global Head of Cell & Gene Therapy and Bioproduction, Horizon Discovery

Pitching Session

5-Minute Pitch: Meet Tomorrow’s Healthcare Innovators

Join our rapid pitching session to gain access to the latest start-ups working in this space. This segment offers a unique opportunity to connect with new leaders in healthcare innovation.

If you are a start-up interested in pitching, please fill out this application form.

Tickets

All tickets can be purchased here.

Academic, poster, corporate, and start-up tickets are available. If you are not represented by any of these groups, please enquire about general admission at [email protected], for which there are a limited number of tickets available.

Speakers

Kathryn Golden is an accomplished CMC executive with a track record of shepherding complex drug candidates from discovery stage to pivotal trials. Kathryn's expertise includes integrated process development, phase-appropriate quality and regulatory coordination, and management of contract manufacturing organisations.

She has been an early employee at six biotechnology start-ups, including Q32 Bio and Codiak BioSciences. Kathryn is particularly passionate about increasing access to transformative therapies, as evidenced in her current role as SVP, Technical Operations and Cell Manufacturing at bit.bio and her co-founding of Sunflower Therapeutics, a start-up utilising yeast manufacturing technologies to provide biologics at point-of-care to underserved populations.

She received her S.B. in Chemical Engineering and M. Eng. in Bioengineering from the Massachusetts Institute of Technology and holds an M.B.A. from the Sloan School of Management at MIT.

Michael is a Partner specialising in life sciences investments. Before joining CIC he was a Principal in the Healthcare Practice Area at The Boston Consulting Group. Michael has experience in advising multinational businesses across North America, Europe, India, and Japan.

Prior to BCG, Michael was an Investment Analyst at Oxford Capital Partners. Michael was also co-founder of an early-stage biotechnology company focused on developing small molecule drugs that target protein-protein interactions implicated in disease.

Michael earned his DPhil in Zoology in the field of neurobiology from the University of Oxford. He manages CIC's investments in Bicycle Therapeutics (NASDAQ: BCYC), Congenica, Epitopea, Storm Therapeutics and Start Codon. He is also a co-founder of Innovate Cambridge, a locally driven initiative developing an ambitious and inclusive innovation strategy for Greater Cambridge, with the goal of ensuring it remains the leading innovation ecosystem in Europe.

Simon Waddington is Professor of Gene Therapy at University College London. Over the past two decades he has worked on treatments for muscular dystrophy, cystic fibrosis, haemophilia and thalassemia; more recently he and his team have concentrated on therapies for several severe and often fatal genetic diseases which affect young children. He has co-authored more than one hundred and seventy publications and has been principal investigator or co-applicant on grant awards totalling more than fifteen million pounds.

With Professors Ahad Rahim, Manju Kurian and Paul Gissen he has founded a clinical-stage gene therapy company, Bloomsbury Genetic Therapies and is co-inventor of eight patents. He holds an honorary chair at the University of Witwatersrand, South Africa.

Jesús has an extensive career in the biopharmaceutical industry both in therapeutic development and CDMO / CRO organisations, with a particularly strong focus on the design and development of transformative cell & gene therapies.

After completing his PhD at the Autonomous University in Madrid, Jesús spent many years in academia as a scientist, including research positions at CBM-CSIC in Madrid and later at the Universities of Oxford and Cambridge in the UK, where he studied the molecular mechanisms of amyloidosis and other degenerative disorders. He then made his transition to the industry as an entrepreneur, having founded two drug discovery start-ups to develop disease-modifying treatments for metabolic and neurodegenerative disorders (Zyentia, Zapaloid).

Jesús has held senior and executive positions in several global organisations dedicated to the development and manufacture of biological therapies (Lonza, Rentschler Biopharma, Horizon Discovery-Revvity), and championed the adoption of novel technologies and development strategies with innovators and regulatory agencies. He has held executive and board member roles in biotherapeutic start-ups and acted as a mentor and coach for new entrepreneurs. Jesús is a jury member at the European Innovation Council’s start-up Accelerator Programme, dedicated to nurturing innovative businesses with the potential to generate a positive societal impact.

Above all, Jesús is a leukaemia survivor, having been diagnosed with ALL in 2022, and undergone diverse treatments for this condition. He actively supports various charities and is passionate about promoting patient equity and engagement in the design and development of effective treatments. He is keen to engage with bold minds to explore vehicles that help realise his vision: Ensuring patients have access to cell & gene therapies that bring about significant improvements in quality of life which are meaningful to patients and their families.

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