Seizing today’s moment to propel the industry forward
As seen in their leading role in the fight against COVID-19, the hype around cell and gene therapy (C>) is finally translating into reality. The market is thriving with innovation, investment, partnerships and M&A activity. But much remains unclear about how these therapies can deliver full value, and where pharma and biotech leaders should invest energy and resources.
$14bn
Projected size of C> market by 2025.
2,000
Open or planned C> trials.
10–20
Projected new approved C> products in the US each year from 2025.
To help navigate the future, we’ve explored four potential future C> scenarios using our proprietary approach to scenario planning and exploring uncertainty. Based on the insight and input of biochemists, biologists, mechanical engineers, materials specialists, healthcare experts, strategists and more, we formulated four potential views of the future. The aim is to provoke, not predict – to immerse leaders in the future, and identify how they can prepare for and shape it.
To enable future success, leaders need to look beyond immediate challenges to ensure their organisation can compete and continue to bring innovative solutions to patients. This will require careful consideration of key topics such as early research, clinical trials, manufacturing and supply chain, regulations, reimbursement and commercialisation.
The future is bright for C>, but today’s players must actively plan for multiple futures to ensure they’re part of tomorrow’s landscape.
Leaders can use our FutureWorlds™ as a thinking tool to reflect on the capabilities and the strategy they should pursue. In doing so, they’ll be able to respond to any combination of these scenarios, and shape both the industry’s future and their own success.
We analysed uncertainties facing the C> field using two axes – ‘accessibility’ and ‘level of personalisation’ – chosen basd on our commercial and technical insight in this space. This approach produced four extreme points on the axes – and four potential futures.
Bespoke World, where scientific innovations create a better understanding of disease physiology and greater availability to personalised treatments for many diseases, especially in the rare disease space.
Mass-Market World, where advances in cell reprogramming, genetic editing and manufacturing mean affordable off-the-shelf (allogeneic) C>s are available globally for a broad range of diseases and uses.
Eclipse World, where success is limited in off-the-shelf therapies. Successful C>s remain tailored to the patient and, with challenges controlling the cost of manufacturing/supply chain, prices remain high.
Blocker World, where off-the-shelf C>s advance but ultimately come up against hurdles that block their commercial success.
Today’s players must actively plan for multiple futures to ensure they are part of tomorrow’s landscape. Our report explores the considerations for each world, as well as six steps leaders can take now to shape and operate in whatever world emerges.
Editas Medicine, a leading gene editing company based in the US, was preparing to launch the world’s first ever clinical trial using a CRISPR-based gene editing medicine inside the human body. In a period of transition, we led their IT function so...
Ori Biotech, a London and Philadelphia-based innovator in cell and gene therapy manufacturing, is on a mission to enable patient access to this new generation of life saving treatments. As Ori’s design and development partner, we’re accelerating...
We helped precision therapy company Blueprint Medicines to develop a roadmap of IT system needs and clarity around their organizational structures, enabling them to move forward, confident that they had the right structures in place to grow and make...
Discover more about the future of cell and gene therapy and learn about our FutureWorlds™ approach to scenario planning.
