Cell and Gene Therapies: Accelerating uptake

Cell and Gene Therapies: Accelerating uptake

Cell and gene therapies (CAGTs) are delivering on the promise of personalised medicines, meeting high unmet need and delivering powerful and curative treatments. So why is uptake so slow? The obstacles are diverse with the low volume of patients impacting clinical research, evidence generation and manufacturing efficiency, while cost, reimbursement challenges and low HCP knowledge/confidence are all limiting wider adoption. What can be done? How pharma can rethink its commercial and business models is explored by CAGT sector experts in this report.

Companies

Amgen, Novartis, Bristol Myers Squibb, Astellas, Spark Therapeutics, Bluebird Bio, Santen, Kite Pharma, Taysha Gene Therapies, Autolus


Subject synopsis
Research methodology and objectives
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Issues and insights
Clinical trials and evidence generation
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Manufacturing challenges
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Regulatory facilitators and roadblocks
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Reimbursement hurdles
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HCP buy-in
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Commercialisation
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Partnering for accelerating CAGT uptake
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Next-generation CAGTs
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New technologies
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Ethical challenges
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Future market uptake
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