Cell and gene therapies (CGTs) are transformative modalities in personalized medicine. These groundbreaking advancements address unmet needs for life-threatening or debilitating conditions that have limited or no curative options. But manufacturers often find it challenging to commercialize CGTs successfully, with one major set of challenges involving patient access.
Factors affecting access include patients’ lack of awareness or hesitancy to pursue specific therapies. A complex coordination process and financial impact, both on patients and providers, can also negatively impact patient access. For your commercialization strategy to succeed, these challenges can be addressed through strategies such as:
Discover recommendations intended to help you navigate patient access challenges so you can deliver on your CGT’s potential to improve patient lives.
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