Accelerating asset development

In recent years the Pharma and Biotech industries, and the broader healthcare market, have seen some key players successfully bringing new therapies to market significantly faster than previously. A key enabler of this has been successful harnessing of expedited approval pathways, which can reduce asset development and approval timelines by half or up to two-thirds of historical levels. The clear benefits of expedited timelines, along with cost-driven pressure to deliver returns quickly, is eliciting widespread attempts in pursuing alternative and more innovative asset development approaches – from the way clinical trials are designed over the clinical operations itself to regulatory strategies for leveraging expedited approval pathways in respective indications.

As the competition across therapeutic areas and modalities becomes more fierce, the report outlines how PharmaCos and Biotechs can implement concerted and targeted measures to capitalize on clinical acceleration opportunities to remain competitive among three distinct but synergistic deployment layers.

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Considerations to accelerate new assets during clinical development

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