Rare disease trials differ from those in most other
therapeutic areas because the indications are more complex and involve
smaller patient populations. But rare disease trials have one distinct
advantage: these patients are very vocal, with caretakers, family
members, and advocates eager to share their experiences. It is essential
to understand the current disease landscape, the prior research, and
the competitive clinical trial environment when positioning a new
clinical trial within the rare disease space. Drug developers must be
aware of the status of the indication and the location of open trials,
their phases, and the patients they seek.
In a series of white papers, PRA experts discuss the
barriers drug developers face when positioning a new trial in the rare
disease space and how to minimize these while engaging with the right
patients.
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