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Case Studies / Driving Genetic Testing and Patient Identification in an Ultra-Rare Disease
Case Study

Driving Genetic Testing and Patient Identification in an Ultra-Rare Disease

A pharma manufacturer with a first-to-market targeted treatment for APDS — an ultra-rare primary immunodeficiency — needed to find HCPs who may have undiagnosed APDS patients in their care. With a tiny eligible population and fragmented specialist landscape, the challenge was identifying and educating the right physicians before and after launch.

What’s Inside

  • Reaching immunologists, hematologists, and allergists across a fragmented specialist network
  • Multi-format content deployment to drive awareness and genetic testing intent
  • Physician-level engagement data tracked across every content touchpoint
  • Measurable increase in genetic testing referrals among engaged HCPs
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