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Companion diagnostics are poised to be a huge growth area worldwide, with a CAGR of 20.1% over the next 5 years, making it a $6B industry by 2022. These often in-vitro medical devices provide essential information for the efficacy of a corresponding drug or biological product, and are also used for pre-determining the efficacy of treatment. Their growth is being propelled in most countries by a number of favorable factors

In this recording we focus on the area of oncology technologies and pathways. We discuss:

  • Examples of how companies used these new technology regulations in applications
  • Biomarker-driven drug development
  • Lessons from orphan drug development
  • New technologies in play such as next-gen sequencing and liquid biopsy
  • The regulatory context for these developments






Will reimbursement prove to be the biggest barrier as three gene therapies gain regulatory approval?

 

Learn more in the "Trends in Gene Therapy report", available to buy here

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