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Pediatric Cancer Dataset Gaps, FDA ‘High Bar’ Make Use Of External Control Arms Difficult

 
• By Sue Sutter

European data privacy regulations could further complicate efforts to build external control arms using real-world data that are housed outside the US, experts said at advisory committee meeting on use of real-world evidence in pediatric cancer drug development.

Boy with teddy bear
For pediatric cancer drug sponsors, it may be difficult to find a comparator arm outside their study. • Source: Alamy

The ability to leverage real-world evidence as an external control in pediatric cancer drug trials currently is limited by the quality of the underlying datasets, including a lack of genomic and molecular marker information, and the US Food and Drug Administration’s high bar for use of such data to support regulatory decision-making.

In addition, European data privacy regulations could further complicate efforts to build external control arms using real-world data that are...

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What UK’s Clinical Trials Overhaul Means For Orphan Drug Developers

 
• By Eliza Slawther

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Elegy For SACHRP: US HHS Research Protection Panel Tackled Tough Pediatric Trial Questions

 
• By Bridget Silverman

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