World Orphan Drug Congress USA 2018
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World Orphan Drug Congress 2018 ICON Whitepaper

Overcoming the Challenges of Rare Disease Drug Development

 

Rare diseases present unique challenges when conducting clinical trials as a result of the small number of patients affected, and the heterogeneity of the population. Rare disease trials often amplify the challenges of designing a traditional trial, making it more difficult for developers to select treatment outcomes, gather payer evidence, and maintain patient interest.

 

Over the past 10 years, ICON’s highly experienced clinical and therapeutic teams have conducted numerous rare disease trials across a wide range of therapeutic areas, rendering us experts in the field. Learn more about the challenge of rare disease drug development, and how our experienced team can help you to navigate them. 

 

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