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Designing Patient-Centered Endpoint in Rare Disease Trials

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"Designing Patient-Centered Endpoint in Rare Disease Trials"

To make every rare disease trial count, we design patient-centric, relevant strategies for sponsors and caregivers to produce impactful results every time.

Rare diseases affect over 350 million people worldwide and of about 7,000 rare diseases, only 6% have approved treatments. It’s more important than ever to ensure trial strategies and data points are reliable, personal, and efficiently collected. Emmes develops innovative approaches that don’t solely rely on primary endpoints. We design personalized, validated assessments relevant to each patient’s daily life—efficiently producing impactful results every time. Explore new technology and endpoint solutions in our Rare Disease eBook, that helps accelerate new treatment development, identify trial participants, and ease the patient burden for improved retention.


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