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HATTR-PN

Clinical trials for HATTR-PN explained in plain language.

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  • New hope for rare nerve disease: phase 3 trial of nucresiran begins

    Disease control Recruiting now

    This study tests a new medicine, nucresiran, for people with a rare inherited disease that damages nerves (hATTR-PN). About 125 adults will receive either nucresiran or another drug (vutrisiran) to see which better slows nerve damage and improves quality of life. The goal is to c…

    Matched conditions: HATTR-PN

    Phase: PHASE3 • Sponsor: Alnylam Pharmaceuticals • Aim: Disease control

    Last updated May 17, 2026 15:00 UTC

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