The latest from HNF: research updates, patient stories, advocacy wins, events, and CMT community news.
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September 16, 2026
On August 4, CureCMT (HNF) led a Patient-Focused Listening Session with the FDA dedicated entirely to CMT-SORD. Six patients and family members told the agency what the disease costs them, and what a treatment would give back.
May 21, 2026
A South Korean biotech, ENCell, has dosed the first patient in a Phase 2a trial of EN001, a stem cell therapy aimed at the myelin damage behind CMT1A.
May 21, 2026
HNF is hosting an FDA Patient Listening Session for the CMT-SORD community on August 4, giving patients and caregivers a direct line to the agency at a critical moment for the subtype.
May 21, 2026
Over 200 attendees made the 2026 CMT Summit our biggest gathering yet. Thank you to our sponsors, speakers, research participants, and every member of the community who came.
May 21, 2026
If you have a genetic report related to your CMT diagnosis, uploading it to GRIN is one of the most direct contributions you can make to CMT research today. Even negative or inconclusive reports belong.
May 18, 2026
May 18, 2026
May 18, 2026
May 18, 2026
May 1, 2026
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