Hear from Allison Moore, Founder/CEO of the Hereditary Neuropathy Foundation about the past, present and future or CMT research.
On March 19th, at the MDA Clinical and Scientific Conference in Dallas, TX, Dr. Cornett will...
CMT Summit + Retreat 2025: Uniting Patients, Researchers, Regulators, and Industry Leaders to...
Early preclinical research indicates that ALE2 could effectively slow or halt the progression of these debilitating symptoms, offering new hope for patients with these rare forms of CMT.
CMT Simplified is here to make staying informed about Charcot-Marie-Tooth disease (CMT) easier...
NMD670, has been granted Orphan Drug Designation (ODD) by the U.S. Food and Drug Administration (FDA)
NMD Pharma Initiates Phase 2 Study of NMD670 in Patients with Charcot-MarieTooth Disease Type 1...
HNF’s Wearable Tech Study Delivers Strong Results for CMT Clinical Trials The Hereditary...
Seeking Participants for a New CMT Clinical Trial (for the US only): A Chance to Help Advance...
A recent clinical trial has shown promising results for a new treatment option for people living...
Join the thousands of HNF volunteers who are fueling CMT research. The more you share, the more we’ll learn. Complete your GRIN surveys today!
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