Exciting News For The CMT Patient Community
December 20, 2018
Exciting news for the CMT patient community with the first potential treatment ever!
News from the Hereditary Neuropathy Foundation: research updates, clinical trial progress, partnerships, and advocacy wins for the Charcot-Marie-Tooth community.
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December 20, 2018
Exciting news for the CMT patient community with the first potential treatment ever!
December 17, 2018
They will collaborate on research and provide access to genetic testing for CMT.
December 13, 2018
HNF launches GRIN with 4 online clinical studies that are important as we continue with our therapy development pipelines.
December 10, 2018
2018 was a pivotal year for the Hereditary Neuropathy Foundation (HNF) and the entire Charcot-MarieTooth (CMT) Community.
December 8, 2018
True Reply's Voice Activated Technology is an accessible and innovative new platform that captures the patient’s experience with CMT in their own words.
October 8, 2018
HNF to host an educational CMT symposium at AANEM's Annual Conference October 10-13th in Washington, D.C.
October 1, 2018
The Annual RARE Patient Advocacy Summit, hosted by Global Genes, is in its seventh year and will take place on October 3-4 at the Hotel Irvine in Irvine, California.
January 25, 2018
HNF proudly stands with the chronic pain community in protecting access to therapies and treatments.
November 9, 2017
Pharnext completed patient enrollment for the international Phase 3 clinical trial of PXT3003, Pharnext’s lead PLEODRUG ©, for treatment of CMT1A.
July 31, 2017
Join this exclusive research study for people with CMT featuring the AlterG anti-gravity treadmill.
October 31, 2016
For the first time investigators are looking for patients to participate in a pivotal Phase 3 clinical trial of Pharnext’s lead investigational pleodrug, PXT-3003 for the potential treatment of Charcot-Marie-Tooth Disease Type 1A (CMT1A).
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