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Neuropathy, hereditary motor and sensory, type VIc, with optic atrophy

MONDO:0032792

Also known as: CMT 6C, CMT6C, Charcot-Marie-Tooth Disease, Type 6C, HMSN 6C, HMSN6C, neuropathy, hereditary motor and sensory, type VIc, with optic atrophy

7 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Peripheral nervous system disorder (107) Neuromuscular disease (98) Peripheral neuropathy (90) Human disease (14) Hereditary peripheral neuropathy (6) Hereditary neurological disease (5) Hereditary motor and sensory neuropathy (3)

Trials to join now! 5 Not yet recruiting 1 Completed 1

Gene therapy readiness check: new study maps virus immunity in muscle disease patients

Knowledge-focused Not yet recruiting

This study will test blood samples from 450 people aged 6 to 60 with inherited neuromuscular diseases to see if they have antibodies that could block gene therapy viruses (AAVs). The goal is to understand how common these antibodies are and which patients might be good candidates…

Phase: NA • Sponsor: Genethon • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:04 UTC