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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study Evaluating the Predictive Value of the Terminal Latency Index (TLI) for Treatment Response in Patients With Anti-MAG Neuropathynervous system disorder, neuromuscular disease, peripheral nervous system disorder, polyneuropathy associated with IgM monoclonal gammapathy with anti-MAGNot yet recruitingNot stated2026-08-31NCT07794137
Studying Nerve Function and Structure in Charcot-Marie-Tooth Disease, Anti-MAG Neuropathy and CIDPCharcot-Marie-Tooth disease, Charcot-Marie-Tooth disease X-linked dominant 1, Charcot-Marie-Tooth disease type 1A, Charcot-Marie-Tooth disease type 4B2, Charcot-Marie-Tooth disease type 4D, Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, autoimmune disease, autoimmune disorder of the nervous system, central nervous system malformation, chronic inflammatory demyelinating polyradiculoneuropathy, demyelinating disease, hereditary disease, hereditary motor and sensory neuropathy, immune system disorder, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG, polyradiculoneuropathyRecruitingNot stated2026-03-10NCT07461896
Rituximab Therapy in Anti-Myelin Associated Glycoprotein Patients With Characteristics of Good Responderspolyneuropathy associated with IgM monoclonal gammapathy with anti-MAGRecruitingPhase 32025-11-24NCT05136976