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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Feasibility Study to Evaluate a Digital Tool for Monitoring Patients Who Have Discontinued Treatment for Chronic Myeloid Leukemiachronic leukemiaNot yet recruitingNot applicable2026-08-12NCT07760311
Genotype/Phenotype Correlation of MORC2 MutationsCharcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, developmental disability, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neurodevelopmental disorder, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, psychiatric disorderRecruitingNot stated2026-06-18NCT07038239