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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Natural History Study in Participants With Congenital Myasthenic Syndromes (CMS) Due to Mutations in DOK7, MUSK, AGRN, or LRP4Congenital, Hereditary, and Neonatal Diseases and Abnormalities, congenital myasthenic syndrome, hereditary disease, nervous system disorder, neuromuscular disease, neuromuscular junction diseaseRecruitingNot stated2026-09-25NCT06078553
CLEOPATTRA: A Research Study to Look at the Effects of Treatment With a Medicine Called Coramitug (NNC6019-0001) in People With Heart Failure Due to Transthyretin Amyloid (ATTR) AmyloidosisTransthyretin Amyloid Cardiomyopathy (ATTR CM)RecruitingPhase 32026-09-22NCT07207811