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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
A Prospective Longitudinal Study in Adults With Multifocal Motor Neuropathymultifocal motor neuropathyActive, not recruitingNot stated2026-05-29NCT05988073
Long-Term Safety and Efficacy of Tegoprubart in Kidney Transplant RecipientsChronic Disease, Disease Attributes, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Urogenital Diseases, chronic renal failure syndrome, kidney disorder, kidney failure, urinary system disorderEnrolling by invitationPhase 22025-12-10NCT06126380
Safety, Pharmacokinetics, and Efficacy of AT 1501 in Patients Undergoing Kidney TransplantChronic Disease, Disease Attributes, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Urogenital Diseases, chronic renal failure syndrome, kidney disorder, kidney failure, urinary system disorderRecruitingPhase 1 / Phase 22025-06-29NCT05027906