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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Stopping TSC Onset and Progression 2B: Sirolimus TSC Epilepsy Prevention StudyCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Malformations of Cortical Development, Group I, Neoplasms, Multiple Primary, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, epilepsy, hamartoma, hereditary disease, hereditary neoplastic syndrome, inherited neurodegenerative disorder, neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, tuberous sclerosisRecruitingPhase 22026-10-02NCT05104983