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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
TANDem-2: Closing the Gap to Interventions for TANDCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Malformations of Cortical Development, Group I, Neoplasms, Multiple Primary, central nervous system malformation, cerebral cortical dysplasia, hamartoma, hereditary disease, hereditary neoplastic syndrome, inherited neurodegenerative disorder, neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, tuberous sclerosisEnrolling by invitationNot applicable2025-09-22NCT06879665

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Research sitesCityCountryLinked trials
TSC AllianceSilver SpringUnited States2
Tuberous Sclerosis AustraliaBeverly HillsAustralia1