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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Lamivudine as a Novel Clinical Effort for Rett SyndromeCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Rett syndrome, X-linked disease, hereditary disease, inherited neurodegenerative disorder, intellectual disability, nervous system disorderEnrolling by invitationPhase 22026-06-10NCT07640503