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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
An Open-Label Extension Study of BPN14770 in Subjects With Fragile X SyndromeCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Sex Chromosome Disorders, X-linked disease, chromosomal disorder, fragile X syndrome, hereditary disease, inherited neurodegenerative disorder, intellectual disability, nervous system disorderActive, not recruitingPhase 32025-10-03NCT05367960