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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

1 results · Page 1 of 1

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OrganizationsLinked trials
Tetra Discovery Partners1

17 results · Page 1 of 1

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Research sitesCityCountryLinked trials
Amnova Clinical ResearchIrvineUnited States3
Boston Children's HospitalBostonUnited States343
Children's Hospital ColoradoAuroraUnited States312
Cincinnati Children's Hospital Medical CenterCincinnatiUnited States405
Clinic for Special ChildrenStrasburgUnited States2
Emory University School of MedicineAtlantaUnited States47
Greenwood Genetic CenterGreenvilleUnited States2
Icahn School of Medicine at Mount SinaiNew YorkUnited States342
Kennedy Krieger InstituteBaltimoreUnited States41
MIND Institute UC Davis Medical CenterSacramentoUnited States1
Rush University Medical CenterChicagoUnited States283
Suburban Research AssociatesMediaUnited States9
Thompson Autism & Neurodevelopment Center - CHOCOrangeUnited States1
U MassWorcesterUnited States1
University of Kansas Medical CenterKansas CityUnited States240
University of MiamiMiamiUnited States327
University of Utah and Primary Children's HospitalSalt Lake CityUnited States1