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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Observational Study of VYKAT™ XR in Patients With Prader-Willi SyndromeAbnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Imprinting Disorders, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Overweight, Prader-Willi syndrome, chromosomal disorder, hereditary disease, intellectual disability, nervous system disorder, nutritional disorder, obesity disorder, overnutritionEnrolling by invitationNot stated2026-10-08NCT07450664

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OrganizationsLinked trials
Soleno Therapeutics, Inc.2

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