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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of MRM-3379 in Male Participants With Fragile X Syndrome (BLOOM)Congenital 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 disorderRecruitingPhase 22026-09-29NCT07209462