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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of BBP-418 in Patients With LGMD2ICongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, autosomal recessive limb-girdle muscular dystrophy type 2I, hereditary disease, limb-girdle muscular dystrophy, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseActive, not recruitingPhase 22026-07-21NCT04800874

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OrganizationsLinked trials
ML Bio Solutions, Inc.3

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Research sitesCityCountryLinked trials
Virginia Commonwealth UniversityRichmondUnited States38