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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Rhizomelic Chondrodysplasia Punctata RegistryBone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Peroxisomal Disorders, bone disorder, chondrodysplasia punctata, hereditary disease, inborn errors of metabolism, metabolic disease, musculoskeletal system disorder, osteochondrodysplasia, rhizomelic chondrodysplasia punctata, rhizomelic chondrodysplasia punctata type 1, rhizomelic chondrodysplasia punctata type 2, rhizomelic chondrodysplasia punctata type 3, rhizomelic chondrodysplasia punctata type 5RecruitingNot stated2026-08-07NCT04569162

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Research sitesCityCountryLinked trials
NemoursWilmingtonUnited States2