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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
ASO Treatment for Syndromic CraniosynostosesApert syndrome, Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Crouzon syndrome, Limb Deformities, Congenital, Muenke syndrome, Musculoskeletal Abnormalities, Pfeiffer syndrome, Saethre-Chotzen syndrome, bone disorder, craniosynostosis, dysostosis, musculoskeletal system disorder, syndactyly, synostosisRecruitingNot stated2026-09-08NCT07535372

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Research sitesCityCountryLinked trials
Cellular and Experimental Biology UnitRomeItaly1