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Trial Match

Clinical trials test new treatments โ€” sometimes the newest options available for a disease. Find trials that are recruiting now, near you. Open one to see its eligibility rules as simple questions to go through with your doctor.

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30 recruiting trials

for Skeletal Dysplasia

A Natural History Study in Children With a Type II Collagen Disorder With Short Stature NCT05408715n/a2 sites๐Ÿ“ Paris๐Ÿ“ Madrid Innoskel ยท Tests: Natural History Study Relationship Between Circulating Sclerostin and Bone Lesions in Patients With Mastocytosis NCT06440148n/a1 site๐Ÿ“ Lublin Medical University of Lublin ยท Tests: SCLEROSTIN Decoding the Genetic Landscape of Skeletal Diseases NCT05876416n/a1 site๐Ÿ“ Stockholm Karolinska Institutet A Study in Children With Achondroplasia NCT07301463n/a8 sites๐Ÿ“ Beijing๐Ÿ“ Guangzhou๐Ÿ“ Zhengzhou Abbisko Therapeutics Co, Ltd ยท Tests: No Interventions, complete a natural history observation of ACH for at least 6 months and up to 2 years Natural History, Pathogenesis and Outcome of Melorheostosis A Rare Osteosclerotic Disease NCT02504879n/a1 site๐Ÿ“ Bethesda National Institute of Arthritis and Musculoskeletal and Skiโ€ฆ Registry for Patients With Achondroplasia / Hypochondroplasia (OMPR-Ach/Hy) NCT05328050n/a1 site๐Ÿ“ Milan Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico ยท Tests: Registry Clinical Evaluation of Patient-Specific 3D-Printed Titanium Implants for Facial Reconstruction. NCT07654647NA1 site๐Ÿ“ Latakia Latakia University ยท Tests: Patient-specific titanium implants for facial reconstruction Osteogenesis Imperfecta Trial of AGA2115 for ADUlts With COL1A1 and/or COL1A2 GeNetic Variations (IDUN) NCT07062588Phase 226 sites๐Ÿ“ Phoenix๐Ÿ“ New Haven๐Ÿ“ Wilmington Angitia Incorporated Limited ยท Tests: AGA2115, Placebo Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases. NCT04880356n/a1 site๐Ÿ“ Milan Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta ยท Tests: collection of data Fibrous Dysplasia, McCune-Albright Syndrome Patient Registry NCT03231644n/a1 site๐Ÿ“ Bethesda Tovah Burstein Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD) NCT01668186n/a1 site๐Ÿ“ Montreal McGill University Health Centre/Research Institute of the Mโ€ฆ Functional and Morphological Characterization of Multiple Osteochondromas Disorder NCT06703736n/a1 site๐Ÿ“ Bologna Istituto Ortopedico Rizzoli RCDP Natural History Study NCT04031287n/a1 site๐Ÿ“ Wilmington MED-LIFE DISCOVERIES LP Study to Evaluate the Efficacy and Safety of BMN 333 Versus Vosoritide in Children With Achondroplasia NCT07441876Phase 2, Phase 328 sites๐Ÿ“ Oakland๐Ÿ“ Wilmington๐Ÿ“ Chicago BioMarin Pharmaceutical ยท Tests: BMN 333, Vosoritide Injection [Voxzogo] Longitudinal Study of Neurodegenerative Disorders NCT03333200n/a1 site๐Ÿ“ Pittsburgh University of Pittsburgh ยท Tests: Palliative Care, Hematopoetic Stem Cell Transplantation Registry of Ollier Disease and Maffucci Syndrome NCT04134572n/a1 site๐Ÿ“ Bologna Luca Sangiorgi Audio-vestibular Evaluation of Children and Young Adults With Osteogenesis Imperfecta NCT05419960n/a1 site๐Ÿ“ Paris Assistance Publique - Hรดpitaux de Paris ยท Tests: Vestibular Assessment, Petrous bone Computed Tomography (CT), Magnetic Resonance Imaging (MRI) Achondroplasia Natural History Multicenter Clinical Study NCT02597881n/a1 site๐Ÿ“ Baltimore Johns Hopkins University Interventional Study of Infigratinib in Children < 3 Years Old With Achondroplasia (ACH) NCT07169279Phase 212 sites๐Ÿ“ Oakland๐Ÿ“ Baltimore๐Ÿ“ Madison QED Therapeutics, a BridgeBio company ยท Tests: Infigratinib is provided as a single dose of minitablets for oral administration, Infigratinib is provided as sprinkle โ€ฆ FORTIFI-HN01: A Study of Ficerafusp Alfa (BCA101) or Placebo in Combination With Pembrolizumab in First-Line PD-L1-pos, R or M HNSCC NCT06788990Phase 2, Phase 3231 sites๐Ÿ“ Birmingham๐Ÿ“ Phoenix๐Ÿ“ La Jolla Bicara Therapeutics ยท Tests: Ficerafusp alfa, Pembrolizumab (KEYTRUDAยฎ), Placebo A Study of TYRA-300 in Children With Achondroplasia: BEACH301 NCT06842355Phase 225 sites๐Ÿ“ Torrance๐Ÿ“ Aurora๐Ÿ“ Wilmington Tyra Biosciences, Inc ยท Tests: TYRA-300 0.125 mg/kg, TYRA-300 0.25 mg/kg, TYRA-300 0.375 mg/kg, TYRA-300 0.50 mg/kg, TYRA-300 0.625 mg/kg Uncovering Genes Behind Cartilage Tumors and Vascular Anomalies Using Genomic Sequencing NCT06749366n/a1 site๐Ÿ“ Bethesda Eunice Kennedy Shriver National Institute of Child Health aโ€ฆ Screening and Natural History of Patients With Polyostotic Fibrous Dysplasia and the McCune-Albright Syndrome NCT00001727n/a1 site๐Ÿ“ Bethesda National Institute of Dental and Craniofacial Research (NIDโ€ฆ Non-invasive Functional Assessment and Pathogenesis of Morquio A NCT05284006n/a1 site๐Ÿ“ Wilmington Nemours Children's Clinic ยท Tests: Imaging, gait analysis, growth, joint test, hearing test, questionnaire, etc. Salivary Biomarkers in Periodontal Disease Progression NCT07661784n/a1 site๐Ÿ“ Isparta Suleyman Demirel University ยท Tests: Saliva Sampling Registry of Osteogenesis Imperfecta NCT04115774n/a1 site๐Ÿ“ Bologna Luca Sangiorgi ยท Tests: bisphosphonates Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Osteogenesis Imperfecta NCT05927389NA2 sites๐Ÿ“ Montpellier๐Ÿ“ Toulouse University Hospital, Toulouse ยท Tests: Adapted Physical Activity program Data Collection of Patients With Rare Bone Diseases NCT05247645n/a1 site๐Ÿ“ Bologna Luca Sangiorgi Multidisciplinary Evaluation and a Genome-wide Analysis in a Cohort of Idiopathic Short Stature Patients NCT05858606NA1 site๐Ÿ“ Montpellier University Hospital, Montpellier ยท Tests: Evaluation of the prevalence of truly (authentified) idiopathic short stature after multidisciplinary clinico-radiologiโ€ฆ Fibrous Dysplasia: An Epidemiological and Correlational Evaluation of Multimodal Data NCT07569731n/a1 site๐Ÿ“ Bologna Istituto Ortopedico Rizzoli
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