Bone Diseases, Developmental
Bone Diseases, Developmental
Explore linked clinical trials. Standard reference: MESH:M0002777232 results · Page 1 of 10
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Phase 3 Study of LUM-201 in Children With Growth Hormone Deficiency | Bone Diseases, Developmental, Bone Diseases, Endocrine, Dwarfism, bone disorder, brain disorder, central nervous system disorder, endocrine system disorder, hypopituitarism, hypothalamic disorder, musculoskeletal system disorder, nervous system disorder, pituitary dwarfism, pituitary gland disorder | Recruiting | Phase 3 | 2026-10-09 | NCT06948214 | |
| RCDP Natural History Study | Bone 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 | Recruiting | Not stated | 2026-10-09 | NCT04031287 | |
| Screening and Natural History of Patients With Polyostotic Fibrous Dysplasia and the McCune-Albright Syndrome | Bone Diseases, Developmental, bone disorder, fibrous dysplasia, musculoskeletal system disorder, osteochondrodysplasia, polyostotic fibrous dysplasia | Recruiting | Not stated | 2026-10-09 | NCT00001727 | |
| Evaluate the Efficacy and Safety of KK8398 in Patients With Achondroplasia（AOBA Study） | Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, achondroplasia, bone disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia | Active, not recruiting | Phase 3 | 2026-10-08 | NCT06926491 | |
| ES Catheter vs Cryoablation After Pectus Surgery | Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Musculoskeletal Abnormalities, bone disorder, musculoskeletal system disorder, pectus excavatum | Recruiting | Not applicable | 2026-10-08 | NCT06682208 | |
| Comprehensive Study of Post-surgical Pain After Pectus or Spine Surgery | Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Musculoskeletal Abnormalities, Neurologic Manifestations, Pain, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Postoperative Pain, Signs and Symptoms, Spinal Curvatures, bone disorder, musculoskeletal system disorder, pectus excavatum, scoliosis, vertebral column disorder | Active, not recruiting | Not applicable | 2026-10-08 | NCT04031716 | |
| Postoperative and Chronic Pain Genetic Spine and Pectus Surgery Study | Bone Diseases, Developmental, Chronic Pain, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Kyphosis, Musculoskeletal Abnormalities, Neurologic Manifestations, Pain, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Postoperative Pain, Signs and Symptoms, Spinal Curvatures, bone disorder, musculoskeletal system disorder, pectus excavatum, scoliosis, vertebral column disorder | Active, not recruiting | Not stated | 2026-10-08 | NCT02998138 | |
| Ngenla Subcutaneous Injection Special Investigation | Bone Diseases, Developmental, Bone Diseases, Endocrine, Dwarfism, bone disorder, brain disorder, central nervous system disorder, endocrine system disorder, hypopituitarism, hypothalamic disorder, musculoskeletal system disorder, nervous system disorder, pituitary dwarfism, pituitary gland disorder | Active, not recruiting | Not stated | 2026-10-07 | NCT05602766 | |
| Setrusumab vs Placebo for Osteogenesis Imperfecta | Bone Diseases, Developmental, Collagen Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, bone disorder, connective tissue disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia, osteogenesis imperfecta | Active, not recruiting | Phase 2 / Phase 3 | 2026-10-06 | NCT05125809 | |
| Prospective Evaluation of OptiThyDose | Bone Diseases, Developmental, Bone Diseases, Endocrine, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, Graves disease, autoimmune disease, bone disorder, congenital hypothyroidism, disease of orbital part of eye adnexa, endocrine system disorder, exophthalmos, eye disorder, goiter, hereditary disease, hyperthyroidism, hypothyroidism, immune system disorder, musculoskeletal system disorder, thyroid gland disorder | Recruiting | Not applicable | 2026-10-02 | NCT06864351 | |
| FORTIFI-HN01: A Study of Ficerafusp Alfa (BCA101) or Placebo in Combination With Pembrolizumab in First-Line PD-L1-pos, R or M HNSCC | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Head and Neck Neoplasms, Neoplasms by Histologic Type, Neoplasms by Site, bone disorder, carcinoma, epithelial neoplasm, head and neck squamous cell carcinoma, hereditary disease, laryngeal disorder, musculoskeletal system disorder, neoplasm, osteochondrodysplasia, otorhinolaryngologic disease, respiratory system disorder, squamous cell carcinoma | Recruiting | Phase 2 / Phase 3 | 2026-10-02 | NCT06788990 | |
| Natural History, Pathogenesis and Outcome of Melorheostosis A Rare Osteosclerotic Disease | Bone Diseases, Developmental, Skin and Connective Tissue Diseases, bone disorder, connective tissue disorder, hyperostosis, musculoskeletal system disorder, osteochondrodysplasia, osteosclerosis, rheumatic disorder | Recruiting | Not stated | 2026-10-02 | NCT02504879 | |
| Natural History and Genetics of Food Allergy and Related Conditions | Abnormalities, Multiple, Aneurysm, Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Digestive System Diseases, Eosinophilia, Hemic and Lymphatic Diseases, Hypersensitivity, Immediate, Loeys-Dietz syndrome, Musculoskeletal Abnormalities, Skin Diseases, Eczematous, Skin and Connective Tissue Diseases, aortic aneurysm, aortic disorder, atopic eczema, bone disorder, cardiovascular disorder, dermatitis, digestive system disorder, eosinophilic esophagitis, esophageal disorder, esophagitis, food allergy, gastroenteritis, hematologic disorder, hereditary disease, hereditary skin disorder, immune system disorder, leukocyte disorder, musculoskeletal system disorder, osteochondrodysplasia, skin disorder, vascular disorder | Recruiting | Not stated | 2026-10-02 | NCT02504853 | |
| A Study of TYRA-300 in Children With Achondroplasia: BEACH301 | Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, achondroplasia, bone disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia | Recruiting | Phase 2 | 2026-10-01 | NCT06842355 | |
| Uncovering Genes Behind Cartilage Tumors and Vascular Anomalies Using Genomic Sequencing | Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Enchondromatosis, Neoplasms by Histologic Type, Neoplasms, Connective and Soft Tissue, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, bone disorder, chondroma, chondrosarcoma, connective tissue disorder, connective tissue neoplasm, cutaneous mucinosis, hemangioma, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 4, musculoskeletal system disorder, neoplasm, osteochondrodysplasia, sarcoma, vascular cancer | Recruiting | Not stated | 2026-10-01 | NCT06749366 | |
| Trial Investigating the Efficacy and Safety of Weekly Lonapegsomatropin Compared to Daily Somatropin in Children and Adolescents With Short Stature or Growth Failure Due to Growth Hormone Sufficient Disorders | Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Dwarfism, Failure to Thrive, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Musculoskeletal Abnormalities, Noonan syndrome, Pathological Conditions, Signs and Symptoms, Sex Chromosome Disorders, Signs and Symptoms, Skin and Connective Tissue Diseases, Turner syndrome, Urogenital Abnormalities, Urogenital Diseases, bone disorder, cardiovascular disorder, chromosomal disorder, congenital heart disease, connective tissue disorder, disorder of sexual differentiation, endocrine system disorder, gonadal disorder, gonadal dysgenesis, heart disorder, hereditary disease, musculoskeletal system disorder, sex chromosome disorder of sex development | Recruiting | Phase 3 | 2026-09-30 | NCT07221851 | |
| Treatment for "Asymmetric Crying Facies" | Bell's palsy, Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Crouzon syndrome, DNA Virus Infections, Herpesviridae infectious disease, Infections, Musculoskeletal Abnormalities, Stomatognathic Diseases, bone disorder, cranial nerve neuropathy, craniofacial microsomia, dysostosis, facial nerve disorder, mandibulofacial dysostosis, mouth disorder, musculoskeletal system disorder, nervous system disorder, viral infectious disease | Recruiting | Not applicable | 2026-09-28 | NCT07802639 | |
| Setrusumab in Pediatric Japanese Subjects With Osteogenesis Imperfecta | Bone Diseases, Developmental, Collagen Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, bone disorder, connective tissue disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia, osteogenesis imperfecta | Active, not recruiting | Phase 3 | 2026-09-28 | NCT06636071 | |
| A Prospective Natural History Study of Lymphatic Anomalies | Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Hemic and Lymphatic Diseases, Lymphatic Abnormalities, Osteolysis, Essential, Peritoneal Diseases, bone disorder, bone resorption disease, chylous ascites, digestive system disorder, intestinal disorder, lymphangiectasis, lymphatic system disorder, lymphedema, lytic metastatic bone lesion, musculoskeletal system disorder, protein-losing enteropathy | Recruiting | Not stated | 2026-09-28 | NCT05731141 | |
| Pregnancy in Women With Rare Multisystemic Vascular Diseases: COGRare5 Study | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Marfan syndrome, Skin and Connective Tissue Diseases, arteriovenous hemangioma/malformation, bone disorder, cardiovascular disorder, central nervous system disorder, congenital heart disease, connective tissue disorder, heart disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary hemorrhagic telangiectasia, lymphatic system disorder, lymphedema, musculoskeletal system disorder, nervous system disorder, telangiectasis, vascular disorder, vascular hemostatic disease, vascular malformation | Recruiting | Not stated | 2026-09-28 | NCT04194619 | |
| The AgRP and GH/IGF-1 Axis in Children | Bone Diseases, Developmental, Bone Diseases, Endocrine, Dwarfism, bone disorder, brain disorder, central nervous system disorder, endocrine system disorder, hypopituitarism, hypothalamic disorder, musculoskeletal system disorder, nervous system disorder, pituitary dwarfism, pituitary gland disorder | Not yet recruiting | Not stated | 2026-09-25 | NCT05645211 | |
| Anterior Cervical Disectomy And Fusion Using The Tritanium® C Anterior Cervical Cage For One Or Two-Levels | Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Klippel-Feil syndrome, Musculoskeletal Abnormalities, bone disorder, cervical disk degenerative disorder, dysostosis, intervertebral disk degenerative disorder, musculoskeletal system disorder, vertebral column disorder | Active, not recruiting | Not applicable | 2026-09-25 | NCT04214535 | |
| Study to Evaluate the Efficacy and Safety of BMN 333 Versus Vosoritide in Children With Achondroplasia | Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, achondroplasia, bone disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia | Recruiting | Phase 2 / Phase 3 | 2026-09-24 | NCT07441876 | |
| A Study to Learn About Somatrogon in Patients With Pediatric Growth Hormone Deficiency (p GHD) in India. | Bone Diseases, Developmental, Bone Diseases, Endocrine, Dwarfism, bone disorder, brain disorder, central nervous system disorder, endocrine system disorder, hypopituitarism, hypothalamic disorder, musculoskeletal system disorder, nervous system disorder, pituitary dwarfism, pituitary gland disorder | Recruiting | Not stated | 2026-09-24 | NCT06587035 | |
| Frontal Reconstruction Without Orbital Advancement for Moderate Metopic Craniosynostosis | Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Metopic Synostosis, Musculoskeletal Abnormalities, Trigonocephaly, Nonsyndromic, bone disorder, craniosynostosis, dysostosis, musculoskeletal system disorder, synostosis | Not yet recruiting | Not applicable | 2026-09-23 | NCT07837453 |