Camurati-Engelmann disease
Camurati-Engelmann disease
Explore linked clinical trials. Standard reference: MONDO:000754212 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| 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 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 | |
| The Role of Transforming Growth Factor- Beta (TGF- β) Expression in Renal Biopsy of Lupus Nephritis Patients | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Skin and Connective Tissue Diseases, Urogenital Diseases, autoimmune disease, bone disorder, connective tissue disorder, glomerulonephritis, hereditary disease, immune system disorder, kidney disorder, lupus nephritis, musculoskeletal system disorder, nephritis, osteochondrodysplasia, systemic lupus erythematosus, urinary system disorder | Active, not recruiting | Not applicable | 2026-09-16 | NCT07823556 | |
| A Study Evaluating Ficerafusp Alfa (BCA101) QW in Combination With Pembrolizumab vs Alternative Ficerafusp Alfa Dosing in 1L 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 | 2026-09-08 | NCT07807163 | |
| Salivary Biomarkers in Periodontal Disease Progression | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Infections, Stomatognathic Diseases, bone disorder, gingival disorder, gingivitis, hereditary disease, mouth disorder, musculoskeletal system disorder, osteochondrodysplasia, periodontal disorder, periodontitis | Recruiting | Not stated | 2026-06-22 | NCT07661784 | |
| Losartan to Reduce Radiation Induced Fibrosis in Breast Cancer Patients | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fibrosis, Inflammation, Neoplasms by Site, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Radiation Fibrosis Syndrome, Skin and Connective Tissue Diseases, bone disorder, breast disorder, breast neoplasm, hereditary disease, injury, musculoskeletal system disorder, neoplasm, osteochondrodysplasia, radiation injury, skin disorder | Active, not recruiting | Phase 2 | 2026-06-18 | NCT05637216 | |
| Local Inflammation in Arrhythmogenic Right Ventricular Cardiomyopathy | Bone Diseases, Developmental, Camurati-Engelmann disease, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Inflammation, Pathologic Processes, Pathological Conditions, Signs and Symptoms, arrhythmogenic right ventricular cardiomyopathy, bone disorder, cardiomyopathy, cardiovascular disorder, congenital heart disease, heart disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia | Recruiting | Not applicable | 2026-06-01 | NCT05209776 | |
| Effects of Non-Surgical Periodontal Treatment on Inflammatory and Bone Markers in Periodontitis Patients | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Stomatognathic Diseases, bone disorder, hereditary disease, mouth disorder, musculoskeletal system disorder, osteochondrodysplasia, periodontal disorder, periodontitis | Active, not recruiting | Not applicable | 2026-04-27 | NCT07475013 | |
| An Engineered Sirpα Fused to Anti-Pd-L1 And Tgf-β Fusion Protein (HCB301) in Subjects With Selected Advanced Tumors | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Hodgkins lymphoma, Neoplasms by Histologic Type, bone disorder, hereditary disease, immune system disorder, immunoproliferative disorder, lymphatic system disorder, lymphoma, lymphoproliferative syndrome, musculoskeletal system disorder, neoplasm, osteochondrodysplasia | Recruiting | Phase 1 | 2026-04-13 | NCT06487624 | |
| Assessment of Pancreatic Dysfunction in Patients With Type 2 Diabetes | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, bone disorder, diabetes mellitus, endocrine system disorder, exocrine pancreatic insufficiency, glucose metabolism disease, hereditary disease, metabolic disease, musculoskeletal system disorder, osteochondrodysplasia, pancreas disorder, type 2 diabetes mellitus | Recruiting | Not stated | 2026-04-06 | NCT07512934 | |
| A Study of LY3200882 in Participants With Solid Tumors | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, bone disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia | Active, not recruiting | Phase 1 | 2026-04-03 | NCT02937272 | |
| TGF-beta Resistant Cytotoxic T-lymphocytes in Treatment of EBV-positive Nasopharyngeal Carcinoma / RESIST-NPC | Bone Diseases, Developmental, Camurati-Engelmann disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Head and Neck Neoplasms, Neoplasms by Histologic Type, Neoplasms by Site, Otorhinolaryngologic Neoplasms, Pharyngeal Diseases, Stomatognathic Diseases, bone disorder, carcinoma, epithelial neoplasm, hereditary disease, musculoskeletal system disorder, nasopharyngeal carcinoma, nasopharyngeal disorder, nasopharyngeal neoplasm, neoplasm, osteochondrodysplasia, otorhinolaryngologic disease | Active, not recruiting | Phase 1 | 2026-01-29 | NCT02065362 |