piebaldism
piebaldism
Explore linked clinical trials. Standard reference: MONDO:00082444 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Comparing Regorafenib Combined With Envafolimab to Physician's Choice in Patients With Metastatic Gastrointestinal Stromal Tumors Harboring KIT Exon 17 Mutations Refractory to Standard Treatment | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Digestive System Neoplasms, Eye Diseases, Hereditary, Neoplasms by Histologic Type, Neoplasms, Connective and Soft Tissue, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, albinism, connective tissue neoplasm, digestive system disorder, digestive system neoplasm, gastrointestinal stromal tumor, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, neoplasm, piebaldism, skin disorder, skin pigmentation disorder | Recruiting | Phase 2 | 2026-04-30 | NCT07559864 | |
| Allergy and Immunology Natural History Study | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Hypersensitivity, Immediate, Nutritional and Metabolic Diseases, Respiratory Hypersensitivity, Skin Diseases, Eczematous, Skin and Connective Tissue Diseases, albinism, anaphylaxis, angioedema, asthma, atopic eczema, autoimmune disease, bronchial disorder, cardiovascular disorder, dermatitis, food allergy, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, immune system disorder, inborn disorder of amino acid metabolism, inborn error of immunity, inborn errors of metabolism, lung disorder, metabolic disease, obstructive lung disease, piebaldism, respiratory system disorder, skin disorder, skin pigmentation disorder, skin vascular disease, urticaria, vascular disorder | Recruiting | Not stated | 2026-02-04 | NCT05584488 | |
| A Study of the c-Kit Specific Antibody-Drug Conjugate NN3201 for Advanced and/or Metastatic Solid Tumors Known to Express c-Kit | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Digestive System Neoplasms, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Connective and Soft Tissue, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, Thoracic Neoplasms, Urogenital Diseases, Urogenital Neoplasms, Uveal Neoplasms, adenocarcinoma, adenoid cystic carcinoma, albinism, benign urinary system neoplasm, bronchial neoplasm, bronchogenic carcinoma, carcinoma, chromophobe renal cell carcinoma, clear cell renal carcinoma, connective tissue neoplasm, digestive system disorder, digestive system neoplasm, epithelial neoplasm, eye disorder, gastrointestinal stromal tumor, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, kidney cancer, kidney disorder, lung disorder, lung neoplasm, melanocytic neoplasm, melanoma, metabolic disease, neoplasm, neuroendocrine neoplasm, ocular cancer, piebaldism, primitive neuroectodermal tumor, renal cell carcinoma, respiratory system disorder, respiratory tract neoplasm, skin disorder, skin pigmentation disorder, small cell lung carcinoma, urinary system disorder, uveal disorder, uveal melanoma | Recruiting | Phase 1 | 2025-09-23 | NCT06805825 | |
| Preoperative Imatinib Mesylate Combined With Rectal-sparing Surgery in Patients With c-KIT Gene-mutant Rectal GIST | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Digestive System Neoplasms, Eye Diseases, Hereditary, Neoplasms by Histologic Type, Neoplasms, Connective and Soft Tissue, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, albinism, connective tissue neoplasm, digestive system disorder, digestive system neoplasm, gastrointestinal stromal tumor, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, neoplasm, piebaldism, skin disorder, skin pigmentation disorder | Not yet recruiting | Phase 3 | 2023-08-01 | NCT05970900 |