An Interventional Study of Infigratinib in Children With Hypochondroplasia
An Interventional Study of Infigratinib in Children With Hypochondroplasia
Enrolling by invitation · NCT06873035 · Registry updated 2026-07-16Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| An Interventional Study of Infigratinib in Children With Hypochondroplasia | Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, bone disorder, connective tissue disorder, cutaneous mucinosis, endocrine system disorder, hereditary disease, hypochondroplasia, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 4, musculoskeletal system disorder, osteochondrodysplasia | Enrolling by invitation | Phase 2 / Phase 3 | 2026-07-16 | NCT06873035 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| QED Therapeutics, a BridgeBio company | 5 |
24 results · Page 1 of 1
Research sites
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