progeroid syndrome
progeroid syndrome
Explore linked clinical trials. Standard reference: MONDO:00153333 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| A Study Observing Disease Progression in a Patient With Hutchinson-Gilford Progeria Syndrome (HGPS) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, laminopathy, metabolic disease, progeroid syndrome | Not yet recruiting | Not stated | 2026-09-24 | NCT07839351 | |
| Creating Stem Cells From a Progeria Patient's Blood to Test Candidate Treatments in the Lab | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, laminopathy, metabolic disease, progeroid syndrome | Not yet recruiting | Not stated | 2026-09-10 | NCT07803432 | |
| Phase I/II Trial of Everolimus in Combination With Lonafarnib in Progeria | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, laminopathy, metabolic disease, progeroid syndrome | Enrolling by invitation | Phase 1 / Phase 2 | 2026-04-02 | NCT02579044 |