NCT04512963
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Repair-Deficiency Disorders, Genetic Diseases, Inborn, +7 more
- Locations
-
- PRG S&T Investigational Site Glendale, California, United States
Clinical trial condition
Hutchinson-Gilford Progeria Syndrome
Explore clinical trials studying Hutchinson-Gilford Progeria Syndrome. Study availability and eligibility vary by location and protocol.
4 public trials
0 recruiting studies
Hutchinson-Gilford Progeria Syndrome trial results
NCT03871972
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hutchinson-Gilford Progeria Syndrome, +5 more
- Locations
-
- Bundang CHA Medical Center Seongnam-si, Gyeonggi-do, South Korea
NCT00731016
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hutchinson-Gilford Progeria Syndrome, +5 more
- Locations
-
- Laboratoire de Génétique Moléculaire - Hopital de la Timone Marseille, France
Active, Not Recruiting
Study to Determine Optimal Dose and Evaluate Safety, Tolerability, and Pharmacokinetics of Progerinin in Patients With Hutchinson-Gilford Progeria Syndrome (HGPS)
NCT06775041
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hutchinson-Gilford Progeria Syndrome, +5 more
- Locations
-
- Boston Children's Hospital Boston, Massachusetts, United States