4 results ยท Page 1 of 1

Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Glycogen Storage Disease Type Ia (GSDIa) Disease Monitoring ProgramCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, disorder of glycogen metabolism, glucose metabolism disease, glycogen storage disease I, glycogen storage disease due to glucose-6-phosphatase deficiency type IA, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, metabolic diseaseRecruitingNot stated2026-08-26NCT06636383
Accuracy of Home Lactate Meter and Accu-chek Glucometer in Patients With Glycogen Storage DiseaseCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Fanconi renotubular syndrome, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Urogenital Diseases, disorder of glycogen metabolism, glycogen storage disease I, glycogen storage disease Ib, glycogen storage disease due to GLUT2 deficiency, glycogen storage disease due to glucose-6-phosphatase deficiency type IA, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, kidney disorder, metabolic disease, renal tubular transport disease, urinary system disorderRecruitingNot stated2026-06-01NCT07459582
Accuracy of Lactate Meter in GSDIaglycogen storage disease due to glucose-6-phosphatase deficiency type IARecruitingNot stated2026-03-06NCT06843330
A Phase 1/2, Dose-Exploration Study to Evaluate the Safety and Efficacy of BEAM-301 in Patients With Glycogen Storage Disease Type Ia (GSDIa)glycogen storage disease due to glucose-6-phosphatase deficiency type IARecruitingPhase 1 / Phase 22025-12-15NCT06735755