1 active not recruiting, 1 completed, 1 not yet recruiting, 1 recruiting. 1 Phase 2.
| Phase | Trials | Status |
|---|---|---|
| Phase 2 | 1 | Withdrawn 1 |
Follow Glycogen Storage Disease IB: new trials by email Literature Review of Glycogen Storage Disease IB trials Research Report on Glycogen Storage Disease IB
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| Effects of the Carbohydrate Counting Method on Blood Glucose Regulation, Quality of Life, Urinary Glc4 and Other Biomarkers in Children With GSD1 Glycogen Storage Disease Type I, Glycogen Storage Disease Type IB | Not yet recruiting | Şükrü Arman AKSOY | 8 | 2026-10-30 | 2026-10-15 | |
| Accuracy of Home Lactate Meter and Accu-chek Glucometer in Patients With Glycogen Storage Disease Lactate Meter, Accu Chek - Glycogen Storage Disease Type IA, Glycogen Storage Disease Type I | Recruiting | Connecticut Children's Medical Center | 10 | 2026-08-01 | 2026-06-01 | |
| Efficacy and Safety of Empagliflozin in GSD-Ib Patients Empagliflozin - Glycogen Storage Disease Type IB | Phase 2 | Withdrawn | Xinhua Hospital, Shanghai Jiao Tong University School of Medicine | 2023-07-15 | 2026-06-18 | |
| Prospective Collection of Biospecimen in Pediatric Patients and Adult Guardians Diagnosed With Glycogen Storage Disease Type 1B (GSD1b) Specimen Donation - Glycogen Storage Disease Type IB | Terminated | Sanguine Biosciences | 6 | 2023-04-27 | 2024-04-19 | |
| Prospective Cohort Study of Children With GSD1b Receiving Empagliflozin Empagliflozin - Glycogen Storage Disease Type IB | Unknown | Hong Kong Children's Hospital | 11 | 2021-08-08 | 2021-08-16 | |
| Early Check: Expanded Screening in Newborns Confirmatory Testing - Spinal Muscular Atrophy, Fragile X Syndrome | Active not recruiting | RTI International | 30000 | 2018-10-15 | 2026-07-01 | |
| Sleep and Quality of Life in Patients With Glycogen Storage Disease on Standard Versus Modified Uncooked Cornstarch Glycosade - Glycogen Storage Disease Type IA, Glycogen Storage Disease Type IB | Completed | John Mitchell | 11 | 2013-11-01 | 2015-09-25 |
Glycogen Storage Disease Type I (3) · Hepatorenal form of glycogen storage disease (3) · 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (1) · 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (1) · 3-methylcrotonyl CoA carboxylase 1 deficiency (1) · 3-methylcrotonyl CoA carboxylase 2 deficiency (1) · Acidemia, isovaleric (1) · Acrodermatitis enteropathica (1) · Adenine phosphoribosyltransferase deficiency (1) · Adrenal hyperplasia, congenital, type 5 (1) · Adrenocorticotropic hormone deficiency (1) · Amaurosis congenita of Leber, type 2 (1) · Anemia, Sickle Cell (1) · Angelman Syndrome (1)
Carbohydrate Metabolism, Inborn Errors (4) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (4) · Genetic Diseases, Inborn (4) · Metabolic Diseases (4) · Metabolism, Inborn Errors (4) · Nutritional and Metabolic Diseases (4) · Glycogen Storage Disease (3) · Female Urogenital Diseases (2) · Female Urogenital Diseases and Pregnancy Complications (2) · Kidney Diseases (2) · Male Urogenital Diseases (2) · Renal Tubular Transport, Inborn Errors (2) · Urogenital Diseases (2) · Urologic Diseases (2) · Abnormalities, Multiple (1)
empagliflozin (2)
Connecticut Children's Medical Center (1) · Hong Kong Children's Hospital (1) · John Mitchell (1) · RTI International (1) · Sanguine Biosciences (1) · Xinhua Hospital, Shanghai Jiao Tong University School of Medicine (1) · Şükrü Arman AKSOY (1)
United States (3) · Canada (1) · China (1) · Hong Kong (1) · Turkey (Türkiye) (1)
Curt Scharfe, MD, PhD (1) · John J Mitchell, MD (1) · Malaya Mount, MS, RD, CDN (1) · Mei Kwun Kwok (1) · Rebecca Riba-Wolman, MD (1) · Wenjuan Qiu, MD PhD (1)