Glycogen Storage Disease Type I
Showing 1 - 25 of >10,000
Glycogen Storage Disease Type IB Trial in Shanghai (Empagliflozin)
Recruiting
- Glycogen Storage Disease Type IB
-
Shanghai, Shanghai, ChinaXinhua Hospital, Shanghai Jiao Tong University School of Medicin
Jul 17, 2023
Glycogen Storage Disease Type I Trial in Durham (Triheptanoin)
Completed
- Glycogen Storage Disease Type I
-
Durham, North CarolinaDuke University Medical Center
Dec 14, 2021
Glycogen Storage Disease Type IA Trial in Groningen ([6,6-2H2]glucose)
Completed
- Glycogen Storage Disease Type IA
- [6,6-2H2]glucose
-
Groningen, NetherlandsUniversity of Groningen, UMC Groningen
Feb 10, 2022
Glycogen Storage Disease Type IA Trial in Worldwide (genetic, other, drug)
Recruiting
- Glycogen Storage Disease Type IA
- DTX401
- +3 more
-
Orange, California
- +16 more
Jan 13, 2023
Biomarker for Glycogen Storage Diseases (BioGlycogen)
Active, not recruiting
- Fructose Metabolism, Inborn Errors
- +9 more
-
Rostock, Germany
- +3 more
May 12, 2021
Mucopolysaccharidosis I, Mucopolysaccharidosis II, Mucopolysaccharidosis IV A Trial in San Francisco (There is no intervention)
Recruiting
- Mucopolysaccharidosis I
- +7 more
- There is no intervention
-
San Francisco, CaliforniaUniversity of California San Francisco
Nov 9, 2022
MPS I, MPS II, MPS IVA Trial in San Francisco (Aldurazyme (laronidase))
Recruiting
- MPS I
- +8 more
- Aldurazyme (laronidase)
-
San Francisco, CaliforniaUniversity of California
Apr 21, 2022
Myozyme® and of Aldurazyme® in Male and Female Participants of
Recruiting
- Pompe Disease
- Mucopolysaccharidosis Type I (MPS I)
-
Italy, ItalyInvestigational site Italy
May 3, 2022
Pompe Disease, Muscle Loss, Obesity Trial (Multi-ingredient supplement (PDT-MIS), Placebo (PLA))
Not yet recruiting
- Pompe Disease
- +7 more
- Multi-ingredient supplement (PDT-MIS)
- Placebo (PLA)
- (no location specified)
Nov 8, 2023
Glucose 6 Phosphatase Deficiency Trial in Warsaw (Empagliflozin)
Not yet recruiting
- Glucose 6 Phosphatase Deficiency
-
Warsaw, PolandThe Children's Memorial Health Institute
Jun 18, 2021
Biospecimen in Pediatric Patients and Adult Guardians Diagnosed
Recruiting
- Glycogen Storage Disease Type IB
- Specimen Donation
-
Woburn, MassachusettsSanguine BioSciences, Inc.
Jun 22, 2023
Long-Term Development of Muscular Dystrophy Outcome Assessments
Not yet recruiting
- LGMD1A
- +33 more
-
Richmond, VirginiaVirginia Commonwealth University
Aug 3, 2023
Glycogen Storage Disease VI, GLYCOGEN STORAGE DISEASE IXa1, GLYCOGEN STORAGE DISEASE IXa2 Trial in Durham (No intervention)
Recruiting
- Glycogen Storage Disease VI
- +4 more
- No intervention
-
Durham, North CarolinaDuke University
Jul 27, 2022
Carbon-13 Magnetic Resonance Spectroscopy in Glycogen Storage
Recruiting
- Glycogen Storage Disease
- +2 more
- No intervention
-
Copenhagen, Copenhange, DenmarkNeuromuscular Research Unit, 8077
Oct 26, 2022
Pompe Disease, Glycogen Storage Disease Type II (GSD-II), Acid Maltase Deficiency Disease Trial in Gainesville, Decatur, Detroit
Completed
- Pompe Disease
- +2 more
- alglucosidase alfa
-
Gainesville, Florida
- +2 more
Jul 29, 2022
Baby Detect : Genomic Newborn Screening
Recruiting
- Congenital Adrenal Hyperplasia
- +126 more
-
Liege, Wallonia, BelgiumCRMN, Hôpital La Citadelle
Jan 24, 2023
Pompe Disease -Non-invasive Magnetic Resonance Exploratory Pilot
Not yet recruiting
- Pompe Disease
- McArdle Disease
- Siemens Magnetom 7T Plus
-
Vienna, AustriaMedical University of Vienna
Jul 5, 2023
Hypoglycemia in Glycogen Storage Disease Type III
Recruiting
- Glycogen Storage Disease Type III
- No Intervention
-
Philadelphia, Pennsylvania
- +1 more
Jul 22, 2022
Glycogen Storage Disease Type IV, Adult Polyglucosan Body Disease Trial in Durham (No intervention)
Recruiting
- Glycogen Storage Disease Type IV
- Adult Polyglucosan Body Disease
- No intervention
-
Durham, North CarolinaDuke University Medical Center
May 20, 2022
Adeno-Associated Virus Antibody Study in Subjects OTC
Recruiting
- Ornithine Transcarbamylase Deficiency
- +2 more
-
Akron, Ohio
- +2 more
Jul 22, 2022
Glycogen Storage Disease Type II, Pompe Disease (Late-onset) Trial in Milan (Inspiratory Muscle Training (IMT), Inspiratory
Recruiting
- Glycogen Storage Disease Type II
- Pompe Disease (Late-onset)
- Inspiratory Muscle Training (IMT)
- Inspiratory Muscle Training (IMT) + Air Stacking
-
Milan, ItalyIRCCS S. Maria Nascente - Fondazione Don Carlo Gnocchi
Jul 11, 2023
Glycogen Storage Disease Type III Trial in Worldwide (biological, other, drug)
Recruiting
- Glycogen Storage Disease Type III
- UX053
- +4 more
-
Orange, California
- +9 more
Jul 22, 2022
Pompe Disease, Pompe Disease (Late-onset), Glycogen Storage Disease Type 2 Trial in Worldwide (Neutralizing Antibody to SPK-3006
Completed
- Pompe Disease
- +5 more
- Neutralizing Antibody to SPK-3006 capsid
-
Phoenix, Arizona
- +17 more
Jul 14, 2021
Glycogen Storage Disease Type I Trial in Porto Alegre (sweet polvilho, Cornstarch)
Unknown status
- Glycogen Storage Disease Type I
- sweet polvilho
- Cornstarch
-
Porto Alegre, RS, BrazilIda Vanessa D Schwartz
Feb 14, 2020