Crick
HomeTrialsGenesDrugs23andMeGraphBlogContact
  • Home
  • Trials
  • Genes
  • Drugs
  • 23andMe
  • Graph
  • Blog
  • Contact
Crick

An open-source clinical intelligence platform. Explore clinical trials, gene networks, and molecular structures using public data sources.

Data Sources

  • ClinicalTrials.gov
  • OpenTargets
  • ClinVar
  • PubChem

Links

  • Contact
  • Privacy

© 2026 Crick. All rights reserved.

Crick is for educational purposes only. Not medical advice.

Results for “Glycogen Storage Disease Type I”

Filters

Phase
Early Phase 1
Phase 1
Phase 2
Phase 3
Phase 4
Status
Recruiting
Active, Not Recruiting
Not Yet Recruiting
Completed
Enrolling by Invitation

Showing 11 of 0 results

Very early researchStudy completedNCT03665636
What this trial is testing

Anaplerotic Therapy Using Triheptanoin for Patients With Glycogen Storage Disease Type I

Who this might be right for
Glycogen Storage Disease Type I
Areeg El-Gharbawy 4
Not applicableStudy completedNCT01961076
What this trial is testing

Overnight Feeding Study in Glycogen Storage Disease Type 1

Who this might be right for
Glycogen Storage Disease Type 1 (GSD 1)
University of Zurich 5
Not applicableNot Yet RecruitingNCT07739394
What this trial is testing

Diazoxide in the Treatment of Type 1 Glycogenosis

Who this might be right for
Glycogen Storage Disease Type I
Central Hospital, Nancy, France 15
Not applicableStudy completedNCT05073783
What this trial is testing

Assess the Safety of Myozyme® and of Aldurazyme® in Male and Female Participants of Any Age Group With Pompe Disease or With Mucopolysaccharidosis Type I (MPS I) in a Home-care Setting

Who this might be right for
Pompe DiseaseMucopolysaccharidosis Type I (MPS I)
Sanofi 57
Large-scale testing (Phase 3)Study completedNCT05139316
What this trial is testing

Adeno-Associated Virus Serotype 8-Mediated Gene Transfer of Glucose-6-Phosphatase in Patients With Glycogen Storage Disease Type Ia (GSDIa)

Who this might be right for
Glycogen Storage Disease Type IA
Ultragenyx Pharmaceutical Inc 49
Not applicableStudy completedNCT02176096
What this trial is testing

Comparison of the Effect of a Novel Starch (Glycosade) Versus Gastrostomy Tube-Dextrose Infusion on Overnight Euglycaemia Control in Children With Glycogen Storage Disease Type I: Open Label Demonstration Trial

Who this might be right for
Glycogen Storage Disorder Type 1HypoglycemiaCornstarch+1 more
University of Manitoba 4
Not applicableStudy completedNCT03871673
What this trial is testing

The Use of Uncooked Sweet Manioc Starch to Treat Hepatic Glycogen Storage Diseases

Who this might be right for
Glycogen Storage Disease Type I
Hospital de Clinicas de Porto Alegre 11
Not applicableWithdrawnNCT02385162
What this trial is testing

Biomarker for Glycogen Storage Diseases (BioGlycogen)

Who this might be right for
Fructose Metabolism, Inborn ErrorsGlycogen Storage DiseaseGlycogen Storage Disease Type I+7 more
CENTOGENE GmbH Rostock
Not applicableLooking for participantsNCT05085704
What this trial is testing

Brain Metabolism Observed at 3 Tesla or 7 Tesla in Health and Metabolic Disease

Who this might be right for
Glut1 Deficiency Syndrome 1Glucose Metabolism DisordersEpilepsy+4 more
Weill Medical College of Cornell University 20
Not applicableLooking for participantsNCT01793168
What this trial is testing

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

Who this might be right for
Rare DisordersUndiagnosed DisordersDisorders of Unknown Prevalence+340 more
Sanford Health 20,000
Not applicableLooking for participantsNCT07459582
What this trial is testing

Accuracy of Home Lactate Meter and Accu-chek Glucometer in Patients With Glycogen Storage Disease

Who this might be right for
Glycogen Storage Disease Type IAGlycogen Storage Disease Type IGlycogen Storage Disease Type IB+1 more
Connecticut Children's Medical Center 10