Condition (MeSH)
Glycogen Storage Disease Type VI
ClinicalTrials.gov lists 2 trials for Glycogen Storage Disease Type VI or a narrower condition beneath it. CENTOGENE GmbH Rostock has the most among industry and government lead sponsors, with 1.
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Rows recorded per section
3 sections measured, none recorded · 1 not measured yet · 1 not computed
2 of the 2 trials are tagged with Glycogen Storage Disease Type VI itself; the rest are tagged with a narrower condition beneath it.
When did Glycogen Storage Disease Type VI trials start? (2)
Shown in this order: most recent first, 1990 onwards. 2026 is partial: trials registered with a 2026 start date so far, not a full year.
| Year | Trials started |
|---|---|
| 2020 | 1 |
| 2018 | 1 |
No forecast is made for this condition: it averages 0.0 trial starts a year over the five years to September, under the 5 a year the method needs.
Recruitment duration, a model prediction: none of the 2 trials evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Glycogen Storage Disease Type VI trials in? (1)
Shown in this order: phase order.
| Phase | Trials |
|---|---|
| Observational | 2 |
How many Glycogen Storage Disease Type VI trials are recruiting? (2)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Recruiting | 1 |
| Withdrawn | 1 |
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which lead sponsors run the most Glycogen Storage Disease Type VI trials? (1)
Shown in this order: most trials first. Lead sponsors the registry classes as industry, NIH, US federal, other government or network. A hospital or university the registry files as government can appear here. Sponsors it classes as academic or other are shown on the full page, because that class cannot separate an institution from a named investigator.
| Sponsor | Trials |
|---|---|
| CENTOGENE GmbH Rostock | 1 |
Prevalence (9)
Shown in this order: jurisdiction, then disease name. Orphanet observation for the mapped ORPHA concept; the mapping relation column says whether that concept is exactly this condition or broader or narrower.
| Orphanet disease | Type | Class | Geography | Jurisdiction | Mapping relation |
|---|---|---|---|---|---|
| Glycogen storage disease due to liver glycogen phosphorylase deficiency | Point prevalence | Unknown | Worldwide | Not stated | Exact |
| Glycogen storage disease due to liver glycogen phosphorylase deficiency | Prevalence at birth | 1-9 / 100 000 | Specific population | Not stated | Exact |
| Glycogen storage disease due to liver glycogen phosphorylase deficiency | Prevalence at birth | 1-9 / 100 000 | Specific population | Not stated | Unspecified |
| Glycogen storage disease due to liver glycogen phosphorylase deficiency | Prevalence at birth | 1-9 / 100 000 | Israel | Not stated | Exact |
| Glycogen storage disease due to liver glycogen phosphorylase deficiency | Point prevalence | Unknown | Worldwide | Not stated | Unspecified |
Showing 5 of 9 prevalence observations.
Rare-disease identity (2)
Shown in this order: exact, broader, narrower, other.
| Orphanet disease | ORPHA code | Relation | Source |
|---|---|---|---|
| Glycogen storage disease due to liver glycogen phosphorylase deficiency | 369 | Exact | Orphanet Rare Disease Ontology (ORDO) |
| Glycogen storage disease due to liver glycogen phosphorylase deficiency | 369 | Exact | Orphadata Science knowledge files, Product 1 |
Not on this page
Not measured: delivery record.
Checked, with nothing recorded for this condition: serious adverse events in this condition's trials, publications, and sub-conditions in mesh.
Not computed for conditions with fewer than 10 trials: drugs tested.