An Extension Study of S-606001 in Participants With Late-onset Pompe Disease (LOPD)
← catalyst calendarNCT07750990 · readout in 743 d
Sponsored by Shionogi (industry) · 4507.T — their whole pipeline →.
Phase
Phase 2
Status
Not yet recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
60estimated
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-08-31 | estimated | When the study began enrolling |
| Primary completion | 2028-08-31 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-08-31 | estimated | The whole study's end, after follow-up |
| First posted | 2026-08-06 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-06 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Pompe Disease
Interventions
- Drug: S-606001
- Drug: ERT
Primary outcome
what the primary-completion date above is the date OFNumber of Participants With Treatment-emergent Adverse Events
measured Baseline through Week 96
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