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A Study to Evaluate the Effect of Venglustat Tablets on Neuropathic and Abdominal Pain in Male and Female Participants ≥16 Years of Age With Fabry Disease

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NCT05206773

Sponsored by Sanofi (industry) · SNY — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
122actual
Sites
58
Countries
Argentina, Australia, Austria +18

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
DateFiledBasisWhat it is
Start2022-03-11actualWhen the study began enrolling
Primary completion2025-12-17actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-01-04estimatedThe whole study's end, after follow-up
First posted2022-01-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-04actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Fabry Disease

Interventions

  • Drug: Venglustat (GZ402671)
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Percent change from baseline at 6 months in the most bothersome symptom of 3 Fabry Disease Patient-Reported Outcome (FD-PRO) items (neuropathic pain in upper extremities, neuropathic pain in lower extremities, or abdominal pain)
measured From baseline to 6 months
Percent change from baseline at 12 months in the most bothersome symptom of 3 Fabry Disease Patient-Reported Outcome (FD-PRO) items (neuropathic pain in upper extremities, neuropathic pain in lower extremities, or abdominal pain)
measured From baseline to 12 months

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