Skip to content

avalglucosidase alfa Special Drug Use Investigation for patients with pompe disease

avalglucosidase alfa Special Drug Use Investigation for patients with pompe disease - avalglucosidase alfa Special Drug Use Investigation for patients with pompe disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000047301
Enrollment
50
Registered
2022-03-28
Start date
2022-02-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pompe disease

Interventions

None listed

Sponsors

Sanofi K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with Pompe disease who are newly treated with Nexviazyme

Exclusion criteria

Exclusion criteria: -Individuals participating in or enrolling in other clinical trials involving therapeutic interventions of Nexviazyme -Those with off-label use of Nexviazyme

Design outcomes

Primary

MeasureTime frame
Safety (Adverse Drug Reaction)

Secondary

MeasureTime frame
Efficacy

Countries

Japan

Contacts

Public ContactPublic contact for Drug use surveillance Public contact for Drug use surveillance

Medical Affairs Post-authorization regulatory studies

Sanofi_Medical@sanofi.com03-6301-3867

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026