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An multicenter open-label long-term continuous administration study to investigate the safety and tolerability of lucerastat in Japanese Fabry disease patients

Phase 3
Conditions
Fabry disease
Registration Number
JPRN-jRCT2080224890
Lead Sponsor
Idorsia Pharmaceuticals Japan Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
other
Sex
All
Target Recruitment
20
Inclusion Criteria

Patients who complete the preceding study and continue its eligibility

Exclusion Criteria

Patients with a risk of worsening of clinical symptoms due to an organ lesion during the study period at the discretion of the investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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