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RecruitingNCT07187440

A Study of Agalsidase Alfa Enyzme Replacement Therapy in Chinese Children and Adults With Fabry Disease

A Prospective, Multi-center, Observational Study to Evaluate the Clinical Outcomes of Agalsidase Alfa Enzyme Replacement Therapy Among Chinese Patients With Fabry Disease in Real-world Clinical Practice

Status
Recruiting
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
Takeda · Industry
Sex
All
Age
7 Years
Healthy volunteers
Not accepted

Summary

Fabry Disease is a rare blood disorder that some people are born with. People with Fabry disease have low levels of an enzyme called alpha-galactosidase A. This enzyme helps to cut down fat-like substances. Without alpha-galactosidase A, large forms of these substances build up and clot in blood vessels. Over time, this can affect vital organs (especially the heart, kidneys, and brain) causing serious health problems with advancing age. Agalsidase alfa (Replagal®) is a human enzyme made in the laboratory and may provide higher levels of alpha-galactosidase A. Replagal® works the same way as natural alpha-galactosidase A does. The main aim of this study is to learn more about the treatment with Replagal® in Chinese children and adults with Fabry disease. The study aims to assess the heart and kidney function in people with Fabry disease who are routinely treated with Replagal®. Other aims are to learn about the change in heart and kidney function, impact on quality of life, how the treatment with Replagal® works for people with Fabry Disease, and how safe the treatment with Replagal® is in routine real-world settings. Participants will receive with Replagal® per the routine treatment settings in China. No study-specific visits to the clinical are scheduled.

Conditions

Interventions

TypeNameDescription
OTHERNo interventionThis is a non-interventional study

Timeline

Start date
2025-11-01
Primary completion
2028-11-30
Completion
2028-11-30
First posted
2025-09-23
Last updated
2026-01-02

Locations

18 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07187440. Inclusion in this directory is not an endorsement.

A Study of Agalsidase Alfa Enyzme Replacement Therapy in Chinese Children and Adults With Fabry Disease (NCT07187440) · Clinical Trials Directory