Nexviazyme has been applied for domestic permission
By Lee, Tak-Sun | translator Choi HeeYoung
21.10.02 06:00:40
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The effectiveness has been significantly improved compared to the existing treatment Myozyme
FDA approved for late-onset patients in August
According to the MFDS on the 1st, Sanofi Aventis Korea submitted a report on the results of clinical trials by Nexviazyme (Avalglucosidase alfa-ngpt) and applied for permission.
This drug is a Pompe's disase treatment. Pompe's disease is a genetic disorder in which respiratory failure and myocardial disease appear due to muscle strength loss and muscle atrophy. It is a rare disease that is reported to be about one person per 40,000 people worldwide, and it is known that there are about 1,300 patients in
Lee, Tak-Sun(hooggasi2@dailypharm.com)
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