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Nexviazyme®
(avalglucosidase alfa)
Forced Vital Capacity (FVC)

Nexviazyme has shown improved respiratory function in patients with LOPD vs Myozyme (P=0.06, not significant)1

Nexviazyme vs Myozyme: a 2.43% difference* in FVC (% predicted) (P=0.06, not significant).1

CI, confidence interval; FVC, forced vital capacity; LOPD, late-onset Pompe disease; LS, least square; SD, standard deviation; SE, standard error.

  1. Nexviazyme Australian Approved Product Information.

Please review full Nexviazyme Product Information before prescribing. Full Product Information is available from sanofi-aventis australia pty ltd here or by contacting 1800 818 806.

â–¼ This medicinal product is subject to additional monitoring in Australia. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse events at www.tga.gov.au/reporting-problems.

 

 

Please review full Myozyme Product Information before prescribing. Full Product Information is available from sanofi-aventis australia pty ltd here or by contacting 1800 818 806.

Life Saving Drugs Program - Pompe disease - Guidelines are available at www.health.gov.au/resources/publications/lsdp-pompe-guidelines.

Nexviazyme® and Myozyme​​​​​​​® are registered trademarks of Sanofi.

MAT-AU-2201155 - 2.0 - 05/2024