• The results of two phase III clinical trials evaluating new-generation double-blind enzyme therapies in late-onset Pompe disease against Myozyme were published in December 2021.
• Both treatments were well tolerated and they preserved or even improved patients’ walking and breathing capacity after one year of treatment.
- Avalglucosidase alfa (Nexviadyme), evaluated in the COMET trial in 100 enzyme-naïve participants, showed non-inferiority to Myozyme over one year. The authors point out that several clinical parameters support avalglucosidase alfa. The extension of the trial will allow the evolution of the therapeutic response to be followed over time. In France, avalglucosidase alfa is available under temporary authorization for use.
- Cipaglucosidase alfa, combined with miglustat (AT-GAA) was evaluated in the PROPEL trial, both in people already treated with Myozyme and in people naïve to any enzyme therapy. As with avalglucosidase alfa, it is not possible to conclude on the superiority of the treatment compared to Myozyme, except for patients previously treated with Myozyme.
Voir aussi « Maladie de Pompe : l’arsenal thérapeutique s’agrandit »