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Η Φαρμακευτική Εταιρεία NS Pharma ανακοίνωσε χθες την έγκριση του VILTEPSO™ (viltolarsen) από τον FDA των ΗΠΑ για τα άτομα με Μυϊκή Δυστροφία Duchenne, που η μετάλλαξή τους επιδέχεται αγωγή για exon skipping 53. 

Διαβάστε το Δελτίο Τύπου της Εταιρείας:

 https://nspharma.com/pdfs/Viltepso_Approval_Press_Release.pdf

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