Revance
États-Unis
Site web: http://www.revance.com
Catégorie
- Injectables: Toxines botuliniques
- Injectables: Produits de comblement
- Pratiques de gestion: Services commerciaux - Logiciels
Profil de l'entreprise
In the Phase 3 SAKURA clinical trials, DAXI achieved unrivalled efficacy, including a median 24-week duration of effect in treating glabellar lines. Revance’s open-label, long-term safety study, SAKURA 3, was the largest clinical program of an aesthetic neuromodulator, and included nearly 2,700 patients and more than 3,800 treatments.
Revance anticipates commercial launch in 2020 upon FDA approval.