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Revance to Present Clinical Da - GuruFocus com

Revance to Present Clinical Da - GuruFocus com
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Revance to Present Data on DaxibotulinumtoxinA for Injection and Hyaluronic Acid Fillers at American Academy of Dermatology VMX Meeting 2021

Revance to Present Data on DaxibotulinumtoxinA for Injection and Hyaluronic Acid Fillers at American Academy of Dermatology VMX Meeting 2021
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United statesUnited kingdomBeverly hillsBritish columbiaSan diegoManhattan beachSan franciscoLaurence wattsShannon humphreyAva shambanConorj gallagherRichard glogauJessica brownTheda kontisSusan weinkleDerek jones

Revance to Present Data on DaxibotulinumtoxinA for Injection and Hyaluronic Acid Fillers at American Academy of Dermatology VMX Meeting 2021

Revance to Present Data on DaxibotulinumtoxinA for Injection and Hyaluronic Acid Fillers at American Academy of Dermatology VMX Meeting 2021
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Revance to Showcase Phase 3 Results Evaluating DaxibotulinumtoxinA for Injection for the Treatment of Cervical Dystonia at the American Academy of Neurology Annual 2021 Virtual Meeting

Revance to Showcase Phase 3 Results Evaluating DaxibotulinumtoxinA for Injection for the Treatment of Cervical Dystonia at the American Academy of Neurology Annual 2021 Virtual Meeting
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United statesRush university medical centerBaylor college of medicineDomenico vitarellaLaurence wattsToddm grossRomang rubioJessica serraRoman rubioRoberta hauserSara fahyCynthia comellaJoseph jankovicAllergan incDepartment of neurologyMovement disorders center

Revance Reports Positive Efficacy and Duration Results from Phase 2 Upper Facial Lines Study

Revance Reports Positive Efficacy and Duration Results from Phase 2 Upper Facial Lines Study Revance Reports Positive Efficacy and Duration Results from Phase 2 Upper Facial Lines Study Revance Therapeutics, Inc. (Nasdaq: RVNC), a biotechnology company focused on innovative aesthetic and therapeutic offerings, today announced positive topline efficacy and safety results from its Phase 2 multicenter, open-label study of investigational drug candidate DaxibotulinumtoxinA for Injection for the combined treatment of upper facial lines, which are comprised of glabellar (frown) lines (GL), dynamic forehead lines (FHL) and lateral canthal lines (LCL), commonly known as crows feet lines. In the Phase 2 study, 48 subjects were enrolled to receive a single treatment of DaxibotulinumtoxinA for Injection with a total study duration of 36 weeks. Subjects received 40, 32, and 48 units of DaxibotulinumtoxinA for Injection respectively in the glabellar complex, forehead and lateral canthal are

United statesJeffreys doverJessica serraLaurence wattsRoman rubioSara fahyNadine toskJeanie herbertAllergan incClinical program in upper facial linesDrug administrationClinical development at revanceExchange commissionGilmartin groupRevance therapeutics incSecurities exchange