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GaldermaAnnouncesU.S.FDAAcceptanceofRelabotulinumtoxinABiologicsLicenseApplicationResubmission
===2026/2/3 10:03:21===
xpertise and heritage in the neuromodulator space to develop next-generation aesthetic solutions that address evolving needs.







“We pioneered the development of RelabotulinumtoxinA to address the growing demand for faster-acting and longer-lasting anti-wrinkle solutions. We’re excited about the potential to bring this innovative neuromodulator to the U.S., offering advanced performance and ease of use and building on our portfolio of neuromodulators that meets the full spectrum of injector and patient needs.”



BALDO SCASSELLATI SFORZOLINI, M.D., PH.D.

GLOBAL HEAD OF R&D

GALDERMA







The filing is based on data from the robust, large-scale READY (REelabotulinumtoxin Aesthetic Development StudY) clinical trial program, which is composed of four phase III trials, enrolling more than 1,900 participants.1-4Results demonstrated that RelabotulinumtoxinA deliver
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