All primary and secondary endpoints were met for second Phase 3 study (M21-310) and results were consistent with findings from first Phase 3 study (M21-309).
–Results support onabotulinumtoxinA as a potential treatment option for moderate to severe platysma prominence.–Data will be included as part of an upcoming U.S. Food and Drug Administration regulatory submission expected near the end of the year. If approved, onabotulinumtoxinA will be the first and only neurotoxin for this indication.
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.