AbbVie IncEU approval of Boey, a novel rapid-onset short-duration neurotoxin, expands AbbVie's product portfolio and competitive edge in aesthetics.

Allergan Aesthetics, an AbbVie company, announced that the European Commission has approved Boey (trenibotulinumtoxinE) for the temporary improvement of moderate to severe glabellar lines in adults when these have an important psychological impact. The centralized procedure decision applies across all 30 European Economic Area countries, following a prior approval in Canada in June of this year. Boey is the first and only rapid-onset and short-duration botulinum neurotoxin serotype E approved in Europe, with onset of effect observed as early as eight hours after treatment and effects lasting approximately two to three weeks. The approval is supported by two Phase 3 clinical trials enrolling 725 patients, where the co-primary efficacy measure was a two-grade or greater improvement in glabellar line severity at maximum frown at Day 7. Allergan Aesthetics is preparing to launch Boey across Europe and will support healthcare professionals through education and training.
AbbVie IncEU approval of Boey, a novel rapid-onset short-duration neurotoxin, expands AbbVie's product portfolio and competitive edge in aesthetics.