Evolus Phase III European – Canadian Head-to-Head Trial of prabotulinumtoxinA Compared to Botox® Meets Primary Endpoint

Evolus (NASDAQ:EOLS) a medical aesthetics company focused on delivering advanced aesthetic procedures and treatments to physicians and consumers, today announced the presentation of data from the European and Canadian Phase III EVB-003 head-to-head comparative trial demonstrating that its investigational prabotulinumtoxinA 900 kilodalton (kDa) neuromodulator met its primary endpoint of non-inferiority at Day 30 in subjects with moderate to severe glabellar lines, also known as “frown lines,” compared to onabotulinumtoxinA (Botox®).

As quoted in the press release:

The results were presented today in a poster titled “A Multicenter Phase III Study Comparing prabotulinumtoxinA and onabotulinumtoxinA for the Treatment of Glabellar Lines” by Dr. Patricia Ogilvie, M.D., dermatologist and Principal Investigator of the study, at the 2018 Aesthetic & Anti-Aging Medicine World Congress (AMWC), being held April 4-7 in Monte-Carlo, Monaco. The results presented at AMWC expand upon the initial results presented at the American Academy of Dermatology (AAD) annual meeting in February 2018.

“Analysis of this study presented at AMWC shows that prabotulinumtoxinA met its primary endpoint in efficacy as well as its secondary endpoints. In particular, the secondary endpoint of subject satisfaction is important because it represents the opinions of consumers who underwent the treatment,” commented Patricia Ogilvie, M.D. “Based on these findings, we believe that prabotulinumtoxinA represents a compelling and innovative option for the aesthetic treatment of glabellar lines.”

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