Evolus Broadens Its International Presence with Nuceiva® Launch in Great Britain
Evolus, Inc. (NASDAQ: EOLS) has initiated its commercial operations in Great Britain, marking a significant milestone in its global expansion strategy. The company has shipped its first orders for Nuceiva® (botulinum toxin type A), targeting the UK's largest aesthetic neurotoxins market. Evolus will also launch in Germany and Austria later in 2023 and aims for further European expansion. The company’s commitment to education for healthcare professionals is evident through its Innovator and Early Adopter programs, designed to enhance product understanding and application.
- Launched commercial operations in Great Britain, the largest market for aesthetic neurotoxins in Europe.
- First customer orders for Nuceiva® shipped, indicating strong market entry.
- Plans for expansion into Germany and Austria within 2023, supporting growth objectives.
- Challenges related to regulatory approvals and market competition in Europe.
- Risks associated with COVID-19 impacting business operations and market dynamics.
Geographic expansion represents a significant step toward becoming a leading, global, multi-product performance beauty company
“Worldwide, the aesthetics market sector continues to rapidly evolve. We are excited to introduce Nuceiva® to
In the
“It’s refreshing to have a new type of aesthetics company to engage with,” said Dr.
“Starting commercialization in one of Europe’s biggest aesthetics markets gives practitioners another choice in the neuromodulator they offer to their patients,” said
Nuceiva® (botulinum toxin type A) is approved for the temporary improvement in the appearance of moderate to severe vertical lines between the eyebrows seen at maximum frown (glabellar lines), when the severity of the facial lines has an important psychological impact in adults below 65 years of age. The safety and efficacy of Nuceiva® was evaluated through the company’s TRANSPARENCY program, the largest head-to-head pivotal study versus BOTOX® to date.
About
Forward-Looking Statements
This press release contains forward-looking statements as defined under the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, are statements that could be deemed forward-looking statements, including statements that relate to the status of regulatory processes, future plans, events, prospects or performance and statements containing the words “plans,” “expects,” “believes,” “strategy,” “opportunity,” “anticipates,” “outlook,” “designed,” or other forms of these words or similar expressions, although not all forward-looking statements contain these identifying words. The company’s forward-looking statements include, but are not limited to, statements related to the company’s prospects, customer and consumer acceptance of Nuceiva®, regulatory approvals and commercial launch timing.
The forward-looking statements included herein involve risks and uncertainties that could cause actual results or experiences to differ materially from those expressed or implied by the forward-looking statements. Factors that could cause actual results or experience to differ materially from that expressed or implied by the forward-looking statements include uncertainties associated with our ability to address all of our losses, costs, expenses, liabilities and damages resulting from the settlement agreement with Daewoong and our ability to comply with the terms and conditions in the Allergan/Medytox Settlement Agreements, the continued impact of COVID-19 on our business and the economy generally, uncertainties related to customer and consumer adoption of Nuceiva® / Jeuveau®, the efficiency and operability of our digital platform or commercialization strategies, competition and market dynamics, and our ability to maintain regulatory approval of Nuceiva® / Jeuveau® and other risks described in Evolus’ filings with the
Jeuveau® and Nuceiva® are registered trademarks of
Hi-Pure™ is a trademark of Daewoong Pharmaceutical Co, Ltd.
BOTOX® (Botulinum toxin type A) is a registered trademark of
* PAS (Post Approval Safety Study)
▼ This medicine is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse events. Reporting forms and information can be found at mhra.gov.uk/yellowcard.
View source version on businesswire.com: https://www.businesswire.com/news/home/20221004005189/en/
Investor Contact:
Vice President, Investor Relations
Tel: +1-949-966-1798
Email: david.erickson@evolus.com
Media Contact:
President/CEO,
Tel: +1-562-304-0301
Email: asampson@sampsonprgroup.com
Communications Consultant,
Tel: +447738506476
Email: janet.kettels@evolus.com
Source:
FAQ
What recent expansion plans has Evolus announced for 2023?
What product is Evolus introducing in Great Britain?
What is Nuceiva® approved for?
How is Evolus supporting healthcare professionals with its new product?