Evolus, Inc. ((EOLS)) announced an update on their ongoing clinical study.
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Evolus, Inc. is conducting a non-interventional post-authorization safety study (PASS) titled ‘Non-Interventional Post-Authorisation Safety Study of NUCEIVA for the Treatment of Moderate-to-Severe Glabellar Lines.’ The study aims to further characterize the long-term safety of NUCEIVA, a treatment for glabellar lines, in real-world clinical settings. This research is significant as it provides insights into the safety profile of NUCEIVA, which is crucial for its continued use and acceptance in the market.
The intervention being tested is prabotulinumtoxinA, a botulinum toxin type A, used for injection to treat moderate-to-severe glabellar lines. This treatment is intended to reduce the appearance of these lines, offering a cosmetic solution for patients seeking such outcomes.
This study is observational and prospective, involving approximately 750 patients across 20 sites in the UK and EU over 18 months. It does not involve allocation or masking, as it is designed to observe the safety of NUCEIVA in a real-world setting without intervention from the researchers.
The study began on March 15, 2023, with a primary completion date not specified, and the last update was submitted on August 4, 2025. These dates are crucial as they guide investors on the timeline for potential results and subsequent market actions.
The update on this study could positively impact Evolus, Inc.’s stock performance by reinforcing investor confidence in NUCEIVA’s safety profile. As the cosmetic treatment market is competitive, demonstrating long-term safety can provide Evolus with a competitive edge, potentially influencing market dynamics and investor sentiment.
The study is ongoing, and further details are available on the ClinicalTrials portal.