Welcome to our dedicated page for Revance Therapeu news (Ticker: RVNC), a resource for investors and traders seeking the latest updates and insights on Revance Therapeu stock.
The RVNC news page on Stock Titan provides an archive of announcements and transaction-related communications concerning Revance Therapeutics, Inc., a biotechnology company focused on aesthetic and therapeutic offerings. These news items document Revance’s role in the aesthetic injectables market, its product portfolio, and the corporate events that led to its acquisition by Crown Laboratories, Inc.
Readers can review press releases describing Crown’s commencement of a cash tender offer to acquire all outstanding shares of Revance, subsequent extensions of the tender offer, and an increase in the offer price that was unanimously approved by the Revance Board of Directors. Additional news items cover competing interest from Teoxane SA, reminders to Revance stockholders about tendering their shares, and joint announcements by Crown and Revance regarding the expiration of the tender offer and satisfaction of its conditions.
The archive also includes Crown’s announcements of the successful closing of the acquisition and completion of the second-step merger, in which Crown stated that Revance’s common stock will be delisted from the NASDAQ Global Select Market and deregistered. These releases provide context on how Revance, as the issuer of RVNC, transitioned from an independent publicly traded biotechnology company to a Crown-owned business within a larger skincare and aesthetics platform.
For investors and researchers, the RVNC news feed serves as a historical record of key milestones, including strategic reviews by the Revance Board, tender offer mechanics, and the ultimate outcome of the Crown transaction. Users interested in the evolution of Revance’s aesthetic and therapeutic portfolio, its partnerships with Teoxane SA, Viatris Inc., and Shanghai Fosun Pharmaceutical, and the terms of the acquisition can use this page to trace the sequence of public communications around the deal.
Revance Therapeutics has submitted a supplemental Biologics License Application (sBLA) to the FDA for DAXXIFY™ to treat cervical dystonia, a painful condition affecting neck muscles. The application is based on the ASPEN Phase 3 clinical program, showcasing DAXXIFY’s median response duration of 24 weeks. The company anticipates a PDUFA target action date in 2023. Successful approval could position Revance in the nearly $1 billion U.S. muscle movement disorder market, significantly reducing treatment frequency for patients.
Revance Therapeutics (RVNC) appointed Dr. David A. Hollander as Chief Medical Officer to enhance clinical development and regulatory strategies. This leadership change comes as the company prepares for the commercial launch of Daxxify™, recently approved by the FDA for glabellar lines, and the advancement of its biosimilar to Botox®. Dr. Hollander brings over 20 years of experience, having previously held prominent roles in R&D and regulatory affairs at Aerie Pharmaceuticals and Allergan. His extensive background is expected to bolster Revance's growth in aesthetics and therapeutics.
Revance Therapeutics (RVNC) presented two video abstracts on DAXXIFY™ at the ASDS Annual Meeting, showcasing its efficacy and safety across diverse patient subgroups. Highlights of the presentations include strong patient satisfaction and successful elimination of glabellar lines in black patients, reaffirming DAXXIFY™ as a pioneering treatment in aesthetic medicine. DAXXIFY™ is a FDA-approved long-lasting neuromodulator, promising year-long results with limited treatments. Revance continues to emphasize their commitment to innovation in facial aesthetics.
Revance Therapeutics, Inc. (NASDAQ: RVNC) will participate in the Guggenheim Nantucket Therapeutics Conference from September 27 to 29 in Nantucket, MA. CEO Mark Foley is scheduled to present on September 28 at 9:00 A.M. EST. A live audio webcast will be accessible from the Investor Relations section of the company's website and a replay will be available for 30 days post-event. Revance focuses on innovative aesthetic and therapeutic solutions, including products like DAXXIFY™ and a biosimilar to BOTOX®.
Revance Therapeutics (NASDAQ: RVNC) announced the publication of two peer-reviewed articles in Aesthetic Surgery Journal regarding the effects of DAXXIFY™ on glabellar lines. The studies showed DAXXIFY™ significantly improved eyebrow position with a response duration of over 24 weeks across various age and race subgroups. In a post-hoc analysis, patients experienced a positive reduction in frontalis muscle activity. The safety profile was consistent across demographics, with common adverse events including headache and injection site reactions.
Revance Therapeutics presented positive results from its Phase 2 JUNIPER clinical trial for DAXXIFY™, targeting upper limb spasticity in adults post-stroke or brain injury. The 500U dose showed a median response duration of 24 weeks and was well tolerated. The drug's effectiveness may potentially reduce treatment frequency by 50% annually. Results will be shared at the MDS Congress on September 16, enhancing the company's prospects in a market valued at $756 million, projected to exceed $1 billion by 2025.
Revance Therapeutics announced the closing of its public offering of 9.2 million shares at $25.00 per share, raising gross proceeds of $230 million. The offering saw the complete exercise of the underwriters' option for 1.2 million additional shares. The shares were offered under an automatic shelf registration statement previously filed with the SEC on November 27, 2020. Goldman Sachs, Cowen, Guggenheim, and Barclays acted as joint book-running managers for this offering, with full details available on the SEC's website.
Revance Therapeutics has priced an upsized public offering of 8,000,000 shares of common stock at $25.00 per share, aiming to raise approximately $200 million in gross proceeds. The offering is expected to close around September 15, 2022, subject to customary conditions. Proceeds will fund the commercialization of DAXXIFY™, the RHA® Collection of dermal fillers, and OPUL®, alongside general business operations, research, and development. The underwriters have a 30-day option to purchase an additional 1,200,000 shares at the same price.
Revance Therapeutics (RVNC) announced a proposed underwritten public offering of $150 million of its common stock, with a potential for an additional 15% from underwriters. The proceeds will fund commercialization of DAXXIFY™, the RHA® Collection, and OPUL®, alongside general corporate purposes. The offering is subject to market conditions and completion is not guaranteed. Goldman Sachs, Cowen, Guggenheim Securities, and Barclays are managing the offering. The offering is being made under an automatic shelf registration statement.
Revance Therapeutics, Inc. (RVNC) has received FDA approval for DAXXIFY™ (daxibotulinumtoxinA-lanm), the first long-acting neuromodulator for treating moderate to severe frown lines in adults. This product showcases a median efficacy duration of six months, with some patients experiencing results lasting up to nine months. DAXXIFY™ is formulated with Peptide Exchange Technology™ and does not contain animal-derived components. The approval strengthens Revance's position in the $3.2 billion U.S. facial injectables market and indicates potential for future therapeutic applications.