ZORYVE, the first FDA-approved medication for eczema, psoriasis, and dermatitis, wins Allure's 2025 Best of Beauty Breakthrough Award.
Quiver AI Summary
Arcutis Biotherapeutics, Inc. announced that ZORYVE, the first FDA-approved medication for atopic dermatitis, plaque psoriasis, and seborrheic dermatitis, has received the 2025 Best of Beauty Breakthrough Award from Allure magazine. This award recognizes ZORYVE as a groundbreaking innovation in skincare and highlights its effectiveness as the top prescribed branded topical therapy for these inflammatory skin conditions. ZORYVE is a once-daily, steroid-free topical treatment available in both cream and leave-in foam forms, suitable for all skin and hair types. It offers rapid symptom relief while maintaining a unique safety profile. The award highlights the product's transformative impact on patient care and the ongoing commitment of Arcutis to develop advanced therapeutics in dermatology.
Potential Positives
- ZORYVE has received the prestigious Allure Best of Beauty Breakthrough Award, recognizing it as a significant innovation in the skincare industry.
- It is the first FDA-approved medication to win this award for treating eczema, plaque psoriasis, and seborrheic dermatitis, highlighting its unique positioning in the market.
- ZORYVE is the number one prescribed branded topical therapy for three major inflammatory dermatoses, demonstrating strong market acceptance and physician endorsement.
- The product offers a safe, effective, and easy-to-use alternative to traditional treatments, addressing critical unmet patient needs in dermatology.
Potential Negatives
- Despite the accolade, ZORYVE's recognition may create high customer expectations, which could lead to disappointment if the product does not meet these expectations during real-world use.
- The press release highlights common adverse reactions, which may raise concerns among potential patients about the safety and tolerability of ZORYVE.
- Forward-looking statements imply uncertainty regarding the future market performance and acceptance of ZORYVE, pointing to potential risks that could affect the company's growth and reputation.
FAQ
What is ZORYVE approved for?
ZORYVE is FDA-approved for treating eczema, plaque psoriasis, and seborrheic dermatitis in patients aged 6 and older.
Why did ZORYVE win the Best of Beauty Breakthrough Award?
ZORYVE won the award for its innovative formulation and versatility in treating multiple inflammatory skin diseases effectively.
How is ZORYVE applied on the body?
ZORYVE can be applied once daily anywhere on the body, making it convenient for diverse skin and hair types.
What sets ZORYVE apart from other therapies?
ZORYVE is a steroid-free, highly selective topical therapy designed for safety and rapid symptom relief in inflammatory skin conditions.
Who manufactures ZORYVE?
ZORYVE is developed and manufactured by Arcutis Biotherapeutics, Inc., a company specializing in dermatological treatments.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$ARQT Insider Trading Activity
$ARQT insiders have traded $ARQT stock on the open market 34 times in the past 6 months. Of those trades, 6 have been purchases and 28 have been sales.
Here’s a breakdown of recent trading of $ARQT stock by insiders over the last 6 months:
- HOWARD G. WELGUS has made 0 purchases and 7 sales selling 59,347 shares for an estimated $859,962.
- MASARU MATSUDA (See Remarks) has made 0 purchases and 4 sales selling 49,290 shares for an estimated $775,663.
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- PATRICK J HERON has made 6 purchases buying 19,888 shares for an estimated $269,900 and 0 sales.
- DAVID JOSEPH TOPPER (Chief Financial Officer) sold 9,600 shares for an estimated $151,698
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- LATHA VAIRAVAN (SVP Chief Financial Officer) sold 89 shares for an estimated $1,275
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$ARQT Hedge Fund Activity
We have seen 122 institutional investors add shares of $ARQT stock to their portfolio, and 134 decrease their positions in their most recent quarter.
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$ARQT Analyst Ratings
Wall Street analysts have issued reports on $ARQT in the last several months. We have seen 3 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- Needham issued a "Buy" rating on 08/07/2025
- Guggenheim issued a "Buy" rating on 04/03/2025
- HC Wainwright & Co. issued a "Buy" rating on 04/03/2025
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$ARQT Price Targets
Multiple analysts have issued price targets for $ARQT recently. We have seen 3 analysts offer price targets for $ARQT in the last 6 months, with a median target of $19.0.
Here are some recent targets:
- Serge Belanger from Needham set a target price of $22.0 on 08/07/2025
- Richard Law from Goldman Sachs set a target price of $18.0 on 07/25/2025
- Douglas Tsao from HC Wainwright & Co. set a target price of $19.0 on 04/03/2025
Full Release
- First FDA-approved medication for atopic dermatitis (eczema), plaque psoriasis, and seborrheic dermatitis to win prominent “Breakthrough Award”
- ZORYVE is the number one prescribed branded topical therapy across three major inflammatory dermatoses combined—eczema, plaque psoriasis, and seborrheic dermatitis
- Cream and leave-in foam options are uniquely formulated to be used anywhere on the body once per day and on diverse skin and hair types
- ZORYVE was shown to be safe and well-tolerated and to provide rapid and reliable symptom relief and has been chosen by healthcare providers over 1 million times
WESTLAKE VILLAGE, Calif., Sept. 16, 2025 (GLOBE NEWSWIRE) -- Arcutis Biotherapeutics, Inc. (Nasdaq: ARQT), a commercial-stage biopharmaceutical company dedicated to developing meaningful innovations in immuno-dermatology, today announced that ZORYVE was presented with a 2025 Best of Beauty Breakthrough Award by Allure magazine , which is globally recognized as the most distinguished beauty award by industry professionals and consumers. ZORYVE is the first prescription topical medication for eczema, plaque psoriasis, and seborrheic dermatitis to win the prestigious Allure Best of Beauty Breakthrough Award, which highlights groundbreaking innovations transforming the skincare category.
“ZORYVE earning the Allure Best of Beauty Breakthrough Award is a powerful acknowledgment of its truly unique profile in dermatology. ZORYVE stands apart in its versatility and safety profile, providing patients with a single, effective, and well-tolerated option that can be used across multiple inflammatory skin diseases and applied anywhere on the body. This recognition underscores not only innovation in topical drug delivery but also meaningful progress in addressing unmet patient care needs,” said Adam Friedman, MD, FAAD, professor and chair of dermatology at The George Washington University School of Medicine & Health Sciences .
ZORYVE is the number one prescribed branded topical therapy across three major inflammatory dermatoses combined—eczema, plaque psoriasis, and seborrheic dermatitis.
"We are thrilled that ZORYVE has been recognized with Allure’s prestigious Best of Beauty Breakthrough Award, which celebrates truly first-of-its-kind innovation," said Frank Watanabe, president and chief executive officer of Arcutis. "ZORYVE is a highly selective and potent phosphodiesterase-4 (PDE4) inhibitor with a unique, moisturizing formulation—specifically designed without ingredients that could further compromise the fragile skin barrier in conditions like atopic dermatitis, psoriasis, and seborrheic dermatitis. By offering a safe, effective, and easy-to-use alternative to steroids and medicated shampoos, ZORYVE is redefining how inflammatory skin diseases are treated. This award is a powerful testament to the ingenuity of our team at Arcutis and our unwavering commitment to delivering advanced targeted topicals that raise the bar in dermatology."
ZORYVE is a once-daily, steroid-free topical foam or cream that can be used anywhere on the body, for any duration, and is suitable for all skin and hair types. ZORYVE’s novel, water-based, non-greasy formulation has moisturizing properties and contains no penetration enhancers, ceramide-stripping properties, fragrances, ethanol, or propylene glycol.
For more information including prescribing information, visit www.zoryve.com .
About the Allure Best of Beauty Awards
For 29 years, the Allure Best of Beauty Awards have sought to highlight the best beauty products between skin, body, hair, makeup, nails, tools, and scent. The products are rigorously tested, and the editors consult a panel of professional judges—including top dermatologists, makeup artists, hairstylists, and cosmetic chemists—to determine which products are the best. The Best of Beauty Breakthrough is a distinct category of the awards that seeks the most revolutionary beauty products over the same categories. Fewer than 10 products typically win the Breakthrough category, making it one of the most selective and prestigious honors in beauty, reserved for game-changing innovations that have real impact on the lives of consumers.
About ZORYVE
®
(roflumilast)
ZORYVE is the number one prescribed branded topical therapy across three major inflammatory dermatoses combined—eczema, seborrheic dermatitis, and plaque psoriasis. ZORYVE is a next-generation, highly potent, and selective topical PDE4 inhibitor. PDE4, an established target in dermatology, is an intracellular enzyme that increases the production of pro-inflammatory mediators and decreases the production of anti-inflammatory mediators.
ZORYVE cream 0.3% is approved by the U.S. Food and Drug Administration (FDA) for the topical treatment of plaque psoriasis, including intertriginous areas, in patients 6 years of age and older. ZORYVE cream 0.15% is approved by the FDA for the topical treatment of mild to moderate atopic dermatitis in patients 6 years of age and older. In 2024, ZORYVE cream 0.15% was awarded Glamour’s Beauty and Wellness Award for “Eczema Product.” ZORYVE topical foam 0.3% is uniquely formulated for use anywhere on the body, including hair-bearing areas, and is indicated for the treatment of plaque psoriasis of the scalp and body in patients 12 years of age and older, as well as seborrheic dermatitis in patients 9 years of age and older. Recently, both ZORYVE cream 0.3% and ZORYVE foam 0.3% were awarded the National Psoriasis Foundation’s Seal of Recognition—the first FDA-approved product to receive the honor.
INDICATIONS
ZORYVE topical foam, 0.3%, is indicated for the treatment of plaque psoriasis of the scalp and body in adult and pediatric patients 12 years of age and older.
ZORYVE topical foam, 0.3%, is indicated for the treatment of seborrheic dermatitis in adult and pediatric patients 9 years of age and older.
ZORYVE cream, 0.3%, is indicated for topical treatment of plaque psoriasis, including intertriginous areas, in adult and pediatric patients 6 years of age and older.
ZORYVE cream, 0.15%, is indicated for topical treatment of mild to moderate atopic dermatitis in adult and pediatric patients 6 years of age and older.
IMPORTANT SAFETY INFORMATION
ZORYVE is contraindicated in patients with moderate to severe liver impairment (Child-Pugh B or C).
Flammability : The propellants in ZORYVE foam are flammable. Avoid fire, flame, and smoking during and immediately following application.
The most common adverse reactions (≥1%) for ZORYVE foam 0.3% for plaque psoriasis include headache (3.1%), diarrhea (2.5%), nausea (1.7%), and nasopharyngitis (1.3%).
The most common adverse reactions (≥1%) for ZORYVE foam 0.3% for seborrheic dermatitis include nasopharyngitis (1.5%), nausea (1.3%), and headache (1.1%).
The most common adverse reactions (≥1%) for ZORYVE cream 0.3% for plaque psoriasis include diarrhea (3.1%), headache (2.4%), insomnia (1.4%), nausea (1.2%), application site pain (1.0%), upper respiratory tract infection (1.0%), and urinary tract infection (1.0%).
The most common adverse reactions (≥1%) for ZORYVE cream 0.15% for atopic dermatitis include headache (2.9%), nausea (1.9%), application site pain (1.5%), diarrhea (1.5%), and vomiting (1.5%).
ZORYVE is for topical use only and not for ophthalmic, oral, or intravaginal use.
Please see full Prescribing Information for ZORYVE cream and full Prescribing Information for ZORYVE foam.
About Arcutis
Arcutis Biotherapeutics, Inc. (Nasdaq: ARQT) is a commercial-stage medical dermatology company that champions meaningful innovation to address the urgent needs of individuals living with immune-mediated dermatological diseases and conditions. With a commitment to solving the most persistent patient challenges in dermatology, Arcutis has a growing portfolio of advanced, targeted topicals approved to treat three major inflammatory skin diseases. Arcutis’ unique dermatology development platform coupled with our dermatology expertise allows us to invent differentiated therapies against biologically validated targets and has produced a robust pipeline with multiple follow-on clinical programs for a range of inflammatory dermatological conditions. For more information, visit
www.arcutis.com
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Forward-Looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. For example, statements contained in this press release regarding matters that are not historical facts are forward-looking statements. These statements are based on the Company’s current beliefs and expectations. Such forward-looking statements include, but are not limited to, statements regarding the potential real-world use of ZORYVE and the potential for ZORYVE cream or foam to advance the standard of care in eczema, plaque psoriasis, and seborrheic dermatitis. These statements are subject to substantial known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance, or achievements to be materially different from the information expressed or implied by these forward-looking statements. Risks and uncertainties that may cause our actual results to differ include risks inherent in our business, reimbursement and access to our products, the impact of competition and other important factors discussed in the “Risk Factors” section of our Form 10-K filed with the U.S. Securities and Exchange Commission (SEC) on February 25, 2025, as well as any subsequent filings with the SEC. Any forward-looking statements that the Company makes in this press release are made pursuant to the Private Securities Litigation Reform Act of 1995, as amended, and speak only as of the date of this press release. Except as required by law, we undertake no obligation to revise or update information herein to reflect events or circumstances in the future, even if new information becomes available.
Contacts
Media
Amanda Sheldon, Head of Corporate Communications
[email protected]
Investors
Brian Schoelkopf, Head of Investor Relations
[email protected]
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