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Arcutis Submits Supplemental New Drug Application for ZORYVE® (roflumilast) Cream 0.3% to Expand Indication for Treatment of Plaque Psoriasis in Children Ages 2 to 5

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Arcutis Biotherapeutics (NASDAQ:ARQT) has submitted a supplemental New Drug Application (sNDA) to the FDA to expand the indication of ZORYVE® (roflumilast) cream 0.3% for treating plaque psoriasis in children ages 2 to 5. Currently approved for adults and children aged 6 and above, if approved, ZORYVE would become the first topical PDE4 inhibitor indicated for plaque psoriasis in children as young as 2.

The sNDA submission is supported by data from a 4-week Maximal Usage Systemic Exposure (MUSE) study in children aged 2-5 years and a long-term open-label study. The once-daily, steroid-free cream has demonstrated consistent favorable long-term safety, tolerability, and efficacy across age ranges, particularly beneficial for sensitive areas like intertriginous skin where psoriasis commonly presents in children.

Arcutis Biotherapeutics (NASDAQ:ARQT) ha presentato alla FDA una domanda di nuova indicazione supplementare (sNDA) per estendere l'uso della ZORYVE® (crema di roflumilast 0,3%) al trattamento della psoriasi a placche nei bambini di età compresa tra 2 e 5 anni. Attualmente approvata per adulti e bambini dai 6 anni in su, se autorizzata ZORYVE diventerebbe il primo inibitore topico della PDE4 indicato per la psoriasi a placche nei bambini a partire dai 2 anni.

La sNDA si basa sui dati di uno studio di esposizione sistemica a uso massimo (MUSE) di 4 settimane condotto in bambini di 2-5 anni e su uno studio a lungo termine in aperto. La crema, applicata una volta al giorno e priva di steroidi, ha mostrato un profilo favorevole e coerente di sicurezza, tollerabilità ed efficacia a lungo termine nelle varie fasce d'età, risultando particolarmente utile nelle aree delicate come le regioni intertriginose dove la psoriasi si presenta spesso nei bambini.

Arcutis Biotherapeutics (NASDAQ:ARQT) ha presentado a la FDA una solicitud complementaria de nuevo fármaco (sNDA) para ampliar la indicación de ZORYVE® (crema de roflumilast 0,3%) para el tratamiento de la psoriasis en placas en niños de 2 a 5 años. Actualmente aprobada para adultos y niños de 6 años en adelante, si se autoriza, ZORYVE sería el primer inhibidor tópico de PDE4 indicado para la psoriasis en placas en niños a partir de los 2 años.

La sNDA está respaldada por datos de un estudio MUSE (exposición sistémica con uso máximo) de 4 semanas en niños de 2 a 5 años y por un estudio abierto a largo plazo. La crema, de uso diario y sin esteroides, ha demostrado una seguridad, tolerabilidad y eficacia a largo plazo consistentes y favorables en todos los grupos de edad, siendo especialmente beneficiosa en zonas sensibles como las áreas intertriginosas donde la psoriasis suele manifestarse en la infancia.

Arcutis Biotherapeutics (NASDAQ:ARQT)ZORYVE® (로플루미라스� 크림 0.3%)� 적응증을 2세부� 5세까지 소아� 판상 건선 치료� 확대하기 위해 FDA� 보완 신약신청�(sNDA)� 제출했습니다. 현재 성인 � 6� 이상 소아� 승인되어 있으�, 허가� 경우 ZORYVE� 2세부� 사용 가능한 최초� 국소 PDE4 억제제가 됩니�.

이번 sNDA 제출은 2~5� 소아� 대상으� � 4주간 최대 사용� 전신 노출(MUSE) 연구와 장기 개방� 연구� 데이터에 근거합니�. 하루 � � 바르� 무스테로이드 크림은 연령대 전반� 걸쳐 장기적으� 일관되게 우수� 안전�, 내약� � 유효성을 보였으며, 소아에서 건선� 자주 발생하 겨드랑이 접촉부 � 민감� 부위에 특히 유리합니�.

Arcutis Biotherapeutics (NASDAQ:ARQT) a soumis une demande d'autorisation complémentaire (sNDA) à la FDA afin d'étendre l'indication de ZORYVE® (crème de roflumilast 0,3%) au traitement du psoriasis en plaques chez les enfants de 2 à 5 ans. Actuellement approuvée pour les adultes et les enfants à partir de 6 ans, ZORYVE deviendrait, en cas d'approbation, le premier inhibiteur topique de la PDE4 indiqué pour le psoriasis en plaques dès l'âge de 2 ans.

La sNDA s'appuie sur les données d'une étude MUSE (exposition systémique en utilisation maximale) de 4 semaines chez des enfants de 2 à 5 ans et sur une étude ouverte à long terme. La crème sans stéroïdes, appliquée une fois par jour, a démontré une sécurité, une tolérance et une efficacité favorables et constantes à long terme dans toutes les tranches d'âge, et se révèle particulièrement bénéfique sur les zones sensibles comme les zones intertrigineuses où le psoriasis apparaît souvent chez l'enfant.

Arcutis Biotherapeutics (NASDAQ:ARQT) hat bei der FDA eine ergänzende Zulassungsanfrage (sNDA) eingereicht, um die Indikation von ZORYVE® (Roflumilast-Creme 0,3%) zur Behandlung von Plaque-Psoriasis bei Kindern im Alter von 2 bis 5 Jahren zu erweitern. Die Creme ist derzeit für Erwachsene und Kinder ab 6 Jahren zugelassen; bei Genehmigung wäre ZORYVE der erste topische PDE4-Inhibitor, der für Plaque-Psoriasis bei Kindern ab 2 Jahren angezeigt ist.

Die sNDA stützt sich auf Daten einer 4-wöchigen Maximalnutzungs-Studie zur systemischen Exposition (MUSE) bei 2�5 Jahre alten Kindern sowie auf eine langfristige offen durchgeführte Studie. Die einmal täglich angewendete, steroidfreie Creme zeigte über verschiedene Altersgruppen hinweg durchweg günstige Langzeitsicherheit, Verträglichkeit und Wirksamkeit und ist besonders vorteilhaft in sensiblen Bereichen wie intertriginösen Hautpartien, in denen Psoriasis bei Kindern häufig auftritt.

Positive
  • First potential topical PDE4 inhibitor for plaque psoriasis in children as young as 2
  • Demonstrated favorable long-term safety and efficacy in clinical trials
  • Addresses significant unmet need in pediatric psoriasis treatment
  • Unique steroid-free formulation suitable for sensitive skin areas
Negative
  • None.

Insights

Arcutis' sNDA for ZORYVE in children 2-5 years could capture an underserved pediatric psoriasis market with first PDE4 inhibitor option.

Arcutis' supplemental New Drug Application (sNDA) for ZORYVE cream 0.3% to treat plaque psoriasis in children ages 2-5 represents a strategic market expansion into an underserved demographic. Currently, limited FDA-approved options exist for children under 6 with plaque psoriasis, creating a significant opportunity if approved.

The significance lies in ZORYVE's potential to become the first and only topical PDE4 inhibitor approved for this age group. This positioning is particularly valuable given that children's psoriasis often presents in sensitive areas like the face and intertriginous regions, where long-term steroid use raises safety concerns. ZORYVE's steroid-free formulation addresses this clinical challenge while avoiding sensitizing excipients.

Supporting the application is data from a 4-week Maximal Usage Systemic Exposure study and a long-term open-label study, which demonstrated consistent safety, tolerability, and efficacy persistence - critical factors for pediatric dermatology treatments where safety profiles are heavily scrutinized.

This submission aligns with Arcutis' broader strategy to establish ZORYVE as a foundational therapy across multiple inflammatory skin conditions and age groups. The company is systematically addressing gaps in pediatric dermatology treatment, where many therapies historically weren't studied in children.

If approved, this would strengthen Arcutis' competitive position by expanding ZORYVE's addressable market and potentially increasing prescription volume through pediatric dermatologists and general practitioners treating younger patients.

  • If approved, ZORYVE cream would be the first and only topical PDE4 inhibitor indicated for plaque psoriasis in children as young as 2, offering patients and caregivers an important alternative to topical steroids and vitamin-D analogs
  • ZORYVE cream is uniquely formulated to be effective, safe, and well tolerated for all areas of the body, including sensitive areas such as intertriginous skin, where plaque psoriasis often presents in children

WESTLAKE VILLAGE, Calif., Sept. 03, 2025 (GLOBE NEWSWIRE) -- Arcutis Biotherapeutics, Inc. (Nasdaq: ARQT), a commercial-stage biopharmaceutical company focused on developing meaningful innovations in immuno-dermatology, today announced the submission of a supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) to expand the indication of ZORYVE® (roflumilast) cream 0.3% for the treatment of plaque psoriasis in children down to the age of 2. If approved, ZORYVE cream 0.3% would be the first and only topical PDE4 inhibitor treatment indicated for plaque psoriasis in children down to age 2.

“Today, there are very limited FDA-approved treatment options for plaque psoriasis for children under 6, who often present with disease on sensitive skin such as the face and intertriginous areas. There is a significant unmet need for non-steroidal options that can effectively treat plaque psoriasis over the long-term,� said Adelaide Hebert, MD, professor and chief of pediatric dermatology at UTHealth Houston. “If approved, investigational ZORYVE cream could be an important first-line treatment option for children as young as age 2.�

Plaque psoriasis is the most common form of psoriasis in young children and presents with similar clinical features to those seen in adults. However, in children � particularly those under 6 � psoriasis often appears in sensitive areas, such as the face or intertriginous areas, increasing the challenge of safe long-term management.

ZORYVE cream is a once-daily, steroid-free, non-greasy cream that does not include sensitizing excipients or irritants such as propylene glycol, polyethylene glycol, ethanol, or fragrances. It is the only topical treatment specifically indicated for intertriginous psoriasis and has demonstrated efficacy, safety, and tolerability across adults and children.

“This submission represents another important step forward in our goal to establish ZORYVE as foundational therapy for young children suffering with inflammatory skin diseases,� said Frank Watanabe, president and CEO at Arcutis. “Historically, many treatments for inflammatory skin diseases were not studied in children, creating challenges for the clinicians who treat these vulnerable patients. Arcutis is committed to helping to address this gap in treatment through conducting trials of ZORYVE in pediatric patients across a range of inflammatory skin diseases.�

ZORYVE cream 0.3% is currently approved for plaque psoriasis in adults and children down to age 6. The sNDA is supported by data from a 4-week Maximal Usage Systemic Exposure (MUSE) study in children aged 2 to 5 years with plaque psoriasis, as well as data from a long-term open-label study. Results from the long-term study demonstrate consistent favorable long-term safety and tolerability as well as persistence of efficacy across the age ranges studied.

About Plaque Psoriasis

Psoriasis is a common, chronic, inflammatory skin disease that affects nearly 9 million people in the United States. Symptoms include itch, scaling, redness, flaking, and pain. On darker skin tones, plaques may appear more grayish, purplish, or brown. Psoriasis can appear anywhere on the body, including the knees, elbows, torso and thin-skinned areas like the face, genitals and intertriginous areas, which are areas where skin touches skin, such as the armpits, under the breasts, stomach folds, between the buttocks, and in the groin area. In children, psoriasis more commonly affects these sensitive areas and intertriginous regions, posing treatment challenges and quality-of-life burdens for patients and families.

About ZORYVE® (roflumilast)
ZORYVE is the number one prescribed branded topical therapy across three major inflammatory dermatoses combined � atopic dermatitis, 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 production of anti-inflammatory mediators.

ZORYVE (roflumilast) cream 0.3% is approved by the FDA for the topical treatment of plaque psoriasis, including intertriginous areas, in patients 6 years of age and older. ZORYVE (roflumilast) 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 awardedұdzܰ’sBeauty and Wellness Award for “Eczema Product.� ZORYVE (roflumilast) topical foam 0.3% is uniquely formulated for use anywhere on the body, including hair-bearing areas, and is indicated for 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.

ٱ䴡ձ
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.

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.

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 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%).

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%).

Please see fullfor ZORYVE cream and fullfor 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 develop differentiated therapies against biologically validated targets, and has produced a robust pipeline for a range of inflammatory dermatological conditions. For more information, visitor follow Arcutis on,,, and.

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 FDA approval for ZORYVE cream 0.3% as a treatment for plaque psoriasis in children ages 2 to 5 years. 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

Investors
Brian Schoelkopf, Head of Investor Relations


FAQ

What is the current FDA approval status of ZORYVE cream for psoriasis treatment?

ZORYVE cream 0.3% is currently approved for plaque psoriasis in adults and children down to age 6. Arcutis has submitted an sNDA to expand treatment to children ages 2-5.

What makes ZORYVE unique for treating pediatric plaque psoriasis?

ZORYVE is a once-daily, steroid-free cream specifically indicated for intertriginous psoriasis, without sensitizing excipients or irritants, making it suitable for sensitive skin areas where psoriasis commonly presents in children.

What clinical data supports Arcutis' sNDA for ZORYVE in young children?

The sNDA is supported by data from a 4-week Maximal Usage Systemic Exposure (MUSE) study in children aged 2-5 years and a long-term open-label study showing favorable safety, tolerability, and sustained efficacy.

Why is ARQT expanding ZORYVE's indication to younger children?

There are currently very limited FDA-approved treatment options for plaque psoriasis in children under 6, creating a significant unmet need for non-steroidal options that can effectively treat the condition long-term.

How does plaque psoriasis present differently in young children compared to adults?

While plaque psoriasis has similar clinical features in children and adults, in children under 6 it often appears in sensitive areas such as the face or intertriginous areas, making safe long-term management more challenging.
Arcutis Biotherapeutics, Inc.

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Biotechnology
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WESTLAKE VILLAGE