ZORYVE fuels Arcutis (NASDAQ: ARQT) Q1 2026 $105M revenue and cash-flow positive quarter
Filing Impact
Filing Sentiment
Form Type
8-K
Rhea-AI Filing Summary
Arcutis Biotherapeutics reported strong first quarter 2026 growth driven by its dermatology franchise ZORYVE. Net product revenue was $105.4 million, up 65% from Q1 2025 but down 17% from Q4 2025 due to typical first-quarter deductible resets and insurance changes.
By product, Q1 2026 revenue was $32.7 million from ZORYVE cream 0.3%, $49.6 million from ZORYVE foam 0.3%, $21.7 million from ZORYVE cream 0.15%, and $1.4 million from ZORYVE cream 0.05%. Net loss narrowed to $11.3 million or $0.09 per share, compared with a $25.1 million loss a year earlier.
The company generated $2.2 million of positive operating cash flow and ended March 31, 2026 with $224.3 million in cash, cash equivalents, restricted cash, and marketable securities. Arcutis reaffirmed its expectation for 2026 net product revenue between $480 million and $495 million and highlighted pipeline progress, including an sNDA for ZORYVE cream 0.05% in infants, a June 29, 2026 PDUFA date for ZORYVE cream 0.3%, enrollment completion for a pediatric MUSE trial, and initiation of a Phase 1a/1b study of investigational biologic ARQ-234.
Positive
- Robust revenue growth and improving profitability: Net product revenue reached $105.4 million in Q1 2026, up 65% year over year, while net loss narrowed to $11.3 million from $25.1 million and operating cash flow was positive $2.2 million.
- Clear pipeline and regulatory momentum: The company submitted an sNDA for ZORYVE cream 0.05% in infants, has a June 29, 2026 PDUFA date for ZORYVE cream 0.3%, is advancing multiple Phase 2 studies, and initiated a Phase 1a/1b trial for biologic ARQ-234.
Negative
- None.
Insights
Arcutis posts strong ZORYVE growth, narrows losses, and advances its pipeline.
Arcutis delivered Q1 2026 net product revenue of $105.4 million, up 65% year over year, driven by ZORYVE across cream and foam formulations. The 17% sequential decline versus Q4 2025 is explicitly tied to typical first-quarter deductible resets and insurance changes, rather than weaker demand.
Net loss improved to $11.3 million from $25.1 million a year earlier, while operating activities generated positive cash flow of $2.2 million. Cash, cash equivalents, restricted cash, and marketable securities totaled $224.3 million as of March 31, 2026, giving the company a meaningful liquidity buffer to fund commercialization and R&D.
The company maintained full-year 2026 net product revenue guidance of $480–$495 million and reported multiple pipeline and regulatory milestones, including a submitted sNDA for ZORYVE cream 0.05% in infants, a June 29, 2026 PDUFA date for ZORYVE cream 0.3%, and initiation of a Phase 1a/1b trial for ARQ-234. These steps underscore a strategy of expanding ZORYVE into broader age groups and indications while adding a biologic candidate in atopic dermatitis.
8-K Event Classification
2 items: 2.02, 9.01
2 items
Item 2.02
Results of Operations and Financial Condition
Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01
Financial Statements and Exhibits
Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Key Figures
Net product revenue: $105.4 million
ZORYVE cream 0.3% revenue: $32.7 million
ZORYVE foam 0.3% revenue: $49.6 million
+5 more
8 metrics
Net product revenue
$105.4 million
Quarter ended March 31, 2026; 65% increase vs Q1 2025
ZORYVE cream 0.3% revenue
$32.7 million
Q1 2026 product revenue component
ZORYVE foam 0.3% revenue
$49.6 million
Q1 2026 product revenue component
Net loss
$11.3 million
Q1 2026, improved from $25.1 million loss in Q1 2025
Operating cash flow
$2.2 million
Net cash provided by operating activities in Q1 2026
Cash and investments
$224.3 million
Cash, cash equivalents, restricted cash, and marketable securities as of March 31, 2026
2026 net product revenue guidance
$480–$495 million
Full-year 2026 outlook reiterated by the company
R&D expenses
$30.6 million
Quarter ended March 31, 2026; includes $10.0 million milestone for ARQ-234 trial
Key Terms
net product revenue, supplemental New Drug Application (sNDA), Maximum Usage Systemic Exposure (MUSE), Phase 1a/1b, +2 more
6 terms
net product revenue financial
"Q1 2026 net product revenue for ZORYVE was $105.4 million, a 65% increase"
Net product revenue is the money a company actually earns from selling its products after subtracting returns, discounts, rebates and other sales-related allowances. It shows the real cash-generating sales performance—like the amount a store keeps after giving change for coupons and refunds—and matters to investors because it drives profitability, helps forecast future cash flow and reveals whether reported sales are sustainable or inflated by temporary price cuts or promotions.
supplemental New Drug Application (sNDA) regulatory
"Submitted supplemental New Drug Application (sNDA) for ZORYVE cream 0.05% to the U.S. Food and Drug Administration"
A supplemental new drug application (snda) is a formal request made to regulatory authorities to make changes to an already approved medication, such as adding new uses, adjusting dosages, or improving manufacturing processes. It’s similar to updating a product’s packaging or instructions after it has been approved for sale. For investors, an snda signals ongoing development or improvements that could impact a company’s future sales or regulatory approval prospects.
Maximum Usage Systemic Exposure (MUSE) medical
"Completed enrollment in ZORYVE foam 0.3% Maximum Usage Systemic Exposure (MUSE) trial in children"
Phase 1a/1b medical
"Initiated Phase 1a/1b, first-in-human study to evaluate safety and tolerability for investigational ARQ-234"
Phase 1a/1b are the earliest human clinical trial stages that test a new drug’s safety, how the body handles it, and the right dosage. Think of phase 1a as a careful test drive in healthy volunteers to find safe dosing, and phase 1b as expanded testing—often in people with the target condition—to confirm dosing and look for early signs the treatment works; investors watch these stages because they determine safety, dosing decisions, and the next funding or development milestones.
Prescription Drug User Fee Act target action date regulatory
"Prescription Drug User Fee Act target action date for ZORYVE cream 0.3% ... is assigned for June 29, 2026"
gross-to-net sales deductions financial
"Year-over-year increases were due to strong unit demand as well as improvements in gross-to-net sales deductions"
Earnings Snapshot
Net product revenue: $105.4 million · Guidance included
Q1 2026
Net product revenue
$105.4 million
+65% year over year vs Q1 2025
Total revenues
$105.4 million
up from $65.8 million in Q1 2025
Net loss
$11.3 million
improved from $25.1 million net loss in Q1 2025
Net loss per share
$0.09
improved from $0.20 in Q1 2025
Operating cash flow
$2.2 million
positive in Q1 2026; not specified for Q1 2025
Guidance
Company continues to anticipate 2026 net product revenue between $480 million and $495 million.
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
___________________________________________
FORM 8-K
___________________________________________
CURRENT REPORT
Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): May 6, 2026
___________________________________________
(Exact name of registrant as specified in its charter)
___________________________________________
(State or other jurisdiction of incorporation) | (Commission File Number) | (IRS Employer Identification Number) | ||||||
(Address of principal executive offices, including Zip Code)
Registrant’s telephone number, including area code: (805 ) 418-5006
___________________________________________
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instructions A.2. below):
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) | |||||
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) | |||||
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) | |||||
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) | |||||
Securities registered pursuant to Section 12(b) of the Act:
Title of each class | Trading Symbol(s) | Name of each exchange on which registered | ||||||||||||
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter). Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
On May 6, 2026, Arcutis Biotherapeutics, Inc. (the “Company” or “Arcutis”) issued a press release relating to its financial results for the quarter ended March 31, 2026. The full text of the press release is furnished herewith as Exhibit 99.1.
The information in this Item 2.02 of this Form 8-K and the Exhibit 99.1 attached hereto shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that Section, or incorporated by reference in any filing under the Securities Act of 1933, as amended (the “Securities Act”), or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
Exhibit No. | Description | |||||||
| 99.1 | Press Release May 6, 2026. | |||||||
| 104 | Cover Page Interactive Data File (formatted as Inline XBRL). | |||||||
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
ARCUTIS BIOTHERAPEUTICS, INC. | |||||||||||
| May 6, 2026 | By: | /s/ Latha Vairavan | |||||||||
| Latha Vairavan | |||||||||||
Chief Financial Officer | |||||||||||
Arcutis Announces First Quarter 2026 Financial Results and Provides Business Update
•Q1 2026 net product revenue for ZORYVE® (roflumilast) was $105.4 million, a 65% increase compared to Q1 2025, and a 17% decrease compared to Q4 2025
•Continued strong demand for ZORYVE despite typical Q1 seasonality, with continued growth in share of branded non-steroidal topical treatments
•Submitted supplemental New Drug Application (sNDA) for ZORYVE cream 0.05% to the U.S. Food and Drug Administration (FDA) to expand the indication for the treatment of atopic dermatitis in infants ages 3 to 24 months
•Completed enrollment in ZORYVE foam 0.3% Maximum Usage Systemic Exposure (MUSE) trial in children with plaque psoriasis of the scalp and body ages 2 to 11 years
•Initiated Phase 1a/1b, first-in-human study to evaluate safety and tolerability for investigational ARQ-234 in healthy volunteers and adults with moderate to severe atopic dermatitis
•Completed expansion of dermatology sales force at the beginning of May and initiated the build-out of a primary care and pediatrics-focused organization including the hiring of the head of Primary Care Franchise
•Maintained positive operating cash flow for the quarter
Westlake Village, CA, May 6, 2026 – Arcutis Biotherapeutics, Inc. (Nasdaq: ARQT), a commercial-stage biopharmaceutical company focused on developing meaningful innovations in immuno-dermatology, today reported financial results for the quarter ended March 31, 2026, and provided a business update.
“Strong product revenue in the first quarter was driven by continued robust demand for ZORYVE, which remains the leading prescribed branded topical across its three approved indications. During the quarter, we also advanced our pipeline with the initiation of a Phase 1 trial for ARQ‑234, our biologic candidate for atopic dermatitis, submission of an sNDA to the FDA to expand the ZORYVE cream indication in atopic dermatitis to patients as young as 3 months, and progress on our Phase 2 proof-of-concept studies of ZORYVE in potential new indications,” said Frank Watanabe, president and chief executive officer. “We also continued to generate positive cash flow, underscoring our focus on financial and operational discipline as we continue to advance our corporate strategy.”
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
First Quarter 2026 Financial Results and Business Highlights
Commercial Highlights
ZORYVE — a highly potent and selective phosphodiesterase-4 (PDE4) inhibitor in once-daily cream and foam formulations, approved in the United States and Canada for the treatment of plaque psoriasis, atopic dermatitis, and seborrheic dermatitis.
•ZORYVE net product sales for the first quarter of 2026 were $105.4 million, reflecting a 17% sequential decline versus the fourth quarter of 2025 and 65% year-over-year growth. The sequential decline was primarily due to typical first-quarter patient deductible resets and insurance changes.
•The dermatology sales force expansion has been completed, with representatives in the field at the beginning of May, to optimize prescriber targeting and call frequency in order to deepen adoption of ZORYVE.
•Began the build-out of an internal, targeted sales team dedicated to primary care and pediatric healthcare providers with the hiring of Katie Swolfs as the head of Primary Care Franchise. Katie brings an incredible breadth and depth of commercial experience to the role, having held a series of strategic and operational senior leadership positions for dermatology-focused companies.
Clinical and Regulatory Developments
•Submitted an sNDA for ZORYVE cream 0.05% to the FDA to expand the indication for the treatment of mild to moderate atopic dermatitis in infants ages 3 to 24 months.
•Presented new results from the INTEGUMENT-INFANT Phase 2 trial in infants with atopic dermatitis in a late-breaking session at the 2026 American Academy of Dermatology (AAD) Annual Meeting, highlighting that investigational ZORYVE cream 0.05% was well tolerated, improved signs and symptoms of mild to moderate atopic dermatitis, and demonstrated a rapid improvement in itch in as little as 10 minutes in nearly half of infants, as reported by caregivers.
•Prescription Drug User Fee Act target action date for ZORYVE cream 0.3% for the treatment of plaque psoriasis down to 2 years of age is assigned for June 29, 2026.
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
•Completed enrollment in the 0.3% ZORYVE foam MUSE trial in children with plaque psoriasis of the scalp and body ages 2 to 11 years intended to serve as the basis for an sNDA submission to expand the indication for this age group.
•The Company continues to enroll patients in Phase 2 proof-of-concept studies with ZORYVE foam 0.3% for the treatment of vitiligo and hidradenitis suppurativa, and expects to report results, as well as decisions on program advancement in these indications, in the fourth quarter of 2026 and the first quarter of 2027, respectively.
•Initiated Phase 1a/1b, first-in-human study to evaluate safety and tolerability for investigational ARQ-234, a fusion protein that is a potent and highly selective checkpoint agonist of the CD200 receptor, in healthy volunteers and adults with moderate to severe atopic dermatitis.
Corporate Updates
•ZORYVE cream 0.05% received a strong recommendation in the AAD Clinical Practice Guidelines for the management of pediatric atopic dermatitis.
•Sustained positive cash flow, generating $2.2 million of positive cash flow from operating activities in Q1 2026.
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
First Quarter 2026 Summary Financial Results
Net Product revenues for the quarter ended March 31, 2026 were $105.4 million compared to $63.8 million for the corresponding period in 2025. Revenues for the quarter were $32.7 million for ZORYVE (roflumilast) cream 0.3%, $49.6 million for ZORYVE (roflumilast) topical foam 0.3%, $21.7 million for ZORYVE (roflumilast) cream 0.15%, and $1.4 million for ZORYVE (roflumilast) cream 0.05%. Year-over-year increases were due to strong unit demand as well as improvements in gross-to-net sales deductions. In addition, the first quarter of 2025 included Other revenues of $2.0 million related to license revenues received in connection with the Huadong Pharmaceutical collaboration and licensing agreement covering China and Greater Asia.
Cost of sales for the quarter ended March 31, 2026 were $9.8 million compared to $8.8 million for the corresponding period in 2025, due to increased ZORYVE sales.
Research and development (R&D) expenses for the quarter ended March 31, 2026 were $30.6 million compared to $17.5 million for the corresponding period in 2025. The year-over-year increase was primarily due to the $10.0 million milestone obligation to former stockholders of Ducentis triggered by the dosing of the first patient in the ARQ-234 Phase 1a/1b trial.
Selling, general, and administrative (SG&A) expenses for the quarter ended March 31, 2026 were $74.1 million compared to $64.0 million for the corresponding period in 2025. The year-over-year increase was primarily due to compensation and personnel-related expenses and to higher sales and marketing expenses related to the Company's continued commercialization efforts for ZORYVE.
Net loss was $11.3 million, or $0.09 per basic and diluted share, for the quarter ended March 31, 2026 compared to $25.1 million, or $0.20 per basic and diluted share, for the corresponding period in 2025.
Cash, cash equivalents, restricted cash, and marketable securities were $224.3 million as of March 31, 2026, compared to $221.3 million as of December 31, 2025. Net cash provided by operating activities was $2.2 million during the first quarter.
Financial Guidance
The Company continues to anticipate net product revenue of between $480 million and $495 million for the full year 2026.
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
Conference Call and Webcast
Arcutis management will host a conference call and webcast today at 4:30 PM ET to discuss the financial results for the quarter and provide a business update. The webcast for this conference call may be accessed in the “Events” section of the Company’s website. A replay of the webcast will be available on the Arcutis website following the call.
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, visit www.arcutis.com or follow Arcutis on LinkedIn, Facebook, Instagram, and X.
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
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 to address large markets with significant unmet need; the development, submission, and potential approval, and potential commercialization of product candidates and expanded indications; the potential commercial success and growth of ZORYVE in plaque psoriasis, seborrheic dermatitis, and atopic dermatitis; anticipated net product sales for 2026; the expansion of the Company's dermatology sales force and the success of the Company's efforts in primary care and pediatric health care providers; the Company's ability to maintain positive operating cash flow on a quarterly basis; the building and advancement of the Company's pipeline; and the timing of regulatory filings. These statements involve 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 and you should not place undue reliance on our forward-looking statements. Risks and uncertainties that may cause our actual results to differ include risks inherent in the clinical development process and regulatory approval process, the timing of regulatory filings, the timing, expenses, and success of our commercialization efforts, including uncertainty of future commercial sales and related items that can impact net sales, and our ability to defend our intellectual property. For a further description of the risks and uncertainties applicable to our business, see the “Risk Factors” section of our Form 10-K filed with U.S. Securities and Exchange Commission (SEC) on February 25, 2026, 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.
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
Contacts:
Media
Amanda Sheldon, head of Corporate Communications
media@arcutis.com
Investors
Brian Schoelkopf, head of Investor Relations
ir@arcutis.com
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
ARCUTIS BIOTHERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(in thousands)
(unaudited)
| March 31, | December 31, | ||||||||||
| 2026 | 2025 | ||||||||||
ASSETS | |||||||||||
Current assets: | |||||||||||
Cash and cash equivalents | $ | 34,762 | $ | 42,907 | |||||||
| Restricted cash | 308 | 308 | |||||||||
| Marketable securities | 189,238 | 178,075 | |||||||||
| Trade receivable, net | 144,377 | 146,229 | |||||||||
| Inventory | 37,391 | 22,634 | |||||||||
Prepaid expenses and other current assets | 31,980 | 21,079 | |||||||||
Total current assets | 438,056 | 411,232 | |||||||||
| Property and equipment, net | 1,040 | 1,043 | |||||||||
| Intangible assets, net | 14,250 | 14,812 | |||||||||
Operating lease right-of-use asset | 4,361 | 4,467 | |||||||||
Other assets | 2,296 | 1,419 | |||||||||
Total assets | $ | 460,003 | $ | 432,973 | |||||||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | |||||||||||
Current liabilities: | |||||||||||
Accounts payable | $ | 18,296 | $ | 12,528 | |||||||
| Current portion of long-term debt, net | 7,950 | 1,000 | |||||||||
| Accrued and other current liabilities | 136,957 | 116,310 | |||||||||
Total current liabilities | 163,203 | 129,838 | |||||||||
| Operating lease liability, long-term | 5,251 | 5,266 | |||||||||
| Long-term debt, net | 101,470 | 107,959 | |||||||||
| Other long-term liabilities | 431 | 431 | |||||||||
Total liabilities | 270,355 | 243,494 | |||||||||
| Stockholders’ equity: | |||||||||||
| Common stock | 12 | 12 | |||||||||
Additional paid-in capital | 1,339,529 | 1,327,595 | |||||||||
| Accumulated other comprehensive loss | (514) | (44) | |||||||||
Accumulated deficit | (1,149,379) | (1,138,084) | |||||||||
| Total stockholders’ equity | 189,648 | 189,479 | |||||||||
| Total liabilities and stockholders’ equity | $ | 460,003 | $ | 432,973 | |||||||
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
ARCUTIS BIOTHERAPEUTICS, INC.
Condensed Consolidated Statements of Operations
(in thousands, except per share data)
(unaudited)
| Three Months Ended March 31, | |||||||||||
| 2026 | 2025 | ||||||||||
| Revenues: | |||||||||||
| Product revenue, net | $ | 105,398 | $ | 63,846 | |||||||
| Other revenue | — | 2,000 | |||||||||
| Total revenues | 105,398 | 65,846 | |||||||||
| Operating expenses: | |||||||||||
| Cost of sales | 9,784 | 8,830 | |||||||||
| Research and development | 30,627 | 17,543 | |||||||||
| Selling, general, and administrative | 74,076 | 64,002 | |||||||||
| Total operating expenses | 114,487 | 90,375 | |||||||||
| Loss from operations | (9,089) | (24,529) | |||||||||
| Other income (expense): | |||||||||||
| Interest income | 2,275 | 2,537 | |||||||||
| Interest expense | (4,368) | (2,982) | |||||||||
| Other income (expense), net | (20) | 193 | |||||||||
Loss before income taxes | (11,202) | (24,781) | |||||||||
Provision for income taxes | 93 | 279 | |||||||||
| Net loss | $ | (11,295) | $ | (25,060) | |||||||
| Net loss per share, basic and diluted | $ | (0.09) | $ | (0.20) | |||||||
| Weighted-average shares used in computing net loss per share, basic and diluted | 129,365 | 126,037 | |||||||||
3027 Townsgate Road, Suite 300 Westlake Village, CA 91361 | arcutis.com
FAQ
How did Arcutis (ARQT) perform financially in Q1 2026?
Arcutis reported Q1 2026 net product revenue of $105.4 million, up 65% year over year. Net loss narrowed to $11.3 million, or $0.09 per share, compared with a $25.1 million loss in Q1 2025, reflecting higher sales and controlled operating performance.
What drove Arcutis (ARQT) ZORYVE revenue in the first quarter of 2026?
ZORYVE generated $105.4 million in Q1 2026 net product revenue, with $32.7 million from cream 0.3%, $49.6 million from foam 0.3%, $21.7 million from cream 0.15%, and $1.4 million from cream 0.05%. Growth reflected strong unit demand and improved gross-to-net deductions.
What is Arcutis (ARQT) guidance for 2026 net product revenue?
Arcutis continues to anticipate 2026 net product revenue between $480 million and $495 million. This outlook is based on expected continued commercial performance of ZORYVE across approved indications and geographies throughout the year, as highlighted in the company’s business update.
How strong is Arcutis (ARQT) cash position after Q1 2026?
As of March 31, 2026, Arcutis held $224.3 million in cash, cash equivalents, restricted cash, and marketable securities. The company also generated $2.2 million of positive cash flow from operating activities during the quarter, supporting ongoing commercialization and development plans.
What key regulatory milestones are upcoming for Arcutis (ARQT) products?
Arcutis has a PDUFA target action date of June 29, 2026 for ZORYVE cream 0.3% in plaque psoriasis down to age two. It also submitted an sNDA for ZORYVE cream 0.05% in infants with atopic dermatitis and completed enrollment in a pediatric MUSE trial.
What are the main R&D developments for Arcutis (ARQT) in Q1 2026?
Arcutis submitted an sNDA for ZORYVE cream 0.05% in infants, advanced Phase 2 proof-of-concept trials for ZORYVE foam 0.3% in vitiligo and hidradenitis suppurativa, and initiated a Phase 1a/1b trial of ARQ-234, a CD200 receptor checkpoint agonist for atopic dermatitis.