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Arcutis Announces Third Quarter 2026 Financial Results and Provides Business Update

Higher sales supported quarterly profitability and positive operating cash flow, while marketing and personnel spending increased.

Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

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Arcutis Biotherapeutics (Nasdaq: ARQT) reported third-quarter 2026 ZORYVE net product sales of $143.9 million, reflecting growth across its products. Sales rose 45% year over year and 11% sequentially, primarily on increased unit demand. Net income reached $8.8 million versus $7.4 million a year earlier; diluted earnings per share remained $0.06. Operating activities generated $18.9 million in cash.

The company raised its 2026 net product sales outlook to $535 million–$545 million from $525 million–$540 million. Selling, general and administrative expenses increased to $99.6 million from $62.4 million. Arcutis initiated a Phase 3 trial in moderate to severe atopic dermatitis and expects vitiligo results and an advancement decision by year-end. The FDA set February 23, 2027, as its target action date for expanding ZORYVE cream 0.05% use to infants aged 3 to 24 months.

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16 points · 1 major

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Rhea-AI Sentiment measures something else, the tone of the wording.

0 major · 6 points

Hollow bars mark forward-looking points. How the balance works

Positive

  • Major point. Forward-looking: it has not happened yet and may not happen.Arcutis raised 2026 sales guidance to $535 million–$545 million from $525 million–$540 million.
  • Moderate pointQ3 ZORYVE sales of $143.9 million rose 45% year over year and 11% sequentially.
  • Moderate pointPhase 3 trial initiated for ZORYVE cream 0.3% in adults and children with moderate to severe atopic dermatitis.
  • Minor pointQ3 net income increased to $8.8 million from $7.4 million; diluted EPS remained $0.06.
  • Minor pointQ3 operating cash flow was positive at $18.9 million.
11 minor points
  • Minor pointCash, restricted cash and marketable securities reached $259.8 million versus $221.3 million at December 31, 2025.
  • Minor pointQ3 operating income increased to $9.436 million from $8.526 million a year earlier.
  • Minor pointNine-month net product revenue increased to $379.178 million from $244.569 million in 2025.
  • Minor pointNine-month net income reached $12.515 million versus a $33.536 million loss in 2025.
  • Minor point. Forward-looking: it has not happened yet and may not happen.Arcutis expects vitiligo Phase 2 results and an advancement decision by year-end 2026.
  • Minor point. Forward-looking: it has not happened yet and may not happen.Arcutis expects hidradenitis suppurativa Phase 2 results and an advancement decision in Q1 2027.
  • Minor pointARQ-234 Phase 1a/1b enrollment continues, with progression to the multiple ascending dose portion.
  • Minor pointPhase 4 INTEGUMENT-ITCH enrollment continues, evaluating itch improvement in adults with atopic dermatitis.
  • Minor point. Forward-looking: it has not happened yet and may not happen.Arcutis is preparing enrollment for a Phase 2 trial treating checkpoint inhibitor-related skin adverse events.
  • Minor pointOne new U.S. patent obtained in Q4 2026 covers topical PDE4 inhibitor foam compositions.
  • Minor pointQ3 interest expense decreased to $2.959 million from $3.071 million a year earlier.

Negative

  • Moderate pointQ3 selling, general and administrative expenses rose to $99.6 million from $62.4 million.
  • Moderate pointInfant indication expansion remains pending FDA action, with a February 23, 2027, target date.
  • Minor pointQ3 research and development expenses rose to $22.4 million from $19.6 million.
  • Minor pointQ3 cost of sales increased to $12.5 million from $8.7 million as ZORYVE sales volume increased.
  • Minor pointNine-month interest expense increased to $10.733 million from $9.082 million in 2025.
  • Minor pointCurrent long-term debt increased to $6.950 million from $1.000 million at December 31, 2025.

News Explained

In its third-quarter results, Arcutis reported cash, cash equivalents, restricted cash and marketable securities of $259.8 million at September 30, 2026, versus $221.3 million at December 31, 2025, a larger reported asset pool at quarter-end.

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Market Reaction – ARQT

$28.61 – $34.80 Day Range
$3.75B Mkt Cap at Last Price

On Nov 4, the day this news came out, the latest delayed price for ARQT is 12.39% below the previous close. Our momentum scanner has recorded 70 alerts for this stock so far that day. The latest delayed price is $29.83.

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Key Figures

Net product revenue: $143.9 million Year-over-year revenue growth: 45% Sequential revenue growth: 11% +5 more
Net product revenue
$143.9 million
Q3 2026
Year-over-year revenue growth
45%
Q3 2026 versus Q3 2025
Sequential revenue growth
11%
Q3 2026 versus Q2 2026
FY 2026 net product sales guidance
$535 million–$545 million
Raised from $525 million–$540 million
Net income
$8.8 million
Q3 2026
Diluted earnings per share
$0.06
Q3 2026
Cash provided by operating activities
$18.9 million
Q3 2026
FDA target action date
February 23, 2027
Supplemental application for ZORYVE cream 0.05% in infants aged 3 to 24 months

Previous Earnings Reports

4 past events · Latest: Aug 05
Same Type 4 events
  1. Aug 05

    Q2 earnings

    24h Move
    -2.5%

    ZORYVE revenue grew, guidance was raised, and operating cash flow was positive.

  2. May 06

    Q1 earnings

    24h Move
    -14.5%

    ZORYVE revenue grew year over year and the company reported positive operating cash flow.

  3. Feb 25

    Q4 and FY earnings

    24h Move
    +5.8%

    ZORYVE revenue grew and 2026 net product sales guidance was introduced.

  4. Oct 28

    Q3 earnings

    24h Move
    +27.0%

    ZORYVE revenue grew year over year and the company reported net income.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

pde4 inhibitor, supplemental new drug application, gross-to-net, multiple ascending dose
4 terms
pde4 inhibitor medical
"a highly potent and selective phosphodiesterase-4 (PDE4) inhibitor"
A PDE4 inhibitor is a drug that blocks an enzyme (PDE4) involved in turning off certain cell signals linked to inflammation and brain activity; blocking it lets those signals persist and can reduce inflammation or alter nerve-cell behavior. Investors care because this drug class underlies treatments for conditions like chronic inflammatory and neurological disorders, so clinical trial results, regulatory decisions, or patent news can strongly affect a company’s drug pipeline value and stock outlook.
supplemental new drug application regulatory
"for the supplemental New Drug Application to expand the indication"
A supplemental new drug application is a request submitted to regulatory authorities to make changes to an existing approved medication, such as adding new uses, strengths, or formulations. For investors, it signals that a pharmaceutical company is seeking approval for new product developments or expanded applications, which can impact the company's future sales, market potential, and stock value.
gross-to-net financial
"modest improvements in gross-to-net (GTN) deductions"
Gross-to-net describes the difference between a product’s total billed sales (the “sticker” or list price) and the cash a company actually keeps after subtracting discounts, rebates, returns and other deductions. For investors it matters because large or growing deductions can make reported sales look strong on paper while actual revenue and profit are much smaller, similar to a store advertising high prices but taking many coupons at checkout.
multiple ascending dose medical
"progressed to the multiple ascending dose portion of the trial"
A multiple ascending dose is a method used in testing new medicines where small groups of people receive gradually larger amounts of the drug over time. This approach helps researchers find the safest and most effective dose without causing too many side effects. For investors, it signals ongoing steps in drug development that can impact a company's potential success or approval prospects.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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  • Continued strong ZORYVE® (roflumilast) net product revenue growth, with Q3 revenues of $143.9 million, +45% versus Q3 of 2025, and +11% versus Q2 of 2026, driven by strong demand growth
  • Raised 2026 full-year net product sales guidance to $535 million–$545 million
  • Partnered with World Champion gymnast Simone Biles to launch the Skin to Believe In awareness campaign for individuals living with inflammatory skin conditions
  • Remains on track to disclose topline results from Phase 2 trial of ZORYVE foam 0.3% in individuals with vitiligo and decision on program advancement in Q4 of 2026
  • Maintained positive operating cash flow for the quarter with $18.9 million of net cash provided by operating activities

WESTLAKE VILLAGE, Calif., Nov. 04, 2026 (GLOBE NEWSWIRE) -- 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 September 30, 2026, and provided a business update.

“Yet another strong quarter of performance reflects the consistent execution of our corporate strategy and further strengthens our financial position. ZORYVE continues to lead the branded non-steroidal topical segment driven by its efficacy and tolerability across multiple inflammatory skin conditions and patient populations. We are very excited to launch a new awareness campaign with Simone Biles, a World Champion gymnast who uses ZORYVE herself, to raise awareness of inflammatory skin diseases and of advanced targeted topicals like ZORYVE,” said Frank Watanabe, president and chief executive officer. “Looking ahead, with a potential FDA approval of ZORYVE cream 0.05% for infants as young as 3 months in the first quarter of 2027, the progress of our indication expansion trials, and the advancement of our ARQ-234 Phase 1 trial, we are well positioned to drive continued growth.”

Third Quarter 2026 Financial Results and Business Updates

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 third quarter of 2026 were $143.9 million, reflecting 45% year-over-year growth and an 11% sequential increase versus the second quarter of 2026. The year-over-year and sequential increases were driven by increasing demand across products.
  • Launched the Skin to Believe In campaign with Simone Biles to raise awareness of seborrheic dermatitis and eczema and to encourage individuals to talk to their doctor about long-term, steroid-free, topical treatment options for their skin conditions, including ZORYVE.

Clinical and Regulatory Developments

  • The Company initiated a pivotal Phase 3 trial with ZORYVE cream 0.3% for the treatment of adults and children with moderate to severe atopic dermatitis, distinct from the current indication of ZORYVE cream 0.15% for the treatment of adults and children 6 years of age and older with mild to moderate atopic dermatitis.
  • The FDA has set a target action date of February 23, 2027, for the supplemental New Drug Application to expand the indication for ZORYVE cream 0.05% for mild to moderate atopic dermatitis to infants aged 3 to 24 months.
  • The Company continues to enroll patients in a Phase 4 study evaluating quality and speed of itch improvement with ZORYVE cream 0.15% in adult patients with atopic dermatitis (INTEGUMENT-ITCH).
  • The Company remains on track to disclose topline results from the Phase 2 proof-of-concept study of ZORYVE foam 0.3% for the treatment of vitiligo and share its decision on program advancement by the end of 2026.
  • The Company continues to enroll patients in the Phase 2 proof-of-concept studies of ZORYVE foam 0.3% for the treatment of hidradenitis suppurativa, and expects to report results, as well as a decision on program advancement, in the first quarter of 2027.
  • The Company is preparing to enroll a Phase 2 trial evaluating the safety and efficacy of ZORYVE foam 0.3% in the treatment of cutaneous adverse events due to checkpoint inhibitors.
  • The Company continues to enroll patients in the Phase 1a/1b study of ARQ-234, a potent and highly selective checkpoint agonist of the CD200 receptor, for the treatment of atopic dermatitis and has progressed to the multiple ascending dose portion of the trial.

Corporate Updates

  • Appointed Rob Lisicki, a commercial and executive leader with over 30 years of biopharmaceutical industry experience, as chief commercial officer, effective November 4, 2026.
  • Appointed Rob Scott, MD, a global pharma industry leader and pioneer, to the Board of Directors in October 2026.
  • ZORYVE cream 0.15% received the 2026 "Best Prescription Skin Solution" Award from Marie Claire magazine, the first time a prescription drug has been recognized by this prestigious publication.
  • Sustained positive cash flow, generating $18.9 million of cash flow from operating activities in the third quarter of 2026.
  • Obtained one new U.S. patent in the fourth quarter of 2026 related to topical PDE4 inhibitor foam compositions.

Third Quarter 2026 Summary Financial Results

Product revenues for the quarter ended September 30, 2026 were $143.9 million compared to $99.2 million for the corresponding period in 2025, an increase of 45%. All products grew in the quarter, with revenues for the quarter of $37.8 million for ZORYVE cream 0.3%, $27.3 million for ZORYVE cream 0.15%, $3.7 million for ZORYVE cream 0.05%, and $75.1 million for ZORYVE topical foam 0.3%. The year-over-year and quarter-over-quarter increases were predominantly due to increased unit demand, as well as modest improvements in gross-to-net (GTN) deductions.

Cost of sales for the quarter ended September 30, 2026 was $12.5 million compared to $8.7 million for the corresponding period in 2025, due to increasing ZORYVE sales volume.

Research and development (R&D) expenses for the quarter ended September 30, 2026 were $22.4 million compared to $19.6 million for the corresponding period in 2025. The year-over-year increase was primarily driven by ARQ-234 clinical development expense and investment in medical affairs to support medical education related to our roflumilast programs.

Selling, general, and administrative (SG&A) expenses for the quarter ended September 30, 2026 were $99.6 million compared to $62.4 million for the corresponding period in 2025. The year-over-year increase was driven by greater marketing spend primarily in support of the Skin to Believe In celebrity awareness campaign and by increased personnel-related expenses resulting from the dermatology sales force expansion and launch of the primary care provider and pediatric sales team.

Net income was $8.8 million, or $0.07 basic and $0.06 diluted earnings per share, for the quarter ended September 30, 2026, compared to net income of $7.4 million, or $0.06 basic and diluted earnings per share, for the corresponding period in 2025.

Cash, cash equivalents, restricted cash, and marketable securities were $259.8 million as of September 30, 2026, compared to $221.3 million as of December 31, 2025. Net cash provided by operating activities was $18.9 million during the third quarter.

Financial Guidance

  • The Company raised net product sales guidance for the full year 2026 to $535 million–$545 million from $525 million–$540 million.

Conference Call and Webcast

Arcutis management will host a conference call and webcast today at 4:30 p.m. ET to discuss the financial results for the quarter and provide a business update. The webcast for this conference call may be accessed at the “Events” section of the Company’s website. The replay of the webcast will be available on the Company's 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.

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 progression of the development, 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, including peak sales, market access and reimbursement, product demand growth and developments regarding GTN; future product sales guidance; and the timing of regulatory filings and potential approvals. 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 the 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.

Contacts:

Media
Amanda Sheldon, head of Corporate Communications
media@arcutis.com

Investors
Brian Schoelkopf, head of Investor Relations
ir@arcutis.com

ARCUTIS BIOTHERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(In thousands)
(unaudited)

  September 30, December 31,
   2026   2025 
ASSETS    
Current assets:    
Cash and cash equivalents $33,373  $42,907 
Restricted cash  308   308 
Marketable securities  226,087   178,075 
Trade receivables, net  171,281   146,229 
Inventory  45,669   22,634 
Prepaid expenses and other current assets  26,972   21,079 
Total current assets  503,690   411,232 
Property and equipment, net  796   1,043 
Intangible assets, net  13,125   14,812 
Operating lease right-of-use asset  4,145   4,467 
Other assets  2,670   1,419 
Total assets $524,426  $432,973 
LIABILITIES AND STOCKHOLDERS’ EQUITY    
Current liabilities:    
Accounts payable $8,342  $12,528 
Current portion of long-term debt, net  6,950   1,000 
Accrued and other current liabilities  157,065   116,310 
Total current liabilities  172,357   129,838 
Operating lease liability, noncurrent  5,224   5,266 
Long-term debt, net  102,448   107,959 
Other long-term liabilities  431   431 
Total liabilities  280,460   243,494 
Stockholders’ equity:    
Common stock  12   12 
Additional paid-in capital  1,370,692   1,327,595 
Accumulated other comprehensive loss  (1,169)  (44)
Accumulated deficit  (1,125,569)  (1,138,084)
Total stockholders’ equity  243,966   189,479 
Total liabilities and stockholders’ equity $524,426  $432,973 


ARCUTIS BIOTHERAPEUTICS, INC.
Condensed Consolidated Statements of Operations
(In thousands, except per share data)
(unaudited)

  Three Months Ended
September 30,
 Nine Months Ended
September 30,
   2026   2025   2026   2025 
Revenues:        
Product revenue, net $143,919  $99,219  $379,178  $244,569 
Other revenue  —   —   —   2,000 
Total revenues  143,919   99,219   379,178   246,569 
         
Operating expenses:        
Cost of sales  12,460   8,685   33,183   25,007 
Research and development  22,422   19,604   73,404   56,600 
Selling, general, and administrative  99,601   62,404   255,815   195,576 
Total operating expenses  134,483   90,693   362,402   277,183 
Income (loss) from operations  9,436   8,526   16,776   (30,614)
         
Other income (expense):        
Interest income  2,596   2,118   7,150   6,731 
Interest expense  (2,959)  (3,071)  (10,733)  (9,082)
Other income (expense), net  (77)  (83)  (254)  130 
Total other income (expense)  (440)  (1,036)  (3,837)  (2,221)
         
Income (loss) before income taxes  8,996   7,490   12,939   (32,835)
         
Provision for income taxes  195   80   424   701 
         
Net income (loss) $8,801  $7,410  $12,515  $(33,536)
         
Earnings (loss) per share:        
Basic $0.07  $0.06  $0.10  $(0.26)
Diluted $0.06  $0.06  $0.09  $(0.26)
         
Weighted-average shares used in computing earnings (loss) per share:        
Basic  131,011   127,623   130,306   126,891 
Diluted  136,836   132,885   136,192   126,891 

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What were Arcutis ARQT's third-quarter 2026 sales and earnings?

Arcutis reported $143.9 million in net product sales and $8.8 million in net income for the quarter ended September 30, 2026. Sales increased 45% year over year and 11% from the second quarter. Basic earnings per share were $0.07, while diluted earnings per share were $0.06.

What is Arcutis ARQT's updated 2026 sales guidance?

Arcutis raised its full-year 2026 net product sales guidance to $535 million–$545 million, compared with its previous range of $525 million–$540 million.

Why did Arcutis ARQT's selling and administrative expenses increase in Q3 2026?

The increase reflected greater marketing spending and personnel-related expenses. Marketing spending primarily supported the Skin to Believe In celebrity awareness campaign. Personnel expenses increased with the dermatology sales force expansion and the launch of the primary care provider and pediatric sales team.

How much revenue did each Arcutis ZORYVE product generate in Q3 2026?

ZORYVE topical foam 0.3% generated $75.1 million in third-quarter revenue. ZORYVE cream 0.3% generated $37.8 million, cream 0.15% generated $27.3 million, and cream 0.05% generated $3.7 million. All products grew during the quarter.

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