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Arcutis Biotherapeutics, Inc. ARQT Topical roflumilast program costs — R&D

Other product segments

ARQ-234 program costs
$11M
Other program costs
$95K

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Other financials

Income statement

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Revenue$105.4M+60.1%
Gross profit$95.6M+67.7%
Operating income-$9.1M+62.9%
Net income-$11.3M+54.9%
EPS (diluted)-$0.09+55.0%

Balance sheet

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Cash & equivalents$35.1M-34.7%
Total debt$114.7M+3.5%
Total equity$189.6M+32.9%
Total assets$460.0M+33.7%

Cash flow

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Operating cash flow$2.2M+107%
CapEx--100%
Free cash flow$2.2M+107%

Valuation

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Market cap$3.29B+57.5%

Profitability

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Gross margin90.9%+2.5pp
Operating margin-12%-5.7pp
Net margin-13.9%-6.6pp
FCF margin-52.5%-21.9pp

Returns & leverage

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Return on equity-28.2%-13.0pp
Debt / equity0.6×-0.2×
Current ratio2.7×-0.9×

Where this comes from

Reported directly by Arcutis Biotherapeutics, Inc. in its filing.

Tagged under the XBRL concept us-gaap:ResearchAndDevelopmentExpense.

The official record: Arcutis Biotherapeutics, Inc.’s 10-Q, filed May 6, 2026, on SEC EDGAR. View the filing →

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Questions, answered.

What is Arcutis Biotherapeutics, Inc.'s topical roflumilast program costs — R&D?
Arcutis Biotherapeutics, Inc. (ARQT) reported topical roflumilast program costs — R&D of $3.31M in Q1 2026.
How has Arcutis Biotherapeutics, Inc.'s topical roflumilast program costs — R&D changed year-over-year?
Arcutis Biotherapeutics, Inc.'s topical roflumilast program costs — R&D increased by 128.7% year-over-year, from $1.45M to $3.31M.
What is the long-term trend for Arcutis Biotherapeutics, Inc.'s topical roflumilast program costs — R&D?
Over 2 years (2022 to 2025), Arcutis Biotherapeutics, Inc.'s topical roflumilast program costs — R&D has grown at a -63.7% compound annual growth rate (CAGR), from $83.03M to $10.94M.
What does topical roflumilast program costs — R&D mean?
This metric represents the direct research and development expenditures specifically allocated to the topical roflumilast product pipeline. It captures the costs associated with clinical trials, regulatory filings, and formulation development required to advance this specific therapeutic candidate toward commercialization. Monitoring these costs helps investors assess the capital intensity and progress of the company's primary dermatological asset.