Arcutis Biotherapeutics, Inc.

Fundamentals7.0
Price Action6.0
News Sentiment7.0
AI Rating
7.0

Key Drivers

  • Strong liquidity
  • High gross margins
  • Large operating spend

AI
AI Summary

7.0

ARQT has transitioned from a binary clinical-stage biotech into a cash-flowing specialty pharma where ZORYVE commercial execution and margin sustainability now matter as much as pipeline outcomes. The key opportunity is pediatric sNDA-driven market expansion, but single-product concentration, payer/supply risks and rich valuation mean overweight only with consecutive quarters of predictable revenue, gross-margin stability, and positive operating cash flow.

CashFlow
Concentration
Catalyst‍

Price Chart

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Financial Metrics

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Revenue (TTM)
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Net Income (TTM)
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EPS (Q)
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MCAP

Deep Analysis

Research tool. Not personalized advice.

Fundamental Analysis

7.0

Key Financial Insights:

  • Strong liquidity
  • High gross margins
  • Large operating spend

ARQT has strong liquidity and very high gross margins but faces large, volatile operating losses and an outsized valuation that make the recent profitable quarter encouraging yet insufficient to offset material earnings and valuation risk.

OperationalMomentum
RichValuation

Price Behavior

6.0
Research tool. Not personalized advice. Technical analysis is for informational purposes only.

Key Price Behavior Insights:

  • Downtrend persist
  • Trading at lows
  • Elevated volatility

ARQT is in a clear short-term downtrend over the last month (≈ −12.5%), trading at recent lows that mark $22.24 support and near-term resistance around $24.6–$24.8 (with stronger resistance $26.9–$28.6) amid elevated short-term volatility.

bearish
Support Level: $22.24
Resistance Level: $24.6–$24.8; $26.9–$28.6

Rapid decline from late‑February highs to

Sentiment & News

7.0

Key News Insights:

  • Strong sales
  • Profitability shift
  • Pipeline progress

Arcutis crushed Q4 with $127.5M ZORYVE sales, turned GAAP profitable, raised 2026 guidance and signaled sustainable positive cash flow while advancing pediatric/first‑in‑human clinical programs and expanding commercialization.

ZORYVE

The results and guidance upgrade materially de‑risk the commercial story, supporting a premium valuation as sales momentum and upcoming regulatory/clinical catalysts reduce execution risk