Day One Biopharmaceuticals, Inc (DAWN) Stock Analysis
Healthcare · Biotechnology
Sell if holding. Engine safety override at $21.50: a dimension score below its floor triggers a hard block regardless of the otherwise-positive setup — overall score 5.3/10. Specifically: Below-average business quality; Rich valuation.
Day One Biopharmaceuticals develops targeted oncology therapeutics, with OJEMDA (tovorafenib) as its first FDA-approved product (April 2024) for relapsed/refractory pediatric low-grade glioma. OJEMDA generated ~$212.6M in cumulative product sales through December 31, 2025;... Read more
Sell if holding. Engine safety override at $21.50: a dimension score below its floor triggers a hard block regardless of the otherwise-positive setup — overall score 5.3/10. Specifically: Below-average business quality; Rich valuation. Chart setup: No recognized chart pattern (not a breakout, bounce, continuation, recovery, falling knife, or range) — technicals mixed. Score 5.3/10, moderate confidence.
Passes 7/8 gates (positive momentum, clean insider activity, no SEC red flags, news events none recent, earnings proximity no date, semi cycle peak clear, materials cycle peak clear). Fails on favorable risk/reward ratio. Suitability: aggressive.
Recent Developments — Day One Biopharmaceuticals, Inc
Material events (past 30 days)
- Apr 23, 2026 HIGH Item 5.01: Change of control completed: Servier Pharmaceuticals' tender offer for all DAWN shares at $21.50/share expired April 22, 2026 and the merger closed. Day One becomes an indirect wholly-owned subsidiary of Servier S.A.S. No successor management named.
Generated 2026-05-20T20:21:21Z.
Thesis
Key Metrics
Quality Signals
Options Flow
Concentration Risks(10-K Item 1A)
- HIGHProductOJEMDA10-K Item 1A: 'Our near-term revenues are highly dependent on, and a meaningful portion of the value of our company relates to, our ability to successfully commercialize OJEMDA in the United States'
Material Events(8-K, last 90d)
- 2026-04-23Item 5.01HIGHChange of control completed: Servier Pharmaceuticals' tender offer for all DAWN shares at $21.50/share expired April 22, 2026 and the merger closed. Day One becomes an indirect wholly-owned subsidiary of Servier S.A.S. No successor management named.SEC filing →
Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results. Full disclaimer
Rating Breakdown
3 floor-breakers·1 ceiling hit
Priced at a premium — multiples above sector norms. Needs delivery on growth + margins to justify.static
Technicals below the gate floor. Component breakdown shows what dragged the score down.static
Clinical-stage biotech: losses expected pre-commercialisation. Quality floor doesn't distinguish R&D investment from operational decay — components above tell the real story.static
Price Targets
Position Sizing
Risk Alerts
Earnings
Verdict History
Frequently Asked Questions
Sell if holding. Engine safety override at $21.50: a dimension score below its floor triggers a hard block regardless of the otherwise-positive setup — overall score 5.3/10. Specifically: Below-average business quality; Rich valuation. Chart setup: No recognized chart pattern (not a breakout, bounce, continuation, recovery, falling knife, or range) — technicals mixed. Prior stop was $21.47. Score 5.3/10, moderate confidence.
Take-profit target: $24.76 (+15.0% upside). Prior stop was $21.47. Stop-loss: $21.47.
Concentration risk — Product: OJEMDA; Target reached (-13.1% upside); Quality below floor (3.6 < 4.0).
Day One Biopharmaceuticals, Inc trades at a P/E of N/A (forward -504.1). TrendMatrix value score: 2.0/10. Verdict: Sell.
13 analysts cover DAWN with a consensus score of 2.6/5. Average price target: $22.
What does Day One Biopharmaceuticals, Inc do?Day One Biopharmaceuticals develops targeted oncology therapeutics, with OJEMDA (tovorafenib) as its first FDA-approved...
Day One Biopharmaceuticals develops targeted oncology therapeutics, with OJEMDA (tovorafenib) as its first FDA-approved product (April 2024) for relapsed/refractory pediatric low-grade glioma. OJEMDA generated ~$212.6M in cumulative product sales through December 31, 2025; FIREFLY-2 Phase 3 confirmatory trial enrolls through early 2026 with newer pipeline assets Emi-Le (ADC, ACC) and DAY301.