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 5.1/10. Specifically: Below-average business quality; Rich valuation.
Day One Biopharmaceuticals is a commercial-stage biopharmaceutical company; its first product OJEMDA (tovorafenib) was FDA-approved in April 2024 for relapsed/refractory pediatric low-grade glioma. As of December 2025, the company had generated ~$212.6M in cumulative OJEMDA... 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 5.1/10. 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 5.1/10, moderate confidence.
Passes 5/7 gates (positive momentum, clean insider activity, no SEC red flags, news events none recent, semi cycle peak clear). Fails on favorable risk/reward ratio and earnings proximity 5d<=7d. Suitability: aggressive.
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'
Material Events(8-K, last 90d)
- 2026-04-23Item 5.01HIGHServier Pharmaceuticals' tender offer for all Day One shares at $21.50/share expired April 22, 2026. Servier acquired all outstanding shares per Merger Agreement dated March 6, 2026. Change of control completed.SEC filing →
- 2026-04-23Item 1.02MEDIUMMaterial agreement terminated upon completion of Servier merger on April 22-23, 2026, per Merger Agreement. No separate reason cited beyond merger closing.SEC filing →
- 2026-04-23Item 5.02MEDIUMDirector/officer departures upon Servier merger completion effective April 22-23, 2026; expected consequence of change-of-control closing per Merger Agreement from March 6, 2026.SEC filing →
Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results. Full disclaimer
Rating Breakdown
4 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
Negative sentiment — recent news tone and/or analyst downgrades drag the composite below neutral.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 5.1/10. 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 5.1/10, 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 (3.4 < 4.0).
Day One Biopharmaceuticals, Inc trades at a P/E of N/A (forward -177.6). 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 is a commercial-stage biopharmaceutical company; its first product OJEMDA (tovorafenib) was...
Day One Biopharmaceuticals is a commercial-stage biopharmaceutical company; its first product OJEMDA (tovorafenib) was FDA-approved in April 2024 for relapsed/refractory pediatric low-grade glioma. As of December 2025, the company had generated ~$212.6M in cumulative OJEMDA product sales; Phase 3 trials for front-line pLGG (FIREFLY-2) and MDD (Emerge, Ascend) are ongoing.