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Day One Biopharmaceuticals (DAWN) Company Overview and Recent Developments

#biopharmaceutical #clinical_trials #acquisition #financial_performance #healthcare #biotechnology
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US Stock
January 6, 2026

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Day One Biopharmaceuticals (DAWN) Company Overview and Recent Developments

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Based on my searches, I was unable to locate a specific Form 8-K filing by Day One Biopharmaceuticals (DAWN) dated January 6, 2025. This could indicate the filing may not exist on that exact date, may be indexed differently, or there may be a date discrepancy.

However, I can provide you with relevant information about Day One Biopharmaceuticals that may be helpful for understanding the company’s current status and what types of developments typically appear in Form 8-K filings for biopharmaceutical companies.


Day One Biopharmaceuticals (DAWN) — Company Overview
Current Market Position
  • Ticker:
    DAWN (NASDAQ)
  • Market Cap:
    $876.85M
  • Current Price:
    $8.54 (as of January 6, 2026) [0]
  • Sector:
    Healthcare — Biotechnology
Recent Financial Performance

Quarterly Results (Q3 FY2025, reported November 2025):

  • EPS:
    $-0.19 (beat estimate by +31.75%)
  • Revenue:
    $39.80M (beat estimate by +4.18%) [0]
  • Cash Position:
    $451.58M (as of Sept 30, 2025) [0]
Key Product: OJEMDA™ (tovorafenib)

Day One’s flagship therapy is OJEMDA (tovorafenib), targeting pediatric low-grade glioma (pLGG). The company reported

positive 3-year follow-up results from the pivotal Phase 2 FIREFLY-1 trial
in December 2025 [0].


What Form 8-K Filings Typically Disclose for Biopharma Companies

Although I couldn’t locate the specific January 6, 2025 filing, Form 8-K reports for biopharmaceutical companies commonly include material events such as:

  1. Clinical Trial Updates

    • Initiation, completion, or termination of clinical trials
    • Interim or final efficacy/safety results
    • Regulatory interactions (FDA feedback, breakthrough therapy designations)
  2. Regulatory Milestones

    • FDA/EMA submissions (NDA, MAA, sNDA)
    • Regulatory approvals or complete response letters
    • Advisory committee meeting outcomes
  3. Corporate Actions

    • Mergers and acquisitions
    • Licensing agreements or partnerships
    • Management or board changes
  4. Financial Matters

    • Public offerings or private placements
    • Material changes to cash position or burn rate guidance
    • Significant collaborations with milestone payments

Relevant Recent Developments for DAWN (Based on Available Data)
1.
Mersana Therapeutics Acquisition

Day One announced a definitive agreement to acquire Mersana Therapeutics. Under the terms:

  • Consideration:
    $25 per share in cash at closing + 1 non-tradable CVR per share
  • Potential Total Value:
    Up to $55.25 per share in cash
  • Total Equity Value:
    ~$129 million at closing [0]

This transaction expands Day One’s pipeline with

Mersana’s radioconjugate platform
, including:

  • [225 Ac]Ac-AKY-1189
    for Nectin-4 expressing tumors
  • [225 Ac]Ac-AKY-2519
    for B7-H3 expressing tumors [0]

Impact on Investor Assessment:

  • Positive:
    Broadens oncology pipeline beyond pediatric CNS tumors; adds differentiated radioconjugate platform
  • Risk:
    Integration execution risk; potential dilution of focus; milestone payment obligations under CVR structure
2.
Clinical Progress of OJEMDA

The

3-year follow-up data from FIREFLY-1
demonstrated durable responses in pediatric low-grade glioma, reinforcing the commercial potential of OJEMDA [0].

3.
Financial Position
  • Strong cash reserves
    ($451.58M as of Q3 2025) support ongoing clinical development activities [0]
  • Narrowing losses:
    EPS improved from -$0.69 (Q4 2024) to -$0.19 (Q3 2025) [0]
  • Revenue growth:
    Q3 2025 revenue of $39.80M vs $29.21M in Q4 2024 [0]

Implications for Investor Assessment

If a Form 8-K filing on January 6, 2025 did exist, it would likely have addressed one or more of the following areas affecting investor sentiment:

Potential Disclosure Area Possible Impact on Clinical/Commercial Outlook
Positive clinical readout
Accelerates path to regulatory submission; enhances commercial launch expectations
Regulatory milestone achievement
Validates development pathway; may shorten timeline to market
Partnership/collaboration announcement
Non-dilutive capital; validates science; expands commercial reach
Manufacturing/supply update
Addresses commercial readiness; mitigates launch risk
Safety signal or trial setback
Could delay regulatory timeline; increase development costs; alter risk profile

Recommendation: Locate the Specific Filing

If you’re looking for the exact contents of a specific filing, I recommend:

  1. Direct SEC EDGAR Search:

    • Visit SEC.gov/EDGAR
    • Search for “Day One Biopharmaceuticals” or CIK: 1845337
    • Filter by date range around January 6, 2025
  2. Investor Relations:

  3. Financial Data Providers:

    • Bloomberg, Reuters, or other financial news aggregators often summarize key 8-K disclosures

Data Sources:

  • [0] Company financial data and market information from broker API
  • [1] Mersana acquisition announcement from company investor relations

Would you like me to attempt a more targeted search with additional details, or would you prefer to enable

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to access more comprehensive SEC filing databases and historical disclosures for DAWN?

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Insights are generated using AI models and historical data for informational purposes only. They do not constitute investment advice or recommendations. Past performance is not indicative of future results.