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Novavax Q1 2025 Earnings Report
Novavax reported a significant increase in revenue and net income for Q1 2025, primarily driven by the termination of APAs with Canada and New Zealand, and revenue from the Sanofi CLA.
Key Takeaways
Novavax, Inc. reported a net income of $518.6 million on total revenue of $666.7 million for the three months ended March 31, 2025. This represents a substantial increase compared to a net loss of $147.6 million and total revenue of $93.9 million in the same period last year. The significant revenue growth was primarily due to the termination of advance purchase agreements (APAs) with Canada and New Zealand, and initial revenue recognition from the Sanofi Collaboration and License Agreement.
Total revenue for Q1 2025 increased by $572.8 million to $666.7 million, up from $93.9 million in Q1 2024.
The company achieved a net income of $518.6 million in Q1 2025, a significant improvement from a net loss of $147.6 million in Q1 2024.
Product sales were $621.7 million, primarily driven by the termination of APAs with Canada ($575.7 million) and New Zealand ($27.3 million).
Licensing, royalties, and other revenue increased by $41.0 million to $45.0 million, mainly due to the Sanofi CLA.
Revenue by Segment
Revenue by Geographic Location
Forward Guidance
Novavax anticipates continued focus on its Sanofi partnership, leveraging its technology platform for additional partnerships, and advancing its early-stage pipeline. The company expects to fund operations through milestone payments, royalties, product sales, and potential equity financings.
Positive Outlook
- Anticipates a $175 million milestone payment from Sanofi upon BLA approval for COVID-19 Vaccine Product in pre-filled syringe from U.S. FDA.
- Expects an additional $50 million in combined milestones from Sanofi upon transfers of marketing authorization for U.S. and European Union markets in Q4 2025.
- Entered into an Amended Takeda CLA, improving financial terms, including a $20 million upfront payment and annual milestone payments plus royalties on net sales.
- Signed an additional Material Transfer Agreement (MTA) for Matrix-M® with a top-tier pharmaceutical company, expanding scope to viral pathogens and entering a preclinical collaboration for cancer vaccine candidate.
- Completed enrollment for Phase 3 trial of COVID-19-Influenza Combination and stand-alone seasonal influenza vaccine candidates, with initial cohort data expected by mid-2025.
Challenges Ahead
- Potential for further delays in U.S. FDA approval for prototype vaccine and NVX-CoV2601 due to information requests for post-marketing commitments.
Historical Earnings Impact
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Avg. Return Before/After Earnings
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