US FDA asks Novavax to complete new clinical trial for delayed COVID-19 shot, WSJ reports
ByAinvest
Friday, Apr 25, 2025 9:30 pm ET1min read
NVAX--
The FDA's request for new data gives Novavax room to negotiate for a smaller, less expensive study, potentially costing only a few million dollars [1]. The vaccine maker has responded to the FDA's Post Marketing Commitment (PMC) request and is awaiting feedback from the agency. Novavax believes its Biologics License Application is approvable and looks forward to moving to full approval as soon as possible [1].
Shares of Novavax fell nearly 6% to close at $6.67 on Friday, following the WSJ report [1]. The stock was down more than 1% in after-market trade. However, shares rose 20% on Wednesday after the company said in a securities filing that it believed its Biologics License Application is approvable based on conversations with the FDA [2].
The request for additional clinical trials is part of a broader review process that has been affected by changes in the FDA's leadership under Health and Human Services Secretary Robert F. Kennedy Jr. [1]. The company wants to convert its emergency authorization into full approval to allow for expanded use and to better compete against messenger RNA vaccines from rivals such as Moderna and Pfizer [1].
Novavax's protein-based technology offers an alternative to the mRNA vaccines, which received full approvals in 2021 and 2022, respectively. The company's vaccine has been approved for emergency use but faces challenges in gaining full approval [1].
References:
[1] https://www.tradingview.com/news/reuters.com,2025:newsml_L4N3R31UC:0-us-fda-asks-novavax-to-complete-new-clinical-trial-for-delayed-covid-19-shot-wsj-reports/
[2] https://www.marketwatch.com/story/novavax-slips-after-wsj-report-on-fda-request-for-another-vaccine-study-7b55f5e5
US FDA asks Novavax to complete new clinical trial for delayed COVID-19 shot, WSJ reports
The U.S. Food and Drug Administration (FDA) has requested that Novavax NVAX conduct an additional clinical trial on its COVID-19 vaccine, according to a report by the Wall Street Journal [1]. The request comes after the FDA missed its April 1 deadline to approve the shot, which has raised concerns about its prospects.The FDA's request for new data gives Novavax room to negotiate for a smaller, less expensive study, potentially costing only a few million dollars [1]. The vaccine maker has responded to the FDA's Post Marketing Commitment (PMC) request and is awaiting feedback from the agency. Novavax believes its Biologics License Application is approvable and looks forward to moving to full approval as soon as possible [1].
Shares of Novavax fell nearly 6% to close at $6.67 on Friday, following the WSJ report [1]. The stock was down more than 1% in after-market trade. However, shares rose 20% on Wednesday after the company said in a securities filing that it believed its Biologics License Application is approvable based on conversations with the FDA [2].
The request for additional clinical trials is part of a broader review process that has been affected by changes in the FDA's leadership under Health and Human Services Secretary Robert F. Kennedy Jr. [1]. The company wants to convert its emergency authorization into full approval to allow for expanded use and to better compete against messenger RNA vaccines from rivals such as Moderna and Pfizer [1].
Novavax's protein-based technology offers an alternative to the mRNA vaccines, which received full approvals in 2021 and 2022, respectively. The company's vaccine has been approved for emergency use but faces challenges in gaining full approval [1].
References:
[1] https://www.tradingview.com/news/reuters.com,2025:newsml_L4N3R31UC:0-us-fda-asks-novavax-to-complete-new-clinical-trial-for-delayed-covid-19-shot-wsj-reports/
[2] https://www.marketwatch.com/story/novavax-slips-after-wsj-report-on-fda-request-for-another-vaccine-study-7b55f5e5

Stay ahead of the market.
Get curated U.S. market news, insights and key dates delivered to your inbox.
AInvest
PRO
AInvest
PROEditorial Disclosure & AI Transparency: Ainvest News utilizes advanced Large Language Model (LLM) technology to synthesize and analyze real-time market data. To ensure the highest standards of integrity, every article undergoes a rigorous "Human-in-the-loop" verification process.
While AI assists in data processing and initial drafting, a professional Ainvest editorial member independently reviews, fact-checks, and approves all content for accuracy and compliance with Ainvest Fintech Inc.’s editorial standards. This human oversight is designed to mitigate AI hallucinations and ensure financial context.
Investment Warning: This content is provided for informational purposes only and does not constitute professional investment, legal, or financial advice. Markets involve inherent risks. Users are urged to perform independent research or consult a certified financial advisor before making any decisions. Ainvest Fintech Inc. disclaims all liability for actions taken based on this information. Found an error?Report an Issue

Comments
No comments yet