Moderna Says That FDA, Due To Administrative Constraints, Does Not Expect To Complete Its Review Of mRNA-1345, Respiratory Syncytial Virus Vaccine, By May 12, The FDA Has Informed Moderna That It Is Working To Conclude The Review By The End Of May
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Moderna has announced that the FDA, due to administrative constraints, will not complete its review of mRNA-1345, a vaccine for Respiratory Syncytial Virus, by the initially expected date of May 12. The FDA aims to conclude the review by the end of May.
May 10, 2024 | 11:06 am
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The delay in the FDA's review of Moderna's mRNA-1345 vaccine may cause temporary investor concern, potentially impacting Moderna's stock price in the short term.
Delays in regulatory approvals, especially for significant products like vaccines, can lead to investor uncertainty and short-term negative sentiment towards a company's stock. In this case, the delay is attributed to administrative constraints, not to concerns about the vaccine's efficacy or safety, which might mitigate the negative impact. However, the delay still introduces uncertainty regarding the timeline for potential revenue from the vaccine, which can lead to short-term volatility in Moderna's stock price.
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