Pfizer and Valneva report promising Phase 3 Lyme disease vaccine results
The company plans to submit the vaccine for regulatory review
The company plans to submit the vaccine for regulatory review
Previously, Arexvy was authorized for adults 60 and older, and for those 50–59 with heightened risk
The two companies will collaborate to evaluate Hopewell’s ttLNPs for clinical applications
Moderna will appeal to the Federal Circuit to assert that its government-contractor immunity limits liability under federal law
The order will cover the manufacturing of bulk vaccine in 2026
The data highlights its RSV vaccine cuts hospitalizations in older adults
mNEXSPIKE is the third Moderna vaccine authorized in the European Union, strengthening the Company's respiratory vaccine portfolio in Europe
The FDA’s Center for Biologics Evaluation and Research (CBER) cited Moderna’s choice of a licensed standard-dose flu vaccine as the comparator in its Phase 3 trial, saying it “does not reflect the best-available standard of care.”
Signed Memorandum of Understanding supports "Plan Mexico," Mexico's strategic initiative to build a local mRNA ecosystem and strengthen health security
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