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Moderna Receives U.S. FDA Approval for Updated 2026-2027 Spikevax and mNEXSPIKE COVID-19 Vaccines
NASDAQ: $MRNA CAMBRIDGE, MA / ACCESS Newswire / August 27, 2026 / Moderna, Inc. (NASDAQ:MRNA) today announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental Biologics License Applications (sBLA) for the 2026-2027 formulas for… Source: Read More
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A Breakthrough in Oncology: Merck and Moderna Report Positive Phase 3 Results for Personalized Cancer Vaccine
NYSE: $MRK A Major Milestone in Cancer Treatment The landscape of cancer therapy is evolving rapidly, and a recent announcement from Merck and Moderna marks a significant turning point. The companies have officially announced that the Phase 3 INTERPATH-001 trial, investigating their investigational individualized neoantigen therapy (INT), known as mRNA-4157 (telixavastat/intismeran), combined with the immunotherapy…
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FDA Approves mFLUSIVA (influenza vaccine, mRNA) for the Prevention of Seasonal Influenza
NASDAQ: $MRNA CAMBRIDGE, MA / ACCESS Newswire / August 5, 2026 / Moderna, Inc. (NASDAQ:MRNA) today announced that the U.S. Food and Drug Administration (FDA) has approved mFLUSIVA® (mRNA-1010), a new vaccine against seasonal influenza, for use in all adults… Source: Read More
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A New Milestone in Melanoma Treatment: 5-Year Data for mRNA-4157 and Keytruda
Breaking Down the Long-Term Results In a significant development for oncology, Moderna and Merck have released updated 5-year follow-up data from the Phase 2b KEYNOTE-942 clinical trial. This study investigates the combination of mRNA-4157 (V940), an investigational individualized neoantigen therapy, alongside Keytruda (pembrolizumab), Merck’s anti-PD-1 therapy, for patients with resected high-risk melanoma. What the Data…