Moderna

Behind every cancer diagnosis is a person, a family and the hope for more options. This World Cancer Research Day, David Berman, Chief Development Officer, reflects on the questions driving cancer research forward — from finding new ways to harness the immune system to exploring whether we could intervene earlier in the cancer journey. Read David’s perspective: https://lnkd.in/e84EUJjy #WorldCancerResearchDay

We’ve always believed mRNA has the power to change medicine and make a meaningful difference for patients.   That belief has driven us from the beginning—and continues to push us to explore what’s possible for human health.   We’re proud to be named to Fortune’s 2026 Change the World list, recognizing companies working to address some of the world’s biggest challenges through their business.   Thank you to our teams around the world who bring this work forward every day. Read more: https://lnkd.in/eqzYdCu6

Today we announced that three abstracts on intismeran autogene, our investigational mRNA-based individualized neoantigen therapy, have been accepted for presentation at ESMO - European Society for Medical Oncology Congress 2026, which will be held October 23–27 in Madrid, Spain. Read more: https://lnkd.in/eR2vk8QJ

What does learning at Moderna look like? 📚 💻   We recently wrapped up Learning Days in Cambridge and Norwood—two days designed to give our colleagues dedicated time to step away from the day-to-day, build new skills, connect with one another, and invest in their growth.   Across both sites, colleagues heard from our CEO, Stéphane Bancel, participated in hands-on workshops and interactive learning sessions, and connected with colleagues from across the organization.   While Learning Days may be over, growth never stops. We continue to invest in new and meaningful ways for our people to learn and develop—building the skills and capabilities that will help shape what’s next at Moderna.   Interested in growing and learning with us? Explore career opportunities: https://lnkd.in/ezXF4KRK

Read our latest press release: https://lnkd.in/gxcSqvjX

Today we announced that the U.S. Food and Drug Administration has approved the supplemental Biologics License Applications for the 2026-2027 formulas for Spikevax® (COVID-19 Vaccine, mRNA) and mNEXSPIKE® (COVID-19 Vaccine, mRNA), containing the JN.1-lineage XFG subvariant of SARS-CoV-2 to help prevent COVID-19. Read more: https://lnkd.in/gFyRcjAH

Read our latest press release: https://lnkd.in/gYv7uzFg

Along with our partners at Merck, we announced positive results from the Phase 3 INTerpath-001 study of intismeran autogene, our investigational individualized neoantigen therapy, in combination with pembrolizumab as adjuvant treatment in patients with completely resected Stage IIB-IV melanoma. This marks the first and only combination regimen to demonstrate a clinically meaningful improvement over pembrolizumab alone, a current standard-of-care for these patients. In our latest IR Insights, members of our executive team sat down to reflect on what this means: https://lnkd.in/geACX55k

Moderna and Merck today announced positive topline results from the Phase 3 INTerpath-001 trial evaluating adjuvant treatment with intismeran autogene, a novel investigational mRNA-based individualized neoantigen therapy jointly developed by Merck and Moderna, in combination with KEYTRUDA® (pembrolizumab), Merck's anti-PD-1 therapy, in patients with completely resected Stage IIB-IV melanoma.    Read more: https://lnkd.in/gTivr_bx

Today we announced that the U.S. Food and Drug Administration has approved mFLUSIVA® (mRNA-1010), a new vaccine against seasonal influenza, for use in all adults 50 years and older.   This approval follows unanimous recommendations from the FDA's Vaccines and Related Biological Products Advisory Committee supporting mFLUSIVA for adults 50 years of age and older.   Read more: https://lnkd.in/gJvvNnUp