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Moderna stock soared early in the pandemic thanks to sales of its coronavirus vaccine. After soaring to success in the early ...
The Department of Health and Human Services has defended cuts to vaccine research with statements that mislead on the safety ...
The label expansion for Moderna’s jab arrives at a juncture in America’s changing vaccine regulatory landscape.
The agency’s decision to clear Moderna’s shot for use in certain younger adults is a much-needed win for a company that’s ...
Moderna vaulted to the forefront of biotech, becoming a major pillar of the region’s economy. But Robert F. Kennedy Jr.’s ...
FDA drug alerts in infectious diseases, including new drug approvals, safety warnings, recalls, and changes in indications.
Expanded indication builds on existing U.S. FDA approval of mRESVIA for adults aged 60 and older CAMBRIDGE, MA / ACCESS ...
The Food and Drug Administration (FDA) has approved Moderna’s next-generation mRNA COVID-19 vaccine mNexspike ®.
The main reason for the downturn in Moderna’s stock is a significant drop in the demand for its COVID-19 vaccine.
Interest in what caused the coronavirus pandemic has many political dimensions today, with President Trump saying genetic ...
Explore why Novavax, Inc. faces profitability challenges despite a promising tech platform, with uncertain revenue streams.
(HealthDay News) — The U.S. Food and Drug Administration has approved a new lower-dose vaccine for active immunization against COVID-19 caused by severe acute respiratory syndrome coronavirus 2.
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