Moderna announced today that Taiwan's Food & Drug Administration (FDA) has approved an updated formulation of the COVID-19 mRNA vaccine, Spikevax, targeting the JN.1 variant, in people aged six months and over.
In April 2024, the World Health Organization (WHO) Technical Advisory Group on COVID-19 Vaccine Composition (TAG-CO-VAC) issued guidelines recommending the use of a monovalent JN.1 for the antigenic composition of COVID-19 vaccines.
Regulatory submissions for Moderna's updated vaccine are currently under review by regulatory agencies worldwide, with decisions expected in the coming weeks, the laboratory points out.
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Moderna, Inc. is a biotechnology company specialized in research and development of therapeutics and vaccines for cancer, infectious, autoimmune and cardiovascular diseases. Net sales break down by type of revenue as follows:
- revenue from product sales (96.1%);
- revenue from collaboration agreements (1.5%);
- revenue from royalties and licensing (1.3%);
- revenue from grants (1.1%).
At the end of 2024, the group's portfolio comprises 37 products in clinical development, of which 10 in phase I, 18 in phase II and 9 in phase III, 3 products in preclinical development, and 4 products in commercial phase.
Net sales are distributed geographically as follows: the United States (55.1%), Europe (18.5%) and other (26.4%).
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