Moderna Inc. announced today that the U.S. FDA’s Vaccines and Related Biological Products Advisory Committee meeting to review the safety and efficacy data package for mRNA-1273 will likely be scheduled for December 17, 2020.
The Company anticipates that the shipping of the mRNA-1273 vaccine to designated distribution points throughout the U.S. will occur shortly after an Emergency Use Authorization is granted. By the end of 2020, the Company expects to have approximately 20 million doses of mRNA-1273 available in the U.S. and remains on track to manufacture 500 million to 1 billion doses globally in 2021.