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This week, the FDA posted a blog post about that meeting, emphasizing its "renewed unwavering commitment to the rare disease community." Advisors on FDA's Vaccines and Related Biological Products Advisory Committee are meeting on Thursday, 18 June, to discuss whether to recommend approval of Moderna's MFLUSIVA mRNA influenza vaccine for adults ages 5064 and accelerated approval for adults 65 and older

In general, intravenous infusions or injections are not prohibited if they are legitimately received in the course of a hospital treatment, surgical procedure or clinical investigation or if they do not exceed 100 mL per 12 hour period

Others are immune modulators, with peptides known to move macrophages from an inflammatory state to a repair state, reducing local cytokine production

The most important factor for any research protocol is consistency, so administering it at the same time each day is recommended