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FDA won't comment on status of Emergency Use Authorizations for two antibody treatments

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Last updated 21 setembro 2024
FDA won't comment on status of Emergency Use Authorizations for two antibody treatments
The US Food and Drug Administration told CNN Thursday morning that the agency doesn’t have any comments on the applications for Emergency Use Authorizations for Eli Lilly and Regeneron antibody treatments.
The coronavirus pandemic has brought countries to a standstill. In many places, as countries reopen, Covid-19 cases are on the rise. Follow here for the latest.
FDA won't comment on status of Emergency Use Authorizations for two antibody treatments
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