FDA14 Nov 2020 18:24
https://www.fda.gov/media/136832/download
The FDA and other government partners are working with industry to make treatment options available to patients and providers who are not able to participate in clinical trials, including through expanded access under investigational new drug (IND) applications.
Additionally, if certain statutory criteria are met, the FDA may issue an emergency use authorization (EUA) to allow unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life- threatening diseases or conditions caused by chemical, biological, radiological, or nuclear threat agents when, among other factors, there are no adequate, approved, and available alternatives.
As of September 16, 2020, the FDA has authorized six EUAs, and revoked one of the initial six, to treat COVID and serious conditions caused by COVID-19: