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Description

It is normally withdrawn, mixed with the drug, and then that mixture is injected (usually intramuscularly or subcutaneously, as indicated for the drug)

The panel voted yes

Batch-specific data are provided on the Certificate of Analysis (CoA)

The FDA is not bound by the committee's recommendation and may decline to add these compounds to the 503A bulks list

Retatrutide is in Phase 3 clinical trials through Eli Lilly, and cagrilintide is in Phase 3 trials through Novo Nordisk (both as monotherapy and as part of CagriSema)