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marzan

11/29/18 8:32 PM

#164125 RE: OldYeller187 #164119

Thanks for everything OldYeller. Ask Elizabeth whether they are submitting or already submitted cvd efficacy evidence to FDA fulfilling the Anchor control. This is a much faster route to reach 70M+ U.S. patients that are >200 Tg. While they work on the ReduceIt sNDA and the 10 month long waiting period to get approval from FDA, Anchor label can get us the much needed scripts in the interim, imo.