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Re: Tatsumaki post# 389123

Tuesday, 09/20/2022 3:52:39 PM

Tuesday, September 20, 2022 3:52:39 PM

Post# of 429367
T. Its been awhile but the FDA refused to approve the Anchor indication ( TG's below 500 mg/dl ) because they felt patients would be using Vascepa this way to reduce CV event risk ...rather than risk of Pancreatitis ( TG's over 500 mg/dl ) .

So they forced AMRN to complete the R-IT trial to prove that Vascepa would reduce CV events

Kiwi
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