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Re: DewDiligence post# 7326

Tuesday, 05/28/2013 1:45:37 PM

Tuesday, May 28, 2013 1:45:37 PM

Post# of 427228
FDA has rejected a prior EPA/DHA combo that raised LDL in treatment of 200-500. Extremely unlikely a combo would be approved with a mono product that increases LDL.

This is Pronova territory and likely not patentable again. The only way this will help AZN is if they end up with Amarin. I don't see PFE losing the bid.
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