Bird and Marjac, Correct me If I'm wrong, but I'm not sure Bird's final conclusion is entirely accurate. I believe the FDA reneged on its promise, allowing Amarin to sell Vascepa through the Reduce-It trial completion, if the Marine Trial was a success, which it was. Their reasoning for reneging: Emerging data showing Triglyceride lowering alone does not equal event reduction, so they were disallowing another TG lowering drug from being approved. Amarin was always going to have to prove event reduction, regardless of Triglyceride lowering benefits. However, instead of selling Vascepa through the 5 year Reduce-it trial for TG's >500, they (WE) had wait it out. All the while, scheduling additional stock offerings. With that being said, the FDA approving "another" TG lowering drug for 500 and above TG's, in the form of generic V is a bit bewildering.
Webster