Do you know how additional patents for new methods ad uses would affect that agreement?
I did not see the agreement, but it is about the launch of generic V (ANDA product) and I do not think that any, new patent will effect the agreement.
TEVA's gV will get the same label that will be for V (in 2029) … the usage of both wil be identical.
contractual relationships tying up most existing EPA supply, wouldn't AMRN create a significant barrier to entry for most generic manufacturers? Or do you think that the supply will be easily expandable at that point, and generics will have the same effect on V sales as they have had on Lipitor?
2029/30 is far away … I am sure that a lot of "fish-oil" production company will restructure their operation - especially if V will be as widely used as we think - and will produce pure EPA for Pharma (for higher profit) instead of DS, food, etc. industry.
Meanwhile Amarin could keep the x % of the market the profit will be significantly less.
e.g. Currently it looks like as (per annualized patient, $): NR: 1,500 / year COGS: 300 / year Gross Profit: 1,200 / year (80%)
to keep the "100"% of the market they have to reduce the price and it will looks like: NR: 420 / year COGS: 300 / year Gross Profit: 120 / year (28.5%)