infringement via inducement and chronic conditions
since amarin already has vascepa on the market, could another entity perform a study of EPA for new indication (an indication not currently patented by amarin) with the intent of marketing that new indication themselves WITHOUT inducing providers to infringe with vascepa Rx's?
i think, if not, any new EPA indications go to vascepa.
example:
trial sponsor: Prostrivity (made up) API marketed name: PROSEPA trial: does PROSEPA significantly reduce prostrate inflammation? trial outcome: success assume FDA approval: to significantly reduce prostrate inflammation due to ... DTC commercials: see your doctor for a new drug, PROSEPA, for A, B, and C. placebo-like side effects
patient goes to doctor: doc, i want an Rx for PROSEPA. well. mr. SoandSo, you're already taking vascepa so i don't believe you'll need PROSEPA to get the benefits of prostrate inflammation reduction.