Ned Pagliarulo@NedPagliarulo Sept. 3, 2020
Dive Brief:
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A federal appeals court on Thursday upheld an earlier court
ruling that had invalidated six patents covering Amarin's heart drug Vascepa,
increasing the likelihood that generic competitors could soon launch copycat
versions of the fish oil-derived pill in the U.S.
·
Tough questions from the three-judge panel on Wednesday had sunk
Amarin shares by nearly a third, and news of the decision just one day later
dragged the company's stock down further. Amarin has lost 80%, or roughly $7
billion, of its value since late last year as investor hopes Vascepa could
become a blockbuster drug for the company dimmed.
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Vascepa is Amarin's only drug, approved since 2012 for lowering
high triglycerides. In mid-December, the Food and Drug Administration cleared its use for reducing the risk of
events like heart attacks or strokes, dramatically widening the number of
people who could potentially benefit from treatment.
Dive Insight:
Two years ago, Amarin surprised
many with news Vascepa significantly reduced major cardiovascular adverse
events in a trial known as REDUCE-IT.
That Vascepa, a highly purified
form of an acid contained in fish oil, would prove so beneficial for heart
health wasn't expected. The study results, which were later published in The New England Journal of Medicine, changed
Amarin's fortunes overnight, raising the company's value by billions and
putting it in position to widely sell a heart pill that compared favorably to
more expensive drug options already on the market.
A district court ruling in March
put that all at risk. Judge Miranda Du of the U.S. District Court for the
District of Nevada found that patents held by Amarin on
Vascepa were invalid due to "obviousness," a term indicating the
information contained would be readily apparent to an expert in the field and therefore
undeserving of legal protection.
Amarin had argued that the
unexpectedly large benefit shown in REDUCE-IT justified its patents, but Du
disagreed.
Now, three judges on the U.S.
Court of Appeals for the Federal Circuit have upheld Du's decision, making it
more likely that generic drugmakers Hikma Pharmaceuticals and Dr. Reddy's could
soon launch a generic version of Vascepa.
In a statement, Hikma said is "working
towards" a launch of its copycat drug, which the FDA approved in
May.
Amarin, though, isn't giving up,
indicating Thursday it expects to request an "en banc" hearing by all
12 appeals court judges. The company added that it doesn't believe its would-be
competitors can readily make large supplies of generic Vascepa, so it will
continue its current marketing efforts around the drug.
While the decision dims Amarin's
prospects in the U.S., the company is putting greater emphasis on the potential
for sales of Vascepa in Europe, Canada and elsewhere. No generic litigation is
pending outside the U.S., Amarin said.
Earlier this summer, the company
opted to commercialize Vascepa in Europe on its own, rather than seeking a large
drugmaker as a partner. The drug is currently under review by EU
regulators.
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