FTC v. Actavis
On June 17, the Supreme Court ruled that reverse payment settlements
between brand name and generic drug manufacturers were not presumptively
unlawful, but were subject to scrutiny under the “rule of reason.” This
holding overruled the United States Court of Appeals for the Eleventh
Circuit’s dismissal of the case, resolving a circuit split.
JD Supra explains the Court’s holding. HealthAffairs describes the background of the industry and the history of the case. FDA Law Blog predicts its implications on future litigation.
Actavis addresses the uncertain legality of “reverse payment
settlements.” Such settlements are common when a generic drug
manufacturer announces its intention to produce a patented drug and
declares that it believes the patent to be invalid in an Abbreviated New
Drug Application (“ANDA”) to the FDA, as required by the Hatch-Waxman
Act. Actavis, slip op. at 2–4. This declaration constitutes
infringement, and the patent owner can immediately sue to prevent the
generic drug from entering the market. Id. at 3–4.
In many such cases, the patent owner agrees to pay the potential
infringer in exchange for a promise not to produce the patented drug
until the expiration of the patent term. Reverse payment settlements
allow the parties to avoid potentially costly litigation, at the cost
(to everyone else) of allowing invalid drug patents to remain
effectively enforced as government-granted monopolies.
Actavis involved Solvay Pharmaceuticals, the manufacturer of a
patented drug called AndroGel, and three generic manufacturers —
Actavis, Inc. (“Actavis”), Paddock Laboratories (“Paddock”), and Par
Pharmaceutical (“Par”). Id. at 5. When Actavis and Paddock filed
ANDAs in 2003 seeking approval to market a generic version of AndroGel
and claiming that Solvay’s patent was invalid, Solvay sued. Id. In
2006, the parties settled, agreeing that the generic manufacturers
would promote AndroGel to urologists and would not market generic
versions of AndroGel until 2015, 65 months before the patent’s
expiration date. Id. In return, Solvay agreed to pay $12 million
to Paddock, $60 million to Par, and up to $30 million annually for nine
years to Actavis. Id. at 5–6.
The FTC filed a lawsuit against all parties in 2009, arguing that the
purpose of the payments was to compensate the generic manufacturers for
their agreement not to compete with Solvay. Id. The District
Court and the Eleventh Circuit dismissed the case, holding that “a
reverse settlement is immune from antitrust attack so long as its
anticompetitive effects fall within the [term] of the patent” because of
the inherent anticompetitive goals of the patent system and the policy
of encouraging settlement. Id. at 6–7 (quoting FTC v. Watson
Pharmaceuticals, Inc., 677 F.3d 1298, 1312 (11th Cir. 2012)). The Court
granted certiorari to resolve the split between courts applying this
logic and other courts holding reverse payment settlements presumptively
unlawful. Id. It heard oral arguments in March 2013 (previously covered by the Digest).
The Court declined to adopt either position of the lower courts, endorsing instead a “rule of reason” test. Id.
at 20. The Court first rejected the idea that settlements within the
term of the patent were presumptively valid, noting that while valid
patents would grant a holder legitimate monopoly rights, “[t]he patent
here may or may not be valid, and may or may not be infringed.” Id.
at 8. However, it also rejected the FTC’s proposed “quick look” rule,
which would have found reverse payment settlements to be presumptively
invalid; the “complexities” of the settlements’ consequences merited a
case-by-case determination of anticompetitive effects. Id. at 20–21.
The Court held that courts should balance patent and antitrust goals.
Settlements “amount[ing] to . . . a rough approximation of the
litigation expenses saved” or compensating “for other services that the
generic has promised to perform” weighed against a finding of
anticompetitive effects, id. at 17; however, “unexpectedly large” reverse payments could show a desire to maintain “supracompetitive prices,” id.
at 19. The Court found that the FTC’s case should have been allowed to
continue, given the special incentives of Hatch-Waxman, the suspicious
characteristics of the settlement, and the potentially unjustified
competitive consequences, and remanded the case for further proceedings.
Id. at 16–21.
Dissenting, Chief Justice Roberts endorsed the Eleventh Circuit’s test. Id. at 1–3. He argued that the validity and scope of a patent were not antitrust principles but questions for patent law. Id.
at 5–6. Roberts further argued that the majority’s rule would
disincentivize patent litigation settlements, and therefore invalidity
suits, by decreasing their reward. Id. at 11. His dissent also
noted that the majority’s decision could discourage patent challenges,
and prohibiting litigation of validity disputes constitutes a public
harm would undermine the entire idea of patent licensing. Id. at 11, 14, 17–18.
Commentators, such as Patently-O and FDA Law Blog, suggest that the Court’s decision in Actavis
will increase uncertainty for parties contemplating reverse-payment
settlements, as the opinion offers little guidance to indicate how the
“rule of reason” will actually apply to these settlements. Going
forward, those looking to enter into such agreements will likely want to
be extra cautious of the potential antitrust issues such settlements
implicate.
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