1. “[T]he specific restraint at issue has the ‘potential for genuine adverse effects on competition.’” Justice Breyer found that Solvay’s settlement with both of the initial filers of ANDAs removed the competitors with the most to gain and thus the greatest motivation to challenge the patents covering AndroGel®. Put another way, the Hatch-Waxman framework provides inducement for a patentee to pay an accused infringer to settle a patent infringement claim, something that almost never occurs outside of the pharmaceutical context.
2. “[T]hese anticompetitive consequences will at least sometimes prove unjustified.” The amount of the settlement or presence of consideration other delay of entry from the generic company—such as distributing the patented drug or providing marketing services—may suggest that a reverse payment settlement is not anticompetitive. But these facts would be considered as part of the “rule of reason” analysis
3. “[W]here a reverse payment threatens to work unjustified anticompetitive harm, the patentee likely possesses the power to bring that harm about in practice.” In other words, the patentee is willing and able to enter into a reverse payment because it is able to reap higher profits than would be possible with normal competition.
4. “An antitrust action is likely to prove more feasible administratively than the Eleventh Circuit believed.” There was significant concern regarding how courts applying a rule of reason analysis may have to delve into the strength of the asserted patents. Justice Breyer indicates that the size of the reverse payment settlement itself “may provide a workable surrogate for a patent’s weakness.”
5. “The fact that a large, unjustified reverse payment risks antitrust liability does not prevent litigating parties from settling their lawsuit.” Justice Breyer suggests that settlements can be reached that allow the generic company to enter the market before patent expiration without a reverse payment. But if a reverse payment is preferred by the parties, the courts should examine the reasons behind that preference.
These considerations led the majority to reject the “scope of the patent” test applied by the Eleventh Circuit.
However, the majority also rejected the FTC’s position that reverse payment settlements are presumptively unlawful. Justice Breyer explained that the likelihood of a reverse payment settlement leading to anticompetitive effects depends upon the amount of the settlement, its scale in relation to the patentee’s future litigation costs, whether the generic company is providing consideration other than delayed entry into the market in return for the payment, and any other convincing justification. Thus, the lower courts are left with—depending on your viewpoint—discretion to consider all the circumstances surrounding the settlement or little guidance to assess whether the settlement is anticompetitive.
The Chief Justice’s Dissent
Chief Justice Roberts, joined by Justices Scalia and Thomas, dissented, emphasizing that patents represent an exception to the antitrust law: “The point of patent law is to grant limited monopolies as a way of encouraging innovation.” Thus, reviewing the same case law as the majority, the Chief Justice came to the conclusion that the “scope of the patent” test is the proper test based on the existing precedent. The Chief Justice went on to criticize the analysis of the five considerations listed above as suggesting “a regime where courts ignore the patent, and simply conduct an antitrust analysis of the settlement without regard to the validity of the patent.”
The Chief Justice then went on to explain that exposing a patent settlement to an antitrust challenge would require the parties to relitigate the question of patent validity as a defense to the antitrust complaint. Such a process would create significant disincentives to reverse payment settlements and encourage pharmaceutical patentees to avoid settlements. That, leads to the ironic conclusion, as pointed out by the Chief Justice, that the Actavis decision may actually discourage generic drug companies from challenging pharmaceutical patents at all.
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