Showing posts with label Overbreadth. Show all posts
Showing posts with label Overbreadth. Show all posts

Tuesday, March 5, 2024

Obviousness Attack Succeeds: Overbreadth and Wilful Misleading Fail

Valley Blades Ltd v Usinage Pro-24 Inc (Nordik Blades) 2023 FC 1749 St-Louis J

2,856,940 2,965,426 2,992,233 / Segmented Snow Plow Blades

Valley Blades and Nordik Blades are direct competitors in the market for snowplow blades [206]. Valley Blades brought a declaratory action seeking to have Nordik’s 940 patent declared invalid, and Nordik responded with an action claiming that Valley Blades infringed Nordik’s 426 and 233 patents. The patents are all related — the 426 is a divisional of the 940 and the 233 is a divisional of the 426 [46] — and the actions were consolidated Patent [46]. The action was bifurcated and infringement was conceded [7].

St-Louis J found that all the asserted claims were obvious in a very straightforward decision which turned entirely on the facts [88]–[174]. Indeed, that part of the decision was so straightforward that I won’t bother to summarize it. This post will deal with the two other validity attacks, while a subsequent post will address the defendant’s claim under the Trademarks Act s 7(a) for damages for business lost as a result of demand letters sent by Nordik to Valley Blades’ clients.

Overbreath

The first of the other validity attacks was based on overbreadth. In a two part article I have argued that the overbreadth requirement is almost always redundant: Overbreadth in Canadian Patent Law, 33 IPJ 21 and 33 IPJ 147. But the FCA in Seedlings 2021 FCA 154 [50], held that overbreadth is indeed an independent ground of invalidity, and since then parties attacking the patent have been trying to find a way to use overbreadth to launch novel attacks on the patent, so far without success.

In this case, St-Louis J summarized the law of overbreadth as follows:

[175] The law of overbreadth is rooted in the patent bargain; an inventor shall not reap the benefits of an expanded monopoly without a corresponding sufficient disclosure to the public (Seedlings Life Science Ventures, LLC v Pfizer Canada ULC, 2020 FC 1 at para 167).

[178] To identify whether an element goes to the “core of the invention,” the Court ought to consider whether implementing the invention without those elements would require inventive ingenuity (Seedlings FCA at para 63).

This is a fair summary of those decisions, but it is also a fair summary of the sufficiency requirement.

On the facts, Valley Blades argued that the claims at issue were “broader than the invention actually made by [the inventor]. It argues this is because the tapered shape of the Nordik Blades’ blades is not claimed in any of the Disputed Claims” [180]. Valley Blades relied on the inventor’s evidence: “during his examination for discovery in July 2020, [the inventor] was clear that he considered the shape of the Nordik Blades’ blades to be a part of his purported invention” [181]. This passage suggests that Valley Blades was arguing that “the invention” is what the inventor subjectively believed the invention to be. This is an outlandish argument. In the first place, the inventor very often does not know their true invention, because the inventor is not always aware of the complete prior art and so is not necessarily aware of their true contribution. Second, even if the inventor did have a more advanced invention in their head, how can that invalidate the patent they actually were granted? If Sargon invented the wheel, but the idea of a spoked wheel passed through his mind, a patent on the wheel would still be valid. That would be true whether he thought of the spoked wheel either before or after he filed his application for the wheel. It would also be true if he had said to a friend, “My invention is the spoked wheel” after filing his patent; and the same would be true if he had said that before filing the patent.

In response Nordik argued that “nothing demonstrates that the tapered shape is an essential element for the invention to work as claimed in the Nordik Patents” [186]. This seems to be saying that the patent was not overbroad because the claimed invention had utility even without the tapered shape. On this view, overbreadth seems to be a lack of utility argument in a different guise, which, as I explain in my article, is often the case. St-Louis J accepted Nordik’s position, saying “when I factor in all the evidence, I am not convinced on balance that the blades’ tapered shape was an omitted essential element of the invention and that the claims are invalid for claiming more than the invention that was made” [188].

Section 53 Wilful misleading

Valley Blades argued that the patents were invalid for wilful misleading under s 53(1) because some statements in the specifications exaggerated the benefits of the invention [192]. St-Louis J had no difficulty dismissing this attack. She noted that the threshold for establishing wilful misleading is high, and “even assuming that Nordik Blades somehow exaggerated the blade movement, the system’s efficiency, and the blade’s wear-and-tear, I find nothing amounts to the required threshold for statements violating section 53" [197].

In making this argument, Valley Blades relied on Ratiopharm v Pfizer 2009 FC 711, which St-Louis J distinguished on the basis that “the misstatements referred to in Ratiopharm appear considerably more serious—particularly as they relate to pharmaceutical products—than what has been raised against Nordik Blades” [197]. I’d also point out that the FC decision in Ratiopharm is not good authority in any event. While the decision was affirmed on appeal, the s 53 analysis was not. In Ratiopharm 2010 FCA 204 noted that:

[34] Pfizer expressed concern that the trial judge’s determination pursuant to subsection 53(1) of the Act was based on an overly broad interpretation of that subsection. I am of the view that the determination is confined to the unique and particular circumstances of this matter. It has limited, if any, value as a precedent.

Monday, December 11, 2023

Redundancy between Overbreadth and Utility

NCS Multistage Inc v Kobold Corporation 2023 FC 1486 McVeigh J

2,693,676 / 2,820,652 / 2,738,907 / 2,766,026 / 2,820,704 (NCS) / 3,027,571 (Kobold)

My last post provided an overview of this decision and address several miscellaneous issues. This post addresses the overbreadth argument. McVeigh J held a number of claims of the 704 patent to be invalid for overbreadth. I have argued that overbreath in Canadian law is almost always redundant with some other ground of invalidity. In this case, McVeigh J held most of the overbroad claims to also be invalid for lack of utility, and I will argue that overbreadth was indeed redundant. The details are interesting to see how the two separate tests for overbreadth and utility ended up functionally converging, and to see why some claims were overbroad but nonetheless useful.

The key question on overbreadth is whether a feature of the invention is essential, not in the sense of claim construction, but “whether that feature is so key to the invention described in the disclosure that a Claim that omits it encompasses embodiments that were not contemplated in the disclosure”: Seedlings 2021 FCA 154 [54], quoted at [167]. McVeigh J summarized this as asking whether the whether the feature in question is “at the core of the invention actually invented or disclosed” [1458]. This strikes me as a good summary of Seedlings, which puts the question in a positive form. In utility, the question is whether the invention is useful, which in this case boiled down to whether it was operable, ie whether it worked. In principle, these are two distinct questions. But what does it mean to ask whether the feature lies “at the core of the invention”?

To see how McVeigh J answered this question, we need to turn to the facts. There were five features implicated in the overbreadth and utility attacks, namely three components of the fracturing valve — the wedge, plug, and seal — as well as the the alignment mechanism and the means for holding the mandrel stationary. We can ignore the wedge, as both attacks failed.

Seals

On overbreadth, McVeigh J held as follows:

[1467] The placement of the seals and the number of seals goes to the very core of the 704 Patent invention. The 704 Patent discloses a fracturing valve and both parties agree that the lower seal is essential to allow the fracturing valve to operate as disclosed. The 704 Patent does not disclose any method by which the invention could operate without the described lower seal placement. The lower seal is an essential element that goes to the very core of the invention.

The claims that did not specify a seal were therefore invalid for overbreadth [1470]. That means that those claims were overbroad because they were inoperable. The claims without seals were also invalid for lack of utility [1514] for the same reason: “There are no operable embodiments of the 704 Patent Claims that do not include a seal” [1511]. It is not just that the claims happened to be invalid on both grounds: they were invalid on both grounds for the same reason, namely inoperability. Thus overbreadth was functionally redundant in light of the utility requirement.

(Note that Claim 15 was listed as being invalid for overbreadth [1470] but not lack of utility [1514], but in light of McVeigh J’s reasoning, I think this must have been an inadvertent omission from the utility list.)

Equalization Valve or Plug

The equalization plug “goes to the very core of the invention, such that the fracturing valve cannot operate without an equalization plug” [1475]. Again, it is “core” because it is necessary for operability. Consequently, “those claims that do not explicitly claim an equalization plug are invalid for overbreadth” [1478]. Those claims were invalid for lack of utility for the same reason: “the 704 Patent Claims that do not claim an equalization plug cannot perform the claimed fracturing function; they will not operate” [1517]. Again, overbreadth and the lack of utility are functionally the same — both turn on inoperabilty — and the overbreadth attack is redundant.

Alignment Mechanism

Similarly, McVeigh J found that the alignment mechanism goes to the core of the invention because it was necessary for the tool to work [1483], and the claims at issue lacked utility for exactly the same reason [1520]. Again, overbreadth was functionally redundant.

(In the listing of invalid claims at [1486], [1521] claims 24–27 were listed as being invalid for overbreadth but not lack of utility. In light of the reasoning, this seems to have been an oversight.)

Stationary Mandrel

McVeigh J found that a component for holding the mandrel stationary was core to the invention because “there must be some kind of component that provides frictional resistance against the wellbore that allows the mandrel to remain stationary for the invention to operate” [1494]. Claims that did not specify a means for holding the mandrel stationary were therefore invalid for overbreadth [1495].

However, lack of utility was not proven:

[1525] There was insufficient evidence on this issue to demonstrate that the 704 Patent will not work where the mandrel is not held stationary. This is likely due to the fact that Kobold raised this issue in construction and it was not argued substantively by either party in closing.

[1526] Therefore, without more evidence on this specific issue, I find that Kobold has not met its burden to demonstrate inutility on this issue.

So, in discussing overbreadth, McVeigh J found that the tool would not operate if the mandrel was not held stationary, but in discussing utility she could not arrive at that conclusion on the evidence. It is not clear to me why the evidence that McVeigh J relied on in the overbreadth context did not allow her to come to the same conclusion in respect of lack of utility. Nonetheless, it is clear that the functional question was the same under both overbreadth and utility — would the invention work if the mandrel was not held stationary — and the only difference was in respect of the evidence.

In summary, notwithstanding that McVeigh applied separate analyses with separate tests for overbreadth and utility, overbreadth is functionally redundant in light of the utility requirement. I would expect similar results in contexts where there is overlap with novelty or anticipation: eg it seems very reasonable to say that a feature that is the only point of distinction between the prior art and the claimed invention would be considered “core” to the invention.

Thursday, September 28, 2023

Another Failed Attempt to Give Independent Meaning to Overbreadth

GreenBlue Urban North America Inc v DeepRoot Green Infrastructure, LLC 2023 FCA 184 Gleason JA: Woods, Mactavish JJA varg 2021 FC 501 McDonald J

2,552,348 / 2,829,599 / Integrated Tree Root and Storm Water System

DeepRoot’s 348 and 599 patents relate to a landscaping system to promote healthy urban trees using a subsurface structural cell system that supports the hardscape (eg sidewalk and paving). At trial, McDonald J held DeepRoot’s patents to be valid and infringed, in a straightforward decision which turned on the facts: see here.

At trial, GreenBlue argued that the patents were overbroad. This argument was dismissed by McDonald J on the facts after a brief discussion [FC 255]–[261]. The FCA decision further illuminates the nature of the argument (my emphasis):

[65] Finally, with respect to overbreadth, GreenBlue asks us to reach a different conclusion from the Federal Court and to find that metal rods, which were not claimed in the two Patents, are essential for the invention to work.

[66] This submission is premised on the assertion that the evidence established that without the metal rods, the invention would not function. In support of this contention, GreenBlue relies on the fact that the load testing report related to DeepRoot’s final commercial product showed that the product failed without the inclusion of the metal rods attached to the lid.

The FCA dismissed the appeal on this point on the straightforward basis that there was evidence to support McDonald J’s finding on the facts [69].

Of more general interest, this is another failed attempt to give some independent content to the concept of overbreadth. In Seedlings 2021 FCA 154, the FCA affirmed that “overbreadth is a distinct ground of invalidity that must be considered separately” [50]: see here. Ever since then, parties attacking a patent have been trying to give some content to overbreadth as a distinct ground of invalidity, largely without success. (The closest thing to success was in Rovi Guides v BCE Inc 2022 FC 1388: see here.) In this case, we see another failed attempt. This kind of argument would traditionally have been framed as inoperability, which is to say lack of utility. No doubt it would have failed if framed that way as well.

Monday, May 22, 2023

Sufficiency, Overbreadth, or Utility?

Eli Lilly Canada Inc v Teva Canada Limited 2022 FC 1398 St-Louis J

2,226,784 / tadalafil / CIALIS / NOC

I’m back to blogging again after an end of term vacation—still catching up on the backlog from my longer hiatus over the winter. In my last post on this case I discussed the meaning of “or”. This post turns to validity. St-Louis J held the 784 patent to be invalid for overbreadth [120] and insufficiency [149], while declining to address utility. I have argued that overbreadth is almost always functionally duplicative of another established ground of invalidity, and this case illustrates that point once again, as the facts supporting the finding of overbreadth were the same as those supporting insufficiency.

The facts are reasonably straightforward. The 784 patent relates to the use of tadalafil for the treatment of ED. Claim 2, which is representative for present purposes, is to a pharmaceutical composition for the treatment of ED in a male animal, comprising “[tadalafil] or a physiologically acceptable salt or solvate thereof.” All asserted claims include the phrase “or a physiologically acceptable salt.”

St-Louis J found on the facts that it is not possible to make a physiologically acceptable salt of tadalafil [118]. Tadalafil does not have an ionisable functional group and consequently it is very difficult to make a salt form [103]. It may be possible to make one or two salts, but only under extreme conditions that would result in the degradation of the tadalafil such that the resultant salt would not be sufficiently pure and stable to be considered physiologically acceptable [118]. As a result, St-Louis J held the 784 patent to be invalid for overbreadth [120] and insufficiency [149], while declining to address utility.

As discussed in my last post, St-Louis J concluded that a physiologically acceptable salt is an essential element of the claim. While I have my doubts about that conclusion, once we accept that, the claim is effectively to a physiologically acceptable salt of tadalafil, and insufficiency then follows directly from the fact that it is not possible to make even one physiologically acceptable salt. This is the classic “how to make” variety of sufficiency. If you claim “Compound X” you have to tell a skilled person how to make Compound X, or the claim is invalid for insufficiency. The traditional view is that the purpose of the disclosure is to ensure that the public would have benefit of the invention after the term expired: see eg Minerals Separation [1947] ExCR 306, 316. If a skilled person cannot make the claimed compound with the guidance provided by the specification, the patentee could get the benefit of patent protection during the term, while keeping its monopoly through secrecy after the term expired. There is an extremely difficult question as to whether the invention has to be enabled across the full scope of the claim. But that doesn’t concern us here, as the specification did not provide sufficient instruction to allow a skilled person to make any physiologically acceptable salt.

A standard statement of the sufficiency requirement is that the specification must enable the skilled person to practice “the invention” [133]; citing s 27(3) and Teva 2012 SCC 60 [51]. But what is “the invention”? That term is notoriously ambiguous: “The word ‘invention’ has many meanings and nuances,” as Henderson pointed out in Patent Law of Canada (1994) 7–8. It can mean the inventive concept, which is to say the information disclosed in the patent which is the quid pro quo for the grant; it can means the invention as claimed, which is the set of all existing or future embodiments of the claimed invention; or it can mean a particular embodiment: see British United Shoe Machinery Co Ltd v A Fussell & Sons Ltd (1908) 25 RPC 631 (CA) 649–51. This led to a debate in this case in which Lilly argued that insufficiency was not available as an attack because the Defendants had not established the nature of the invention [139]. Lilly’s argument isn’t fleshed out in enough in St-Louis J’s decision for me to fully understand it, but I suspect the point is that the inventive concept was the discovery that tadalafil is an effective treatment for ED, and not the discovery of how to make a salt form of a compound that was already known to be effective. If that is indeed what Lilly was arguing, it is effectively another angle on the “or” argument, and one which, in my view, is better framed in terms of claim construction (as discussed in my last post) rather than sufficiency. So, given St-Louis J’s conclusion on the meaning of “or”, I would say she was right to reject Lilly’s argument on this point [143], to focus on whether the specification instructed how to make the salt [144]–[148]. And since the answer to that on the facts is “no,” I agree with her conclusion that the patent is invalid for insufficiency [149] (given her conclusion on the construction of “or”).

With all that said, the ambiguity as to the meaning of “the invention” made this part of the decision more convoluted that it needed to be. Given the ambiguity of the phrase “the invention, I suggest it might be desirable for the courts to simply stop using it altogether, in any context in which precision is necessary—which is to say, especially in defining validity doctrine. Instead, the law should specify “the invention as claimed” or “an embodiment of the invention,” or “the inventive concept,” as appropriate to the particular doctrine. That is a clarification that would probably have to be done by the FCA, since many authoritative statements of the law use the ambiguous term “invention.”

On that note, I would also point out that the law of sufficient disclosure has several threads that need to be disentangled, and the meaning of “the invention” isn’t necessarily the same for each aspect of the disclosure requirement. The SCC in Consolboard [1981] 1 SCR 504, 518, noted that the statutory provision, s 27(3) “gives the impression of a mélange of ideas gathered at random rather than an attempt to enunciate, clearly and concisely, a governing principle or principles.” While the Court in Consolboard at 518 suggested that the haphazard nature of the statutory provision might be the product of amendment over a period of many years, I think the truth is that the case law gives a similar impression of a mélange of ideas. This is illustrated by Thorson P’s well-known summary of the disclosure requirement established by the case law in Minerals Separation [1947] ExCR 306, 316–17. I won’t repeat it here, but it is plain on its face that it runs together several concepts that are sometimes only tangentially related.

Moving on, St-Louis J also held the asserted claims to be invalid for overbreadth:

[120] As I conclude that it is more probable than not that physiologically acceptable salts of tadalafil cannot be made I conclude, as the Defendants argue, that such a salt was not invented. The Asserted Claims therefore claim broader than what was invented and are thus invalid for overbreadth.

In my article Overbreadth in Canadian Patent Law: Part I (2020) 33 IPJ 21 and Part II (2021) 33 IPJ 147, I argued that a finding of invalidity for overbreath is almost always redundant with another established ground of invalidity. And so it is here. All the evidence St-Louis J reviewed in the context of overbreadth went to the question of whether went to whether a physiologically acceptable salt could be made [114]–[119]. Exactly the same facts that results in a finding of insufficiency—that the claim compound could not be made—was also the basis for the finding of overbreadth.

The problem with overbreadth is that it remains ill-defined. St-Louis J noted that “There are two (2) ways that a patent claim can fail for overbreadth (or overclaiming): it can be broader than the invention disclosed in the specification, or it can be broader than the invention made by the inventor” [109]. It seems that in this case she was relying on the second prong, as she noted that

Under the claims broader than invention made, it is a question of fact as to what the inventor actually invented [112].

But what does “actually invented” mean? As I argued in my Overbreadth article, if the patentee has sufficiency disclosed and claimed subject-matter that is new, useful and non-obvious, how could it be said that they had not “invented” the claimed subject-matter? Overbreadth has an air of being something distinct only because of the ambiguity in the phrase “the invention.” It sound very reasonable to say that the patentee cannot claim more than it invented, but if we try to define exactly what is meant by “invention,” it is difficult to give this proposition any content that is independent of the standard grounds of invalidity.

In any event, as noted, this is another case in which overbreadth is redundant as turning on the same analysis as another ground of invalidity, in this case insufficiency.

The third issue is as to utility. The utility argument turned entirely on the point that a physiologically acceptable salt could not be made: the Defendants argued that “the failure of the 784 Patent to indicate which of the many possible salts can be made as a physiologically acceptable salt of tadalafil” renders the asserted claims invalid for a lack of utility [154], while Lilly argued that “the Defendants have not met their burden to establish that a physiologically acceptable salt of tadalafil cannot be made” [159]. That is, the argument was that the invention lacked utility because a physiologically acceptable salt could not be made; it really just recapitulated the sufficiency argument. To my mind, this conflates utility and sufficiency. (This is not a criticism of St-Louis J, as this is the way the case was argued.) I have to admit, this conflation is very common. There was really no distinction between the two in early English practice, before the development of claims; if the specification describes a device that is not operable, there is no distinction to be made between a case where the patentee had devised a useful invention but failed to disclose it and a case where the specification disclosed the invention precisely, and the invention itself was useless, unless recourse is had to extrinsic evidence.

But with the advent of claims, we can distinguish between the two. The utility requirement asks whether the claimed invention works (or can be soundly predicted to work). Sufficiency asks whether the claimed invention can be made. These are different. Suppose, for example, that in the early days of genetic engineering, the patentee claims “Pure human insulin.” The claimed subject-matter, pure human insulin, is undoubtedly very useful. If the patentee cannot actually make it, the patent is invalid for insufficiency, but not for lack of utility. On the other hand, it may be easy to make something that lacks utility. If the patent claims “Oregano oil for the treatment of cancer,” the claim is sufficient, because oregano oil can be made and administered with the intent of treating cancer, but invalid for lack of utility because oregano oil does not in fact treat cancer. Applications for impossible inventions, like a perpetual motion machine, are traditionally rejected for both lack of utility and insufficiency; in my view, they should be rejected for insufficiency alone. After all, a device with greater power output than input would be extraordinarily useful—if it is could be built. With all that said, I acknowledge that there is a lot of confusion in the caselaw on this issue, stemming ultimately, in my view, from the fact that the distinction could not be drawn prior to the introduction of claims.

Ultimately, St-Louis J, wisely, in my view, declined to address the utility argument. The Defendants argued that”a claim must fail if, in addition to claiming something that is useful, it also claims something that is useless” [173]. In other words, the question is whether utility has to be established across the full scope of the claim. St-Louis J reviewed the caselaw and noted the uncertainty on the question of whether a claim is invalid if it claims a single inoperable species [175]–[178]. Given that she had already held the asserted claims invalid on two other grounds, she refrained from deciding this point of law, and so she declined to rule on the utility ground [178]. This is a difficult question, which is better left to a case in which it is the focus of the argument.

Thursday, November 24, 2022

A (Kind Of) Successful Overbreadth Attack

Rovi Guides, Inc v BCE Inc 2022 FC 1388 Lafrenière J

2,336,870 / 2,339,629 / 2,425,482 / 2,514,585 / Interactive Television Program Guide / Internet Protocol Television

As discussed in my last post, in this decision Lafrenière J held that all of the asserted claims of Rovi’s patents were invalid for anticipation and / or obviousness. The last post focused on remedial issues. This post discusses overbreadth.

As Lafrenière J put it, “A claim is overly broad and invalid if it asserts ‘exclusive property or privilege in something the inventor did not actually invent’” [298]. In my articles on Overbreadth in Canadian Patent Law (2020) 33 IPJ 21 and (2021) 33 IPJ 147, I showed that overbreadth is functionally redundant in almost all cases in which it is invoked; that is, in almost all cases, the factual basis and reasoning leading to a finding of invalidity for overbreadth is exactly the same factual basis and reasoning leading to a finding of invalidity on some other standard ground, such as anticipation: see eg BVD v Canadian Celanese [1937] SCR 221. (The historical exception is Amfac (1986) 12 CPR(3d) 193 (FCA), which I argued was wrongly decided.)

Now, even though overbreadth is functionally redundant in almost all cases, that does not mean it is necessarily functionally redundant all cases; so, in my article I gave the example of the ‘roads to Brighton’ problem in which overbreadth might in principle play an independent role. In Seedlings 2021 FCA 154 [50] the FCA held that “overbreadth remains a proper ground of invalidity,” but at the same time Locke JA acknowledged that “the overlap with other grounds of invalidity makes it difficult to define circumstances in which a patent claim would be invalid for overbreadth but not also invalid on other grounds” [52]. Since Seedlings, parties attacking a patent have attempted to give some independent force to an overbreadth attack, so far without success.

In this case the defendants made overbreadth attacks on two patents, one of which failed and one of which succeeded, albeit in obiter.

The overbreadth attack on the 870 patent was novel. The factual basis for the Defendants’ attack was that the 870 patent claims priority from US provisional application 60/092,807 (the ‘807 Application’). One of the inventors of the 870 patent admitted that “the invention he made in July 1998 was limited to that which he described in the 807 Application” [300]. It was undisputed that the matter disclosed in the 807 Application has very limited overlap with the 870 patent: [301]–[302]. What the inventors claimed in the 870 Patent was therefore significantly broader than the 807 Application, and the Defendants argued that the 870 Claims are invalid on that basis [303].

Lafrenière J rejected this; he agreed with Rovi that “the ‘invention made’ is to be determined as of the filing date, not the priority date” [304]. This must be right, or overbreadth would swallow the claim date rules. The claim date is the filing date unless priority is claimed to a prior application “disclosing the subject-matter defined by the claim”: s 28.1(1)(a)(i),(ii). If the subject-matter disclosed by the application as filed is broader than that in the priority document, the only consequence is that priority cannot be claimed. And that is on a claim by claim basis, as the term “claim date” indicates. Claims that are directed to subject-matter that was disclosed in the priority document can still claim priority. To invalidate the entire patent would upend that well-established system.

The overbreadth attack on the 482 patent was different in nature. The 482 patent relates to a system and method for automatic retrieval of on-demand media data so as to avoid interruption to prevent unacceptable delays in the display of the video-on-demand listings during periods of higher traffic or low bandwidth connections. Lafrenière J rejected a construction which would have included “manual only” retrieval of on-demand data, but nonetheless considered and accepted the Defendants’ argument that if the 482 claims covered manual retrieval, they would be overbroad: [556]–[563].

On the claim construction point, as I understand it, Rovi wanted to argue that the claims included user-initiated download of on-demand data, presumably to bolster their infringement argument: see [562]. The claim at issue expressly requires “automatically retrieving” the on-demand data [473]–[474], and Rovi’s expert had admitted that user initiated retrieval was not automatic retrieval [500]. So, the argument that the patent covered manual retrieval was a complete dud. This makes it a bit difficult to grasp the overbreadth argument, since the premise that the claim encompasses manual retrieval is without foundation.

Lafrenière J’s discussion was understandably brief, given his holding on claim construction. Much of his discussion reviewed the evidence to the effect that the patent was entirely addressed to technology using automatic retrieval, which is of course consistent with Lafrenière J’s finding on claim construction. Manual retrieval simply was not addressed.

With this background, the key discussion was that

[561] I agree with [the Defendants’ expert] that the Skilled Person would understand that the invention described in the 482 Patent requires “automatically retrieving” at least some of the on-demand media data without a user indication to access it because “manual only retrieving” the on-demand media data causes the very undesirable consequences that the 482 Patent seeks to avoid.

[563] Dr. Robinson’s uncontested evidence is that there is no disclosure in the 482 Patent about manually retrieving on-demand media data. Therefore, to the extent such a claim is made in the 482 Patent, the claim is broader than any invention disclosed.

So, the gist of it seems to be that the 482 patent made no mention of manual downloading, so if it had claimed manual downloading, it would have been overbroad, in much the same way as the 482 patent would have been overbroad had it claimed a compound that cures cancer on the basis of a description focusing entirely on interactive television guide technology.

More broadly, a claim is overbroad if it claims subject-matter that is entirely unrelated to the disclosure. That seems reasonable enough, but the question is whether this raises overbreadth as an independent ground of invalidity. I suspect that in the vast majority of cases, a patent that claims subject-matter unrelated to the disclosure would be invalid for insufficiency. Put another way, is it possible for a patent to have claim to subject-matter that is entirely unrelated to the disclosure, in which the claim is nonetheless not invalid on any traditional ground? What if the 482 patent in this case had omitted the word “automatically” in the claim, and it was held that the claim, properly construed, encompassed manual retrieval. Suppose also that automatic retrieval was technically difficult, and the disclosure exclusively addressed automatic disclosure without mentioning manual retrieval; but at the same time, manual retrieval was not technically difficult and could easily be implemented by a skilled person in light of their common general knowledge. Would that patent be invalid simply on the basis the description did not mention manual downloading ie even if manual downloading was novel and non-obvious? I’m not sure.

My sense is that the success of the overbreadth argument in this case turned on the fact that it was premised on a claim construction that had no foundation in the patent. This makes it difficult to draw broader lessons from the analysis. It’s not very surprising that if we give a claim a construction that has no basis in the patent, the claim will be invalid in light of that patent. I doubt that observation is going to generate any independent role for overbreadth in the context of a properly construed claim.

Thursday, August 18, 2022

What Is the Date for Assessing Sufficiency?

Pharmascience Inc v Bristol-Myers Squibb Canada Co 2022 FCA 142 Locke JA: de Montigny, Monaghan JJA affg 2021 FC 1 Zinn J FC Selection

2,461,202 / 2,791,171 / apixaban / ELIQUIS

My previous post addressed issues of selection patents raised by this decision. This post discusses the insufficiency attack on the 202 patent, and concludes with a brief discussion of the 171 patent, which reveals another failed attempt to give independent effect to overbreadth as a ground of attack. As described in my last post, the patents in suit relate to the anticoagulant compound apixaban which is used in treating thromboembolic disorders, including stroke. The 202 patent claims the compound apixaban as such, as well as its use in the treatment of thromboembolic disorders [4]. The 171 patent claims various formulations of apixaban. Only validity was at issue.

Insufficiency attack on the 202 patent

Pharmascience argued that the 202 patent was invalid for insufficiency because it did not indicate that the focus of the invention was apixaban at either the filing date or the publication date [22]. Apixaban was merely one of hundreds of examples, and the claims focusing on it were not introduced until shortly before the patent issued [22].

The answer to this argument is that it is the validity of the granted patent that must be considered. Saying that validity on one ground or the other is assessed as of a particular date does not change that. So, when we say that the claims must be novel as of the claim date, we do not mean that the claims as they existed at that date must be novel, but rather that the claims in the granted patent must claim subject-matter that was novel as of the claim date [31]. The same applies to sufficiency: it is the specification of the issued patent that must adequately disclose the invention [32]–[33]. If we say that sufficiency is assessed as of the filing date (of which, more below), that means that the specification as granted must enable a person skilled in art to make the invention in light of their common general knowledge as of the filing date.

Consequently, this point should have been framed as an added matter objection: “[t]he real debate here should be whether the addition of claims specific to apixaban introduced new matter to the specification of the 202 Patent that could not reasonably be inferred from the application as filed” [37]. It was problematic to raise this on appeal without having raised it at trial [37], but in any event, Locke JA noted that an added matter objection probably could not be sustained, as apixaban was specifically described in Example 18 and that would seem sufficient to support the introduction of claims thereto [37].

That all makes sense. But the decision also has a relatively lengthy discussion of the appropriate date for assessing sufficiency. Pharmascience relied on the decision of Hughes J in Zoledronate 2013 FC 283 [179]–[188], which implied that the correct date is the publication date [23]. Locke JA discounted the Zoledronate decision for various reasons (eg the discussion was obiter), without actually saying it was wrong and without specifically stating the law as to the appropriate date for assessing sufficiency [26]–[28]. For example, Locke JA noted that Hughes J did not address the view expressed by MacKay J in Merck v Apotex 59 CPR(3d) 133 (FCTD) that the date of issue is the appropriate date for assessing insufficiency [28], but only by way of indicating that Hughes J’s analysis was incomplete.

This seems a bit strange because, as indicated in my post on Zinn J’s decision, I thought the point was settled in Idenix v Gilead 2017 FCA 161 [46] affg 2015 FC 1156. In that case, the patentee, Idenix, had not actually synthesized any of the claimed compound as of the filing date: see here. Gilead, therefore, made a classic “how to make” insufficiency argument, and Annis J held that the disclosure was not sufficient to allow a skilled person to synthesize the compounds, and held the patent invalid for that reason. This was even though, by the time of trial, the claimed compound could be synthesized by three different pathways [FCA 46]. I’ve taken a look through Annis J’s (very long) decision, and it is not clear to me what date he took to be the appropriate date; the focus of the discussion is on showing that “retrosynthetic analysis”, based on the specification plus routine experimentation, was not sufficient to enable a skilled person to make the claimed compounds. The first public disclosure of how to make the compounds was in January 2005 [FC 501], so the patent would have been sufficient as of that date, at least if the skilled person were taken to be aware of that public disclosure. The 191 patent at issue had a filing date of June 2003 and a publication date of January 2004, so the patent would have been insufficient as of those dates, but sufficient as of the date of issue. This implies that we can at least rule out the date of issue as the appropriate date for assessing sufficiency.

The FCA affirmed the finding of insufficiency saying:

[46] Though reversed on other points, this Court held in [Viagra] 2010 FCA 242 at paragraph 79. . . that courts must “determine whether the disclosure was sufficient as of the date of filing. As a result, anything which occurred subsequent thereto is of no relevance.” In my view, Idenix’s argument reflects the benefit of hindsight rather than the knowledge of the skilled person at the relevant date.

This clearly indicates that the appropriate date is the filing date, though the result is consistent with using the publication date.

I find it peculiar that, in this case, Locke JA did not mention the FCA decisions in either Idenix or Viagra. It is true that neither of those cases analyzes the issue—the statements of the appropriate date are conclusory—while the FC decisions of MacKay J Merck v Apotex and Hughes J in Zoledronate do have an extended discussion. But still, the express statements by the FCA are directly on point, even if not fully reasoned.

I suspect Locke JA chose to avoid Idenix or Viagra because their endorsement of the filing date sits uneasily with his response to Pharmascience’s argument:

[33] [Pharmascience] notes that subsection 27(3) identifies the requirements of the “specification”, and argues that subsection 27(2) indicates that it is the specification as filed that must meet those requirements. However, such an argument does not withstand scrutiny. Firstly, it would effectively read out subsection 27(6), which contemplates amendments to bring the application into compliance with the sufficiency requirements. Secondly, a similar argument would seem to apply to the requirements for novelty (the opposite of anticipation) and inventiveness (the opposite of obviousness). Sections 28.2 and 28.3, which address these issues, both refer to requirements for “[t]he subject-matter defined by a claim in an application for a patent.” PMS’s focus on the specification as filed for determining sufficiency would also imply a focus on the claims as filed for anticipation and obviousness, since the relevant provisions mention “a claim in an application”. I can see no reason that the approach that PMS urges for sufficiency would not apply similarly to anticipation and obviousness.

I’ll take the second point first. It is perfectly clear that novelty and inventiveness are assessed as of the claim date. But it is the claims as granted that must have been new and inventive as of the claim date; there is no requirement that the claims as they existed as of the claim date must be new and inventive. The same point applies to sufficiency. The specification as granted (including any amendments as per 27(6)) must have been sufficient at the relevant time (whenever that is). That means that in assessing the sufficiency of the specification as granted, we must consider whether it would have allowed the skilled person to practice the invention at the relevant date, without the assistance of new techniques or knowledge that emerged after that date. Turning to the first point, saying that the relevant date for sufficiency is the filing date does not read out 27(6). To say that the relevant date is the filing date does not mean that it is the specification as it existed as of that date that must be sufficient, just as saying that the relevant date for utility is the filing date does not mean that it is the claims as they existed at that date that must claim useful subject-matter. It simply means that in assessing the sufficiency of the specification as granted, common general knowledge arising after the filing date cannot be taken into account. (I note also that while 27(6) permits amendments, that is subject to 38.2, which only permits the addition of matter that can reasonably be inferred from the specification as filed. Consequently, I suspect it would be difficult, and perhaps impossible, to amend a specification that is insufficient as of the filing date so as to render it sufficient at some subsequent date. But that is an aside.) So, the fact that claims can change post-filing does not mean that the relevant date for assessing novelty is post-filing; similarly, the fact that the specification may be amended post-filing does not mean that the relevant date for assessing sufficiency is not the filing date.

At the end of the day, I’m inclined to think that the appropriate date for assessing sufficiency is indeed the filing date. But I suppose the fact that the FCA in this case ignored Idenix and Viagra means that the point should now be considered open.

171 patent

The 171 patent relates to a formulation of apixaban with, inter alia, a specified particular size. Locke JA affirmed Zinn J’s holding on the facts that it was not obvious-to-try [39]–[59]. Pharmascience also argued that the patent was invalid for ambiguity on the basis that the method for determining particle size was not specified, and different methods could give different results. Locke JA dismissed this argument, pointing out that the specification did describe a particular measuring method and a skilled person would understand this to be the method to use [66].

Finally, Pharmascience made an overbreadth attack. In Seedlings 2021 FCA 154 (blogged here) the FCA affirmed that “overbreadth remains a proper ground of invalidity” [50]. Consequently, we are now seeing overbreadth raised regularly as a ground of invalidity. But parties attacking the validity of a patent have struggled to find an approach to overbreadth which gives it any independent force. This case is another example. Locke JA remarked that “The nature of [Pharmascience’s] argument on overbreadth of the 171 Patent is not entirely clear” [69]—which is not entirely surprising, given that the concept of overbreadth itself is not clear. In any event, Locke JA’s discussion was brief, so I’ll just note that Locke JA, after dismissing it on the facts, indicated that the attack “would seem to relate to the sufficiency of the 171 Patent, rather than overbreadth” [71]. Another attempt to give some effect to overbreadth as an independent ground of invalidity has failed.

UPDATE: see my follow-up post on the date for assessing sufficiency.

Monday, July 4, 2022

Accounting Denied

Rovi Guides Inc v Videotron Ltd 2022 FC 874 Lafrenière J

2,337,061 / 2,339,629 / 2,730,344 / 2,336,870

In this decision Lafrenière J held all the asserted claims of Rovi’s patents to be invalid as being anticipated and/or obvious [7] for reasons that turned entirely on the facts. Some of the claims would have been infringed had they been valid. The most interesting aspects of the decision related to remedies, and in particular the question of whether Rovi was entitled to an accounting and his assessment of a reasonable royalty. Lafrenière J’s analysis of these issues strikes me as being entirely sound and a very helpful development of the law.

The patented inventions relate generally to “interactive television program guides” [IPG]—the familiar interactive menus used to select current and upcoming programs. Television listings were originally provided in paper, then in a non-interactive linear scrolling on screen guide [9]–[16]. Interactive guides, as the name suggests, allow the user to scroll through the menu in the way that is familiar to all of us today. Rovi’s patents, which date from the late 1990s, were directed to high-level concepts. For example the 061 claims “focus on a user using a device located outside the home, such as a laptop or smartphone, with a limited IPG to schedule a recording on a device inside the user’s home” [303]. “According to Rovi, there is no pay-TV provider ‘anywhere in the world’ with an IPG who does not need a license from Rovi to operate” [552].

The defendant Videotron is a cable TV service provided operating primarily in Quebec [25]. Videotron initially took a licence from Rovi, effective April 2010 [564], primarily to avoid litigation risk [369], but declined to renew the licence, which expired in 2016, considering that there was little value in the increasingly obsolete portfolio [577], [579].

Most of this long decision is devoted to the details of the prior art and the asserted technology, but in broad terms, it was perfectly clear to everyone in the field that interactive program guides were the future, and development was limited primarily by limitations on bandwidth and hardware [154]. The 1990s were “a period of great innovation in the field of interactive digital audio-visual applications and services” [316] and the kind of conceptual innovations reflected in Rovi’s patents were natural developments as the field responded to consumer demand and improvements in bandwidth and other hardware; consequently, the claimed invention had already been proposed by others, or were obvious extensions of existing technologies. That’s all I’ll say about anticipation and obviousness, which were the main substantive issues.

Overbreadth

Before turning to remedies, I’ll note that Videotron tried yet another variant of the overbreadth argument which was really an (unsuccessful) added matter argument. Videotron produced the file history of the 870 patent which showed that hundreds of claims had been added. Videotron argued that “the inventors were not consulted about the amendments and that the 870C Claims are not described in the disclosure,” and “[a]ccording to Videotron, this raises an issue whether the claims are broader than the invention made or disclosed” [364]. Lafrenière J held that even if the inventors had nothing to do with the application after it was filed “a claim is not invalid simply because it was added without the involvement of the inventor after a patent application is filed” [369]. Even though s 38.2 was not mentioned in the decision, this was really an added matter argument, and Lafrenière J’s conclusion is consistent with O'Reilly J’s holding in Western Oilfield 2019 FC 1606 [236] that “the factual circumstances surrounding the amendments were not relevant to this issue. It is a matter of logic, not fact, whether the amendments are reasonably inferable.” Perhaps Videotron characterized the issue as being one of overbreadth rather than added matter in an attempt to avoid this rule. In any event, this represents another failed attempt at giving independent effect to overbreadth as a ground of invalidity.

Remedies

The most interesting part of the case is Lafrenière J’s discussion of remedies; while the issue was moot, given his holding on the merits, he discussed it for the sake of completeness [544]. The first issue was whether Rovi should be permitted to elect an accounting, or should rather be restricted to damages, in this case a reasonable royalty. While it is very well established that an accounting is a discretionary remedy, there isn’t a lot of jurisprudence on when an accounting should be granted in the patent context that goes beyond the accepted general rules of equity, such as laches or bad faith. It is usually desirable that the law develop incrementally, and it is convenient that Lafrenière J’s holding on the merits allowed him to discuss the issue in some detail, in obiter, in the context of a tricky case.

By way of background, the product at issue is a ‘complex product’ in the sense that the patented technology contributes only a relatively small part of the value of the product embodying the technology. This is opposed to a product, like pharmaceuticals, which are not simple in a technical sense, but rather in the sense that the patented technology accounts for a large part of the value of the product in which it is embodied. Complex products raise some special challenges in terms of remedies, as discussed in Biddle et al (eds), Patent Remedies and Complex Products: Towards a Global Consensus (Cambridge University Press, 2019) (open access).

Rovi provides products, such as the supply of IPG software and program data [549], and Rovi and its predecessors made very significant investments and contribution to the relevant technology over the years [21], [23]. Rovi also provides licensing services, “allowing customers to license patents that they own” [549]. This evidently includes licensing by customers, such as Videotron, who do not use Rovi’s products. Rovi significantly grew its patent licensing business from 2003 to 2013 [549]. Rovi’s business model is to licence its entire portfolio at a rate that does not vary based on the number of patents that Rovi has or the licensee practices. [550]

Rovi and Videotron initially entered into a 5 year licence agreement in 2010 [564]. Videotron’s primary motivation for entering into this agreement was reduction of litigation risk—“Videotron did not want patent issues, including the threat of an injunction, to distract the company from completing its important project” [567]. Videotron did not consider the market value of different features covered by the patents in the Rovi portfolio: “freedom from suit was the primary motivating factor that led Videotron to accept to pay the royalty rates that were ultimately negotiated, and not the value of any particular patents in Rovi’s portfolio” [568].

When Rovi and Videotron entered into renewal negotiations prior to the expiry of the licence agreement, Rovi wanted to nearly double the royalty rate [572]. Videotron asked for a one-year extension to allow it to assess the value of the licensed technology [572]. Videotron repeatedly asked Rovi “to identify those patents Rovi considered to have particular value to Videotron and that were specific to its platform,” but never received a satisfactory answer [575]. Videotron therefore “declined to enter into another long-term licence for what appeared to be aging patents taken from an increasingly obsolete IPG patent portfolio” [576]. In the end, Videotron was licensed through 2016.

It was against this background that Lafrenière J addressed the question of whether Rovi should be allowed to elect an accounting. There’s a bit of schizophrenia in the law relating to the patentee’s election of an accounting. It is perfectly clear that a patentee does not have a right to an accounting for profits [580] and it is true that in principle “the patentee bears the burden of proving their entitlement to an accounting of profits” [581]. But on the other hand, as Lafrenière J noted, “the Court should not decline to exercise its discretion to award an accounting of profits to a party in the absence of any compelling reasons of doing so” [580]. For this point Lafrenière J cited Philip Morris 2016 FCA 55 ¶ 8, a trademark case, which in turn cited Apotex v Bristol-Myers Squibb 2003 FCA 263, a patent case, which noted that although equitable remedies, such as an accounting, cannot be elected as of right “a discretionary remedy is not an arbitrary remedy. In the absence of proof of a bar to equitable relief, a claimant can expect to be granted the remedy it seeks in accordance with the principles governing its availability.” In practice, in a standard patent case, such as an innovator pharmaceutical company bringing an action against a generic, the successful patentee will normally be allowed to elect an accounting, subject to any traditional equitable bar (though even then there are a few cases idiosyncratically denying an accounting). In non-standard cases, the equitable analysis comes more to the fore. There is no doubt the traditional equitable considerations of laches or bad faith are applicable, but these have traditionally had a fairly high bar. But equity does allow for flexibility both in the application of traditional criteria and in developing new criteria.

In this case, Lafrenière J applied a four-factor analysis, drawn from Apotex v Bristol-Myers Squibb 2003 FCA 263 [15] (reformatted for clarity):

[581] These factors include:

(i) whether there has been undue delay in commencing or prosecuting the litigation;

(ii) the patentee’s conduct;

(iii) the infringer’s conduct;

(iv) whether the patentee practiced the invention of the patent in Canada; and

(v) complexity of calculating an accounting of profits.

The first three factors are related to the traditional grounds of laches or bad faith, though perhaps more broadly interpreted, while the last two are more specific to patents and the remedy of an accounting. I should note that neither the FCA in Apotex v Bristol-Myers Squibb nor Lafrenière J in this case suggested that these considerations are exhaustive.

(a) undue delay

There was no suggestion of undue delay by Rovi in commencing litigation [583]–[584], though there was delay by Rovi in prosecuting its patents, which Lafrenière J discussed under the next heading.

(b) Rovi’s conduct

Rovi’s conduct was an important factor in Lafrenière J’s decision to refuse to allow an election of an accounting:

[587] the evidence before me establishes that Rovi has a reputation of using hard-ball legal tactics to pressure third parties to license its patent portfolio. Rovi was known for its business model of aggregating patent portfolios, seeking licences, and relying on its prior licences and aggressive use of litigation to drive risk-avoiding businesses into deals that are consistent with its schedule of royalty fees. It would spend in the tens of millions of dollars annually on patent litigation.

Playing “hard-ball” is not close to the kind of bad faith conduct by the plaintiff that is more traditionally invoked in equity; this is perhaps an illustration of interpreting a traditional equitable ground broadly in the context of an election of an accounting.

This is not a criticism. The broader point here is that if the parties negotiating this kind of licence know that a court would grant an accounting rather than a reasonable royalty, this gives additional leverage to the patentee in the negotiations. This makes it more likely that the royalty will reflect the value of avoiding litigation, rather than the value of the technology itself. This is undesirable. The point of patents is to provide an incentive to create valuable new inventions for the benefit of society, by providing a reward commensurate with the value of that technology. This gives the inventor high-powered incentives to develop technology that consumers actually want—the better the invention, the greater the reward. Giving the patentee a reward that reflects the value of avoided litigation costs, rather than the value of the underlying technology, is therefore contrary to the purpose of patent law. So, as Professor Taylor put it, “reasonable royalties should reflect the value of patented technology rather than patent rights” (49 Ga Law Rev 79, 89, original emphasis); see also Ch 4 of Complex Products. The principle applies whether the reward is reflected in a legal remedy, such as a reasonable royalty, or is reflected in a royalty, which, after all, is negotiated ‘in the shadow of the law.’

A second factor relied on by Lafrenière J “is Rovi’s apparently deliberate strategy of delaying the prosecution of its patents,” which were issued 13–17 years after filing. This kind of submarine patenting is problematic because it means that potential licensees may be locked in to the technology when negotiations start, with the result that the patentee can leverage the threat of an injunction to extract sunk costs, a problem known as “holdup”. In this case, “Rovi’s own expert witness confirmed that patent holdup was a problem because once a potential infringer has launched a product it reduces flexibility and an opportunistic patent holder can then try to extract a larger, unreasonable licencing fee” [591]. Holdup is certainly a problem when it occurs, and the real debate is as to whether holdup is a pervasive problem, or rare and idiosyncratic. Given the evidence before him, it was certainly appropriate for Lafrenière J to take this into account.

Lafrenière J noted “When it came time to negotiate terms of renewal of the licence, Videotron repeatedly sought specific information about the value of the Rovi patents. Its attempts to substantiate and validate the terms for which Rovi wanted a multi-year contract . . . were rebuffed. It is quite apparent to me that the reason why Rovi declined to reveal to Videotron a complete list of specific patent claims it considered infringed was to prevent Videotron from designing around them. Rovi took the position that even after all four patents in suit expire, Videotron would not be free to continue carrying on its current activities as there were always other patents that Rovi would be able to assert against Videotron” [592]–[593]. This illustrates both the holdup problem and that Rovi wanted to avoid negotiating over the value of the technology itself.

In the end, Lafrenière J held that “Rovi’s questionable business practices cannot help but serve to colour my view of the value of the features that it claims in the Patents. This factor weighs heavily against Rovi.” This conclusion strikes me as entirely sound.

(c) Videotron’s conduct

Rovi argued that Videotron was a willful infringer, and this should weigh in favour of an accounting [596], relying Monsanto v Rivett 2009 FC 317 where Zinn J gave the following reasons for granting an accounting:

[23] there is no deterrent from infringing the patent if what the infringer is required to hand over is the sum he would otherwise have paid to Monsanto to buy the seed and the licence. In fact, this would almost be counter to the purpose of deterrence. It is much like saying, as the plaintiffs put it in their oral submission, “Catch me if you can”. If caught, the defendant would be required to pay the sum he would have paid to use the patent in any event. When not caught, he is left with a windfall. The accounting remedy would lack any deterrent effect if defendants could use patented technology and retain the profits from such use subject only to paying a license fee as compensation if and when they are caught.

This is an important point, but it is not complete. First, there are other disincentives to infringement, even if the potential licensee knows it would be practising the invention. An infringer will be liable for their own direct costs of litigation and some part of the patentee’s costs, as well as the indirect costs of management distraction and business uncertainty. In this case, for example, Videotron initially licenced simply to avoid the business risk from litigation. Second, a reasonable royalty is intended in principle to reflect the amount the infringer would have paid as a licensee, but, because of information problems, the reasonable royalty is unlikely to exactly reflect the royalty that would actually have been awarded, try as the court might. This means that the ‘catch-me-if-you-can’ strategy entails considerable risk. Further, if an injunction is a prospect in a sunk costs scenario, the infringer may have to settle for an amount considerably more than it would have paid for a licence. Consequently, it is not clear that an award greater than a reasonable royalty is necessary to avoid the ‘catch-me-if-you-can’ problem: see generally Ch 3 of Complex Products.

Further, the ‘catch-me-if-you-can’ problem is not really at issue if the putative licensee did not know of the patent, or believed in good faith that the patent was invalid or that it did not infringe; note that in Rivett [8] it seems clear that the defendant was an intentional infringer. An award greater than a reasonable royalty therefore risks an unnecessary chilling effect on a party who believes in good faith that they are not infringing.

Accordingly, in this case Lafrenière J considered that Videotron’s conduct did not weigh in favour an accouting:

[599] I disagree that Videotron’s conduct was inappropriate, let alone that it wilfully infringed Rovi’s patents. The evidence suggests that Videotron’s motives to refuse to renew the licence agreement with Rovi were well-founded. Its decision was based on a reasonable assessment of the necessity of the patents.

This strikes me as entirely sound.

(d) Whether Rovi practiced the invention of the patents in Canada

Videotron argued that “where the patentee does not practice their patents and only licenses them, it is ‘almost a rule of law’ to assess damages in terms of a reasonable royalty [602]. Lafrenière J considered this to be a neutral factor, as the evidence was mixed as to the extent that Rovi actually practised the invention in Canada [603], [604]. Since this issue is tricky and it turned on the facts in this case, I won’t comment further.

(e) Complexity of Calculating an Accounting of Profits

Lafrenière J noted that there is caselaw holding that the complexity of calculating an accounting may be a factor, because “the inventor is only entitled to that portion of the infringers’ profit which is causally attributable to the invention, i.e. ‘perfect compensation’” [605]. I take this to mean that complexity means uncertainty, and uncertainty means that the patentee may be over or under-compensated. However, “the calculation of damages can be just as complex as the accounting of profits” [605] This suggests it is not complexity, but relative complexity, that is important. As de Montigny J said in Philip Morris v Marlboro [2015] FCJ No 1564, cited by Lafrenière J, “the Court is essentially concerned with the proportionality of the accounting remedy in view of the length or extent of the infringing activity and the likely benefit of the accounting exercise.”

I’ll note that lost profit damages and an accounting are very similar in structure – it is the differential profit that is to be calculated, and the only difference is whether it is the patentee’s or infringer’s differential profits. The difficulty of assessing causation, and assessment of revenue and apportionment of costs, are likely to be equally difficult to calculate. Reasonable royalty damages, however, are assessed instead on the basis of a hypothetical negotiation, and so might be more or less complex that lost profit damages or an accounting, depending on the facts.

In this case, Lafrenière J held on the facts that “While the complexity of the evidence could be overcome, I am not satisfied that using any methods proposed by Rovi’s expert to calculate profits, which would be fraught with insufficient, speculative, and contradicted evidence would allow me to arrive to reliable and appropriate amount reflecting Videotron’s profits” [607], and accordingly he held this weighed against awarding an accounting. In other words, a patentee who wishes to elect an accounting should propose a sound methodology. This point strikes me as compelling.

I note that in general a reasonable royalty might also be very difficult to calculate in this type of case, where the patentee is claiming a reasonable royalty for the use of one relatively minor feature that is part of a complex product, depending eg on whether good comparables are available—though on the facts in this case Lafrenière J was able to arrive at a reasonable royalty relatively easily, as discussed below. So while I agree with Lafrenière J’s analysis in this case, in general the relevance of the complexity of calculation is a point that needs more development.

C. Reasonable Royalty

After deciding that Rovi was not entitled to an accounting, Lafrenière J went on to assess a reasonable royalty.

Videotron argued that should a particular Videotron system feature be found to infringe a valid claim, the appropriate remedy “is a one-time reasonable royalty, capped at no more than Videotron’s cost to remove or design-around the subject-matter of the relevant asserted patent claim” [612]. Lafrenière J accepted this submission. The evidence was that “the absence of such features would not impact the subscriber base for Videotron” [614] and “subscribers do not make choices around staying or leaving based on the kind of functionality at issue in this case” [615]. It is implicit that the only impact of the patented features on Videotron’s revenue is through the subscriber base and not on the rates that it would charge.

With one caveat, this approach is consistent with the standard hypothetical negotiation framework for assessing a reasonable royalty. The potential licensee’s maximum willingness to pay for a feature is the difference between the value of the product with the feature as compared with the best non-infringing alternative (NIA). In this case the NIA is not to include the feature at all. It is significant in this case that the NIA is not another unpatented technology which replicates the functionality of the patented invention; it is simply to remove the feature entirely. This illustrates that the “non-infringing alternative” is simply a way of framing the question of “what would the licensee have done if it had not infringed”? On the facts in this case, it would have removed the patented feature entirely.

There is a small caveat. Though it is not entirely clear from the brief discussion, it seems that the figure of $150,000 represents the ex post design-around cost. That is, are we assuming that the patented feature was already incorporated in the Videotron system, and $150,000 is the cost to remove it. If so, the $150,000 actually represents the holdup cost, rather than the value of the feature, and so is too high; arguably the true value was zero. With that said, Videotron’s submission, which was accepted by Lafrenière J, is not that the design-around cost reflected the value of the patented technology, but rather that the design-around cost “capped” the reasonable royalty. This is strictly correct. On the facts, a reasonable royalty reflecting the value of the invention is necessarily less than the ex post design-around cost, because the best non-infringing alternative is to remove the feature entirely. No doubt establishing the design-around cost was the simplest way for Videotron to establish a quantum, and safer than arguing that the correct royalty was zero.

The uncontroverted evidence was that the approximate cost for such a design change would have been $150,000 per feature [612], and accordingly that is the royalty that Lafrenière J would have awarded [624].

Monday, June 6, 2022

Overbreadth Overlaps with Utility on the Facts

Janssen Inc v Sandoz Canada Inc 2022 FC 715 Pallotta J

2,659,770 / macitentan / OPSUMIT / NOC

In this NOC proceeding Sandoz conceded infringement and challenged the validity of the 770 patent on the basis of obviousness, lack of utility, overbreadth and insufficiency [8]. All attacks failed on the facts. One point of more general interest is that Pallotta J followed and applied the recent decision in Abiraterone 2021 FCA 45 [41] (discussed here), in holding that a statistical analysis of the results, or statistical significance, is not required to establish a reliable basis for a sound prediction [234]. Also, the overbreadth attack once again failed to gain any independent traction, as it was held on the facts to be simply a rehash of the utility argument.

There are three known biological pathways affecting pulmonary blood pressure, namely the prostacyclin, nitric oxide and endothelin pathways [119]–[122]. PDE5 inhibitors work through the nitric oxide pathway [121]. Macitentan is an endothelin receptor antagonist (ERA), which, as the name suggests, works through the endothelin pathway [3]. The 770 patent relates generally to the use of combination therapy consisting of macitentan and a PDE5 inhibitor (such as sildenafil) to treat diseases involving vasoconstriction, particularly pulmonary hypertension [6], [113], [171]. So, claim 26 is to the use of macitentan in combination with sildenafil for the treatment of pulmonary hypertension [87].

Drugs operating through all three pathways were known and the main question in respect of obviousness was whether it would have been obvious to use, or at least try, a combination therapy. Pallotta J held on the facts that it was not obvious, as the evidence relating to the efficacy of combination therapies was limited and would not have provided an acceptable level of confidence that a combination therapy would work [159], [164], [185], [186]. The desirability of using a combination of an ERA and a PDE5 inhibitor consequently was not obvious [188], and even if it was, the choice of macitentan in particular was not obvious [191], as it was “effectively unknown to the skilled person” at the relevant time [193]. Nor was the invention obvious to try; even if it was obvious to try a combination therapy (and Pallotta J did not hold that it was), it was not obvious to try macitentan in particular from amongst the known ERAs [199], [206].

The utility attack was to the effect that the data disclosed in the patent was not sufficient to establish a sound prediction of utility, and particularly that the rat studies disclosed in the patent were not probative of benefit in humans, primarily on the basis that the studies themselves were flawed, and partly on the basis that animal studies (especially when flawed) are not adequately probative of efficacy in humans [221]. Pallotta J rejected these arguments on the facts [229]–[237]. The main point of general interest is that Pallotta J noted that a statistical analysis of the results, or statistical significance, is not required to establish a reliable basis for a sound prediction [234], citing Abiraterone 2021 FCA 45 [41] (discussed here.)

While utility was soundly predicted, Pallotta J held that utility had not been demonstrated, on the basis that the asserted claims relate to use of the combination for the treatment of diseases in humans, and the rat studies would not necessarily translate to the same effect in humans. However, she acknowledged that the line between sound prediction and demonstrated utility is vague, and she stated expressly that “I do not intend to suggest that there is a bright line that requires, in every case, testing in human patients in order to support demonstrated utility for a drug intended to treat a disease in humans” [246]. Her conclusion was only that the evidence in this case was not sufficient to demonstrate utility in humans [246].

In my article Overbreadth in Canadian Patent Law: Part I (2020) 33 IPJ 21, I argued that overbreadth is almost always overlaps with some other ground of invalidity. However, in Seedlings 2021 FCA 154 (blogged here) the FCA affirmed that “overbreadth remains a proper ground of invalidity” [50]. Consequently, we are now seeing overbreadth raised regularly as a ground of invalidity. But parties attacking the validity to of a patent have struggled to find an approach to overbreadth which gives it any independent force. That pattern continues in this case, in which Pallotta J held that all the overbreadth arguments were really a restatement of utility arguments, and she dismissed them for the same reason [250]–[253]. There was one overbreadth argument which she declined to consider because it had not been properly raised [252]; this also looks like a utility argument to me.

Pallotta J dismissed the insufficiency argument very briefly [254]–[260]. Sandoz’s argument is a bit difficult to understand from Pallotta J’s brief description. It strikes me as being another rehash of the utility argument.

Tuesday, April 19, 2022

Liability of the Parent Corporation / Implied Obligation of Confidence

Angelcare Canada Inc v Munchkin Inc 2022 FC 507 Roy J

2,640,384 / 2,855,159 / 2,936,415 / 2,936,421 / 2,937,312 / 2,686,128 / Diaper pail cassette

In this decision Roy J held many claims of Angelcare’s six patents to be valid and infringed by Munchkin. The holding turned largely on the facts, but there are a few points of interest relating to inducement, liability of the parent corporation, an implied obligation of confidence and overbreadth.

Overview

The invention at issue relates to diaper pail cassettes. A cassette is an insert filled with plastic film which fits into a diaper pail, forming a diaper pail assembly, that dispense plastic bags bags to contain soiled diapers that are put into the pail. The cassettes are replaced once the film is used up, just as the cartridge in an ink jet printer is replaced one the ink is dry.











Angelcare held six patents, consisting of the 128 patent, and a family of divisional patents with 384 patent being the parent [32], [42]. The 128 patent was originally owned by Playtex, and was transferred to Angelcare in 2019 [8]. The claims at issue mostly relate to the cassette, but some relate to the assembly of the cassette and pail. Angelcare or related companies sold diaper cassettes and pails under the Diaper Genie brand. Munchkin’s cassettes were designed with the aim of being compatible with the Diaper Genie pails [14]. Until Munchkin launched its own line of pails in 2016, the Munchkin cassettes were compatible only with Diaper Genie pails: [16], [18].

Claim construction turned almost entirely on the facts. Munchkin argued non-essentiality in respect of only one element of the 128 patent [110]. After noting the presumption of essentiality [109], Roy J found that this element was essential, on the basis that a variant would have a material effect on the way the invention worked: see [38]–[39], [112]–[115]. Infringement followed on the facts in light of claim construction: see eg [163], [191].

The anticipation argument largely failed on the facts. One twist is that four claims of the 384 patent were anticipated by Angelcare’s own 138 patent” [303], [326]. While the decision is not explicit on this point, it appears that it was a matter of anticipation rather than double patenting because the 138 patent was a co-pending application owned by Playtex at the claim date of the 138 patent. These were the only infringed claims that were held invalid on any ground.

The obviousness attack failed on the facts. There was generally no difficulty in identifying the inventive concept of the patents: [394], [396], [403], [404]. The claimed invention was an improvement on the original Captiva/Diaper Genie II system that had been developed by Playtex and Angelcare, and that original system was accordingly the closest prior art [50], [407]. There was some dispute as to whether this was part of the common general knowledge, but that issue made no real difference, as it was not contested that the Captiva/Diaper Genie II system was part of the prior art, and Munchkin was consequently entitled to rely on it as the basis for the obviousness attack [382]. Roy J found on the facts that the differences between that system and the claimed inventions were not obvious.

Roy J had no difficulty in disposing of very tenuous arguments relating to insufficiency, ambiguity, utility and double patenting.

Inducement

Angelcare alleged that Munchkin’s sale of cassettes to end-users had induced infringement of certain assembly claims by those end-users [250]. The cassettes were suitable for use only in combination with patented assemblies (whether used with Angelcare or Munchkin pails) [256]. In the US, this would give rise to what is now usually called contributory infringement—sale of a component especially adapted for use in a patented invention contrary to 35 US § 271(c). However, as Roy J noted, in Canada, in MacLennan 2008 FCA 35 ¶ 33, the FCA stated that “the courts have consistently held that selling a component intended to be incorporated in a patented combination (or process) without anything further, does not constitute an inducement to infringement, even where this component cannot be used for any other purpose.” Consequently, in Canada, such situations are treated as turning on inducement, which requires some additional encouragement beyond mere sale of the part.

Now, it is true that the courts have often stated that contributory infringement in the US sense is not part of Canadian law, but as I pointed out in my article Contributory Infringement in Canadian Law (2020) 35 CIPR 10, there are very few cases which actually decline to impose liability in that scenario, with the most recent being Permacon [1988] 2 FC 179, decided over thirty years ago. Instead, whenever the part sold by the indirect party has no substantial non-infringing use, the courts have consistently found the necessary inducement, sometimes on a slender basis, such as rudimentary assembly instructions in Windsurfing (1985) 8 CPR(3d) 241 (FCA), or the equivalency table in MacLennan.

In this case, Roy J found influence sufficient to establish inducement primarily on the basis of the label affixed on the Munchkin cassettes which clearly directed the end-user to use the Munchkin cassettes with the Diaper Genie diaper pails [266]. [267]. As Roy J noted, this finding is entirely consistent with MacLennan, and the many pharma cases which have found inducement on the basis of the product monograph [268]–[270]. This confirms that, at least in the case of a product especially adapted to infringe, any indication by the indirect party that the product will be used in a patented combination will be sufficient to establish the necessary influence.

The third prong, knowing inducement, was easily established on the facts [272].

Liability of Parent Corporation

To this point I’ve omitted mention of the corporate structure of the defendants, who I have referred to as Munchkin. To be more precise, there are two defendants, Munchkin, Inc, a US company, and Munchkin Baby Canada Ltd, its Canadian subsidiary [11]–[12]. The infringing cassettes were designed by Munchkin Inc [14]–[22], but it was not established that Munchkin Inc had any role in the manufacture, use or sale of the Munchkin cassettes or diaper pails in Canada [281]. (Munchkin Canada distributed and sold the products in Canada; it’s not clear to me where the products were made or by whom [282].) Roy J held Munchkin Inc liable on the basis of its role in the design of the infringing products. The entirety of his analysis on the issue is as follows (my underlining):

[282] The Plaintiffs do not address this issue directly in their closing arguments. However, the evidentiary record they mounted contained information about design decisions that came directly from Munchkin, Inc. in California, which resulted in the infringing products sold in Canada. The Court heard testimony from Mr. Johnson and Mr. Dunn, two Munchkin Inc. Officials, about how Munchkin’s cassettes were designed to be compatible with Diaper Genie’s diaper pails. Mr. Johnson testified that, to his knowledge, there have never been designers at Munchkin Canada (Johnson, TT Vol. 21, p. 2:17-21). Mr. Carvelho testified that all of the Munchkin products distributed in Canada are designed at Munchkin, Inc.’s Los Angeles headquarters (Carvelho, TT Vol. 19, p.183:10-16). He also explained that there are only seven Munchkin Canada employees and that their roles are limited to sales, marketing, and warehousing (Carvelho, TT Vol, 19, p.183:22-28). Moreover, Munchkin Canada’s products are merely a subset of what is offered in the United States; there are no unique items in Canada (Carvelho, TT Vol. 19, p.184:18-25). The Court also heard testimony from Mr. Carvelho about Munchkin’s strategy to advertise that their cassettes are compatible with Diaper Genie pails, with labelling designed to this effect. There was no distinction made between the decisions undertaken for the American market and the Canadian market to this effect. As such, the Plaintiffs advanced evidence that the American parent company made design and marketing decisions that had a direct impact on the resulting infringing activities in Canada. As such, Munchkin, Inc. is liable for any proven infringing activities in Canada.

Roy J cited no authority, and I find this passage puzzling. The gist seems to be in the penultimate sentence, which is to the effect that Munchkin Inc, caused the infringement in Canada, specifically in by (1) designing the infringing cassettes and (2) making the decision to affix labels advertising compatibility with the Diaper Genie pails.

Taking the design issue first, I have difficulty seeing how this in itself can give rise to liability. Suppose a device is patented in Canada, but not in France. If I manufacture it in France I am not infringing the Canadian patent. If I then sell and deliver it, in France, to another party who imports it into Canada, I am still not infringing the Canadian patent, even though I have caused the infringement. This point is well-established in the context of the Saccharin doctrine, which establishes that if a process that is patented in Canada is used abroad to make a product which is itself unpatented, importation and use in Canada of the product is an infringement. At the same time, it is well established that the user of the invention abroad is not an infringer under the Saccharin doctrine, even though the product is ultimately imported by another party: see Hospira v Kennedy Trust / infliximab 2020 FCA 30 ¶ 33–37 rev’g on this point Hospira v Kennedy Trust / infliximab 2018 FC 259; Cefaclor liability 2009 FC 991 ¶ 281–84; Saccharin Corporation v Reitmeyer & Co (1900) 17 RPC 606 (Ch) 612. It is for this reason that the Saccharin doctrine does not violate the principle that patent rights are territorial: Hospira v Kennedy Trust / infliximab 2020 FCA 30 ¶ 36. Accordingly, it is clear that if Munchkin Inc manufactured the cassettes in the US, that would not in itself give rise to liability for infringement of the Canadian patent, even if the cassettes are ultimately imported. It’s difficult to see how design rather than manufacture could lead to a different result.

The second point concerns the labels instructing use in an infringing combination. It may be that a party can be found liable for inducing infringement in Canada by virtue of acts abroad, but it’s not clear that this can support Roy J’s conclusion either. First, Roy J did not undertake an inducement analysis, so it does not appear that this was the basis on which he imposed liability. Second, liability based on inducement would at most support liability for the assembly claims, which were found to be infringed by inducement. Further, liability based on inducement, even for the assembly claims, gives rise to significant issues of extraterritoriality. Suppose a drug is patented in Canada but not in the US, and a generic pharma company sells the drug in the US accompanied by instructions to use it in a way that would infringe the Canadian patent. It sells the same drug in Canada with a skinny label that excises the infringing instructions. A Canadian vacationing in the US reads the PM in the US, and, as a result, uses the drug in an infringing manner on returning home to Canada. Imposing inducement for liability in such circumstances would certainly raise serious issues of extraterritoriality. Munchkin’s decision to affix the labels in the US is perhaps distinguishable, on the basis that the decision was specifically aimed at Canada. But whether that is sufficient to overcome the extraterritoriality concerns would require a full analysis. Finally, the decision to affix labels, taken abroad, is similar to the design decision, also taken abroad. If the latter does not give rise to liability, it is not clear why the former should be any different.

Implied Obligation of Confidence

Roy J’s decision provides some guidance on the question of when an obligation of confidence can be implied so that a disclosure is not a disclosure to the public. While Roy J applied established law and his decision turned on the facts, it is nonetheless helpful, as there is relatively little caselaw on this point in the patent context.

The inventor, a Mr. Morand, had emailed a CAD file of a prototype of the patented cassette to Initial, a third party prototype manufacturing company located in France, more than a year before the earliest filing date [332]. Munchkin argued this disclosure was anticipatory, and Angelcare responded that it was not a disclosure to the public because it was subject to an obligation of confidentiality [336].* There was no express non-disclosure agreement, so the question was whether an obligation of confidentiality could be implied [342].

Relying on Corlac 2011 FCA 228 and Lac Minerals [1989] 2 SCR 574, Roy J held that there was an implied obligation of confidence. This was based in part on the view that “The manufacture of articles by a party for another would fall prima facie in that category carrying an obligation of confidentiality” [339], but he emphasized more specifically not just third party manufacturing, but manufacturing of prototypes:

Initial was in the business of making prototypes, which inherently suggests that an obligation of confidentiality is present” [348]

See similarly [351]. This is even though this was the first interaction between Morand and Intial, or at least very early in the relationship [340], [347].

Mr Morand also sent the same file to a different firm, Plasti-Lax, to create technical drawings for mould-making [333]. This was also found to be subject to a obligation of confidence, though the issue was easier because there was a “longstanding business relationship of trust and cooperation” between the parties.

Roy J also found that the Plaintiffs’ reliance on article 1434 of the CCQ was not helpful, because it added nothing to the test set out in Lac Minerals, and “The legal test set out in Lac Minerals, which is consistent with art. 1434 CCQ and the jurisprudence that Quebec’s courts have developed on it, should continue to guide the Court” [346].

Overbreadth

Munchkin also argued that the claims of several of the patents at issue were overbroad. [445] Roy J began by noting at [445] that “in some quarters it was argued that overbreadth does not constitute a proper ground of invalidity.” This is perhaps an oblique reference to my article Overbreadth in Canadian Patent Law 33 IPJ 21, 33 IPJ 147, in which I showed that the overbreadth argument is almost always redundant, and argued that there is no clear justification for striking down a patent which is otherwise new, useful, non-obvious and properly disclosed. As Roy J went on to point out, this argument was rejected by the FCA in Seedlings 2021 FCA 154 (blogged here), in which Locke JA expressly affirmed that “overbreadth remains a proper ground of invalidity” [50]. But as Locke JA acknowledged “[o]verbreadth often overlaps with other grounds of invalidity,” and this “makes it difficult to define circumstances in which a patent claim would be invalid for overbreadth but not also invalid on other grounds” [50], [51]. With Seedlings having given new life to overbreadth, the law will have to wrestle with new questions: What exactly constitutes overbreadth? What is the test? How it is distinct from other invalidity attacks? What justification is there for invalidating a patent to an invention which is new, useful, non-obvious and fully disclosed?

Roy J’s decision in this case does not really advance the law on those points, simply because the more difficult questions were not engaged on the facts. Roy J did begin with a general analysis, saying that “To determine whether a patent is overbroad, the Court assesses whether the claims, read fairly on what the patent discloses in the disclosure and the figures, are too wide and claim more than was invented. . . . As discussed recently by Justice Grammond, findings of overbreadth will usually occur when the patent fails to claim an essential element of the invention” [452]. This does not explain how overbreadth is different from other grounds of invalidity; in particular, if the patent fails to claim an esssential element of the invention, it will normally—dare I say inevitably?—be invalid for anticipation or obviousness.

Munchkin’s arguments on the facts were difficult to understand: so, Roy J started his analysis by saying “It is unclear how it can be said that more than this invention is claimed” given the facts acknowledged by Munchkin itself [454], and Roy J dismissed the overbreadth attack on other patents by noting that “Munchkin has not shown how these two Patents are overbroad in that the claims are broader than the invention disclosed in the specification or broader than the invention” [456]. Without going into the details reviewed by Roy J, I will say that I agree with his analysis, and his conclusion that Munchkin failed to make out any real case for overbreadth.

My sense is that what is going on is that parties seeking to attack the validity of a patent recognize that they have a new weapon in the overbreadth attack, but no one is really sure what that new weapon is, or how it should be used. I expect we will continue to see a series of futile overbreadth attacks until one day something sticks, and the law begins to develop more systematically; or nothing ever sticks, and defendants simply give up on the overbreadth attack. Time will tell, but this particular decision does not provide any signposts.

*In my initial post, this sentence reversed the names of the parties. Corrected as of 17 Feb 2023