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19 April 2021
The Federal Court of Appeal (FCA) recently dismissed Apotex's appeal of the Federal Court decision which held that the claims of Canadian Patent 2,527,646 (the 646 patent) were valid and prohibited the minister of health from issuing a notice of compliance to Apotex for its lisdexamfetamine (LDX) product (Shire's VYVANSE) until the expiry of the 646 patent (Apotex Inc v Shire LLC, 2021 FCA 52. For further details please see "Shire's VYVANSE patent valid, prohibition order issued").
The prohibition application under the pre-amended Patented Medicines (Notice of Compliance) Regulations was consolidated with Apotex's action seeking a declaration of invalidity and non-infringement. Apotex appealed both judgments.
Amphetamine was an established treatment for conditions such as attention deficit hyperactivity disorder but as it is an immediate release compound, it requires patients to take doses frequently throughout the day. LDX is a prodrug of amphetamine that provides sustained release and reduces abuse potential.
The Federal Court judge found that the claims at issue were not anticipated by Australian Patent Application 54168/65 (AU 168), which discloses a large class of amino acid conjugates, including LDX. Apotex argued that:
The FCA disagreed and affirmed that the validity analysis does not change depending on whether a patent is classified as a selection patent; a prior art reference discloses the claimed invention when, if performed, the prior art reference would necessarily result in the infringement of the patent claim. LDX was not an example described in AU 168; it was merely one of a large class of "advantageous compounds". Accordingly, the FCA held that claims to LDX and its salts in the 646 patent were not specifically disclosed as there are numerous other ways to "perform" AU 168 without necessarily infringing the claims of the 646 patent.
Apotex also contended that the judge had erred in not finding the claims at issue obvious. Following a review of the claims and the problem that they intended to solve, the judge had held that the inventive concept of the 646 patent was "a sustained release formulation of a therapeutically useful dose of amphetamine that is resistant to abuse". Apotex argued that the judge had erred in doing so on the basis that Section 28.3 of the Patent Act mandates a narrow, claim-based end point, focused solely on the "subject matter of the claim", and that recourse to the specification is not allowed. It noted that unlike some of the unasserted claims, none of the asserted claims related to sustained release or abuse resistance.
The FCA disagreed, holding that Section 28.3 does not narrow the inventive concept to the essential elements of the claim itself. Where there is no agreement on the inventive concept, it must be construed and, where it is impossible to fully grasp its nature solely from the claims as construed, the judge may have regard to the specification. Here, as the claims to LDX and its salts were to bare chemical compounds, the essential element of each of these claims was the chemical formula itself. Therefore, it was necessary to turn to the specification for amplification.
Apotex also argued that the inventive concept was faulty as it made the inventive concept of some of the claims "necessarily redundant". The FCA again disagreed, holding that while there must be a single overarching inventive concept, each claim can give rise to its own inventive concept, and that the inventive concepts of the various claims may overlap or replicate each other. Here, the judge:
There was no reviewable error in the legal framework or in its application to the facts as found.
For further information on this topic please contact Andrea Berenbaum at Smart & Biggar by telephone (+1 416 593 5514) or email (email@example.com). The Smart & Biggar website can be accessed at www.smartbiggar.ca.
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