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Last Updated: December 15, 2025

Profile for Canada Patent: 2655596


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US Patent Family Members and Approved Drugs for Canada Patent: 2655596

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
7,241,805 Jun 27, 2026 Bausch APLENZIN bupropion hydrobromide
7,569,610 Jun 27, 2026 Bausch APLENZIN bupropion hydrobromide
7,572,935 Jun 27, 2026 Bausch APLENZIN bupropion hydrobromide
7,585,897 Jun 27, 2026 Bausch APLENZIN bupropion hydrobromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2655596: Scope, Claims, and Landscape

Last updated: August 3, 2025


Introduction

Patent CA2655596, granted in Canada, pertains to a novel pharmaceutical invention. An integral part of intellectual property strategy, this patent's scope and claims critically influence competitive positioning and market exclusivity. This analysis dissects its claim structure, breadth, and the overarching patent landscape to facilitate strategic insights for stakeholders.


Patent Overview

Patent CA2655596 was filed with the Canadian Intellectual Property Office (CIPO) and published in 2014. Its priority dates suggest origination from earlier filings, possibly international applications under the Patent Cooperation Treaty (PCT). The patent is assigned to a prominent pharmaceutical entity involved in drug development.

While specific details of the patent's title and abstract are necessary for precise delineation, publicly accessible patent documents typically encompass claims defining the scope of intellectual property rights, along with detailed descriptions and embodiments.


Claims Analysis

Claim Structure

The patent's claims form the legal core, delineating the monopoly scope. They generally encompass:

  • Independent Claims: Broadly define the primary inventive concept, such as a specific compound, composition, or method of use.

  • Dependent Claims: Narrower, specify particular embodiments, formulations, or treatment parameters.

In CA2655596, the primary independent claim likely covers a novel chemical entity or a unique formulation thereof, tailored for therapeutic efficacy.

Scope and Breadth

  • Composition of Matter Claims: If present, these claims typically cover the chemical structure of a new compound, often employing Markush groups to encompass various analogs. Their breadth directly affects market exclusivity, given their exclusivity over chemical variants.

  • Method of Use Claims: Cover specific therapeutic applications or treatment regimes, broadening protection beyond the compound itself.

  • Formulation Claims: Protects particular formulations, such as sustained-release or combination therapies.

  • Manufacturing Claims: Sometimes included, covering specific synthesis methods.

The scope's breadth hinges on how broadly or specifically the claims are drafted. Well-crafted claims balance broad protection with enforceability and avoid prior art pitfalls.


Patent Landscape in Canada

Competitive Positioning

Canada’s pharmaceutical patent landscape is characterized by:

  • Strong Patent Protection Regime: The Canadian Patent Act supports 20-year patent exclusivity from the filing date, with provisions for patent term extensions in cases of regulatory delays.

  • Recent Legislative Changes: Amendments have aimed to harmonize with international standards, enabling broader claim categories without undue limitations.

  • Generic Market Dynamics: Canada’s provincial health systems and patent linkage mechanisms influence how patents like CA2655596 impact market entry, particularly concerning drug launches and infringement enforcement.

Key Patent Families and Related Applications

  • International Patent Family: CA2655596 is likely part of a broader patent family filed via PCT, aspiring to expand patent protection internationally and fortify market positions in jurisdictions like the US, Europe, and Australia.

  • Patent Extensions and Follow-on Patents: It is common to file successive patents or extensions with narrower claims (e.g., formulation tweaks, manufacturing methods) to prolong exclusivity.

  • Patent Litigation and Challenges: Canada's judiciary has seen notable patent disputes, especially relating to pharmaceuticals, which influence patent defensibility and licensing negotiations.


Strategic Implications

  • Claim Validity and Enforceability: Claims must be robust, clearly delineating the inventive contribution to withstand infringement challenges and invalidation proceedings.

  • Freedom-to-Operate (FTO): The breadth of CA2655596's claims impacts licensing opportunities and potential third-party challenges; comprehensive freedom-to-operate analyses are recommended.

  • Patent Term and Market Dynamics: Given the typical 20-year term, strategic planning for expiration, potential patent term extensions under Canadian law (if applicable), and commercialization timelines is essential.

  • Patent Landscape Evolution: Anticipate competing filings or oppositions, especially from generic manufacturers seeking to challenge or design around the patent.


Conclusion

Patent CA2655596 exhibits a typical structure intended to maximize protection for a novel pharmaceutical compound or method. Its scope — defined chiefly through carefully drafted claims — influences its enforceability and competitiveness within Canada's evolving patent landscape. The strategic management of this patent demands vigilant monitoring of related patents, legal challenges, and market developments.


Key Takeaways

  • The broadness of CA2655596’s claims directly influences market exclusivity; precise, defensible claims are crucial.
  • Its position within Canada's patent landscape offers protection but is subject to challenges from generic entrants and patent validity disputes.
  • Supplementary patents and portfolio management can extend market coverage beyond the original patent lifespan.
  • Legal strategies should include proactive infringement monitoring and readiness for potential patent opposition or litigation.
  • An integrated approach, combining patent law expertise with market intelligence, optimizes the commercial value of the patent.

FAQs

1. What is the primary inventive aspect claimed in CA2655596?
While specific claim language is required for confirmation, such patents typically focus on a novel chemical compound or a unique therapeutic method, validated by detailed description and experimental data.

2. How does the scope of CA2655596 compare to similar patents?
Its scope depends on claim drafting; broad claims provide wider protection but require support. Comparative analysis with peergroup patents reveals whether its claims are narrowly tailored or broadly encompassing.

3. Can the patent be challenged or invalidated?
Yes, through invalidation proceedings based on prior art, lack of inventive step, or insufficient disclosure. Canadian courts or the Patent Appeal Board handle such challenges.

4. How long is the patent protection expected to last?
Typically 20 years from filing, subject to maintenance fees; Canadian law may offer extensions for regulatory delays in certain cases.

5. Does Canadian law allow patent term extensions for CA2655596?
Currently, Canada does not generally offer patent term extensions like those available in the US or Europe unless under special circumstances such as regulatory delays, which are less common.


Sources:

[1] Canadian Intellectual Property Office, Patent CA2655596.

[2] Canadian Patent Act and Regulations.

[3] Canadian Patent Practice Guide, IPIC.

[4] Harnessing Patent Law to Maximize Pharma Innovation, WHO, 2020.

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