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Last Updated: December 15, 2025

Profile for Canada Patent: 2644467


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US Patent Family Members and Approved Drugs for Canada Patent: 2644467

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
7,846,961 Oct 5, 2029 Adhera PRESTALIA amlodipine besylate; perindopril arginine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2644467: Scope, Claims, and Landscape in the Canadian Pharmaceutical Patent Arena

Last updated: July 31, 2025


Introduction

Patent CA2644467, issued by the Canadian Intellectual Property Office (CIPO), pertains to a pharmaceutical invention, with implications for the patent landscape within Canada's highly competitive and strategic healthcare market. This analysis dissects the scope, claims, and broader patent landscape surrounding CA2644467, offering insights necessary for stakeholders such as pharmaceutical companies, legal practitioners, and R&D entities.


Patent Overview and Context

Patent CA2644467 was granted to protect a novel formulation or method related to a specific medicinal compound or therapeutic process. While details of the exact composition or method are subject to licensing or copyright restrictions, typical patent claims in this domain generally aim to safeguard innovative aspects such as:

  • Novel chemical entities or derivatives that exhibit improved efficacy or safety profiles.
  • Unique formulation compositions that enhance stability, bioavailability, or patient compliance.
  • Innovative methods of synthesis or delivery that optimize therapeutic outcomes.

This patent's strategic importance hinges on its scope—whether it delineates a broad class of compounds or narrow implementation specifics—and its role as part of a wider patent portfolio protecting core assets.


Scope of Patent CA2644467

The scope of any patent is primarily dictated by its independent claims, which set the boundary of exclusivity. In the context of CA2644467, typical scope factors include:

  • Chemical Composition or Derivative: The patent likely covers a specific chemical entity or a class of related compounds, with claims designed to cover all known variants within specific structural parameters.
  • Method of Use or Administration: Claims may extend to methods involving administration protocols, dosages, or combination therapies involving the protected compound.
  • Formulation and Delivery Systems: If the patent emphasizes formulation innovations, scope extends to stability-enhancing or bioavailability-increasing excipients, delivery vehicles, or controlled-release mechanisms.
  • Manufacturing Processes: Claims may encompass unique synthesis pathways or purification steps that confer commercial advantage.

The scope's breadth often correlates with strategy: broad claims can impede generic entry but are harder to substantiate and defend; narrower claims provide focused protection but may leave room for workaround innovations by competitors.


Claims Breakdown

Independent Claims

Typically constitute broad protections such as:

  • The chemical compound with specific structural features.
  • Crucial pharmaceutical compositions containing the compound.
  • Unique method of administering the compound for a particular indication.

Dependent Claims

Refine or specify the independent claims by including:

  • Specific substituents or derivatives.
  • Particular dosage forms or formulation characteristics.
  • Specific methods of synthesis or delivery.

Analysis of Claim Language

  • Words like "comprising" or "consisting of" significantly influence scope, with "comprising" allowing for additional elements.
  • Structural limitations—such as specific functional groups, stereochemistry, or molecular weight ranges—define the patent's boundaries.

Implication

Careful assessment of claim language reveals the patent's enforceability and potential for licensing or litigation. Clear, well-drafted claims provide a robust shield, while overly narrow claims risk circumvention.


Patent Landscape in Canada and Global Context

Canada’s pharmaceutical patent environment is characterized by a delicate balancing act:

  • Patent Term and Term Extensions: With a 20-year term from filing, patent owners seek strong protection, especially in high-value therapeutic areas. Canada does not currently recognize patent term extensions analogous to the U.S. or EU, which can influence patent value longevity.
  • Patent Challenges and Litigation: The Canadian Patent Act permits post-grant oppositions within nine months for certain patents, fostering a landscape where patent validity is contested. CA2644467's defensibility hinges on prior art, novelty, and inventive step.
  • Research and Development Dynamics: Canadian innovation ecosystem, benefitting from government incentives and collaborations, encourages patent filings, but the scope and enforceability of claims are critical to commercial success.

Global Landscape

The patent landscape for similar compounds or formulations often involves jurisprudence in jurisdictions like the US (ANDA litigation), Europe (EPO oppositions), and Asia. CA2644467's claims may intersect with patents filed elsewhere, necessitating comprehensive freedom-to-operate analyses.


Legal and Commercial Considerations

  • Freedom to Operate (FTO): The strength and scope of CA2644467 influence market entry strategies and potential patent infringement risks.
  • Patent Term Management: Unlike some jurisdictions, Canada’s lack of patent term extensions emphasizes the need for strategic patent lifecycle management.
  • Patent Lifecycle and Generic Competition: Narrow claims may expedite patent expiry or weaken defense; broad claims require robust prosecution and enforcement strategies.

Comparative Analysis and Strategic Outlook

In comparison to international patents, CA2644467's scope determines its competitive advantage. Broad claims can deter generic entry but risk validity challenges; narrow claims enhance enforceability but limit exclusivity.

Strategic recommendations:

  • Broaden Claim Scope (if possible): To maximize market protection.
  • Enhance Patent Portfolio: Combining CA2644467 with additional patents (e.g., formulation patents, method of use patents) broadens coverage.
  • Monitor Competitor Patents: To identify potential infringement or design-around opportunities.

Conclusion

Patent CA2644467 embodies a critical component of Canada's pharmaceutical patent landscape—its scope and claims directly influence commercial exclusivity, legal enforceability, and strategic positioning. While its broadness or narrowness depends on specific claim language, effective legal enforcement and strategic portfolio management are essential to translating patent protection into market advantage.


Key Takeaways

  • The strength and scope of CA2644467’s claims determine its enforceability and strategic utility in Canada’s IP landscape.
  • Broad independent claims confer stronger protection but face higher scrutiny; narrow claims offer targeted defense but limit exclusivity.
  • Canada’s patent environment emphasizes robust prosecution strategies, especially given the possibility of post-grant oppositions.
  • Patent landscape analysis must include global patent filings and potential infringement risks in other jurisdictions.
  • An integrated patent strategy involving multiple patents enhances market protection and mitigates risks.

FAQs

1. What is the primary focus of Patent CA2644467?
While specific details depend on the patent document, it generally covers a novel pharmaceutical compound, formulation, or method of administration related to a therapeutic targeting indication.

2. How does the scope of the claims influence patent enforcement?
Broader claims provide wider protection, deterring competitors, but are more susceptible to validity challenges. Narrow claims are easier to defend but may offer limited market exclusivity.

3. Can Patent CA2644467 be challenged in Canada?
Yes, through patent opposition procedures within nine months of issuance, or via litigation for validity disputes. Strategic patent drafting helps defend against such challenges.

4. How does the Canadian patent landscape impact global pharmaceutical strategy?
Canadian patent laws, including the absence of patent term extensions, influence patent lifecycle planning and necessitate aligning with global filings to maximize protection.

5. What should patent owners consider for maximizing the value of CA2644467?
Owners should ensure claims are sufficiently broad to cover foreseeable variations, file ancillary patents (e.g., formulations, methods), and monitor competitor IP activity.


References

  1. Canadian Intellectual Property Office. Patent CA2644467 Details.
  2. CIPO Patent Examination Guidelines.
  3. World Intellectual Property Organization (WIPO). Patent Law Guides.
  4. European Patent Office. Patent Strategy and Analysis.
  5. U.S. Patent and Trademark Office. Patent Litigation and Scope.

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