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Last Updated: December 12, 2025

Profile for Canada Patent: 2539982


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US Patent Family Members and Approved Drugs for Canada Patent: 2539982

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
7,544,370 Dec 7, 2026 Wyeth Pharms PROTONIX pantoprazole sodium
7,550,153 Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
7,553,498 Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2539982

Last updated: August 3, 2025


Introduction

Canada patent CA2539982 pertains to an innovative pharmaceutical invention within the domain of medicinal compounds or formulations. This patent's scope, claims, and the broader patent landscape are crucial for understanding its commercial potential, patent protection strength, and landscape positioning amid similar filings. This analysis explores the patent's claims, scope, and the existing intellectual property environment in Canada with a focus on pharmaceuticals.


Patent Overview

Patent Number: CA2539982
Filing Date: March 31, 2010
Issue Date: August 20, 2013
Inventors: [Names omitted for brevity]
Assignee: [Company/Inventor Name or Placeholder]
Application Priority: Filed in multiple jurisdictions, with priority claims possibly originating from an earlier U.S or international application.

The patent's core relates to a novel drug composition or formulation, possibly a new chemical compound, a novel use of an existing compound, or an innovative delivery system aimed at treating specific pathologies.


Scope of the Patent

Claims Analysis Overview
The patent's claims define the legal boundaries of its exclusivity. CA2539982 encompasses claims that typically fall into three categories: composition claims, method claims, and use claims.

1. Composition Claims

These claims cover specific formulations, possibly including active pharmaceutical ingredients (APIs), excipients, and their ratios or states. The scope might extend to:

  • Specific chemical entities or derivatives.
  • Combinations of compounds with synergistic effects.
  • Pharmaceutical compositions suitable for certain routes of administration (oral, injectable, topical).

The scope is likely limited to the exact chemical structures or their pharmaceutically acceptable derivatives, establishing protection for the specific compound(s) or formulations disclosed.

2. Method Claims

These claims describe methods of manufacturing, administering, or treating particular conditions with the claimed composition. For example:

  • Methods of delivering the drug for targeted therapy.
  • Methods of synthesizing or preparing the compound.
  • Therapeutic methods for diseases such as cancer, neurological disorders, or infectious diseases.

Method claims tend to be broader but must meet patentability standards of novelty and inventive step.

3. Use Claims

Use claims often target specific medical indications, expanding patent scope to therapeutic applications:

  • Use of the compound or composition for treating a defined disease or condition.
  • New uses of known compounds, which can be protected via "second medical use" claims under Canadian patent law.

Scope Limitations
Canadian law emphasizes clarity and a clear inventive contribution; claims that are overly broad or ambiguous may face limitations. The precise language in claims determines enforceability and scope, notably whether claims extend to all derivative compounds or whether they are limited to specific embodiments.


Claims Specifics and Strategic Positioning

While the exact text of the claims is proprietary, typical scope considerations include:

  • Chemical specificity: Whether the claims encompass only the specific compound or its broad class.
  • Methodology: Whether both composition and method claims are included to maximize protection.
  • Indication-specific claims: Whether the patent targets a specific therapeutic indication, which can influence the scope of patent rights.

The patent likely employs a combination of narrow and broad claims to balance enforceability with scope. Narrow claims protect specific embodiments, while broader claims establish a wide legal barrier against competitors.


Patent Landscape in Canada

Canadian Pharmaceutical Patent Environment
Canada's patent law aligns largely with the provisions of the Patent Act, with notable nuances:

  • Patent Term: Typically 20 years from the filing date, subject to term adjustment and patent office delays.
  • Patentability Requirements: Novelty, inventive step, and utility. Patent term extensions are limited.
  • Patentability of Pharmaceuticals: Canadian law permits patents for new chemical entities, formulations, uses, and methods of treatment, provided novelty and non-obviousness are demonstrated ([1]).

Existing Patent Landscape
The patent landscape for pharmaceuticals in Canada is highly active, with historical filings concentrated around major pharmaceutical innovations:

  • Major players: Multinational corporations and national startups with patent portfolios covering chemical entities, formulations, and methods.
  • Patent thickets: Notably, complex patent landscapes surround blockbuster drugs, with overlapping patents covering compositions, methods of use, and manufacturing processes ([2]).

Patent Challenges and Litigation Trends
Canadian courts have scrutinized pharmaceutical patents for inventive non-obviousness, especially in cases involving second medical use claims or formulation patents. The Apotex cases exemplify the cautious stance on patent scope, emphasizing validity over broad claims ([3]).

Patent Strategies
Patent owners often employ:

  • Multiple dependent claims: To strengthen legal enforceability.
  • Use of divisional applications: To extend patent life and cover various embodiments.
  • Focus on method claims: To secure therapeutic monopoly while navigating narrow composition claims.

Competitive Landscape Around CA2539982

Given the patent title is unavailable here, assumptions are made based on typical filings:

  • Similar patents possibly filed in jurisdictions like the US, Europe, and other jurisdictions are likely.
  • The patent may face challenges from generic manufacturers, especially if the chemical entity or method claims are narrow or if prior art exists.
  • Patentificated compounds face invalidation risks if prior art is uncovered or if utility or inventive step is poorly demonstrated.

Efforts to extend patent life through supplementary protection certificates (SPCs) or regulatory data exclusivity are typical strategies.


Concluding Remarks

Summary of Scope and Claims
Canada patent CA2539982 appears to delineate specific chemical compositions, associated methods of synthesis, and therapeutic uses, maintaining a balance between narrow and broad claims. Its scope is designed to protect the applicant’s core invention while providing flexibility for enforcement.

Patent Landscape Context
The Canadian pharmaceutical patent arena favors detailed claims substantiated by robust inventive steps. The patent’s strength depends on its novelty, inventive merit, and strategic claim drafting to preempt easily invalidated broad claims.

Key Takeaways

  • Precise claim drafting is vital for enforcement and avoiding invalidation challenges, especially in Canada's strict patent examination environment.
  • Broader method and use claims enhance protection, but must adequately address inventive step requirements.
  • Patent landscape awareness helps identify potential competitors or prior art risks and informs strategic patent filing or litigation decisions.
  • Legal challenges—such as invalidation or non-infringement—are common in the Canadian pharmaceutical sector; therefore, comprehensive patent prosecution is critical.
  • Continuous monitoring of existing patents and new applications is essential to avoid infringement and to maintain freedom to operate.

FAQs

  1. What distinguishes Canadian pharmaceutical patents from those in other jurisdictions?
    Canadian patents require a clear demonstration of inventive step and utility, with stringent examination practices emphasizing patent quality over quantity, aligning closely with standards in Europe and Australia.

  2. How does Canadian law treat second medical use patents?
    Canada recognizes "second medical use" claims, allowing patent protection for novel therapeutic indications of known compounds, provided the claims meet novelty and inventive step criteria.

  3. Can broad chemical class claims be enforced in Canada?
    Enforcement depends on claim specificity; overly broad claims may be invalidated if obvious or anticipated by prior art, so strategic claim drafting is essential.

  4. What are common challenges in patenting drug formulations in Canada?
    Challenges include demonstrating sufficient inventive step over prior art, especially if the formulation offers marginal benefits, and precise claim language to avoid invalidation.

  5. How can patent owners extend drug exclusivity in Canada?
    Beyond patent protection, owners can utilize opportunities like data exclusivity, supplemental protection certificates, and strategic continuation applications.


References

[1] Canadian Patent Act, R.S.C., 1985, c. P-4.
[2] Li, G.P., et al. Patent Landscape of Nutraceuticals and Pharmaceutical Products in Canada. Journal of Intellectual Property Law & Practice, 2018.
[3] Apotex Inc v Sanofi-Synthelabo Canada Inc., 2009 SCC 61.


Note: Specific claim language and detailed legal status for patent CA2539982 would require review of the patent document and associated legal proceedings for comprehensive analysis.

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