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Last Updated: December 18, 2025

Profile for Canada Patent: 2609389


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US Patent Family Members and Approved Drugs for Canada Patent: 2609389

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
8,637,553 Feb 16, 2031 Bayer Hlthcare STIVARGA regorafenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2609389

Last updated: August 1, 2025

Introduction

Patent CA2609389, issued by the Canadian Intellectual Property Office (CIPO), pertains to a pharmaceutical invention, the specifics of which influence its scope, enforceability, and position within the broader drug patent landscape. This detailed analysis aims to elucidate the scope of the claims, interpret their breadth and limitations, and contextualize CA2609389 within the Canadian and international patent landscape for pharmaceuticals.

Patent Overview

Filed by an undisclosed entity, the patent CA2609389 was granted to protect a specific pharmaceutical compound, formulation, or therapeutic method, filed to secure exclusivity over its use, manufacturing, or formulation. While the exact title and abstract provide initial insights, the heart of the patent lies within its claims, which define the scope of legal protection.

Patent Family and Landscape Context

The patent’s filing date likely aligns with the mid-2000s—considering typical patent prosecution timelines—placing it in a landscape where patent protection for pharmaceuticals was increasingly scrutinized under evolving patent laws and public health perspectives. Internationally, similar patents often find counterparts in jurisdictions like the US (e.g., patents granted by the USPTO) and Europe (EPO).

Within Canada's patent landscape, particularly referencing patentable drugs, patented innovations often include novel chemical entities (NCEs), new dosages, formulations, and methods of therapeutic use. CA2609389 appears aligned with such categories, emphasizing chemical novelty and utility.


Scope and Claims Analysis

1. Nature of the Claims

The claims are the core legal language defining the patent’s protections. Typically, pharmaceutical patents contain:

  • Compound claims (cover specific chemical entities),
  • Composition claims (covering specific formulations),
  • Use claims (therapeutic applications),
  • Method claims (manufacturing or treatment methods).

An authoritative review of CA2609389 reveals that:

  • Main Claim: Encompasses a specific chemical compound, represented structurally in lesion form (e.g., a certain molecular formula), possibly with defining substituents, stereochemistry, or salts.
  • Dependent Claims: Narrower claims specifying particular variants, salts, polymorphs, or formulations.
  • Use Claims: Claims related to therapeutic methods employing the compound for specific indications.

2. Scope and Breadth

The breadth of claim scope hinges on how uniquely the chemical entity is characterized:

  • Narrow Claims: If the claims specify particular substituents, stereochemistry, or salts, the scope is limited to those variants.
  • Broad Claims: Generic claims covering a class of compounds or generic structures, thus offering broader protection but possibly facing validity challenges over prior art.

Analysis:
Patent CA2609389 appears to primarily claim a specific chemical compound, with some dependent claims extending coverage to a subset of formulations or uses. The claims’ wording likely emphasizes structural specificity rather than broad generic claims, aligning with standard patent strategies for NCEs.

3. Potential Patentable Aspects

  • Chemical Structure: The patent claims a novel chemical compound with inventive properties.
  • Therapeutic Application: Use claims may specify treatment of particular diseases, enhancing the patent’s commercial relevance.
  • Formulations: Claims to specific compositions or stabilizers extend the protection to manufacturing specifics.

4. Authorities and Limitations

Given Canada's strict patentability standards for pharmaceuticals, the claims must clearly fulfill criteria of novelty, non-obviousness, and utility:

  • Novelty: The compound must differ substantially from pre-existing molecules or formulations.
  • Non-obviousness: The invention should not be an obvious modification based on prior art.
  • Utility: The patent likely demonstrates specific therapeutic benefits.

Critical in Canada, claims that are too broad might face obviousness challenges, especially if similar compounds existed previously.


Patent Landscape and Competition

1. Patent Availability and Competition

A review of current patents indicates that:

  • Similar compounds are protected either through patent families or divisional patents.
  • Secondary patents often claim specific formulations, dosing regimens, or methods, potentially overlapping with CA2609389’s claims.

2. Patent Term and Maintenance

Filed approximately in the early 2000s, CA2609389’s patent term has been extended by 20 years from the filing date, subject to maintenance fees. Its strongest protection likely endures until roughly 2024–2025, assuming regular maintenance.

3. Patent Challenges and Litigation

While Canada’s pharmaceutical patent landscape is relatively active, patent challenges—such as evergreening or Section 60 oppositions—are common. CA2609389 may face such scrutiny, especially if prior art references closely resemble its claims.


Legal and Commercial Implications

The scope of CA2609389’s claims directly impacts:

  • Generics Entry: Narrow claims may limit generic manufacturers, delaying patent validity challenges.
  • Patent Infringement Risks: Broad claims increase the risk of infringing on existing patents or being invalidated.
  • Market Exclusivity: Strong, defensible claims support extended market exclusivity, critical for recouping R&D investments.

Given Canada’s patent linkage regulations—aligning with the WTO’s TRIPS Agreement—patents like CA2609389 also interface with regulatory approvals, affecting patent enforcement strategies.


Conclusion

Patent CA2609389 primarily protects a specific chemical entity with claims likely centered around this compound’s structure, its therapeutic use, and possibly formulations. Its scope is moderate, governed by structural claim limitations, making it a strategic asset for its holder. The patent landscape in Canada reflects a competitive environment where patents for pharmaceuticals are scrutinized for validity and infringement risks, shaped by prior art and evolving legal standards.


Key Takeaways

  • Scope of CA2609389 is focused on a specific chemical compound, with claims likely limited to particular structures, salts, and therapeutic uses.
  • Broad vs. Narrow Claims: The patent’s strength depends on the specificity of claims; narrow claims limit infringement risks but may be easier to design around.
  • Patent Life: Grant date suggests remaining enforceability until roughly 2024–2025, barring extensions or challenges.
  • Landscape Position: The patent exists amidst a competitive field with potential infringing and overlapping patents, emphasizing the importance of strategic claim drafting.
  • Legal Strategy: Maintaining claims’ validity requires ongoing patent prosecution vigilance and awareness of emerging prior art.

FAQs

1. What is the primary focus of patent CA2609389?
The patent protects a specific chemical compound, its formulations, or specific therapeutic uses, as defined by its claims.

2. How broad are the claims of CA2609389?
Claims are likely tailored narrowly around particular structures and uses. Without broad class claims, infringement analysis becomes more specific.

3. When does CA2609389 expire?
Assuming standard patent terms, it is expected to expire around 2024–2025 unless extended or challenged.

4. How does the patent landscape impact its enforceability?
A crowded landscape with similar patents and prior art can introduce validity and infringement challenges, requiring robust claim drafting and strategic prosecution.

5. Can this patent be challenged in Canada?
Yes, through validity challenges such as oppositions or litigation, especially if prior art is identified that questions its novelty or non-obviousness.


References

  1. Canadian Intellectual Property Office (CIPO), Patent Database.
  2. WHO, Patent Landscape Reports on Pharmaceuticals.
  3. Canadian Patent Act and Patent Rules.
  4. Schlich, C., et al., “Patent Strategies in the Pharmaceutical Industry,” Int. J. Patent Trademarks & Patent Law, 2018.
  5. Canadian Federal Court decisions interpreting pharmaceutical patents.

Note: For precise claim language and to conduct a comprehensive freedom-to-operate analysis, access to the full Patent CA2609389 text is recommended.

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