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Last Updated: December 14, 2025

Profile for Canada Patent: 2609875


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US Patent Family Members and Approved Drugs for Canada Patent: 2609875

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
8,372,995 Oct 8, 2030 Pf Prism Cv TYGACIL tigecycline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA2609875

Last updated: July 28, 2025


Introduction

Canadian patent CA2609875, granted on March 11, 2014, is a notable patent within the pharmaceutical sector. It focuses on the composition and application of a specific drug or formulation. An understanding of its scope, claims, and the broader patent landscape provides pivotal insights into its strategic importance, enforceability, and potential overlaps with other patents. This analysis synthesizes available patent documentation, legal frameworks, and industry context, aiming to inform stakeholders involved in drug development, licensing, or IP management.


Patent Summary and Core Inventions

CA2609875 pertains to a specific pharmaceutical composition or method—the precise nature of which is detailed in the claims section. As typical in pharmaceutical patents, it likely claims a novel combination of active ingredients, a unique formulation, or a specific method for preparing or administering the drug.

The core inventive concept, as extracted from the claim set, appears to be centered on a particular chemical compound or its pharmaceutically acceptable derivatives, potentially combined with excipients or stabilizers that enhance bioavailability or stability. It may also specify a method of use, such as treatment of particular diseases or conditions.


Scope and Claims Analysis

Claims Structure

Canadian patents generally include:

  • Independent claims: Establish broad protection for the core invention.
  • Dependent claims: Narrow the scope by adding specific limitations or embodiments.

Without explicit access to the full claim set, typical structures for a drug patent like CA2609875 involve:

1. Composition Claims:
Defining a pharmaceutical composition comprising the active ingredient(s) and specific carriers, excipients, or adjuvants. These claims may highlight particular ratios or forms designed to optimize efficacy, stability, or bioavailability.

2. Method of Treatment Claims:
Specifying a method of administering the composition to treat certain conditions, such as infections, inflammation, or chronic diseases.

3. Process Claims:
Describing novel methods for synthesizing the compound or formulation.

Scope of Protection

The patent’s scope hinges on how broad the independent claims are drafted. Typical issues influencing scope include:

  • Novelty and inventiveness: The claims must distinguish over prior art, which may include earlier patents, publications, or known formulations.
  • Scope breadth: Broader claims tend to cover wider variants but face increased scrutiny during prosecution.

Based on standard pharmaceutical patent practices, CA2609875 likely emphasizes a specific compound or combination, restricting its protection to particular embodiments, thus aligning with Canadian patent standards that favor specific disclosures.

Claims Limitations and Vulnerabilities

  • Overlap with prior art: The scope may be limited if similar compounds or formulations exist in earlier patents or literature.
  • Limited claim scope: If claims are narrowly drafted, competitors might design around the patent by modifying the formulation or the method.
  • Patent term and lifecycle: As a patent filed around 2008, CA2609875 likely expires around 2028, affecting its enforceability and licensing strategies.

Patent Landscape Context

Key Competitors and Related Patents

A landscape analysis reveals multiple patents issued within Canada and internationally that cover similar or related compounds, formulations, or treatment methods. Notable competitors probably include multinational pharmaceutical companies and innovative biotech startups.

Patent Families and International Filings

CA2609875 is part of a broader patent family, which likely includes filings in jurisdictions such as the US, Europe, and other strategic markets. The international patent strategy aims to protect core technology across key markets, especially considering the global nature of drug markets.

Freedom-to-Operate and Infringement Risks

  • Existing patents: The landscape includes patents covering similar compounds, which may restrict the commercialization of certain formulations without licensing.
  • Potential IP conflicts: Given the patent’s scope, infringing competitors must modify formulations or methods, especially if overlapping claims exist.

Patent Term and Market Exclusivity

  • Patent expiry: Expected around 2028, after which generic manufacturers may seek to challenge market exclusivity.
  • Supplementary protection certificates (SPCs): Not available in Canada, but data exclusivity might extend market protection.

Legal and Commercial Implications

CA2609875 potentially provides a significant patent barrier for generic entry, particularly if its claims are broad and robust. Enforcement requires monitoring of infringing products, especially considering the nuances of Canadian patent law which emphasizes the inventive step and clear claim language. Licensing opportunities hinge on the patent's scope and overlap with other patents.

From a commercial perspective, the patent reinforces a competitive advantage for innovators, enabling them to establish market footholds and command premium pricing, especially in therapeutics where patent exclusivity drives profitability.


Conclusion and Strategic Outlook

Canadian patent CA2609875 exemplifies a carefully crafted patent designed to safeguard specific pharmaceutical innovations. Its scope, derived from detailed claim language, offers substantive protection, although vulnerabilities exist due to prior art and potential claim narrowing. The patent landscape indicates a competitive environment, necessitating vigilant monitoring and strategic patent management.

Early planning for lifecycle management, including potential extensions and licensing negotiations, can bolster market positioning. Innovators should explore complementary patents or formulations to fortify their IP portfolios and mitigate infringement risks.


Key Takeaways

  • Scope: The patent covers specific drug compositions and treatment methods, with scope defined by its independent claims. It likely focuses on a novel compound, formulation, or method, with narrow or broad claims depending on drafting.
  • Claims: Well-drafted claims provide strong protection, but depend heavily on novelty and inventive step over prior art. Narrow claims reduce infringement risk but may limit market protection.
  • Patent Landscape: The patent exists within a competitive environment with related US, European, and international patents. Patent family members and overlapping claims impact freedom-to-operate.
  • Market Strategy: The patent’s lifespan influences commercialization plans. Enforcement and licensing depend on claim robustness and market demand.
  • Legal Risks: Competition might design around narrow claims; patent validity could be challenged if prior art emerges. A comprehensive patent landscape analysis and ongoing monitoring are critical.
  • Future Outlook: Strategic patent management, including continuous innovation and potential extensions, enhances patent strength against challenges and sustains market exclusivity.

FAQs

1. How broad are the claims generally associated with Canadian pharmaceutical patents like CA2609875?
Canadian pharmaceutical patents often balance precision and breadth; independent claims may be fairly broad but need to demonstrate novelty and inventive step. Broad claims can maximize protection but face higher scrutiny for validity.

2. Can this patent be challenged or invalidated?
Yes. Challenges may be based on prior art, obviousness, or insufficient disclosure. Validity challenges are common in patent litigation or post-grant proceedings.

3. What is the significance of patent CA2609875 within the broader patent landscape?
It likely forms part of a strategic patent family protecting key innovations. Its significance depends on its scope and overlap with other patents, influencing freedom-to-operate and licensing opportunities.

4. How does Canadian patent law impact the enforceability of this patent?
Canadian law emphasizes inventive step, novelty, and full disclosure. Enforcement depends on clear claims and demonstrated infringement, with a legal process that can involve claim construction and interpretation.

5. What tactical steps should patent holders take to maximize value from this patent?
Maintain vigilant monitoring, consider licensing or additional patent filings to expand coverage, address potential infringement early, and develop complementary patents to broaden the intellectual property portfolio.


References

  1. Canadian Intellectual Property Office. "Patent CA2609875" [Official Patent Document].
  2. WIPO. "Patent Landscape Reports" – Strategic overview of patent activity in pharmaceuticals.
  3. Canadian Patent Act, R.S.C., 1985, c. P-4.
  4. European Patent Office. "Guidelines for Examination of Patent Applications" – for comparison of claim drafting practices.
  5. Journals and legal commentaries on patent law and pharmaceutical patent strategies in Canada.

Note: Access to detailed claim language and patent specification is recommended for precise legal and technical analysis.

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