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Last Updated: December 30, 2025

Profile for Canada Patent: 2616193


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US Patent Family Members and Approved Drugs for Canada Patent: 2616193

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
8,746,242 Apr 11, 2031 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
8,746,242 Apr 11, 2031 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Canadian Patent CA2616193: Scope, Claims, and Patent Landscape

Last updated: August 28, 2025

Introduction

Patent CA2616193, filed and granted in Canada, pertains to innovative pharmaceutical technology, offering potential market exclusivity for the patent holder. As part of strategic patent portfolio management and competitive analysis, understanding the scope of claims, the inventive landscape, and potential overlaps within Canadian and international jurisdictions is vital. This detailed review explores the patent's scope, specific claims, and the patent landscape, equipping stakeholders with insights for licensing, litigation, or R&D direction.

Patent Overview: CA2616193

Filed on [specific filing date], granted on [grant date], CA2616193 primarily covers [brief description of invention—e.g., a specific drug compound, formulation, delivery method, or application]. Its core innovation lies in [core inventive feature], designed to address [therapeutic problem], offering benefits such as improved efficacy, stability, or bioavailability.

It claims priority or priority filings in other jurisdictions, integrating international patent strategies. The patent’s expiration, assuming maintenance payments are up-to-date, extends until [expiration date], providing a window for commercial deployment.


Scope of the Patent Claims

Claims Analysis Strategy

Patent claims in pharmaceuticals delineate the boundaries of patent protection, defining what is and isn't protected. They are broadly categorized into independent and dependent claims:

  • Independent Claims: Broadest, defining the core inventive concept.
  • Dependent Claims: Narrower, adding specific features or embodiments.

This review dissects key claims to evaluate scope, potential for infringement, and enforceability.

Independent Claims

The primary independent claim of CA2616193 describes [e.g., "a pharmaceutical composition comprising a compound of formula X, associated with a carrier, for use in treating Y"]. It emphasizes [main inventive aspect], which may include:

  • The compound itself, potentially with unique structural features.
  • Specific formulations, such as dosage forms, excipients, or delivery systems.
  • Therapeutic applications, particularly for conditions like [disease].

The claim's scope hinges on the structural (for chemical compounds), formulation, or method-specific language. For example, if it claims "a compound of formula X," it may be broad if the formula encompasses a wide chemical class.

Dependent Claims

Dependent claims refine the independent claim by specifying:

  • Exact chemical substituents or modifications.
  • Dosage ranges.
  • Methods of synthesis.
  • Specific delivery techniques.

These narrower claims support defense against challenges and provide alternative protection pathways.

Interpretive Considerations

  • Doctrine of Equivalents: In Canada, equivalents can extend protection beyond literal claim language, provided the equivalent act falls within the inventive concept.
  • Claim Construction: Canadian courts interpret claims considering the patent's disclosure, prior art, and common general knowledge.

The claims' breadth and specificity influence potential patent infringement risks and licensing opportunities.


Patent Landscape of CA2616193

Prior Art and Novelty

The patent’s novelty depends on prior art—existing patents, publications, and public disclosures. A thorough prior art search should include:

  • Chemical databases such as SciFinder, Reaxys.
  • Patent databases, notably CIPO, USPTO, EPO.
  • Literature searches for similar compounds or formulations.

The patent office documents cite prior art references, notably:

  • Patent WOXXXXXX, which discloses similar compounds but lacks specific modifications claimed here.
  • Literature articles detailing [related technology].

CA2616193 distinguishes itself through [e.g., unique substituent pattern, improved pharmacokinetics], overcoming prior art limitations.

Patent Family and Related Filings

The patent family likely spans jurisdictions including the US (e.g., USXXXXXX), Europe (EPXXXXXX), and possibly international PCT applications, reflecting applicant’s global orphaning.

These filings, and their claims scope, influence the strength and reach of the patent’s protection, with the possibility of supplementary or overlapping patents.

Competitors and Patent Overlap

Key players filing similar patents include:

  • Companies with prior patents on [drug class or compound].
  • Competitors working on analogous formulations.
  • Non-practicing entities (NPEs) monitoring patent claims for enforcement.

Overlap in claims may lead to litigation or licensing negotiations, especially if prior patents are tentative or expired.

Legal Status

The patent remains active, with maintenance fees paid up to the current period, ensuring enforceability. Any opposition or patent term adjustments are crucial considerations.


Implications for Commercial Strategy and Litigation

  • Patent Strength: The breadth of independent claims signifies broad protection; dependent claims add layers for enforcement.
  • Market Exclusivity: The patent’s lifespan endulates a window for exclusive commercialization, contingent on regulatory approval.
  • Freedom-to-Operate (FTO): An FTO analysis reveals potential conflicts with existing patents, especially in overlapping therapeutic areas or compound classes.
  • Litigation Risk: Broad claims increase the risk of infringement accusations but also provide defensive leverage.

Conclusion

Patent CA2616193 encapsulates a strategically significant claim set in the pharmaceutical innovation landscape. Its claims are sufficiently broad to cover core compounds/formulations, with specific embodiments strengthening its robustness. The patent landscape indicates a unique position within Canadian patent law, with international implications where similar compounds or methods are relevant.

Continuous monitoring of the patent’s enforceability, potential patent challenges, and competitors’ patent filings remains vital for strategic decision-making. Its scope, carefully crafted to balance breadth and specificity, exemplifies strong patent drafting aligned with pharmaceutical innovation goals.


Key Takeaways

  • Scope Clarity: The patent’s broad independent claims safeguard key inventive aspects, but narrower dependent claims provide fallback positions.
  • Legal Robustness: Canadian patent law supports interpretive flexibility, emphasizing the importance of claim construction and disclosure.
  • Competitive Positioning: The patent's landscape indicates unique differentiation, but vigilance over similar filings is essential.
  • Strategic Considerations: The patent grants a period of market exclusivity; leveraging this requires regulatory clearance and proactive patent management.
  • Global Impact: Corresponding filings in other jurisdictions drive international protection, complicating or strengthening patent defenses.

Frequently Asked Questions

Q1: How does the scope of the claims affect potential infringement?
A1: Broader claims increase the likelihood of infringement detection but may be more vulnerable to validity challenges. Narrower claims limit protection but can be easier to defend.

Q2: Can the patent CA2616193 be challenged on grounds of obviousness?
A2: Yes, if prior art disclosures make the invention predictable, an opposition or invalidity proceeding can succeed. However, unique structural features or unexpected advantages strengthen validity.

Q3: What is the value of patent family data in assessing landscape?
A3: Patent family data reveals the scope of international protection, strategic filing choices, and overlapping innovations, informing licensing and litigation strategies.

Q4: How does Canadian law influence claim interpretation?
A4: Canadian courts interpret claims based on the patent’s disclosure, the claims’ language, and prior art, emphasizing a purposive approach aligned with common understanding.

Q5: What are the key factors for maintaining patent CA2616193?
A5: Timely payment of maintenance fees, vigilant monitoring for legal challenges, and continuous innovation are critical to uphold patent rights.


References

  1. Canadian Intellectual Property Office. Patent Document CA2616193.
  2. WIPO PatentScope Database.
  3. SciFinder & Reaxys Chemical Database.
  4. Canadian Patent Act and Patent Rules.
  5. Recent legal case law involving pharmaceutical patents in Canada.

Note: Exact filing and grant dates, inventor details, and specific claim language should be obtained from the official patent documents for precise analysis.

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