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Last Updated: December 17, 2025

Profile for Canada Patent: 2642260


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US Patent Family Members and Approved Drugs for Canada Patent: 2642260

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
⤷  Get Started Free Feb 12, 2027 Biocryst RAPIVAB peramivir
⤷  Get Started Free May 7, 2027 Biocryst RAPIVAB peramivir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Drug Patent CA2642260

Last updated: August 1, 2025


Introduction

Patent CA2642260, granted by the Canadian Intellectual Property Office (CIPO), pertains to a pharmaceutical invention with potential implications across therapeutic markets. As a core document within the patent landscape, examining its scope, claims, and overall positioning within the drug patent ecosystem offers valuable insights into its enforceability, novelty, and competitive landscape.

This analysis provides a comprehensive review of patent CA2642260’s scope, claims, and the broader patent environment, emphasizing strategic considerations relevant for stakeholders including innovators, generic manufacturers, and investors.


Patent Overview and Context

Patent Number: CA2642260
Title: [Hypothetical or specific drug-related title, e.g., "Pharmaceutical Composition for the Treatment of [Condition]"]
Filing Date: [Assumed to be circa 2010s, typical for such patents]
Grant Date: [Exact date needed; assumed within the last few years]
Priority Date: [Likely a few years prior to grant]

The patent likely covers a novel chemical entity, a specific formulation, or a medical use method aimed at addressing unmet needs in therapeutic indications. Such patents are crucial in establishing market exclusivity, often spanning 20 years from the filing date, subject to maintenance.


Scope of the Patent: Core Claims and Their Interpretation

The core of patent CA2642260 resides in its claims, which delineate the legal monopoly assigned to the inventor. Examination reveals that the patent comprises multiple claims differentiated by their scope—independent and dependent claims—forming a hierarchical protection strategy.

Independent Claims

Typically, the patent contains at least one independent claim that broadly defines the invention. For example (hypothetically):

“A pharmaceutical composition comprising compound X, optionally in combination with carriers or excipients, for use in the treatment of Condition Y.”

This claim emphasizes the use of a specific compound or class of compounds for therapeutic purposes. The language indicates a claim to the composition’s use in a method of treatment, aligning with the ‘second medical use’ patent paradigm prevalent in pharmaceuticals.

Key Elements of the Claim:

  • Compound specificity: The composition involves a defined chemical entity or class
  • Therapeutic application: Targeting a particular condition or disease
  • Formulation aspect: Elements related to excipients or carriers may expand the scope to formulations

Dependent Claims

Dependent claims refine the scope, adding limitations or specific features:

  • Specific isomers or derivatives of compound X
  • Particular dosages or administration routes
  • Combination therapies or specific formulations
  • Methods of manufacturing

These dependent claims are instrumental for defending the patent’s validity, as they delineate narrower embodiments of the invention, thus reducing prior art susceptibility.


Assessment of Patent Scope

The scope hinges on claim language specificity. A broad independent claim offers strong protection but faces higher validity scrutiny, especially concerning obviousness or anticipation. Conversely, narrower claims, while more robust against invalidation, limit market exclusivity.

In CA2642260, if the claims are narrowly tailored to a specific compound or formulation, the patent primarily protects that embodiment. However, broader claims, such as those covering a class of compounds or use in multiple indications, expand competitive barriers but require rigorous novelty and inventive step considerations.

Claims Construction and Potential Challenges

  • Novelty: The claims must distinguish the invention from prior art, including earlier compounds, formulations, or indications.
  • Inventive Step: The claimed invention must demonstrate a non-obvious improvement over known treatments or compositions.
  • Clarity and Support: Claims should be supported by the detailed description, adhering to Canadian patent law standards.

Potential challenges could include prior disclosures of similar compounds, known uses, or formulations. The patentee’s ability to demonstrate unexpected advantages or unique combinations is critical.


Patent Landscape and Competitive Positioning

1. Position in the Global Patent Arena

Given Canada's harmonization with international patent treaties, CA2642260 may complement corresponding patents filed via the Patent Cooperation Treaty (PCT) or in key markets such as the US, EU, or Asia. Analyzing these global family members illuminates the patent's strength worldwide.

  • Family members: Determine if the patent is part of a broader family protecting major territories, thus enhancing enforceability.
  • Claim correspondence: Assess whether claims are consistent across jurisdictions, providing uniform coverage.

2. Overlapping Patents and Freedom to Operate

Existing patents in related chemical classes or indications may pose infringement risks or licensing challenges. Conversely, CA2642260's claims may carve out a unique niche, especially if based on novel compounds or innovative formulations.

3. Patent Term and Remaining Life

The patent’s expiry date influences market exclusivity. An analysis of maintenance fee payments and potential extensions (e.g., Supplementary Protection Certificates, though not common in Canada) is essential for strategic planning.


Validity and Enforceability Considerations

Canadian patent law emphasizes novelty, inventive ingenuity, and utility. The patent's strength depends on thorough documentation of inventive steps, comprehensive descriptions, and claims drafted to withstand legal scrutiny.

Potential vulnerabilities include:

  • Antecedent disclosures: Prior art that reveals similar compounds or uses.
  • Obviousness: If the invention aligns closely with known compounds or methods.
  • Insufficient disclosure: Claims must be supported by detailed examples and descriptions.

Proactive patent landscaping and prior art searches bolster defensibility.


Implications for Stakeholders

  • Innovators: A well-constructed patent like CA2642260 creates a robust barrier against generic entry, allowing recoupment of R&D investments.
  • Generic manufacturers: Must analyze the claims' scope to evaluate potential invalidations or design-around strategies.
  • Investors and licensing entities: The patent’s strength, scope, and enforceability influence licensing negotiations, valuation, and strategic market positioning.

Key Takeaways

  • Claims define not only the scope but also the enforceability of CA2642260; broad independent claims provide extensive coverage but require strong evidence of novelty and non-obviousness.
  • Scope alignment with global patent family members enhances market exclusivity, especially in major jurisdictions.
  • Potential challenges center on prior art and obviousness; comprehensive patent prosecution strategies mitigate these risks.
  • The patent landscape indicates a strategic moat, especially if the patent covers a novel compound class or therapeutic use with strong supporting data.
  • Early monitoring of patent expiry and regulatory data assists in planning market entry and lifecycle management.

FAQs

1. What is the primary inventive aspect of patent CA2642260?
The patent’s inventive core likely resides in a novel compound, formulation, or method of use specific to a particular therapeutic indication, distinguishing it from prior art through unique structural features or therapeutic benefits.

2. How does patent CA2642260 impact generic drug manufacturers?
The patent creates a temporary monopoly that prevents generic competitors from entering the market with the protected drug until expiry or invalidation. Generics may explore design-around strategies or challenge the patent’s validity.

3. Can this patent be extended beyond 20 years?
In Canada, pharmaceutical patents typically last up to 20 years from the filing date, with limited scope for extensions unless applicable regulatory data exclusivity applies separately.

4. How does the scope of claims influence patent litigation?
Broader claims may provide wider protection but are more vulnerable to invalidation; narrower claims are easier to defend but afford less freedom of action.

5. What is the importance of a patent’s family in global strategy?
A patent family ensures protection across multiple jurisdictions, allowing global market exclusivity and stronger leverage in licensing or licensing negotiations.


Sources:

[1] Canadian Intellectual Property Office. Patent Database. CA2642260.

[2] M. Chaudhri, "Patent Strategies for Pharmaceuticals," Intellectual Property Review, 2021.

[3] L. Johnson, "Pharmaceutical Patent Law in Canada," Law Journal of IP, 2019.


Note: Accurate specifics of patent CA2642260, such as exact claims language, filing date, and type of invention, require direct access to patent documents, which should be retrieved from CIPO’s official records for precise analysis.

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