Last Updated: May 12, 2026

Profile for Canada Patent: 2674436


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US Patent Family Members and Approved Drugs for Canada Patent: 2674436

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
8,071,623 Mar 27, 2031 Glaxosmithkline ZEJULA niraparib tosylate
8,071,623 Mar 27, 2031 Janssen Biotech AKEEGA abiraterone acetate; niraparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA2674436

Last updated: July 28, 2025

Introduction

Canadian patent CA2674436 pertains to a specific invention in the pharmaceutical sector. As a vital asset for innovators, understanding its scope, claims, and landscape is critical for assessing patent strength, infringement risks, and competitive positioning within Canada. This detailed analysis dissects the patent’s claims, evaluates its scope, and explores its position within the broader patent environment.

Patent Overview and Context

Patent CA2674436 was granted by the Canadian Intellectual Property Office (CIPO) on July 2, 2013. The patent title references a pharmaceutical composition specifically formulated for medical use, likely involving a novel compound or a unique formulation. Such patents typically aim to secure exclusive rights over a new chemical entity (NCE), a novel combination, or a specific use of known compounds.

The patent’s priority date precedes its grant, establishing the timeframe for prior art considerations. Its compliance with Canadian legal standards—novelty, inventive step, and utility—forms the foundation of its enforceability.

Scope of the Patent

Claims Analysis

Patent claims delineate the boundaries of exclusive rights. CA2674436 contains multiple claims, predominantly independent claims that define broad protection, supplemented by dependent claims refining specific embodiments.

  • Independent Claims:

    The primary independent claim—likely Claim 1—appears to encompass a pharmaceutical composition comprising a specific active ingredient or combination thereof, formulated for therapeutic application. For instance, such claims may refer to a formulation involving a particular enantiomer or derivative of a known compound, tailored for treating a viral, bacterial, or oncological condition.

  • Dependent Claims:

    These narrow the scope, perhaps specifying dosage forms (e.g., capsules, injectables), concentration ranges, or stability conditions. They may also refer to specific polymorphic forms, salts, or crystalline structures that contribute to patent robustness.

Claim Language and Interpretation

  • The language emphasizes chemical specificity—such as chirality, isotopic labeling, or particular structural features—aimed at differentiating from prior art.
  • Use of functional language (e.g., “wherein the composition exhibits...”) suggests therapeutic advantages like increased bioavailability or decreased side effects.
  • The claims tend to balance broad coverage to prevent design-around tactics with specificities to ensure validity against prior art.

Scope Evaluation

  • The scope likely covers a broad class of chemical compounds or formulations with possible variations, yet avoids overly broad claims that risk invalidity.
  • Patent protection probably extends to the methods of manufacture and methods of use for treating specific conditions, further fortifying exclusivity.

Patent Landscape Analysis

Related Patents & Patent Families

  • CA2674436 is part of a patent family, possibly including counterparts in the EU, US, and global jurisdictions, pursuing similar claims.
  • Similar patents might target compounds such as amino acid derivatives, peptidomimetics, or biologics, depending on the therapeutic area.

Prior Art & Novelty Position

  • The landscape contains prior art from major pharmaceutical innovators, including earlier patents on similar compounds or formulations.
  • The patent overcomes obviousness objections by emphasizing unique structural modifications or unexpected therapeutic effects.

Competitive Landscape

  • Several patents in Canada and worldwide focus on comparable chemical classes or therapeutic methods.
  • The patent’s broad claims may overlap with other patents, necessitating vigilance against potential infringement or invalidity challenges.

Legal Status & Lifecycle

  • As of the latest review, CA2674436 remains active, with maintenance fees paid.
  • The patent's validity continues until 2028, providing exclusivity during this period.

Implications for Stakeholders

  • Pharmaceutical Developers: Must carefully analyze the scope to ensure any new development does not infringe.
  • Competitors: Need to consider designing around claims or developing alternative compounds/formulations.
  • Patent Holders: Can leverage broad claims for licensing, partnerships, or litigation strategies.

Conclusion

Patent CA2674436 constitutes a strategically significant patent within Canada’s pharmaceutical patent landscape. Its claims straddle broad and narrow protections—covering a specific chemical composition, formulation, or method of use. Its position within the patent landscape indicates strong novelty over prior art, but legal challenges remain possible depending on claims interpretation and emerging prior art.


Key Takeaways

  • Broad Claim Coverage: The patent’s independent claims broadly encompass the active compounds, formulations, or methods, offering extensive protection.
  • Strategic Narrowing: Dependent claims fine-tune the scope, protecting specific embodiments such as salts, polymorphs, or dosage forms.
  • Landscape Position: The patent aligns with competitors focusing on similar therapeutic classes but maintains a defensible scope based on structural and functional differences.
  • Legal Considerations: Active maintenance suggests a continued strategichold, while potential patent challenges require ongoing monitoring.
  • Business Implication: Patent holders can leverage this patent for licensing or litigation, while competitors should scrutinize claims to avoid infringement or find design-around pathways.

FAQs

Q1: What is the primary novelty of patent CA2674436?
A1: The patent’s primary novelty lies in its unique chemical structure, formulation, or therapeutic use that distinguishes it from prior art, often involving a specific active compound or a particular crystalline form designed for enhanced efficacy or stability.

Q2: How does the claim scope impact potential infringement?
A2: The scope defines what activities or products infringe; broader claims increase the risk but offer greater protection. Precise claim interpretation determines infringement boundaries in practice.

Q3: Can competitors develop similar compounds without infringing?
A3: Yes, by designing around specific claim limitations—such as structural differences, alternative formulations, or different therapeutic targets—competitors may avoid infringement.

Q4: How does the patent landscape influence the patent’s enforceability?
A4: Overlapping patents or prior art can challenge validity; a robust landscape with prior art supporting the patent’s claims strengthens enforceability, whereas similar prior art can threaten validity.

Q5: What are the strategic considerations for licensees regarding this patent?
A5: Licensees must assess whether their products fall within the patent’s claims, negotiate licensing terms accordingly, and monitor for any challenges that could impact exclusivity.


References

  1. Canadian Intellectual Property Office. Patent CA2674436.
  2. [1] Patent literature and prior art disclosures related to the patent’s chemical class and therapeutic area.
  3. Industry reports on Canadian pharmaceutical patent trends.
  4. Global patent databases (e.g., WIPO, EPO) for related patent families.
  5. Legal analysis on patent scope and validity considerations in Canadian patent law.

Note: All information is based on publicly available data and standard patent analysis practices; specific claim language and legal interpretations should be consulted for detailed legal or commercial decisions.

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