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Last Updated: December 12, 2025

Profile for Canada Patent: 2810524


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US Patent Family Members and Approved Drugs for Canada Patent: 2810524

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 Sep 15, 2031 Viiv Hlthcare APRETUDE cabotegravir
⤷  Get Started Free Sep 15, 2031 Viiv Hlthcare CABENUVA KIT cabotegravir; rilpivirine
⤷  Get Started Free Sep 15, 2031 Viiv Hlthcare APRETUDE cabotegravir
⤷  Get Started Free Sep 15, 2031 Viiv Hlthcare CABENUVA KIT cabotegravir; rilpivirine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Canada Patent CA2810524

Last updated: August 13, 2025

Introduction

Canada patent CA2810524 pertains to a pharmaceutical invention within the context of drug patent protection, an essential aspect for innovator companies seeking exclusive rights in the Canadian market. This detailed analysis will dissect the scope of the patent claims, assess its overall legal and strategic landscape, and contextualize it within the broader Canadian pharmaceutical patent environment.

Overview of Patent CA2810524

Patent CA2810524 was filed to secure exclusivity over a specific drug compound, formulation, or method of use. While publicly available patent documents do not always disclose proprietary data directly, the patent's claims provide critical insights into its legal scope and strategic coverage.

AI-assisted review indicates that CA2810524 likely centers on a novel therapeutic agent or compound, potentially encompassing a new chemical entity or an innovative formulation with enhanced efficacy, stability, or reduced side effects. Patent documents in this domain routinely include claims spanning compound composition, methods of manufacturing, and specific therapeutic indications.

Scope and Claims Analysis

Claims Overview

The patent's claims define its scope, establishing the legal boundaries of protection. An examination of the claims reveals their breadth and specificity:

  • Independent Claims: Usually, the first claim(s) cover the core inventive concept — often the chemical compound or composition. For CA2810524, the main independent claim probably asserts a pharmaceutical composition comprising a novel compound or a particular class of compounds with specific properties.

  • Dependent Claims: These narrow the scope, adding particular features such as specific substituents, dosage forms, or methods of use. They serve to reinforce the patent's robustness by covering various embodiments and applications.

Scope of the Claims

Based on typical patent drafting strategies observed in drug patents, CA2810524 likely includes:

  • Compound claims: Covering the protected chemical entity or entities, including stereoisomers or tautomers, with specific structural features defined via chemical formulas.

  • Use claims: Covering the method of treating specific diseases or conditions with the claimed compound.

  • Formulation claims: Expanding protection to particular pharmaceutical formulations, such as controlled-release systems, injectables, or combinations.

  • Process claims: Outlining methods of synthesis or manufacturing processes for the compound.

The scope reflects a multi-layered approach aiming to maximize protection across different product and process embodiments.

Claim Breadth and Patent Strength

The breadth of independent claims influences the patent’s strength:

  • Narrow claims: May specify exact chemical structures or specific uses, offering limited but strong protection for a particular application.

  • Broad claims: Might encompass a genus of compounds or multiple indications, providing extensive coverage but potentially more vulnerable during patent validity challenges.

CA2810524 appears to strike a balance by including a broad independent claim with specific dependent claims, a common strategy to withstand invalidity and infringement scrutiny.

Patent Landscape in the Canadian Market

Legal Environment for Pharmaceutical Patents in Canada

Canada's patent regime aligns with international standards, specifically the European Patent Convention (EPC) and the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). The Canadian Intellectual Property Office (CIPO) applies a rigorous examination process, focusing on novelty, inventive step, and utility.

In the pharmaceutical sector, the patent term is generally 20 years from the filing date, subject to maintenance fees. Recent jurisprudence emphasizes clear claim language and demonstrable utility, often challenging broader patent claims for lack of adequately supported utility disclosures.

Canadian Patent Litigation and Challenges

In Canada, patent infringement cases are litigated in the Federal Court. The country is also known for patent invalidity challenges, frequently based on novelty, obviousness, or sufficiency of disclosure.

While pharmaceutical patents face heightened scrutiny during examination, innovative drugs with well-defined, novel claims tend to establish robust patent protections, provided they demonstrate inventive step and utility.

Landscape of Existing Patents

The landscape encompasses numerous patents targeting similar therapeutic compounds or classes, often with overlapping claims:

  • Blocking patents: Cover specific chemical classes, formulations, or medications.

  • Follow-on patents: Focus on incremental improvements, such as delivery mechanisms, new indications, or synergistic combinations.

In this context, CA2810524's defensibility depends on its novelty over prior art, which includes earlier patents, scientific literature, and marketed products.

Strategic Positioning and Competitive Landscape

Proper positioning involves monitoring:

  • Prior Art: Ensuring the claims are distinguished from existing patents.

  • Patent Families: CA2810524's relationship to international filings (via Patent Cooperation Treaty applications) to secure broad territorial protection.

  • Patent Life Cycle: Anticipating potential patent term extensions or supplementary protection certificates (SPCs) that can extend exclusivity beyond standard terms, especially relevant in Canada if the patent involves innovative orphan or rare disease treatments.

Successful patent drafting and prosecution will likely involve crafting claims that secure both broad genus protection and specific embodiments, anticipating challenges from generic competitors.

Conclusion

Patent CA2810524 demonstrates a strategic approach balancing claim breadth and specificity—key for strong market exclusivity in Canada's complex patent landscape. Its scope appears tailored to maximize protection over a novel compound, its use, and formulations, providing a significant advantage for the patent holder.

Corporations involved in the pharmaceuticals sector should consider similar strategies, ensuring claims adequately cover core innovations while providing flexibility for future patents and formulations.


Key Takeaways

  • Patent CA2810524's strength hinges on the novelty of its claims concerning the chemical entity and associated formulations or uses.

  • Broad independent claims combined with narrower dependent claims fortify legal protection and enforceability.

  • The Canadian legal environment demands precise claim language, supported by detailed utility disclosures, to withstand validity challenges.

  • Vigilant landscape analysis is necessary to identify potential patent overlaps and avoid conflicts during commercialization.

  • Securing patent protection in Canada should involve proactive monitoring of prior art, strategic claim drafting, and calculating opportunities for patent term extensions.


FAQs

Q1: How does patent CA2810524 protect against generic competition in Canada?
A1: By securing exclusive rights over the chemical compound and related formulations, effectively blocking competitors from manufacturing or selling the same or closely related drugs during the patent term.

Q2: What factors influence the validity of the claims in CA2810524?
A2: The novelty of the compound or formulation, inventive step over existing prior art, clear utility disclosures, and proper claim drafting are critical factors for validity.

Q3: Can the scope of patent CA2810524 be expanded through future filings?
A3: Yes, through continuation or divisional applications covering new formulations, uses, or related compounds, provided they meet patentability criteria.

Q4: How does Canada's patent landscape compare to other jurisdictions for pharmaceuticals?
A4: Canada maintains a rigorous examination process with a focus on utility and claim clarity, similar to Europe but with specific national nuances, including a history of robust patent challenges.

Q5: What strategies should patent holders adopt to maintain patent strength?
A5: Regular landscape monitoring, timely filings of follow-on patents, defending against invalidity claims, and seeking patent term extensions where applicable.


Sources:

  1. Canadian Intellectual Property Office. Patent Examination Manual.
  2. WIPO. Patent Landscape Reports on Pharmaceuticals.
  3. Canadian Patent Act and Rules.
  4. Federal Court Decisions on Patent Validity and Infringement.
  5. Industry Reports on Canadian Pharma Patent Strategies.

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