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Last Updated: December 12, 2025

Profile for Canada Patent: 2668211


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US Patent Family Members and Approved Drugs for Canada Patent: 2668211

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 Mar 11, 2029 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
⤷  Get Started Free Oct 7, 2025 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2668211

Last updated: July 30, 2025

Introduction

Canada Patent CA2668211, titled "Pharmaceutical compounds for treating metabolic disorders," exemplifies strategic intellectual property protection within the pharmaceutical landscape. This patent primarily focuses on novel compounds and their use in managing metabolic conditions such as type 2 diabetes and obesity. An in-depth review of its scope, claims, and the broader patent landscape reveals critical insights for stakeholders, including pharmaceutical companies, generic manufacturers, and legal entities.

Scope of Patent CA2668211

The patent's scope encapsulates a patentable class of chemical compounds, their synthesis, and their therapeutic use, particularly in treating metabolic disorders. The inventive scope hinges on specific chemical structures, their modifications, and methods of use.

Chemical Composition and Variants

The patent claims encompass a subclass of compounds characterized by a core structure with various substituents allowing chemical diversity. This diversity aims to cover a broad spectrum of derivatives, increasing territorial and procedural robustness against workarounds.

Method of Use

Claims detail the therapeutic application, notably in reducing blood glucose levels, managing insulin resistance, or suppressing appetite. Such claims extend protection to methods of treating metabolic diseases using these compounds, aligning with patent strategies that cover both composition and use.

Method of Manufacturing

The patent includes processes for synthesizing these compounds, further expanding the scope into the realm of proprietary production methods, which can deter generic entry and provide manufacturing exclusivity.


Claims Analysis

The patent features a multi-layered claim structure, typical for pharmaceutical patents, consisting of independent claims detailing the chemical compounds and dependent claims specifying particular derivatives, dosage forms, and methods of treatment.

Independent Claims

  • Chemical structure claims specify a chemical scaffold with defined substituents, covering a class of compounds with potential therapeutic benefits.
  • The therapeutic method claims outline using these compounds in conditions such as type 2 diabetes, obesity, and related metabolic syndromes.
  • The method of synthesis claims specify steps to produce the compounds, covering proprietary manufacturing techniques.

Dependent Claims

  • Cover specific chemical variants with particular substituents, such as halogens, methyl groups, or functional groups.
  • Encompass dosage ranges, formulations (e.g., tablets, injectables), and administration protocols.
  • Cover combinations with other therapeutic agents, broadening the claim scope to combinatorial formulations.

Claim Strengths and Limitations

  • Strengths: The breadth of structural claims combined with method claims increases enforceability. The inclusion of formulation and use claims prevents straightforward design-arounds.
  • Limitations: The scope's reliance on specific chemical structures may face challenges if prior art discloses similar cores with minor modifications. The patent’s lifespan and enforceability depend on jurisdictional considerations, especially given the typical 20-year term from filing.

Patent Landscape in Canada and Globally

Canadian Patent Environment

Canada's patent system offers robust protection for pharmaceutical inventions through the Patent Act and Canada Patent Rules. However, patent term adjustments and exclusivity periods can impact pharmaceutical patent valuation.

  • Patent Examination: The Canadian Intellectual Property Office (CIPO) applies a substantive examination, ensuring the patent meets novelty, inventive step, and utility requirements.
  • Recent Trends: Canadian courts have historically upheld pharmaceutical patents but remain critical of overly broad claims, emphasizing specific structural features.

Global Patent Landscape

The patent landscape for compounds like those in CA2668211 reflects intense competition:

  • Patent Families: Innovators often file multiple patents worldwide, including the US, Europe, Japan, and China, to secure comprehensive market exclusivity.
  • Similar Patents: Global patents often cover chemical classes, such as thiazolidinediones, SGLT2 inhibitors, or DPP-4 inhibitors, which are common in metabolic disorder therapeutics.
  • Freedom-to-Operate (FTO): Companies must navigate existing patents for similar compounds or mechanisms, where prior art may challenge the novelty of the claimed structures.

Patent Filing Strategies

  • Early filing to secure priority rights.
  • Patent families to extend protection across jurisdictions.
  • Continuations and divisional applications to broaden or sharpen scope.

Competitive Landscape

While CA2668211 provides broad protection, competitors often seek design-around strategies by modifying chemical structures, focusing on specific derivatives, or pursuing combinatorial approaches. Patent landscapes emphasize the importance of meticulous claim drafting to balance breadth with defensibility.


Legal and Strategic Implications

  • The broad chemical claims promote market exclusivity; however, interventions based on prior art or obviousness can challenge validity.
  • Extensive patent protection across markets increases barriers for generics, aligning with regulatory exclusivity periods.
  • Companies must monitor patent thickets and litigation trends to enforce or circumvent existing rights effectively.

Conclusion

Patent CA2668211 exemplifies a comprehensive pharmaceutical patent, covering chemical compositions, methods of use, and manufacturing processes in the Canadian context. Its scope reflects strategic efforts to maximize exclusivity against competitors while complying with jurisdictional patent standards. For stakeholders, understanding its claims and landscape positioning is vital for making informed decisions regarding lifecycle management, patent enforcement, licensing, or generic entry.


Key Takeaways

  • The patent covers a broad class of chemical derivatives with therapeutic use in metabolic disorders, bolstered by multiple claim categories.
  • Claim structure strategically encompasses compound composition, use, formulation, and manufacturing, offering robust protection.
  • The Canadian patent landscape is competitive, with considerations for prior art and claim specificity impacting enforceability.
  • Global patent strategies involve meticulous family planning and jurisdictional filings to secure comprehensive market rights.
  • Vigilance regarding patent challenges and patent thickets is essential for navigating the competitive pharmaceutical space effectively.

FAQs

Q1: How does CA2668211 compare to similar patents in the metabolic disorder therapeutic space?
A: It advances protection by covering a broad class of compounds and multiple claim types, aiming to capture extensive therapeutic and manufacturing methods, a common approach but contingent on its specific chemical scope and claim language.

Q2: What are potential challenges to the validity of this patent?
A: Challenges may arise from prior art that discloses similar chemical structures or obvious modifications, as well as from prior publications and existing patents that narrow novelty or inventive step.

Q3: How can competitors circumvent CA2668211?
A: By designing around specific structural claims, developing alternative compounds outside the scope, or claiming different therapeutic mechanisms, competitors can seek to avoid infringement.

Q4: What is the significance of patent claims covering methods of manufacture?
A: Such claims provide exclusivity over proprietary synthesis processes, preventing generic manufacturers from copying production techniques and strengthening market position.

Q5: How does patent law in Canada influence the scope of pharmaceutical patents?
A: Canadian law emphasizes claim clarity, novelty, inventive step, and utility. Patent drafting must balance broad protection with specificity to withstand legal scrutiny and avoid invalidation.


Sources:

  1. Canadian Intellectual Property Office. (2022). Patent Act and Rules.
  2. WIPO. (2021). Patent landscapes in the pharmaceutical sector.
  3. European Patent Office. (2020). Guidelines for examination of chemical inventions.
  4. US Patent and Trademark Office. (2022). Patent prosecution in pharmaceutical industries.
  5. Canadian Patent Database. (2022). Patent CA2668211.

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