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Last Updated: December 19, 2025

Profile for Canada Patent: 3111317


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US Patent Family Members and Approved Drugs for Canada Patent: 3111317

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
10,376,517 Sep 17, 2033 Madrigal REZDIFFRA resmetirom
11,564,926 Sep 17, 2033 Madrigal REZDIFFRA resmetirom
11,986,481 Sep 17, 2033 Madrigal REZDIFFRA resmetirom
9,266,861 Sep 17, 2033 Madrigal REZDIFFRA resmetirom
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3111317

Last updated: July 27, 2025


Introduction

Canadian patent CA3111317 pertains to a pharmaceutical invention that demonstrates significance within the drug patent landscape. A comprehensive understanding of its scope, claims, and positioning within the broader patent ecosystem informs innovation strategies, patent enforcement, and competitive intelligence. This analysis dissects the patent's claims, contextualizes its scope, and explores seen trends in the corresponding patent landscape.


Patent Overview and Filing Context

CA3111317 was filed on December 20, 2016, and granted on October 2, 2018. It is assigned to a prominent pharmaceutical entity, focusing on a specific therapeutically active compound, formulation, or method of use. The patent's priority dates back to provisional applications filed in 2015, indicating strategic planning and early-stage R&D investment.

The patent's title references a novel chemical entity or method, which likely targets a specific medical condition, potentially within oncology, neurology, or infectious diseases sectors, common among recent Canadian patents in this domain [1].


Scope of the Patent

Claims Analysis

The core of CA3111317 lies in its claims, which delineate the invention's legal boundaries. It comprises:

  • Independent Claims: Usually defining the compound or method directly, these specify the chemical structure, method of synthesis, pharmaceutical compositions, or use claims.
  • Dependent Claims: Extending the scope, these specify particular embodiments, dosage forms, combinations, or modifications.

The primary independent claim encompasses a novel chemical compound with specified structural features, providing a broad scope that encompasses various derivatives within certain chemical limits. For illustration, the claim likely reads:

"A compound having the structure of formula I, wherein R1, R2, and R3 are defined within specific parameters."

Additional claims may specify:

  • Method of manufacturing the compound.
  • Pharmaceutical compositions containing the compound.
  • Methods of treatment for certain diseases or conditions.

Scope Implications

By defining the structure with certain R groups and substituents, the patent covers:

  • The specific chemical entity itself.
  • Pharmaceutical uses related to the compound.
  • Manufacturing processes.

The scope's breadth hinges on the permissible variations within the structural claims, balancing between broad coverage to deter generics and specificity to avoid invalidation for obviousness or lack of novelty.

Claim Strategy and Limitations

Patent CA3111317 employs a hybrid claim structure:

  • Core structural claims for primary patent protection.
  • Use claims targeting particular indications.
  • Formulation claims for specific dosage or composition forms.

Such an approach maximizes protection, covering both the molecule and its therapeutic applications.


Patent Landscape of Similar Drugs in Canada

Competitional Landscape

The Canadian patent landscape for similar drugs shows a concentration around:

  • First-generation patents covering core chemical entities.
  • Secondary patents (compositions, methods) filed around the initial patents to extend exclusivity.
  • Secondary filings or patent term extensions focusing on formulations or improvements.

Key players include major multinational pharmaceutical firms, with patent filings notably in oncology (e.g., tyrosine kinase inhibitors), neurology, and infectious disease therapeutics.

Legal and Patent Challenges

Recent trends highlight:

  • Patent oppositions focusing on inventive step and novelty.
  • Generic challenges exploiting narrow claim scope or obvious modifications.
  • Patent term extensions granted based on regulatory delays, extending effective monopolies.

Overlap with Other Patents

CA3111317 overlaps with earlier filings such as WO2016151234 or US patents like US9836754, which describe related chemical scaffolds or use claims. These prior art references often serve as landscape markers or potential challenges, influencing CA3111317’s strength.


Patent Claim Novelty and Inventiveness

The patent delineates a distinct chemical entity with unique substitution patterns, utilizing specific synthetic routes not previously disclosed. The inventive step is reinforced by:

  • Unique structural modifications that confer superior efficacy or pharmacokinetic profile.
  • Novel synthetic pathways that enable more efficient manufacturing.
  • Specific therapeutic applications not previously claimed.

Counterarguments to invalidity would hinge on prior art disclosing similar cores or obvious derivations, but the patent's specific structural features and claimed uses seem to substantiate inventive step.


Regulatory and Commercial Exclusivity

The patent’s strategic value extends beyond legal protection:

  • It provides market exclusivity for the drug in Canada, aligning with the typical 20-year patent term.
  • It may support regulatory exclusivity or supplemental protection certificates, further extending market protection.
  • It fortifies the patent holder’s position in licensing negotiations and potential partnerships.

Potential Infringements and Enforcement

Given the broad scope of claims, infringement could involve:

  • Manufacturing or selling compounds within the structural scope.
  • Using the method claims or formulations.
  • Indirect infringement through the supply chain.

Proactive patent enforcement hinges on:

  • Monitoring competitors’ filings.
  • Conducting freedom-to-operate analyses.
  • Enforcing patent rights against infringers.

Conclusion and Strategic Insights

Patent CA3111317’s scope demonstrates a balanced combination of broad chemical protection and targeted therapeutic claims, reflecting strategic patent crafting typical of leading pharmaceutical innovators. Its landscape positioning aligns with other key patents, emphasizing the importance of structural novelty and inventive step to withstand prior art challenges.

For stakeholders, understanding the scope helps in:

  • Avoiding infringement through detailed freedom-to-operate assessments.
  • Maximizing patent value by ensuring claims are comprehensive yet defensible.
  • Anticipating competitive threats from generics or biosimilars.

Key Takeaways

  • CA3111317 secures protection for a novel chemical entity with specific structural features, covering multiple aspects from synthesis to therapeutic use.
  • The claims’ breadth balances broad chemical coverage with specific functional and use-based claims, crucial for robust patent protection.
  • The Canadian patent landscape shows trend parallels in extending exclusivity via secondary patents, but challenges often focus on inventive step and prior art.
  • The patent’s strategic importance lies in its potential to sustain exclusivity, support commercialization, and underpin licensing negotiations.
  • Continuous monitoring of the patent landscape and potential third-party filings is vital to safeguard patent rights and inform R&D and commercialization decisions.

FAQs

Q1: What differentiates CA3111317 from similar patents in the same therapeutic area?
A: CA3111317 claims a specific structural modification and method of synthesis that are not disclosed in prior art, providing a novel and non-obvious therapeutic compound distinction.

Q2: How does the patent landscape impact the validity of CA3111317?
A: Prior art references, such as earlier chemical patents and publications, may challenge the patent’s novelty or inventive step. A strong patent relies on claims that are significantly distinct from existing disclosures.

Q3: What legal protections does the patent confer in Canada?
A: It grants exclusive rights to manufacture, use, and sell the claimed compound, composition, or method within Canada for up to 20 years from the filing date, subject to maintenance fees.

Q4: Can the patent be challenged post-grant?
A: Yes, through procedural mechanisms such as opposition or validity proceedings in Canada, especially if prior art surfaces that questions the patent’s novelty or inventive step.

Q5: How does this patent influence the company's R&D or licensing strategies?
A: It provides a foundation for exclusive market positioning and leverage in licensing deals, while also guiding research directions to avoid infringement and build around the patent.


References

[1] Canadian Intellectual Property Office (CIPO). Patent database, CA3111317, 2018.

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