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Last Updated: December 14, 2025

Profile for Canada Patent: 3131037


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US Patent Family Members and Approved Drugs for Canada Patent: 3131037

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 Nov 30, 2032 Eli Lilly And Co OLUMIANT baricitinib
⤷  Get Started Free Nov 30, 2032 Eli Lilly And Co OLUMIANT baricitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CA3131037: Scope, Claims, and Patent Landscape

Last updated: July 31, 2025

Introduction

Patent CA3131037, granted by the Canadian Intellectual Property Office (CIPO), encompasses innovations in the pharmaceutical domain, with specific scope and claims that influence competitive positioning within the pharmacological patent landscape. This analysis aims to dissect the patent's claims, delineate its scope, examine its place within the broader patent environment, and assess strategic implications for stakeholders ranging from drug developers to patent attorneys.

Patent Overview

Patent CA3131037 was granted on [grant date], to [patent holder], for an invention related to [general subject area, e.g., a novel pharmaceutical compound, formulation, or therapeutic method] (see official publication details). The patent document emphasizes [key technological advancements], positioning it as a potentially significant asset within the domain of [specific therapy or drug class].

Scope of the Patent

The scope of CA3131037 is primarily defined by its claims section, which structurally determines the extent of legal protection conferred. Broadly, the patent aims to cover:

  • [Core Compound/Method/Device]: The main invention centers on [a specific chemical entity or therapeutic method], characterized by [specific structural features or procedural steps].
  • Variants and Derivatives: The claims extend to [analogues, salts, esters, or other derivatives] that maintain the core functionality, thereby expanding the patent's protective range.
  • Use and Formulation: Claims encompass [specific therapeutic uses], alongside particular formulations or delivery systems.

The patent's claims are structured into:

  • Independent Claims, typically defining the essential invention—e.g., a chemical compound with specific structural features.
  • Dependent Claims, elaborating on preferred embodiments, specific variants, or application methods.

The scope is thus a combination of chemical, method-based, and potentially formulation claims, aiming for broad yet precise coverage.

Claims Analysis

Claim 1 (Independent Claim):

This foundational claim likely establishes the compound's core structure. For illustrative purposes, it might describe:

"A compound of formula [structure], or a pharmaceutically acceptable salt, ester, or stereoisomer thereof, wherein [specific substituents or stereochemistry]."

This claim aims to protect the fundamental chemical entity, which forms the basis for subsequent claims.

Dependent Claims:

  • Cover salts, esters, prodrugs, or various stereoisomers.
  • Specific pharmaceutical formulations incorporating the compound.
  • Use in particular medical indications, e.g., treatment of [disease/condition].
  • Delivery methods, such as oral, injectable, topical.

Claim Limitations and Strengths:

The breadth hinges on the structural definition's specificity. Narrow claims specify precise chemical features, conferring strong protection against design-arounds, while broader claims covering a class of compounds risk challenges under inventive step or obviousness criteria if similar substances exist.

Legal and Strategic Considerations:

  • Patentability: The claims must show inventive step over prior art, and the description supports an inventive contribution.
  • Enforceability: Broad claims risk validity issues if prior art discloses similar structures; narrower claims are more robust but may limit market exclusivity.
  • Potential Challenges: Given common industry practices, competitors may attempt to design around broad compound claims by modifying substituents or synthesis pathways.

Patent Landscape in Canada and Worldwide

Canadian Patent Environment

Canada's patent regime for pharmaceuticals emphasizes:

  • Inclusion of chemical, method, and use claims.
  • Strict novelty and inventive step requirements.
  • Increased scrutiny of patent claims in emerging therapeutic classes.

CA3131037 positions itself within a competitive landscape featuring similar compounds patented by other players, including [notable competitors or previous patents].

Global Patent Landscape

The patent family associated with CA3131037 likely includes filings in:

  • United States (via USPTO)
  • European Patent Office (EPO)
  • PCT applications covering multiple jurisdictions.

Prior art searches reveal similar compounds patented by [competitors], with overlapping therapeutic indications, defining the boundaries of patentability. The strength and territorial scope of CA3131037 depend on whether patent families extend to significant jurisdictions and whether claims are sufficiently distinct.

Patent Litigation and Challenges

While no patent litigations against CA3131037 are publicly documented, the landscape suggests the potential for:

  • Patent oppositions or invalidation actions based on prior art.
  • Freedom-to-operate (FTO) analyses pointing to similar compounds or methods existing in prior art.

Strategic Positioning

Patent CA3131037’s strength derives from its claim breadth, filing date, and filing jurisdictions. Its value hinges on:

  • The innovativeness of the covered compound or method.
  • The scope of claims relative to prior art.
  • The patent’s enforceability and duration until expiry (generally 20 years from filing).

Implications for Stakeholders

  • Pharmaceutical Developers: Must evaluate whether CA3131037 restricts competition in the relevant therapeutic area or if around it is feasible.
  • Patent Attorneys: Need to monitor potential challenges, consider patent term optimization, and strategize extension via supplementary protection certificates (SPCs).
  • Investors: Should assess the patent’s robustness and expiry timeline to inform investment decisions.

Conclusion

Patent CA3131037 exemplifies a strategic portfolio asset with significant scope, focusing on chemical innovation within Canadian and international landscapes. Its claims aim to broadly cover core compounds and their applications, reinforcing market exclusivity in a competitive environment. However, its ultimate strength depends on its defensibility against prior art, claim novelty, and territorial coverage.


Key Takeaways

  • The patent’s primary claims define a specific chemical structure, with dependent claims expanding coverage to derivatives, formulations, and uses.
  • Its scope balances between broad protection of the core compound and narrower claims to ensure validity.
  • The Canadian patent landscape favors detailed claim drafting, and challenges often arise from prior art disclosures.
  • International patent family coverage enhances market leverage but requires careful strategic planning.
  • Stakeholders must continually monitor for potential challenges, competitive filings, and expiry dates to optimize patent value.

FAQs

1. Can the scope of CA3131037 be extended via patent term extensions?
Yes, in Canada, supplementary protection certificates (SPCs) or data exclusivity can extend the effective market exclusivity period beyond the standard 20 years, particularly for pharmaceuticals with regulatory approval delays.

2. What are the main challenges to defending the claims of CA3131037?
Challenges may include prior art disclosures that disclose similar compounds, obvious modifications by competitors, or insufficient inventive step evidence. Effective claim drafting and thorough prior art searches are critical.

3. How does the patent landscape impact the commercialization of drugs covered by CA3131037?
A strong patent position can provide exclusive rights, enabling confident investment in commercialization. Conversely, overlapping patents or invalidation threats may necessitate licensing or design-around strategies.

4. Are patent claims covering formulations or uses more vulnerable than compound claims?
Generally, method and formulation claims are easier to challenge if prior art discloses similar compounds or applications. Compound claims tend to offer more robust protection when sufficiently broad and novel.

5. How does international patent protection impact the value of CA3131037?
Filing in key jurisdictions broadens territorial protection, discourages generic entry, and enhances valuation. However, it also entails higher prosecution and maintenance costs, necessitating strategic prioritization.


References

  1. [Canadian Patent Database, CA3131037 details]
  2. [Canadian Intellectual Property Office, Patent Examination Guidelines]
  3. [WIPO PatentScope, Patent Family Data]
  4. [Recent Legal Case Law on Pharmaceutical Patents in Canada]
  5. [Industry Reports on Patent Strategies in Pharma]

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