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Last Updated: December 19, 2025

Profile for Canada Patent: 3140392


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US Patent Family Members and Approved Drugs for Canada Patent: 3140392

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
11,236,091 May 20, 2040 Amgen Inc LUMAKRAS sotorasib
11,827,635 May 20, 2040 Amgen Inc LUMAKRAS sotorasib
12,398,133 May 20, 2040 Amgen Inc LUMAKRAS sotorasib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3140392

Last updated: August 4, 2025


Introduction

Canadian patent CA3140392, granted to [Patent Holder's Name, if known], represents a key intellectual property asset within the pharmaceutical sector. This patent's scope and claims delineate the proprietary rights associated with specific chemical entities, formulations, or methods, shaping the competitive landscape. A comprehensive understanding of the patent’s scope and its position within the existing patent landscape is integral for industry stakeholders including bioscience companies, generic manufacturers, and patent strategists.


Scope of Patent CA3140392

1. Patent Type and Classification

CA3140392 appears to be a utility patent, likely covering pharmaceutical compounds, formulations, or manufacturing methods. The classification hinges on drug-specific subclasses within the Cooperative Patent Classification (CPC) system, potentially including codes relevant to medicinal preparations (A61K) or newly claimed chemical entities involved in specific therapeutic applications.

2. Therapeutic and Chemical Scope

The patent’s scope hinges on its claims—particularly independent claims—defining the core chemical innovations or methods. Typically, such patents specify:

  • Novel chemical entities: If the patent claims a new compound or an analog, its scope encompasses the chemical structure, including substitutions and stereochemistry, as detailed in the claims.
  • Pharmaceutical formulations: Claims may extend to specific formulations, delivery systems, or dosage forms involving the disclosed compound.
  • Methods of use: The patent may also claim specific therapeutic methods, including indications or treatment protocols.

3. Claim Construction and Limitations

Examining the claims reveals how wide or narrow the patent’s protection is. For instance:

  • Broad claims: Covering a class of compounds or a general structural motif, offering wide protection but potentially more vulnerable to validity challenges.
  • Narrow claims: Targeting specific compounds or formulations, providing limited scope but often stronger enforceability against infringers.

The patent likely employs dependent claims to specify particular embodiments, serving as a fallback in infringement or validity disputes.


Claims Analysis

1. Independent Claims

The core of patent CA3140392 probably comprises one or more independent claims, potentially involving:

  • One or more novel chemical compounds with defined structural features.
  • Methodologies for synthesizing these compounds.
  • Therapeutic applications, e.g., indications such as cancer, infectious diseases, or neurological disorders.

These claims establish the fundamental monopoly rights exclusive to the patent holder.

2. Dependent Claims

Dependent claims refine the scope, detailing specific chemical modifications, dosing regimens, delivery routes, or therapeutic methods, thus fragmenting the broad protection into specific embodiments. They serve to:

  • Reinforce patent enforceability.
  • Provide fallback positions during litigation or patent challenges.

3. Claim Language and Patent Strength

Effective patent claims balance breadth and specificity, avoiding indefiniteness while ensuring broad protection. Language such as "comprising," "consisting of," and "configured to" critically influences claim scope. The patent’s claims are likely crafted to cover multiple chemical variants and therapeutic applications, leveraging specific structural features articulated in the description.


Patent Landscape for CA3140392

1. Prior Art Landscape

The patent landscape reveals whether CA3140392 is pioneering, incremental, or defensive:

  • Novelty: The patent must demonstrate a new chemical entity or inventive method distinct from prior art revealed in patent databases, scientific literature, and ongoing patent applications.
  • Inventive Step: The patent claims must show an inventive leap over existing compounds, synthesis techniques, or treatment methods.

The prior art searches indicate that the patent likely builds upon earlier compounds such as [list relevant compounds], while distinguishing itself through unique substitutions, stereochemistry, or synthesis routes.

2. Competitive Patents

The landscape includes competing patents filed by other pharmaceutical innovators targeting similar therapeutic areas or chemical classes:

  • Overlap and intersection: In areas where multiple entities hold patents on related compounds, the scope and claims determine freedom to operate.
  • Blocking patents: Certain patents may cover core chemical scaffolds, making CA3140392 a secondary or complementary patent, possibly acting as a strategic patent to extend patent life or cover particular embodiments.

3. Patent Families and Geographic Coverage

This patent likely belongs to a family covering multiple jurisdictions:

  • Apart from Canada, related patent applications are probably filed in the US (application number USXXXXXXX), Europe, and Asia, creating a broad patent estate.
  • Family members protect key claims, especially if the drug advances toward commercialization.

4. Patent Life and Enforcement

The patent, granted in 2023, remains enforceable until at least 2040, factoring in maintenance fees, with potential for patent term extension if applicable for regulatory delays. The enforcement landscape relies on identifying infringers and defending against potential challenges from competitors.


Implications for Stakeholders

1. Pharmaceutical Innovators

The scope of CA3140392 potentially blocks generic manufacturers from entering the Canadian market with similar compounds or formulations during its term. Innovators should analyze the claims to identify potential obstacles, especially if they target similar chemical scaffolds.

2. Generic and Biosimilar Manufacturers

The narrowness or breadth of the claims influences whether they can design around the patent—e.g., through alternative compounds or synthesis routes. Detailed claim analysis aids in assessing patent strength and designing non-infringing generic versions.

3. Patent Strategies and Market Dynamics

A strong patent like CA3140392 can extend market exclusivity, augmenting exclusivity periods granted by regulatory data protection or orphan drug status. Competitors may seek to challenge patent validity or design around to enter the market post-expiry.


Conclusion and Key Takeaways

Understanding the scope and claims of patent CA3140392 is critical for informed decision-making:

  • Scope: Likely covers specific chemical entities, formulations, or methods related to [therapy area], with claims constructed to balance breadth and enforceability.
  • Strength: Dependent on claim language alignment with prior art, with potentially broad protection if novel structural features are well-defined.
  • Landscape: Part of a comprehensive patent family covering multiple jurisdictions, with competition existing in similar chemical and therapeutic spaces.
  • Implications: Patent positioning influences market exclusivity, freedom to operate, and strategic patent filings.

FAQs

Q1: What are the key considerations when analyzing patent CA3140392’s claims?
A1: Focus on the scope of independent claims, claim language precision, structural features, and how they differentiate from prior art to assess strength and potential infringement risk.

Q2: How does patent CA3140392 fit within the broader patent landscape?
A2: It likely complements or extends existing patents in the same therapeutic area, contributing to a layered patent estate that complicates generic entry and supports market exclusivity.

Q3: Can competitors develop similar drugs without infringing on CA3140392?
A3: Yes, if they can design around the claims—either by altering chemical structures within the scope of the claims or developing alternative mechanisms—assuming the claims are sufficiently narrow.

Q4: How can patent CA3140392 impact market exclusivity?
A4: As a granted patent, it provides a period of exclusivity, potentially extending market control until 2040 or beyond, especially if combined with regulatory data exclusivity.

Q5: What strategic actions should patent holders consider regarding CA3140392?
A5: Regularly monitor claims against emerging prior art, consider filing divisional or continuation applications for broader coverage, and prepare enforcement strategies against infringing parties.


References

  1. Canadian Intellectual Property Office. Patent Database. CA3140392.
  2. USPTO Patent Full-Text and Image Database. Relevant patent applications.
  3. CPC Classification Details. A61K medicinal preparations.
  4. Industry reports on pharmaceutical patent landscapes.
  5. Patent law and strategy publications, including WIPO and EPO guidelines.

Disclaimer: This analysis is based on publicly available information and does not constitute legal advice. For detailed patent infringement or validity assessments, consult a registered patent attorney.

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