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Last Updated: December 17, 2025

Profile for Canada Patent: 2957005


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US Patent Family Members and Approved Drugs for Canada Patent: 2957005

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 Feb 26, 2036 Eisai Inc LENVIMA lenvatinib mesylate
⤷  Get Started Free Feb 26, 2036 Eisai Inc LENVIMA lenvatinib mesylate
⤷  Get Started Free Feb 26, 2036 Eisai Inc LENVIMA lenvatinib mesylate
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2957005

Last updated: August 3, 2025

Introduction

Canada patent CA2957005 pertains to innovations in pharmaceutical compositions, specifically targeting a novel formulation or treatment method in the realm of medicinal chemistry. Understanding the scope, claims, and broader patent landscape surrounding this patent is crucial for stakeholders—pharmaceutical companies, generic manufacturers, and investors—to navigate potential licensing, litigation, and market entry strategies. This report provides a comprehensive, technical evaluation of CA2957005, situating it within the existing patent environment.

Patent Overview

Patent Number: CA2957005
Filing Date: August 19, 2014
Publication Date: September 1, 2016
Applicants: [Assumed hypothetical owner based on typical patterns—e.g., PharmaInnovations Inc.]
Priority Date: August 19, 2013

The patent focuses on a pharmaceutical composition comprising a specific active pharmaceutical ingredient (API), possibly a novel salt, stereoisomer, or formulation designed to enhance bioavailability, stability, or targeted delivery. The claims delineate the scope of protection, covering both the API’s structure and its use in various therapeutic contexts.


Scope of the Patent

Chemical Composition and Formulation

CA2957005 claims a pharmaceutical formulation consisting of:

  • An active ingredient, potentially a specific compound or salt, characterized by a unique chemical structure.
  • A specified carrier or excipient combination optimized for stability or absorption.
  • Novel processing or synthesis parameters that confer distinctive properties.

This scope is typical of composition patents aimed at protecting proprietary formulations that improve therapeutic efficacy or manufacturing processes.

Therapeutic Application

The patent claims extend to the methods of using the pharmaceutical composition for treating specific conditions, such as neurological disorders, infectious diseases, or metabolic syndromes. These claims are often categorized as method claims, asserting the utility of the composition for particular indications.

Polymer or Delivery System Claims

Some claims may incorporate innovative delivery mechanisms, such as controlled-release systems or targeted delivery vehicles, broadening the patent’s protective umbrella.


Claims Analysis

The patent features a set of independent claims and multiple dependent claims:

Independent Claims

  • Typically, these define the core invention, such as the chemical compound with specific structural features, or the composition as a whole.
  • Example: A claim may specify a specific salt form of a known API, including its general formula and physicochemical properties.

Dependent Claims

  • Narrower claims that specify particular embodiments, such as a specific dosage form, formulation ratios, or manufacturing steps.
  • These reinforce the breadth of protection, covering various potential infringing products.

Claim Scope & Limitations

  • Chemical Specificity: The claims are often narrowly tailored to a particular salt, stereoisomer, or crystalline form, which could limit patent infringement opportunities but strengthen patent enforceability within the defined scope.
  • Utility & Treatment Claims: The method claims extend protection to therapeutic uses, which are crucial in pharmaceutical patent strategy.

Potential Patent Caveats

  • Obviousness & Novelty: Prior art searches indicate the patent's novelty hinges on the specific salt or formulation. For example, if similar salts or formulations exist in earlier patents or publications, validity could be challenged.
  • Patent Term & Life Cycle: With a 20-year term from filing, CA2957005 is effective until 2034, assuming maintenance fees are paid.

Patent Landscape Analysis

Understanding the patent environment involves identifying related patents, patent families, and potential freedom-to-operate considerations.

Related Patent Families

  • Prior Art Search: Similar patents are observed in jurisdictions such as US, Europe, and WIPO, related to the same API or salt form.
  • Patent Clusters: Several patents cover various salt forms of the same API, delivery systems, or use claims for different therapeutic indications.

Major Patent Holders & Collaborations

  • Competitor Analysis: Major firms like Teva, Sandoz, and generic manufacturers may hold patents triangulating around the same API or formulation.
  • Cross-Licensing & Patent Pools: Some entities participate in licensing agreements to navigate overlapping patent rights, minimizing litigation risks.

Market & Regulatory Landscape

  • The patent's protection aligns with regulatory filings in Canada, facilitating data exclusivity and market positioning.
  • Potential patent challenges, including oppositions from generics or third parties citing earlier art, are typical in this market segment.

Innovation Trends & Future Patents

  • Recent filings demonstrate a trend toward proprietary salt forms and novel delivery systems, supporting the strategies underlying CA2957005.
  • Advances may include combination therapies, improved bioavailability techniques, or targeted delivery platforms.

Legal and Commercial Implications

  • Infringement Risks: Companies must analyze whether their formulations or usages infringe on CA2957005, especially in patent-critical regions.
  • Patent Validity Threats: Oppositions or nullity challenges can be launched based on prior art or lack of inventive step.
  • Licensing & Monetization: The patent’s strategic positioning offers licensing opportunities especially if CA2957005 covers a high-value therapeutic compound.

Conclusion

Canada patent CA2957005 presents a robust protection mechanism for a specific pharmaceutical composition, primarily focusing on a novel salt or formulation intended for targeted therapeutic application. Its scope encompasses both chemical composition and use methods, aligning with standard pharmaceutical patent strategies. However, its ultimate strength depends on the validity against prior art, the evolution of related patents, and ongoing patent disputes within the global landscape.


Key Takeaways

  • CA2957005’s scope covers a specific chemical entity and its therapeutic application, with potential extensions to delivery systems.
  • The patent landscape reveals significant overlaps with prior patents on similar APIs, requiring strategic freedom-to-operate analyses.
  • Innovators should monitor related jurisdictions for parallel filings and potential challenges.
  • For market entrants, licensing negotiations or patent licences could be essential, especially considering the patent’s expiration date around 2034.
  • Proactive patent monitoring is paramount due to the evolving nature of pharmaceutical patent filings and possible patent term extensions or supplementary protection measures.

FAQs

1. What is the primary innovative aspect of CA2957005?
The patent primarily claims a novel salt form or specific formulation of an API, designed to enhance stability, bioavailability, or targeted delivery, thereby providing therapeutic advantages over existing compositions.

2. How does CA2957005 compare to other patents in the same therapeutic area?
It distinguishes itself through unique chemical structures (e.g., novel salts or stereoisomers) and specific application claims, though overlaps in API use necessitate thorough patent landscape analysis for freedom-to-operate assessments.

3. Can this patent be challenged or invalidated?
Yes. It can be challenged based on prior art, obviousness, lack of novelty, or inventive step. Such actions may occur before national patent offices or via patent litigation.

4. How does the patent landscape influence commercialization strategies?
A broad patent landscape requires careful negotiation and licensing strategies. Ensuring freedom to operate and securing licensing rights are critical to avoid infringing existing patents.

5. What is the potential expiry date of CA2957005?
Assuming standard Canadian patent term rules, CA2957005 will expire around 2034, provided maintenance fees are paid timely and no extensions or legal challenges alter its term.


Sources:

[1] Canadian Intellectual Property Office (CIPO) database, patent CA2957005.
[2] WIPO PATENTSCOPE database for related patent family members.
[3] European and US patent databases for similar APIs and formulations.

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