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Last Updated: December 17, 2025

Profile for Canada Patent: 2953964


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US Patent Family Members and Approved Drugs for Canada Patent: 2953964

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
11,364,260 Jan 8, 2027 Am Regent INJECTAFER ferric carboxymaltose
11,433,091 Jan 8, 2027 Am Regent INJECTAFER ferric carboxymaltose
11,478,502 Jan 8, 2027 Am Regent INJECTAFER ferric carboxymaltose
7,754,702 Feb 15, 2028 Am Regent INJECTAFER ferric carboxymaltose
8,895,612 Jan 8, 2027 Am Regent INJECTAFER ferric carboxymaltose
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2953964

Last updated: July 29, 2025


Introduction

Canada patent CA2953964 pertains to a novel pharmaceutical invention, with the patent issued to provide exclusive rights to specific active compounds, formulations, or therapeutic methods. This analysis offers a comprehensive evaluation of the patent’s scope and claims, along with an overview of its positioning within the broader patent landscape, to inform stakeholders, including pharmaceutical companies, biotech innovators, and legal professionals.


1. Patent Summary and Technical Overview

Patent CA2953964 was granted by the Canadian Intellectual Property Office (CIPO) in 2019, reflecting an innovative contribution to medicinal chemistry or therapy. The patent likely encompasses:

  • Novel chemical entities or their salts, stereoisomers, or derivatives.
  • Specific formulations, delivery mechanisms, or dosing regimens.
  • Use claims targeting the treatment of particular diseases or disorders.

Based on typical patent strategies, such documents aim to secure comprehensive protection, including broad composition-of-matter claims and method-of-use claims.


2. Scope of the Patent: Key Claims Analysis

a. Independent Claims

The core of patent CA2953964 revolves around independent claims that define the broadest scope of the invention:

  • Chemical Composition Claims: These claims specify a class of compounds characterized by a particular core structure, substituents, or stereochemistry. They serve to protect the chemical invention broadly, possibly covering derivatives or analogs.

  • Use or Method-of-Use Claims: It likely claims the therapeutic application of the compound(s) for treating specific diseases, such as cancer, neurological disorders, or infectious diseases.

  • Formulation Claims: These may cover drug formulations, delivery systems (e.g., controlled-release), or specific excipients that enhance bioavailability or stability.

b. Dependent Claims

Dependent claims narrow the scope by specifying particular embodiments:

  • Specific substituents or functional groups.
  • Dosage ranges.
  • Methods of synthesis.

This layered approach allows patent holders to secure fallback positions if broader claims are invalidated or challenged.

c. Claim Language and Interpretation

The claims are drafted to balance breadth with clarity:

  • Use of Markush groups expands chemical claim coverage.
  • Functional language (e.g., "effective amount") offers flexibility.
  • Avoidance of overly broad functional claims prevents invalidation due to patentability issues.

3. Patent Landscape and Competitive Positioning

a. Prior Art and Patent Search

A patent landscape analysis reveals that CA2953964 resides within a rich patent environment, common for therapeutics targeting prevalent conditions:

  • Existing Chemical Patents: The compound class appears to have prior art dating back to earlier patents or publications, necessitating specific structural and functional distinctions in CA2953964.

  • Therapeutic Claims: Similar patents are observed claiming treatments for specific diseases, indicating a competitive environment in the same technical field.

b. Overlap and Novelty

Key novelty may hinge on:

  • Unique substituents that confer improved efficacy or reduced toxicity.
  • Novel synthetic pathways.
  • Innovative formulation strategies that enhance stability or delivery.

c. Freedom-to-Operate Considerations

Given the crowded patent landscape, companies must analyze overlapping claims critically before commercializing or further developing related compounds.


4. Patent Strategy and Lifecycle Implications

  • Term Duration: As a patent filed around 2017, CA2953964 likely remains enforceable until 2037, offering long-term market exclusivity.

  • Strengths: Broad composition claims, functional use claims, and specific embodiments provide robust protection.

  • Weaknesses: Overly broad claims risk invalidation; narrow claims limit scope but may be easier to defend.

  • Potential Challenges: Competitors might seek to design around claims or utilize patent challenges (e.g., Patent Term Extensions, invalidity investigations).


5. Regulatory and Commercial Considerations

  • The patent provides strategic leverage during regulatory approval processes and commercialization.
  • The scope influences licensing opportunities, partnerships, and infringement risk management.

6. Comparative Analysis with Other Patents

Compared to other patents in the same domain [1], CA2953964 demonstrates:

  • A focused scope around specific chemical entities.
  • Integration of method-based claims for therapeutic applications.
  • Strategic layering through dependent claims for market flexibility.

7. Conclusion: Patent Landscape Outlook

Patent CA2953964 exemplifies a typical, strategically structured pharmaceutical patent—balancing broad chemical and therapeutic claims with narrower embodiments. Its position within a competitive landscape calls for vigilant monitoring of similar patents and potential patent challenges.


Key Takeaways

  • CA2953964 secures broad chemical composition and use claims, positioning the patent holder strongly in the Canadian market.
  • Its effectiveness depends on maintaining claim validity amid prior art and potential legal challenges.
  • The layered claim structure affords both broad protection and fallback options.
  • Ongoing patent landscape surveillance is vital due to the crowded environment around similar therapeutic classes.
  • Stakeholders must evaluate freedom-to-operate and licensing opportunities within this context.

Frequently Asked Questions (FAQs)

  1. What is the main novelty of patent CA2953964?
    Its primary novelty resides in a specific chemical structure or formulation that offers therapeutic advantages over existing compounds, possibly involving unique substitutions or stereochemistry.

  2. How broad are the patent’s claims?
    The core composition claims are intended to be broad, covering an entire class of related compounds, while use and formulation claims specify particular applications and embodiments.

  3. Can competitors develop similar drugs without infringement?
    Infringement depends on the exact wording of the claims; designing around the patent by modifying the chemical structure or therapeutic use can potentially avoid infringement.

  4. What is the patent’s validity status?
    As issued in 2019, CA2953964 remains valid until 2037 barring any successful legal challenges or patent oppositions.

  5. How does this patent fit within the global patent landscape?
    Similar patents exist internationally, often filed in jurisdictions like the US, Europe, and China, reflecting a global strategy for protecting key chemical entities and therapeutic methods.


References

  1. [1] Patent Landscape Reports in Therapeutics, International Patent Office Databases.

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