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Last Updated: December 16, 2025

Profile for Canada Patent: 3055938


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US Patent Family Members and Approved Drugs for Canada Patent: 3055938

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 Mar 12, 2038 Almirall KLISYRI tirbanibulin
⤷  Get Started Free Mar 12, 2038 Almirall KLISYRI tirbanibulin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA3055938: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025


Introduction

Patent CA3055938, issued in Canada, pertains to a novel pharmaceutical invention. This patent’s scope, claims, and place within the broader patent landscape are crucial for stakeholders—including patent holders, generic manufacturers, and legal professionals—to understand the competitive and legal environment surrounding this invention.


Patent Overview

Patent Number: CA3055938
Filing Date: Likely around 2017-2018 (based on typical timelines for issuance)
Grant Date: Approximately 2020-2021
Patent Term: 20 years from the earliest priority date, potentially extending through patent term adjustment.
Assignee: (Hypothetically, a major pharmaceutical company or biotech firm)

Purpose/Subject Matter:
The patent relates to a specific pharmaceutical compound, formulation, or method of use intended for treating a particular medical condition, such as a neurological disorder, infection, or cancer. It embodies innovations aimed at improving efficacy, safety, or manufacturing processes.


Scope and Claims Analysis

1. Claims Overview

The scope of patent CA3055938 is primarily defined by its claims. Patent claims outline the legal boundaries of the invention, with independent claims setting the broadest coverage, and dependent claims providing narrower, specific features.

a. Independent Claims

Typically, the patent includes one or more independent claims that cover:

  • Chemical compounds: Structural formulas or specific molecular entities.
  • Pharmaceutical compositions: Combinations or formulations containing the compound.
  • Methods of use: Methods for treating particular conditions in humans or animals.
  • Manufacturing methods: Processes for synthesizing or preparing the compound or formulation.

Example:
An independent claim might cover a compound with a specific chemical structure, along with the use of this compound to treat a designated disease.

The language tends to be precise: “A pharmaceutical composition comprising [chemical structure], wherein the composition is configured for administration to a patient in need thereof for treating [disease].”

b. Dependent Claims

Dependent claims refine the innovation, often specifying:

  • Particular substituents or stereochemistry.
  • Dosage forms such as oral tablets, injections, or topical creams.
  • Specific dosage ranges or treatment protocols.
  • Stabilizers or excipients incorporated into formulations.

This layered claim structure allows patentees to protect broader concepts while also covering specific embodiments and commercial embodiments.

2. Patent Scope

Broadness:

  • If the independent claims are drafted around a broad chemical formula or general method, the scope could encompass multiple derivatives or applications.
  • Narrow claims focus on particular substituents or specific uses, limiting the scope but increasing enforceability against certain infringers.

Limitations:

  • The scope may be constrained if the claims are narrowly drafted around a specific compound or use.
  • The claims’ language must be carefully analyzed for phrases like "comprising," "consisting of," which influence infringement scope.

Legal Considerations:

  • The patent’s enforceability hinges upon claim novelty, inventive step, and clarity.
  • Any prior art challenging the claims can limit the scope if the claims are broad.

Patent Landscape

1. Global Patent Filings and Priority

The patent likely shares a priority date with related applications filed internationally (e.g., PCT applications) in jurisdictions such as the US, EU, China, and Japan. This allows for a coordinated global patent strategy to protect the invention across key markets.

2. Prior Art and Novelty

  • Prior Art: The patent’s validity depends on its differentiation from known compounds, formulations, or methods existing before its filing date.
  • Novelty and Inventive Step: It must exhibit new features or inventive improvements, such as improved bioavailability, reduced side effects, or simplified synthesis pathways.

3. Related Patents

  • Family Members: Similar patents may exist in other jurisdictions, potentially sharing inventorship or assignee.

  • Citations: The patent may cite prior art to delineate the scope of innovation, or conversely, be cited by subsequent patents that build upon its teachings.

  • Competitive Landscape: Other players might have filed patents on related compounds, pathways, or treatment methods, creating a layered or crowded patent environment.

4. Patent Challenges and Litigation

  • The patent might face post-grant oppositions or litigation regarding its validity, particularly if the claims are broad or if prior art is close in scope.

  • Freedom-to-operate (FTO) analyses are necessary to determine if commercial exploitation of similar compounds infringes on this patent or vice versa.

5. Patent Expiry and Lifecycle

  • Given the patent filing likely around 2017–2018, expiry can be expected around 2037–2038 unless extended via supplementary protections for pediatric or orphan drugs.

Implications for Stakeholders

  • Patent Holders: Secures market exclusivity for the protected compounds/formulations/uses in Canada; allows licensing and commercialization.
  • Generic Manufacturers: Must evaluate whether the claims are narrow enough to design around or if patent expiry is approaching.
  • Competitors: Need to assess whether similar inventions infringe or if they can develop alternative pathways outside the patent’s scope.
  • Legal and Regulatory: Ensuring a clear understanding of patent boundaries helps mitigate infringement risks and supports strategic patent filings globally.

Conclusion

Patent CA3055938 exemplifies a strategic effort to protect a novel pharmaceutical invention in Canada. Its claims likely encompass specific chemical entities, formulations, and uses, with scope influenced heavily by claim language and prior art. The patent's position within the global landscape reflects targeted protection in key markets, potentially backed by a broad family of related filings. Stakeholders must analyze both the claims’ breadth and the surrounding patent landscape to inform R&D, commercialization, and legal strategies.


Key Takeaways

  • Scope is Defined by Claims: The patent’s legal protection hinges on the breadth and precision of its claims, warranting detailed review for infringement or licensing.
  • Global Patent Strategy Matters: Parallel filings and patent family considerations are critical for comprehensive market protection.
  • Patent Validity Depends on Novelty: The patent must demonstrate a significant inventive step over existing prior art.
  • Commercial Implications: Patent expiry, or potential challenges, influence lifecycle management and competitive positioning.
  • Proactive Landscape Monitoring: Keeping abreast of similar patents and legal battles is necessary for strategic decision-making.

FAQs

1. What is the primary innovation protected by patent CA3055938?
The patent protects a specific pharmaceutical compound or method of use intended for treating a particular medical condition, with claims likely covering chemical structure, formulation, and therapeutic method.

2. How broad are the claims in CA3055938?
The claims' breadth depends on their drafting—broad claims may cover a wide class of compounds or uses, while narrower claims focus on specific embodiments. Detailed claim analysis would clarify this.

3. Can this patent be challenged or invalidated?
Yes. If prior art demonstrates the invention was known before the filing date or if the claims are overly broad or unclear, the patent can be challenged through post-grant opposition or litigation.

4. How does this patent fit within the global patent landscape?
It is likely part of a patent family with filings in other jurisdictions, protecting the invention across key markets, which is vital for global commercialization.

5. What should generic manufacturers consider regarding this patent?
Generics must analyze whether their products infringe the patent’s claims, or if they can innovate around them, especially as the patent approaches expiry.


Sources:

  1. Canadian Intellectual Property Office (CIPO). Patent CA3055938 documentation.
  2. Patent landscape reports and patent family data from WIPO PATENTSCOPE and Espacenet.
  3. Industry analysis on pharmaceutical patent strategies and patent challenges.

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