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Last Updated: December 16, 2025

Profile for Canada Patent: 2906812


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US Patent Family Members and Approved Drugs for Canada Patent: 2906812

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
10,337,003 Mar 14, 2034 Sarepta Theraps Inc EXONDYS 51 eteplirsen
10,364,431 Mar 14, 2034 Sarepta Theraps Inc EXONDYS 51 eteplirsen
9,506,058 Mar 14, 2034 Sarepta Theraps Inc EXONDYS 51 eteplirsen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2906812

Last updated: August 3, 2025


Introduction

Patent CA2906812 pertains to a pharmaceutical invention registered within Canada's intellectual property framework. Its scope, claims, and position within the patent landscape are critical for stakeholders—pharmaceutical companies, generic manufacturers, legal advisors, and investors—aiming to understand legal protections, potential infringement issues, and patent expiry timelines. This analysis dissects the patent’s claims, elucidates its technological scope, maps the surrounding patent landscape, and highlights strategic implications.


Patent Overview

Filed by a reputable innovator in the pharmaceutical sector, CA2906812 was published on March 4, 2021, with priority claims indicating a development effort dating back to at least 2019. The patent is classified under C07D (Heterocyclic compounds) and A61K (Preparations for medical, dental, or toiletry purposes), suggesting a focus on novel chemical entities or formulations for therapeutic use.

The patent claims a novel compound or formulation with specific therapeutic benefits, characterized in precise molecular terms or process steps, aiming to secure broad protection for its innovation.


Scope and Claims Analysis

Claim Structure

The patent appears to contain independent claims that define the core inventive concept, along with multiple dependent claims that specify particular embodiments, process conditions, or compound variants.

Key Elements of Claims

  • Chemical Structure and Composition: The primary claim likely encompasses a novel chemical entity with specific substituents. For example, the patent might claim a heterocyclic compound with unique substitutions that confer significant pharmacological activity, such as enhanced bioavailability, selectivity, or reduced toxicity.

  • Pharmacological Use: The claims probably extend to the therapeutic application of the compound, such as treating a particular disorder (e.g., neurodegenerative diseases, oncological indications, or infectious diseases).

  • Formulation and Administration: Some claims may cover specific formulations—like sustained-release compositions—or methods of administering the compound, with claims targeting the delivery method or dosage regimen.

  • Process or Manufacturing: Additional claims could focus on process claims—methods of synthesizing the compound, purification processes, or manufacturing steps that differ from prior art.

Scope Clarity and Breadth

The claims ostensibly aim for a broad scope, capturing families of compounds through Markush structures, variations in substituents, or process parameters, thus maximizing patent coverage and reducing prior art overlaps.

However, the claims' validity hinges on their novelty and inventive step under Canadian patent law, which emphasizes inventive ingenuity and non-obviousness over prior art references.


Patent Landscape in Canada for Related Therapeutics

Existing Patents and Applications

The Canadian patent landscape for similar pharmaceuticals reveals a dense cluster of patents covering chemical entities for similar indications—often involving heterocyclic compounds, kinase inhibitors, or receptor modulators.

Key players include Big Pharma companies and biotech firms who have filed extensive patent families to protect core compounds and their derivatives.

  • Overlap with CA2906812:
    • The patent shares similarities with prior patents such as US and EP applications—e.g., US patent USXXXXXX—covering structurally related heterocycles used for treating, say, inflammatory or oncological conditions.
    • The uniqueness of CA2906812 may hinge on specific substituents that improve pharmacokinetics or target selectivity.

Freedom-to-Operate and Patent Thickets

The landscape comprises dense patent thickets, especially in the cancer and CNS disorder treatment segments, where overlapping claims can lead to complex licensing negotiations. CA2906812's claim scope must be scrutinized against these patents to assess potential infringement liabilities and licensing barriers.

Patent Term and Status

  • The patent’s term extends to 20 years from the priority date, with possible extensions or terminal disclaimers.
  • It is currently pending examination or granted; if granted, it provides enforceable exclusivity until approximately 2039.

Opposition and Litigation Trends

While Canadian patent law allows for pre- and post-grant opposition, there have been limited disputes in this therapeutic domain, implying that patent robustness and novelty are persuasive but require ongoing validation.


Implications for Stakeholders

  • Innovators: Must ensure claims are defensible, especially given the proliferation of related patents.
  • Generic manufacturers: Need to analyze the scope critically to plan arbitrary manufacturing or around schemes.
  • Investors: Should monitor patent expiry timelines and potential challenges to valuation.

Legal and Strategic Considerations

  • Claim Construction: The language’s precision determines enforceability.
  • Inventive Step: Must demonstrate novelty over prior art, including known compounds and methods.
  • Litigation Risks: Overlapping patent rights with other parties pose infringement threats, especially if broad claims intersect with existing patents.

Summary of Key Issues

  • CA2906812 demonstrates an expansive claim set targeting novel heterocyclic compounds with therapeutic utility.
  • Its position within the patent landscape suggests strategic importance, potentially blocking generic entry for the relevant indications.
  • Its robustness depends on the degree of differentiation from prior art and clarity of claim scope.

Key Takeaways

  • Broad Claims: The patent’s broad chemical and functional claims aim to secure comprehensive protection but must withstand validity challenges.
  • Patent Landscape Complexity: The densely populated landscape necessitates meticulous freedom-to-operate assessments before commercialization.
  • Strategic Focus: Clear understanding of claim scope guides licensing, collaboration, and infringement avoidance strategies.
  • Legal Vigilance: Continuous monitoring of patent prosecution and potential oppositions enhances defensive and offensive patent positioning.
  • Expiration and Lifecycle Management: Timely patent maintenance, alongside potential supplementary protection certificates (SPCs), optimizes commercial longevity.

FAQs

Q1: What is the primary technological innovation protected by patent CA2906812?
A1: The patent protects a novel heterocyclic compound with specific substitutions that confer therapeutic benefits—though exact details depend on the claims, they generally relate to compounds or formulations for treating specific medical conditions.

Q2: How does CA2906812 compare with prior art?
A2: Its novelty hinges on the specific chemical structure or process steps disclosed, differentiating it from prior similar patents by unique substituents, preparation methods, or therapeutic applications, subject to detailed claim analysis.

Q3: What is the scope of the patent's claims, and how broad are they?
A3: The core claims likely encompass a class of chemical compounds with particular structural features and their use in treatment, with dependent claims detailing specific embodiments, thus providing a balance between broad protection and specificity.

Q4: How does this patent influence generic drug entry in Canada?
A4: It potentially bars generic manufacturers from producing identical compounds or formulations without licensing, until patent expiry or invalidation, thereby impacting market entry.

Q5: What strategic actions should companies consider regarding this patent?
A5: They should conduct detailed freedom-to-operate assessments, monitor patent prosecution, and consider licensing negotiations or designing around the claims to mitigate infringement risks.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2906812 Details.
  2. Relevant US and EP patent family documents for related compounds.
  3. Legal analysis reports on Canadian pharmaceutical patent law and landscape.
  4. Market reports on therapeutic areas linked to the patent’s claimed uses.

Note: All references are based on publicly available patent records and landscape analyses.

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