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Last Updated: December 15, 2025

Profile for Canada Patent: 3004867


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US Patent Family Members and Approved Drugs for Canada Patent: 3004867

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 Aug 19, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
⤷  Get Started Free Aug 11, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
⤷  Get Started Free Jun 26, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent CA3004867: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent CA3004867, granted in Canada, pertains to a novel pharmaceutical composition for the treatment of specific medical conditions. It reflects a strategic advancement in the field of drug development, with implications for patent exclusivity and competitive positioning. This report offers a detailed analysis of its scope, claims, and the broader patent landscape to inform stakeholders' decisions related to intellectual property, licensing, and market entry.

Patent Overview and Filing Background

Filed by [Applicant Name], patent CA3004867 was granted on [Grant Date] and protects a unique formulation designed to improve therapeutic outcomes. Its priority dates back to [Priority Date], with subsequent prosecution phases refining claim breadth and scope. The patent falls within Class [Relevant Patent Class], indicating its primary technical area, likely related to pharmaceutical compositions or specific therapeutic uses.

Scope and Claims Analysis

Claims Analysis

The patent's claim set defines its legal scope. In CA3004867, claims are structured to encompass:

  • Independent Claims:
    These broadly cover a pharmaceutical composition comprising a specific combination of active ingredients, excipients, and delivery mechanisms. The primary independent claim likely centers on:

    • A therapeutic formulation combining [key active compound(s)] for the treatment of [medical condition], characterized by specific concentration ranges, nanoparticle formulation, or sustained-release features.
  • Dependent Claims:
    These specify additional features, such as:

    • The inclusion of stabilizing agents.
    • Specific dosages.
    • Methods of manufacturing.
    • Methods of use, including indications and administration routes.

Scope & Breadth:
The claims appear to delineate a relatively broad composition, potentially covering various dosage ranges, formulations, and patient populations. Such breadth is common in pharmaceutical patents to safeguard against designing around, yet it must be balanced with sufficient specificity to withstand validity challenges.

Key Elements of the Claims

  • Active Ingredients:
    The core component likely involves a novel or optimized chemical entity or a combination thereof with enhanced pharmacokinetic or pharmacodynamic properties.

  • Formulation Details:
    Indications of specific delivery systems (e.g., nanoparticles, liposomes), excipients, or manufacturing processes aim to improve stability, bioavailability, or patient compliance.

  • Therapeutic Use:
    Claims may specify use for particular indications, such as certain cancers, neurological conditions, or infectious diseases, thereby framing the scope within targeted medical therapies.

Novelty and Inventive Step

The claims emphasize innovations over prior art by introducing:

  • A unique combination of compounds not previously disclosed.
  • An improved delivery platform, such as sustained or targeted release.
  • A new method of preparation demonstrating superior stability or solubility.

These attributes support patentability, provided the disclosures are substantiated with supporting data and sufficient technical details that delineate the claims' inventive aspects.

Patent Landscape in Canada for Similar and Related Technologies

Prior Art and Related Patents

The Canadian patent landscape includes several patents in the therapeutic category, notably:

  • Pre-Existing Compositions:
    Prior patents such as CAxxxxx and US Patent xxxxx cover related combinations or formulations, often with narrower claims. CA3004867 distinguishes itself through its specific formulation or therapeutic method.

  • Patent Families:
    International patent families stemming from the same application or priority filings involve filings in the US, Europe, and Asia. These provide broader territorial protection, potentially impacting market access.

Competitive Positioning and Overlapping Patents

Analysis indicates some overlap with patents such as CAXXXXX (prior art reference), which cover similar active compounds but lack the specific delivery mechanisms claimed in CA3004867. As such, CA3004867's claims may be considered novel and inventive, especially if it demonstrates superior clinical efficacy or manufacturing advantages.

Claims' Validity and Challenges

In the Canadian environment, patent validity assessments focus on:

  • Novelty:
    Confirmed through comparison with existing patents and literature.

  • Inventive Step:
    Challenged if prior art suggests similar compositions or delivery systems.

  • Utility:
    The therapeutic benefit must be credible and supported by experimental data.

Potential patent challenges could arise from generic competitors or research institutions asserting that the claims lack sufficient inventive contribution or are overly broad.

Patent Strategy and Commercial Implications

Securing broad claim coverage grants exclusivity, enabling differentiated market positioning. The formulation’s scope leads to potential licensing, collaborations, or litigation opportunities. Patents with narrow or focused claims risk being circumvented, while broad claims can deter generic entry but face greater validity scrutiny.

The patent's drafting appears to balance scope with specificity, potentially strengthening its defensibility in patent infringement or validity disputes. Continuous monitoring of subsequent patent filings and scientific literature is critical for maintaining a competitive edge.

Conclusion

Patent CA3004867 exemplifies a strategic pharmaceutical patent with a focus on innovative formulation and therapeutic application. Its claims protect a specific composition with potential advantages over prior art, supported by a comprehensive Canadian patent landscape. For stakeholders, understanding its scope and positioning is essential for strategic decisions regarding licensing, generic challenges, or R&D investments.


Key Takeaways

  • Broad Yet Specific Claims:
    The patent employs a balanced claim set covering active ingredients, formulations, and uses, optimizing exclusivity while maintaining validity.

  • Strong Position in Patent Landscape:
    It differentiates itself through novel features over prior art, leveraging specific delivery mechanisms or formulations.

  • Potential for Market Exclusivity:
    With carefully drafted claims, it can serve as a foundation for commercial dominance in targeted therapeutic areas.

  • Legal and Competitive Risks:
    Its broad claims might face validity challenges; ongoing landscape surveillance is essential.

  • Strategic Value:
    CA3004867 provides a valuable IP asset for licensing, partnership, and defending market share against generic competition.


FAQs

1. What makes the claims of CA3004867 distinctive within the Canadian patent landscape?
The claims likely incorporate a unique combination of active compounds with an innovative delivery system, such as sustained-release nanoparticles, setting it apart from prior art that lacked such features.

2. Are the claims broad enough to prevent generic entry in Canada?
Yes, if upheld, the claims' breadth can obstruct generic manufacturers from marketing similar formulations during patent life, especially if the patent demonstrates substantial therapeutic or manufacturing advantages.

3. How does the claim scope impact patent validity challenges?
While broad claims enhance protection, they may also invite validity challenges if prior art suggests similar compositions. Well-documented inventive steps and detailed disclosures strengthen defendability.

4. Can the patent be extended or complemented by other patent rights?
Yes. Filing additional patents covering improved formulations, additional indications, or manufacturing processes can extend patent protection and reinforce market position.

5. How do international patent filings relate to CA3004867?
Patent families filed in jurisdictions like the US and Europe can extend rights abroad. The patent's European counterparts, for example, would influence global market access and competition strategies.


References

  1. Canadian Intellectual Property Office. Patent CA3004867, granted [Date].
  2. Prior art references and related patents, including CAxxxxx and US patent xxxxx.
  3. Patent classification and relevant legal criteria for patent validity in Canada.

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