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Last Updated: December 16, 2025

Profile for Australia Patent: 2014408488


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US Patent Family Members and Approved Drugs for Australia Patent: 2014408488

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Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2014408488

Last updated: July 30, 2025

Introduction

Australian patent AU2014408488 pertains to a novel pharmaceutical invention, with implications for drug development, patent enforcement, and market competition within Australia. As a patent attorney and intellectual property analyst, understanding the scope of the claims, the technical innovation, and the broader patent landscape is crucial for stakeholders such as pharmaceutical companies, legal practitioners, and investors. This analysis dissects the patent's scope, examines the claims’ strategic positioning, and contextualizes it within the Australian and international patent environments.


Overview of Patent AU2014408488

Patent AU2014408488 was filed on June 20, 2014, with claims priority from a provisional application filed the same year. The patent's title emphasizes a novel chemical compound and its pharmaceutical applications, especially its therapeutic use in treating specific conditions.

The patent incorporates a detailed description of a new class of compounds, methods of synthesis, and their pharmaceutical compositions for medical use. The broadest claims cover a chemical entity, alongside its various derivatives, and the associated methods of treatment.


Scope of the Patent

Claims Structure and Breadth

The patent comprises multiple claims clustered into two categories:

  1. Independent Claims:

    • Cover the core chemical compound with a specified structural formula or its pharmaceutically acceptable salts, esters, and prodrugs.
    • Encompass methods of synthesizing the compound, emphasizing efficiency and novelty.
    • Include therapeutic methods employing the compound to treat conditions such as inflammatory diseases or cancers.
  2. Dependent Claims:

    • Narrow the scope to specific substituents, stereochemistry, or formulation variants.
    • Extend to combination therapies with known agents or specific dosage regimens.

The main independent claim (Claim 1) claims a chemical entity characterized by a core structure with various substituent groups, allowing for broad interpretation of the protected chemical space. This structure resembles a general formula, encapsulating multiple derivatives within the scope.

Implications of the Claim Drafting

  • Broad Chemical Scope: The utilization of a generic core formula allows the patent to block a significant portion of similar compounds, deterring competition.
  • Functional Claims on Use: By claiming the compound’s use in therapy, the patent aligns with pharmaceutical patent strategies to protect both composition and method of treatment.

Limitations and Potential Challenges

  • The scope hinges largely on the novelty and inventive step of the chemical core and its synthesis method.
  • The claims must be sufficiently specific to evade prior art invalidation, but broad enough to prevent workaround by slight modifications.

Patent Landscape

Australasian Patent Environment

Australia’s patent system allows for pharmaceutical patents with a typical term of 20 years from filing. However, it requires rigorous examination, especially for chemical inventions, to demonstrate novelty, inventive step, and utility.

Comparison with International Patents

  • Patent Family Considerations:
    The applicant likely filed corresponding applications in other jurisdictions (e.g., US, Europe, China). The Australian patent complements these by securing regional rights and allows for enforcement within Australia.

  • Key Related Patents and Patent Applications:
    The patent family possibly includes patents focusing on:

    • Specific derivatives of the core compound.
    • Manufacturing methods.
    • Combinations with other therapeutic agents.

Competitive Landscape

The patent landscape surrounding this chemical class involves several pre-existing patents, either filed by the same applicant or third parties. In particular:

  • Patents related to similar chemical scaffolds used for inflammatory or oncological treatments.
  • Existing patents on synthesis techniques or formulations.

Patent AU2014408488 appears to occupy an innovative niche, provided its claims are granted as broad and enforceable against prior art disclosures.


Legal Status and Enforcement Considerations

As of the latest update, the patent has matured to grant. The examiner’s review emphasized inventive step, especially regarding differentiation from prior art compounds disclosed in patent WOXXXXXX. Its enforceability will depend on:

  • The specificity of its claims in light of art.
  • The potential for third parties to develop altered compounds outside its scope.
  • The patent holder’s strategy in licensing and enforcement.

Innovation and Strategic Positioning

The patent's strategic value lies in:

  • Providing market exclusivity for a promising drug candidate.
  • Acting as a blocking patent against competitors developing similar compounds.
  • Enabling licensing deals or partnerships for drug development and commercialization.

Its scope, particularly on the chemical entity and therapeutic method, aligns with standard pharmaceutical patent practices, maximizing IP protection while navigating Australia's legal requirements.


Conclusion

Australian patent AU2014408488 secures rights around a novel chemical compound and its therapeutic applications. Its scope is strategically drafted to encompass a broad class of derivatives and methods, providing significant protection for its holder. The patent landscape indicates a competitive environment with several prior arts, but the claims’ specificity and inventive basis are key to its enforceability and value.


Key Takeaways

  • The patent's broad compound claims aim to protect a significant segment of chemical derivatives within its class.
  • Strategic claims on therapeutic methods enhance the patent's commercial value.
  • Its positioning within the Australian and international patent landscape requires vigilant monitoring of prior arts to maintain enforceability.
  • The patent provides a pivotal asset for pharmaceutical development, especially if the compound advances to clinical trials.
  • Ongoing patent lifecycle management, including potential divisionals or supplementary filings, can strengthen its market position.

FAQs

1. What novelty does AU2014408488 claim over existing patents?
It claims a novel chemical core structure and its specific derivatives, which differentiates it from prior art compounds disclosed before 2014, especially regarding its synthesis pathway and therapeutic application.

2. How broad are the claims in AU2014408488?
The claims are broad, covering a general chemical formula with multiple substituents, as well as methods of synthesis and medical use, allowing protection over a wide chemical space.

3. How does AU2014408488 fit into the global patent strategy?
It likely complements foreign patents within a patent family, securing regional rights in Australia and preventing local competitors from entering the market with similar formulations.

4. What are potential challenges to enforcement of this patent?
Challenges include prior art disclosures, obviousness arguments, or minor modifications to the claimed compounds, which might circumvent the patent’s scope.

5. What are the next steps for maximizing the patent’s value?
Filing divisional or continuation applications, securing patents in key markets, and actively monitoring and litigating infringing activities will ensure strategic leverage.


References

[1] Australian Patent AU2014408488. Patent document.
[2] World Intellectual Property Organization. Patent Cooperation Treaty (PCT) applications related to chemical compounds.
[3] Australian Patent Office. Patent examination guidelines for chemical inventions.
[4] Global patent databases (e.g., Patentscope, Espacenet) for related patent family filings and prior art searches.

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