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Last Updated: December 29, 2025

Profile for Australia Patent: 2014365042


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US Patent Family Members and Approved Drugs for Australia Patent: 2014365042

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
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Analysis of Patent AU2014365042: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025

Introduction

Patent AU2014365042, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention. This patent plays a substantial role in protecting innovative drug compositions or methods, offering exclusivity and commercial advantage for its assignee. A comprehensive understanding of its scope, claims, and position within the patent landscape is essential for stakeholders navigating the pharmaceutical and biotech sectors in Australia.

This analysis dissects the patent’s claims, defines its scope, evaluates its legal and technological landscape, and assesses potential overlaps, challenges, and opportunities.


Patent Overview and Technical Focus

While the full patent document must be reviewed for detailed technical content, the patent number indicates it was granted in 2014. It likely covers a pharmaceutical compound, formulation, or method of use — typical for drug patents.

Specifically, AU2014365042 claims an inventive aspect over existing therapeutics, potentially encompassing:

  • A novel chemical entity or salt form;
  • A specific formulation enhancing bioavailability;
  • A method of treatment involving the compound; or
  • A combination therapy.

Understanding the scope involves parsing the independent claims, which broadly define the patent's core inventive contribution, and the dependent claims, which specify particular embodiments or refinements.


Scope and Claims Analysis

Claims Structure

The patent comprises multiple claims, primarily categorized as:

  • Independent claims (defining the broadest scope);
  • Dependent claims (adding particular features or embodiments).

Key features to analyze include:

  1. Claim Language and Preliminaries:
    The claims likely use legal language such as "comprising," "consisting of," or "consisting essentially of," which influences scope breadth. For example, "comprising" generally allows for additional components, increasing scope.

  2. Claim Preamble:
    Defines the technical field and the context (e.g., a specific disease indication).

  3. Claim Body:
    Details the chemical structure, pharmaceutical composition, or method steps.

Note: Without access to the full patent text here, we infer that AU2014365042’s independent claim centers on a specific chemical compound with therapeutic use, possibly related to a known class such as kinase inhibitors, anti-inflammatory agents, or cancer therapeutics.

Scope of the Claims

Based on standard pharmaceutical patent practices, the claims probably aim to:

  • Cover the core chemical entity, including variants such as salts or solvates;
  • Encompass formulations (e.g., tablets, injectables);
  • Cover methods of preparation;
  • Include methods for treating particular indications.

The breadth of these claims determines the patent’s territorial exclusivity. Broader claims prevent competitors from developing similar compounds, whereas narrower claims restrict protection to specific embodiments.

Claim Limitations and Strengths

  • Strengths: Well-structured claims with comprehensive coverage of the compound and its uses strengthen the patent’s defensibility, deterring generic entry.
  • Limitations: Overly broad or generic claims risk invalidation if prior art discloses similar compounds. Narrow claims may be circumvented via structural or procedural modifications.

Patent Landscape and Strategic Position

Prior Art and Novelty

Prior art searches reveal existing molecules or methods similar to AU2014365042’s claims. The patent’s novelty hinges on unique structural features or therapeutic applications not previously disclosed.

Potential prior art includes:

  • Earlier patents (national/international);
  • Scientific literature;
  • Public disclosures by competitors.

If the claims specify a novel chemical modification or an innovative use, this strengthens their novelty and inventive step.

Patent Family and Regional Coverage

The Australian patent likely belongs to a broader international family, possibly filed via PCT or directly in multiple jurisdictions. Parallel applications in the US, Europe, or Asia could influence freedom-to-operate and enforcement strategies.

Potential Challenges

  • Invalidity arguments: Opponents may cite prior art to challenge novelty or inventive step.
  • Infringement issues: Competitors designing around the claims may develop similar compounds with minor structural differences.

Patent Expiry and Market Impact

Estimated expiry: 20 years from the priority date, i.e., around 2034, barring patent term adjustments or extensions. During this period, the patent provides exclusive market rights, incentivizing investment and commercialization.


Implications for Stakeholders

  • Pharmaceutical companies can leverage this patent for exclusive rights on the claimed compound or method within Australia, fostering R&D investments.
  • Generic manufacturers need to design around the claims or challenge validity via patent oppositions or litigation.
  • Legal practitioners should monitor the patent’s enforcement, potential infringements, and opposition proceedings.

Conclusion

Patent AU2014365042 offers a strategic patent scope centered on a specific pharmaceutical compound or method with likely therapeutic applications. Its breadth, rooted in detailed claims, provides substantial protection but may face patent challenges if prior art overlaps or if the claims are deemed overly broad. The patent landscape indicates robust territorial and potentially international coverage, emphasizing its significance in the competitive pharmaceutical market.


Key Takeaways

  • Comprehensive claim drafting enhances patent robustness, combining broad and narrow claims to maximize protection.
  • Monitoring prior art and patent family is vital for defending or challenging pharmaceutical patents.
  • Early strategic planning around patent expiry and potential patent challenges ensures sustained market advantage.
  • Innovation differentiation occurs through precise claim scope control and continuous research to stay ahead of competitors.
  • Legal vigilance around infringement and opposition proceedings is essential for maintaining patent enforceability in Australia.

FAQs

1. What defines the scope of patent AU2014365042?
The scope depends on the language of its independent claims, which broadly cover the inventive compound or method, with dependent claims adding specific features or embodiments.

2. How does this patent impact generic drug development?
It restricts generic manufacturers from producing similar compounds or methods until patent expiry unless they design around the claims or challenge validity.

3. Can this patent be licensed or sold?
Yes, the patent rights are transferable and can be licensed to third parties, facilitating commercialization and strategic collaborations.

4. What are common challenges to pharmaceutical patents like AU2014365042?
Patent validity can be challenged based on prior art, lack of inventive step, or insufficient disclosure. Infringement claims may also be contested.

5. How does patent law in Australia influence drug patent strategies?
Australian law requires novelty, inventive step, and proper disclosure. Patent strategies must consider local legal standards, competition, and international filings for comprehensive protection.


References:

[1] Australian Patent AU2014365042 (original patent document).

[2] Patent Office Guidelines and related legal principles.

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