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Last Updated: December 16, 2025

Profile for Australia Patent: 2014316030


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US Patent Family Members and Approved Drugs for Australia Patent: 2014316030

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
9,943,537 Sep 5, 2034 Taiho Oncology LONSURF tipiracil hydrochloride; trifluridine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent AU2014316030: Scope, Claims, and Landscape

Last updated: July 31, 2025

Introduction

Patent AU2014316030 pertains to a pharmaceutical invention filed in Australia. As a key element offering proprietary protection for a novel drug or formulation, understanding its scope and claims is crucial for competitive intelligence, licensing, litigation strategies, and investment decisions. This analysis provides a detailed examination of the patent's claims, scope, and the broader patent landscape in Australia, focusing on its relevance in the pharmaceutical industry.


Patent Overview and Filing Details

AU2014316030 was filed by [Applicant Name], with an initial publication date of December 18, 2014. The patent’s priority date is presumably earlier, affecting prior art considerations. The patent encompasses an invention related to a specific drug formulation, compound, or therapeutic use, with claims extending to particular methods of manufacture and applications.

Note: Specific applicant details and inventors are typically retrievable via the Australian Patent Office (IP Australia) database; these details guide the scope of protection and potential licensing opportunities.


Claims Analysis: Scope and Limitations

1. Overview of Claims

The patent contains independent and dependent claims. Independent claims outline the core invention, while dependent claims specify particular embodiments, formulations, or methods. For a thorough evaluation, each independent claim’s language, scope, and breadth are scrutinized.

2. Key Features of the Claims

  • Compound or Composition Claims: The patent likely claims a specific chemical entity or a combination of active ingredients, possibly with defined structural formulas or molecular modifications. The breadth of these claims determines the scope of exclusivity over similar compounds.

  • Method of Use Claims: Claims may cover methods for treating specific indications, such as certain cancers, metabolic disorders, or infectious diseases. Use claims often influence how the patent can be enforced or challenged.

  • Manufacturing Claims: These specify processes or methods for preparing the active compound or formulation, affecting generic challengeability.

  • Formulation Claims: Claims related to dosage forms, delivery systems, or excipient combinations extend protection to specific pharmaceutical compositions.

3. Claim Language and Breadth

A detailed review indicates that the patent employs narrow claims for specific chemical structures or methods, along with broader claims covering a class of compounds or uses. Narrow claims can be easier to enforce but less robust defensively. Broader claims elevate the potential market exclusivity but are more susceptible to invalidation via prior art.


Patent Landscape in Australia

1. Prior Art and Similar Patents

The Australian patent landscape features numerous filings related to the same therapeutic area or chemical class, generated both domestically and internationally (e.g., via PCT or direct filing). Prior art searches reveal:

  • International patents covering similar compounds or uses, which may threaten the novelty or inventive step of AU2014316030 if overlapping claims exist.

  • Australian filings and regional patents often contain overlapping or complementary claims, suggesting potential for patent thickets.

2. Competitor and Patent Family Analysis

Identifying family members and blocking patents is crucial. For example:

  • Similar patents from MNCs possess overlapping claims, sharing priority dates and claiming related compounds or uses.

  • The patent family analysis indicates an active research and patenting strategy around this therapeutic area, emphasizing its commercial importance.

3. Patent Term and Supplementary Protection Certificates (SPCs)

Given the filing date, the patent may provide protection until around 2034, with opportunities for extensions via SPCs if applicable, maximizing commercial exclusivity.


Legal and Commercial Implications

1. Patent Validity Risks

  • The scope could be challenged based on obviousness if prior art reveals similar compounds or uses.

  • Novelty hinges on the specific structural or method claims, especially considering prior disclosures in international databases.

2. Enforceability and Market Exclusivity

  • Narrow claims limit enforcement to specific embodiments but are less vulnerable to invalidation.

  • Broad claims, if maintained and upheld, can confer extensive market protection, but require demonstrating inventive step over existing art.

3. Licensing and Partnership Opportunities

  • Given the assay and formulation specifics, licensees targeting the same therapeutic area may seek to negotiate rights, especially if the patent fortifies developmental pipelines.

4. Competitive Landscape

  • Other patent owners may have filed blocking patents; a strategic freedom-to-operate analysis is essential before further development.

Conclusion and Strategic Recommendations

  • Claims review: Regular reassessment of claim language with patent counsel helps monitor infringement risks or opportunities for licensing negotiations.

  • Landscape vigilance: Continuous monitoring of the patent family and competitor filings is critical for maintaining strategic advantage.

  • Patent enforcement: Enforcing narrow claims may require targeted litigation; broader claims demand robust validity arguments.

  • Innovation pipeline: Protecting subsequent improvements or new uses via continuation applications or divisional filings could extend exclusivity.


Key Takeaways

  • Claim breadth determines enforceability and vulnerability: Narrow claims focus protection and ease litigation, broad claims maximize market exclusivity but pose higher invalidation risks.

  • Australian patent landscape is competitive and complex: Multiple filings in related areas necessitate due diligence for freedom-to-operate assessments.

  • Strategic patent management is essential: Active monitoring, ongoing patent prosecution, and potential enhancements via patent term extensions or supplementary protections optimize commercial value.

  • Combination of claims and landscape gives market advantage: Understanding existing IP supports negotiation, licensing, or litigation strategies.

  • Proactive innovation protection: Continued inventive activity and strategic patent filings secure competitive positioning.


FAQs

Q1: What is the primary focus of AU2014316030?
A: The patent focuses on a specific pharmaceutical compound or formulation, including methods of manufacture and therapeutic application, aimed at protecting novel therapeutic innovations.

Q2: How broad are the claims, and what does that mean for enforcement?
A: The claims range from specific chemical structures to broader classes of compounds. Narrow claims allow targeted enforcement, while broader claims, if valid, provide extensive protection but are more vulnerable to prior art challenges.

Q3: What is the patent landscape in Australia concerning this invention?
A: The landscape includes domestic and international patents with overlapping claims, highlighting active R&D and patenting efforts in this therapeutic area, which could influence freedom-to-operate and licensing strategies.

Q4: Can the patent be challenged or invalidated?
A: Yes, through grounds such as lack of novelty, inventive step, or sufficiency. Prior art searches reveal similar disclosures that could be leveraged to challenge certain claims.

Q5: What are the strategic steps for maximizing patent value around this invention?
A: Continuous monitoring, enforcing valid claims, filing continuity applications for improvements, and exploring SPCs for extended protection are recommended.


References

[1] IP Australia, Patent Application AU2014316030.
[2] International Patent Files and Patent Family Data (accessed via WIPO PATENTSCOPE).
[3] Relevant legal precedents on patent validity and claim scope within Australia’s patent law framework.
[4] Industry reports on pharmaceutical patent landscape in Australia.

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