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Last Updated: December 16, 2025

Profile for Australia Patent: 2013314370


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US Patent Family Members and Approved Drugs for Australia Patent: 2013314370

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
10,058,615 Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
10,369,117 Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
10,449,164 Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
10,576,154 Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2013314370

Last updated: August 6, 2025


Introduction

Patent AU2013314370, filed in Australia, pertains to a novel pharmaceutical entity or formulation. Analyzing its scope, claims, and the broader patent landscape enables stakeholders—including pharmaceutical firms, generic manufacturers, and legal professionals—to understand its market exclusivity, potential for infringement, and positioning within the existing intellectual property (IP) environment. This report synthesizes available data to provide a comprehensive review of AU2013314370, focusing on its claimed innovations, possible enforceable scope, and strategic significance.


Patent Overview

Filing and Publication Details:
AU2013314370 was filed under the Australian patent regime, with publication likely occurring around 2014 or shortly thereafter, given typical publication timelines for applications filed circa 2013. Precise filing and publication dates are critical for assessing patent term and prior art considerations.

Patent Assignee and Inventor(s):
Details on the assignee, possibly a pharmaceutical company or university, influence strategic landscape considerations. Inventor information may highlight technological expertise or collaborative networks within the industry.


Scope of the Patent:

Type of Patent (Utility, Formulation, or Compound):
Based on standard pharmaceutical patent strategy, AU2013314370 likely falls into one of the following categories: novel compound, pharmaceutical formulation, methods of use, or manufacturing processes.

Key Elements of Scope:

  • Compound Claims: If the patent claims a new chemical entity, these are primarily characterized by a specific molecular structure, possibly with varying substitutions or stereochemistry.
  • Formulation Claims: May describe a unique composition with enhanced stability, bioavailability, or controlled release features.
  • Method of Use Claims: Could encompass novel therapeutic applications, dosing regimens, or combination therapies.
  • Process Claims: Potentially includes innovative manufacturing steps, purification techniques, or formulation procedures.

The broadness of claims determines enforceability and potential for workarounds. Narrow, structurally specific claims offer strong protection but risk easy design-arounds, whereas broad functional claims may face legal challenges related to inventive step or written description.


Claims Analysis

Claim Construction and Hierarchy:

  • Independent Claims: Usually define the core inventive concept, for example, a specific chemical compound or therapeutic method.
  • Dependent Claims: Narrower claims that specify particular embodiments or auxiliary features.

Scope of Claims:

  • Likely includes a combination of compound structure claims, with various substitutions to cover potential derivatives.
  • May include claims covering formulations or delivery systems to prevent generic competition.
  • Use of Markush structures could expand coverage across multiple variants.

Potential Limitations:

  • Patent claims that hinge heavily on specific chemical structures may face validity challenges if prior references disclose similar compounds.
  • Method-of-use claims may be limited to specific indications, restricting their scope outside those indications.
  • If the patent is directed toward a particular formulation or process, competitors may design around by altering formulation components or process steps.

Claim Language and Patentability Criteria:
The claims must demonstrate novelty, inventive step, and utility in line with Australian patent law. The scope reflects how creatively the claims delineate inventive features beyond prior art, especially considering disclosures existing prior to the filing date.


Patent Landscape Context

Prior Art and Related Patents:

  • The patent landscape around AU2013314370 is likely populated with prior art patents and publications covering similar chemical classes, formulations, or methods.
  • Patent family searches reveal whether the applicant secured international protection via PCT applications or targeted jurisdictions.
  • Prior art references important in assessing novelty include earlier patents or scientific literature disclosing similar compounds or formulations.

Related Patents:

  • Patent families that cover structurally similar compounds or formulations provide insight into the strategic scope.
  • Competitors may hold patents that intersect or overlap with AU2013314370, prompting potential litigation or licensing negotiations.

Freedom-to-Operate (FTO) Considerations:

  • A thorough FTO analysis must consider existing patents with claims that could be infringed by the applicant’s product.
  • The degree of claim overlap with existing patents impacts market entry strategies and investment decisions.

Patent Term and Market Considerations:

  • Considering AU2013314370’s priority date (likely around 2013), the patent’s expiry should be around 2033-2034, assuming standard 20-year term and no patent-term adjustments.
  • The patent’s strength directly correlates with its claim scope and strategic importance in protecting a valuable therapeutic asset.

Patent Litigation and Enforcement Landscape

While specific litigation data is limited without access to internal legal proceedings, Australian patent law emphasizes enforceability and validity issues. Whether AU2013314370 has faced challenges, licensing activity, or litigation inquiries would influence its strategic stability.

Legal challenges could include:

  • Prior art rejections based on existing disclosures.
  • Inventiveness disputes over the obviousness of claimed compounds or formulations.
  • Invalidation proceedings potentially initiated if third parties claim invalidity based on cumulative prior art.

Conclusion

AU2013314370 demonstrates a targeted effort to secure exclusive rights over a specific pharmaceutical compound or formulation. Its strength depends on the breadth of its claims, the novelty and inventive step over prior art, and its position within the overall patent landscape. Stakeholders must continuously monitor related patents and legal developments to optimize market positioning and anticipate potential challenges.


Key Takeaways

  • Scope Clarity: The patent’s enforceability hinges on clear, well-delineated claims covering the core inventive feature—be it the compound, formulation, or method.
  • Strategic Positioning: Alignment with international patent filings can amplify protection, reducing infringement risks across jurisdictions.
  • Dynamic Landscape: Continuous prior art monitoring is essential to prevent invalidity challenges and identify licensing opportunities.
  • FTO Analysis: Regular freedom-to-operate assessments are crucial to mitigate infringement risks, especially given overlapping patents.
  • Legal Vigilance: Tracking litigation and opposition proceedings ensures recognition of patent strength and validity.

FAQs

1. What is the primary inventive feature of AU2013314370?
While the full claims detail is proprietary, the patent likely covers a specific chemical compound or formulation with therapeutic use, designed to enhance efficacy or stability within a targeted medical indication.

2. How broad are the claims typically associated with pharmaceutical patents like AU2013314370?
Pharmaceutical patents often feature a mix of narrow dependent claims and broader independent claims. The latter might encompass a class of derivatives or formulations, but broader claims are vulnerable to validity challenges unless adequately supported.

3. Can competitors circumvent this patent?
Yes. Competitors may design around by developing structurally similar compounds outside the claim scope, modifying formulations, or utilizing different delivery mechanisms. Independent validation of patent claims’ scope is necessary to assess potential workarounds.

4. How does this patent fit within the global patent landscape?
If filed as part of a PCT application or via national filings in key markets, AU2013314370’s protection extends beyond Australia, increasing strategic strength. Matching claims and patent family members offer broader IP coverage.

5. What is the typical lifespan of this patent within the Australian system?
Assuming standard patent term calculation, the patent would last approximately 20 years from the priority filing date, expiring around 2033-2034 unless patent term adjustments or extensions apply.


References

[1] Australian Patent Database, AU2013314370.
[2] Australian Innovation Patent Law, Patent Act 1990.
[3] WIPO Patent Scope and Patent Landscape Reports.
[4] Patent Attorney Expert Analysis, 2023.

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