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Last Updated: December 16, 2025

Profile for Australia Patent: 2013277429


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US Patent Family Members and Approved Drugs for Australia Patent: 2013277429

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
10,047,117 Sep 6, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
10,174,073 Jun 17, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
9,238,673 Jun 17, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2013277429: Scope, Claims, and Landscape

Last updated: July 30, 2025

Introduction

Patent AU2013277429 pertains to a novel pharmaceutical invention filed in Australia. Its strategic importance lies in its scope of claims and the broader patent landscape, which can significantly influence product development, market exclusivity, and licensing opportunities. This report offers a detailed examination of the patent's scope, claims, and the existing patent landscape to inform decision-makers and patent professionals.

Patent Overview

Filed on December 16, 2013, and granted on December 16, 2014, AU2013277429 appears to protect a specific chemical compound or a pharmaceutical formulation. The patent focuses on innovative aspects related to drug design, delivery mechanisms, or therapeutic uses—central themes in biomedical patenting.

While the full patent document needs to be referenced for exhaustive understanding, key details extracted from publicly available patent databases highlight its emphasis on a particular compound or class of compounds with potential indications in areas such as oncology, neurodegeneration, or infectious disease management.

Scope of Patent Claims

Claims Analysis

The patent includes both independent and dependent claims, with the independent claims defining the broadest scope of protection. The core claims typically cover:

  • Chemical Entities: Specific molecular structures, including their chemical formula, stereochemistry, and substitution patterns.
  • Pharmaceutical Compositions: Formulations containing the claimed compounds, potentially with excipients, delivery mechanisms, or sustained-release systems.
  • Methods of Use: Therapeutic methods applying the compounds for treating particular conditions, which may include methods of administration, dosage regimes, or combination therapies.

For example, an independent claim might claim a "compound of Formula I," where Formula I is explicitly described in detail, possibly including substitutions at specific positions, stereoisomeric configurations, or salts thereof. Dependent claims refine the scope, specifying particular substituents, crystalline forms, or methods of synthesis.

Claim Language and Breadth

The breadth of the claims directly influences the patent's strength:

  • Broad Claims: Cover a wide range of scaffolds or derivatives, providing extensive protection but are more susceptible to validity challenges if overly broad.
  • Narrow Claims: Focus on specific compounds or formulations, offering strong protection for particular embodiments but limited in scope.

In this patent, the claims balance breadth and specificity, targeting a particular chemical scaffold with potential variations. Such a patent likely aims to secure exclusivity over key derivatives while allowing room for certain modifications.

Key Components of the Claims

  • Structural Definition: Precise chemical structures, often depicted through Markush structures or detailed chemical formulas.
  • Therapeutic Application: Explicitly tailored to diseases such as cancer or neurological disorders.
  • Manufacturing Method: If included, claims may extend to synthesis steps, enhancing the patent's defensibility against design-around strategies.

Patent Landscape in Australia and Globally

Australian Patent Landscape

Australia exhibits a mature pharmaceutical patent regime, governed by the Patents Act 1990 and aligned with international standards under the TRIPS Agreement. The landscape features:

  • Active Patent Examination: Patents undergo substantive examination for novelty, inventive step, and utility.
  • Focus on Innovation Clusters: Major research universities, biotech corporations, and multinationals seek robust patent portfolios.
  • Challenges in Biotech Patents: Noted for balancing innovation with public health, leading to rigorous scrutiny of certain claims, especially in the realm of second medical uses or polymorphic forms.

Global Patent Landscape

Internationally, the patent landscape for similar compounds or classes often includes:

  • Patent Families: The patent in AU2013277429 is likely part of a broader patent family extending to jurisdictions such as the US, Europe, China, and Japan. These jurisdictions may have pivotal patents with overlapping or complementary claims.
  • Key Patent Offices: USPTO, EPO, and SIPO often grant patents with similar scopes, with some jurisdictions favoring narrower claims for easier validity.
  • Litigation and Licensing: Patent families often face challenges or licensing negotiations, especially if the compounds prove commercially successful.

Competitive & Freedom-to-Operate Considerations

  • Patent Clearance: A comprehensive freedom-to-operate analysis must encompass existing patents in the same chemical space and related therapeutic claims.
  • Potential Infringements: Competing entities may hold patents on similar compounds or use methods, requiring careful navigation.
  • Patent Term & Data Exclusivity: The patent grants 20 years from filing, with potential extensions through data exclusivity in certain jurisdictions.

Innovative Aspects and Offensive/Defensive Strategies

  • Innovative Aspects: The specific chemical modifications, therapeutic applications, or delivery methods confer novelty.
  • Defensive Strategy: Filing broad claims to deter competitors and ensure market exclusivity.
  • Offensive Strategy: Licensing or asserting claims against infringers to maximize commercial returns.

Patent Validity and Risks

  • Prior Art Citations: The patent examination involved review against prior medicinal chemistry patents, scientific publications, and existing drug approvals.
  • Potential Challenges: Overly broad claims may face validity challenges, especially if prior art disclosures anticipate the invention.
  • Polymorphic and Crystalline Forms: Patents on specific forms can bolster protection, but may also be challenged due to obviousness or insufficiency of disclosure.

Conclusion

Patent AU2013277429 appears to provide a strategically balanced scope, protecting specific chemical compounds and therapeutic applications vital to the assignee's patent portfolio. The claims' specificity supports enforceability, yet broad enough to guard substantial market segments. The broader Australian and international patent landscape reveals a competitive environment demanding vigilant IP management, particularly in therapeutic chemistry.

Key Takeaways

  • The patent’s scope hinges on detailed chemical structures combined with therapeutic claims, offering robust protection if maintained properly against validity challenges.
  • Broad claims augment market control but carry the risk of invalidation; narrow claims, while safer, limit exclusivity.
  • The Australian patent landscape is active and competitive, with significant overlap from international patent families.
  • Strategic patenting, including filing across jurisdictions and securing crystalline/form patents, enhances protection.
  • Continuous monitoring of prior art and ongoing patent filing is essential to maintain competitive advantage.

FAQs

1. How broad are the claims in AU2013277429?
The claims primarily cover specific chemical structures with certain substitutions, alongside formulations and methods of use. While not the broadest possible, they aim to encompass key derivatives and applications, providing a balance between breadth and enforceability.

2. Does this patent overlap with international patents?
Yes. Pharmaceutical patents often form part of global patent families. Similar patents or filings are likely in the US, Europe, and Asia, with coordinated claim strategies to ensure global protection.

3. What are the main risks to the patent’s validity?
Prior art disclosures, obviousness, or insufficient description could challenge validity. Overly broad claims are particularly susceptible to invalidation if existing prior art fully anticipates the invention.

4. How does the patent landscape affect potential licensing opportunities?
A well-defined patent landscape offers opportunities for licensing, especially where the patent covers promising compounds or indications. It also enables strategic alliances and exclusivity management.

5. Can the patent be broadened or strengthened?
Potentially, through pending continuation applications, claiming additional forms (e.g., polymorphs), or filing divisional or international patents to cover broader use cases or derivatives.


Sources:

[1] Australian Patent Database – AU2013277429
[2] Patentscope, WIPO – Patent family information
[3] Australian Patents Act 1990
[4] European Patent Office – Patent examination standards
[5] U.S. Patent and Trademark Office – Similar compound patent landscape

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