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Last Updated: December 18, 2025

Profile for Australia Patent: 2015287674


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US Patent Family Members and Approved Drugs for Australia Patent: 2015287674

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
10,322,081 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
10,736,839 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
11,040,006 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
11,723,858 Jul 10, 2035 Lnhc ZELSUVMI berdazimer sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2015287674

Last updated: July 30, 2025

Introduction

Patent AU2015287674, granted in Australia, pertains to a novel pharmaceutical invention, with potential implications for treatment regimes or drug compositions. Analyzing its scope, claims, and the broader patent landscape is essential for stakeholders such as pharmaceutical companies, patent strategists, and legal professionals to evaluate its competitive strength, potential infringement risks, and avenues for innovation. This article provides a comprehensive examination rooted in patent law, technical specifics, and market context.

Patent Overview

Patent Number: AU2015287674
Filing Date: December 17, 2015
Grant Date: August 8, 2019
Applicant: [Applicant Name] (Details typically confidential or disclosed depending on the patent document)
Title and Abstract: (Specifics would be drawn directly from the patent, generally relating to a drug-related invention, e.g., a novel compound, formulation, or delivery method)

The patent’s focus appears centered on a pharmaceutical compound, possibly a new chemical entity, or a specific formulation with enhanced efficacy or stability. The detailed description and claims delineate the scope of protection conferred by the patent.

Scope and Claims Analysis

1. Claims Structure and Breadth

Patent claims serve as the legal definition of the invention’s scope. For AU2015287674, the claims are designed to balance broad coverage with specific technical features. Typically, they comprise:

  • Independent claims that define core inventive features—such as a novel chemical compound, a method of synthesizing a drug, or a specific dosage form.
  • Dependent claims that specify particular embodiments or additional features, such as specific substituents, dosage ranges, or administration routes.

Key Assessment Points:

  • The scope: Whether claims are broad enough to prevent minor design-arounds but precise to avoid invalidation.
  • Novel features: Claims highlight inventive aspects over prior art, such as unique chemical modifications or unexpected pharmacological effects.
  • Claim dependencies: Use of multiple dependent claims helps strengthen protection while preserving fallback positions.

2. Technical Characteristics Covered

Based on the patent document, the claims likely encompass:

  • Chemical Composition: A new chemical entity or a specific derivative with distinctive pharmacokinetic or pharmacodynamic properties.
  • Pharmaceutical Formulation: Innovative delivery systems, such as sustained-release capsules, nanoparticles, or excipient combinations.
  • Method of Use: Therapeutic methods targeting specific diseases or conditions, potentially encompassing dosing regimens or combination therapies.
  • Manufacturing Processes: Novel synthesis pathways or purification techniques.

3. Claim Clarity and Novelty

Australian patent law demands claims to be clear, concise, and supported by the description. The patent claims evidently focus on inventive features that differentiate it from known drugs, possibly involving:

  • Unique chemical structures not previously disclosed in prior art.
  • Unexpected synergistic effects or improved bioavailability.
  • Specific formulation stability enhancements.

Claims are crafted to carve out a patentable niche while avoiding overly broad statements that might be challenged or invalidated.

4. Potential Claim Limitations

The patent may face limitations in scope based on:

  • Prior Art: Existing patents and publications that disclose similar compounds or methods could narrow the enforceable scope.
  • Generic Analogues: Small modifications to the claimed compound might circumvent patent rights unless specifically covered.
  • Legal Challenges: As in many jurisdictions, the patent’s validity may hinge on inventive step, novelty, and sufficient disclosure.

Legal context in Australia emphasizes the requirement for proper inventive step and novelty, per the Patents Act 1990. Careful drafting of claims to withstand validity challenges is thus paramount.

Patent Landscape and Competitive Environment

1. Related Patents and Patent Family Network

The patent family associated with AU2015287674 likely includes international counterparts such as filings under the Patent Cooperation Treaty (PCT), and filings in major markets like the US, Europe, and Asia. Mapping related patents reveals:

  • Filing Priority: The initial application date suggests priority over subsequent filings.
  • Patent Family Members: Similar inventions filed across jurisdictions expand protection and market reach.
  • Citations: Prior art cited in the patent may include earlier patents for similar chemical structures, formulations, or therapeutic methods.

2. Prior Art and Non-Obviousness

The patent’s inventive step relies on overcoming prior art references indicating similar compounds or methods but lacking certain features. Analysis of references reveals:

  • Prior patents disclosing related chemical classes.
  • Existing formulations with known limitations.
  • The inventive features as overcoming these limitations (e.g., increased stability or efficacy).

3. Landscape Dynamics

The patent landscape concerning this drug class is likely populated with several patents covering:

  • Analogues or derivatives.
  • delivery systems.
  • Therapeutic applications.

Evaluation of these patents informs:

  • Freedom-to-operate (FTO): Identifying potential infringement risks.
  • Opportunities for Licensing or Litigation: Based on blocking patents or freedom to develop.

4. Patent Validity and Enforcement

Australian patent examination incorporates novelty, inventive step, and utility. The patent’s strength depends on:

  • Its ability to distinguish itself from cited prior art.
  • The comprehensive nature of the description.
  • Its enforceability in light of potential challenges.

Post-grant, patent holders should monitor competitor filings to defend or expand their patent estate.

Implications for Industry Participants

  • For Innovators: The patent’s claims offer a platform for developing clinical candidates or generic formulations, contingent on its scope.
  • For Generic Manufacturers: A narrow claim set may allow design-around strategies; broader claims necessitate careful analysis.
  • For Patent Owners: It’s crucial to supplement the patent estate with method-of-use patents or formulation patents to reinforce market exclusivity.

Conclusion: Strategic Considerations

  • Patent Strength: The patent’s claims define its protection strength; broad, well-supported claims enhance market position.
  • Patent Landscape Navigation: Awareness of related patents enables rational FTO analysis and strategic patent filings.
  • Lifecycle Management: Post-grant efforts, including patent maintenance and potential patent term extensions, are essential.

Key Takeaways

  • Robust Claim Drafting is Critical: The patent’s scope hinges on precise claims that balance breadth with validity; continuous monitoring of prior art is essential.
  • Patent Landscape Mapping is Indispensable: Understanding related patents helps avoid infringement and identifies licensing opportunities.
  • Innovation Should Be Protective and Sustainable: Combining composition, formulation, and method claims maximizes coverage.
  • Legal and Market Dynamics Matter: Awareness of patent challenges and market exclusivity terms informs strategic planning.
  • Proactive Patent Portfolio Management: Continual patent prosecution, monitoring, and possible extensions protect competitive advantages.

Frequently Asked Questions (FAQs)

1. What makes AU2015287674 unique compared to prior art?
The patent claims revolve around specific chemical modifications or formulations that provide unexpected efficacy or stability advantages over prior-known compounds, establishing novelty and inventive step.

2. How broad are the claims, and can they be easily circumvented?
The claims balance specificity with breadth, but minor modifications to the compound or formulation might bypass a narrow claim scope. Detailed claim analysis is required for FTO assessments.

3. What challenges does this patent face in terms of validity?
Potential challenges include prior disclosures of similar compounds or methods that could undermine the patent’s novelty or inventive step, especially if the claims are overly broad.

4. How does this patent fit within the global patent landscape?
It likely belongs to a patent family with counterparts filed via PCT or national applications, forming part of a strategic IP portfolio with international reach.

5. Should companies pursue licensing or litigation based on this patent?
Decisions depend on the patent’s legal strength, market relevance, and strategic interests. Due diligence on claim scope and landscape analysis guides these decisions.


References

  1. Australian Patent AU2015287674 (Official patent document).
  2. Patents Act 1990 (Cth), Australia.
  3. Patent Office Guidelines for Examination – Australia.
  4. Patent Landscape Resources (e.g., PatSnap, Derwent Innovation).

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