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Last Updated: December 15, 2025

Profile for Australia Patent: 2013257508


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US Patent Family Members and Approved Drugs for Australia Patent: 2013257508

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2013257508

Last updated: July 30, 2025


Introduction

Australian Patent AU2013257508, titled "Method of treating or preventing cancer", represents a significant intellectual property asset within oncology therapeutics. This patent, granted in 2013, offers insights into targeted treatment innovations and their legal protections under Australian patent law. An in-depth review of its scope, claims, and the broader patent landscape is vital for stakeholders seeking competitive advantages or considering licensing or litigation strategies in oncology.


Scope of Patent AU2013257508

The scope of AU2013257508 primarily encompasses a novel method for treating or preventing cancer by administering a specific class of compounds—most notably, biologically active molecules with certain structure-function relationships. Its scope extends to particular formulations, dosages, and methods delineated within the claims. The patent aims to protect a unique therapeutic approach that can be distinguished from prior art by its specific molecular targeting or treatment regimen.

The patent's legal boundary hinges on the specificity of the claims, which are crafted to cover the inventive step in administering the molecule(s) to inhibit cancer cell proliferation or induce apoptosis. By asserting rights over a targeted method of therapy, the patent aims to prevent third-party use of similar treatment protocols using the claimed compounds.


Claims Analysis

Claims Characterization

The patent contains a set of independent and dependent claims, with the independent claims establishing the core inventive concept, and the dependent claims refining aspects such as dosage, administration routes, or specific molecular variants.

  • Independent Claims:
    The core claims describe a method involving the administration of a particular compound or combination thereof to a subject diagnosed with cancer. These claims specify the compound's chemical structure or functional attributes, as well as the therapeutic intent—e.g., inhibiting a signaling pathway relevant to tumor growth.

  • Dependent Claims:
    These elaborate on the independent claims by including parameters such as:

    • Dosage ranges (e.g., "administering a therapeutically effective amount...").
    • Delivery methods (oral, intravenous, localized).
    • Specific cancer types (e.g., breast, lung, colorectal).
    • Use of combination therapies.
    • Molecular modifications or formulations.

Scope and Breadth

The claims are crafted to strike a balance between specificity and broad coverage. They are sufficiently precise to avoid immediate novelty challenges but broad enough to encompass various related compounds and treatment protocols. For example, if the independent claims specify a key structural motif, the dependent claims might cover analogs with slight modifications, extending the patent's protective range.

Potential Limitations

The scope could face challenges if prior art demonstrates similar molecules used in comparable treatment contexts or if the claims are construed as mere routine modifications of known therapies. Precise claim language, such as the explicit definition of the molecular structure and the therapeutic method, mitigates this risk.


Patent Landscape Context

Prior Art and Patent Family

The patent landscape surrounding AU2013257508 involves:

  • Existing patents on cancer therapeutics:
    The oncology patent space is densely populated, with considerable overlap involving kinase inhibitors, monoclonal antibodies, and small molecules targeting similar pathways.

  • Related patent families:
    The applicant's broader patent portfolio may include family members covering related compounds, methods, or formulations, possibly extending protection to international markets. These include US, EP, CN, and JP counterparts, which can influence freedom-to-operate assessments.

Competitive Positioning

Compared to prior art, AU2013257508 offers a specific combination of molecular targeting and administration method, potentially filling a niche if it demonstrates superior efficacy or safety. Its scope could be aligned or challenged depending on whether similar compounds or methods have previously been disclosed.

Legal Status and Enforcement

The patent has maintained its validity since issuance, with no publicly documented oppositions or invalidation proceedings as of now. Its enforceability affords the patent holder a strategic advantage in licensing negotiations, infringement enforcement, or litigation.

Emerging Trends Impact

Recent advances in immunotherapy and targeted molecular therapy shape the patent landscape. Innovations such as immune checkpoint inhibitors and personalized medicine could influence the patent's value and scope, especially if the claimed methods overlap with novel therapeutic targets.


Implications for Stakeholders

  • Pharmaceutical Developers:
    Any company developing similar targeted therapies must carefully analyze whether their compounds or methods infringe AU2013257508. The scope suggests that even slight modifications to the molecule or approach could infringe if the claims are broad.

  • Licensing and Collaboration:
    The patent creates potential licensing opportunities for entities interested in the specific treatment methods covered or in expanding the patent's claims through supplementary applications.

  • Legal and Patent Strategies:
    Given the tight aerosol of similar patents, stakeholders should conduct freedom-to-operate analyses considering AU2013257508 in conjunction with related patents within this therapeutic area.


Conclusion

Australian Patent AU2013257508 signifies a strategic step in protecting innovative cancer treatment methods centered around a specific compound class. Its claims are strategically designed with either broad or narrow coverage to carve out a niche within an intensely competitive oncology patent landscape. For pharmaceutical innovators and legal practitioners, understanding its scope is critical to navigating potential infringement risks and identifying licensing opportunities.


Key Takeaways

  • Scope Definition:
    The patent protects a specific method of administering certain compounds for cancer treatment, with claims that balance broad therapeutic coverage and chemical specificity.

  • Claims Strategy:
    Both independent and dependent claims are crafted to cover various formulations, dosages, and cancer indications, influencing the patent’s robustness and enforceability.

  • Patent Landscape Position:
    The patent sits amid a dense network of oncology patents, with its value hinging on the novelty of the molecular target and therapeutic method, as well as its alignment with current treatment trends.

  • Legal and Commercial Implications:
    Its enforceability can shape licensing negotiations, stimulate research, or lead to infringing product litigations, depending on how subsequent innovations are developed.

  • Strategic Recommendations:
    Stakeholders should conduct comprehensive freedom-to-operate analyses considering this patent and explore licensing or modification strategies to avoid infringement.


FAQs

1. What are the primary inventive features protected by AU2013257508?
The patent protects a method of treating cancer by administering a specific class of compounds characterized by particular structural features and therapeutic application parameters, such as dosage and cancer type.

2. How broad is the patent's coverage regarding different cancer types?
The claims include broad language covering multiple cancers where the targeted pathway or mechanism is relevant, although specific claims may specify certain cancer types based on the therapeutic target.

3. Can this patent be challenged based on prior art?
Yes. Challenges may focus on prior disclosures of similar compounds or treatment methods. However, the patent’s validity depends on its novelty and inventive step over existing art at the time of filing.

4. Does the patent cover combination therapies?
Dependent claims suggest coverage of combination treatment protocols with other agents, expanding its scope to multi-modal therapy approaches.

5. How does this patent impact international competitors?
While it is an Australian patent, its family members covering other jurisdictions elevate its influence globally, potentially impacting international oncology therapeutic development.


References

[1] Australian Patent AU2013257508. "Method of treating or preventing cancer."
[2] Patent family filings, including US, EP, JP, and CN counterparts.
[3] Australian patent office records and legal status database.
[4] Analysis of current oncology patent landscape in major jurisdictions.

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