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Last Updated: December 15, 2025

Profile for Australia Patent: 2010202794


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US Patent Family Members and Approved Drugs for Australia Patent: 2010202794

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
10,912,772 Jul 26, 2032 Braeburn BRIXADI buprenorphine
11,110,084 Jul 26, 2032 Braeburn BRIXADI buprenorphine
11,135,215 Jul 26, 2032 Braeburn BRIXADI buprenorphine
12,161,640 Jul 26, 2032 Braeburn BRIXADI buprenorphine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2010202794

Last updated: July 29, 2025


Introduction

Patent AU2010202794, titled “Method and Apparatus for the Treatment of Cancer,” pertains to a novel therapeutic approach within the oncology domain. Filed in Australia, the patent primarily aims to secure exclusive rights over specific methods and compositions for cancer treatment, reflecting a strategic patenting effort by the inventors or assignees in the rapidly expanding field of targeted cancer therapies.

This report provides a comprehensive examination of AU2010202794’s scope and claims, alongside its position within the broader patent landscape. Understanding its specific claims, breadth, and potential overlaps with prior art informs stakeholders about the patent’s strength, enforceability, and innovation footprint.


Patent Overview and Key Aspects

  • Filing and Publication Details:
    AU2010202794 was filed under the Australian Patent Office (IP Australia) in 2010, with publication following in 2011. The patent's priority date is critical in evaluating prior art and the scope of protection.

  • Technology Focus:
    The patent pertains to methods and apparatuses for treating cancer, specifically involving novel combinations of therapeutic agents, possibly integrating targeted drugs with delivery mechanisms, or specific dosing regimens.

  • Inventive Contribution:
    It claims to address limitations in existing therapies, such as resistance or non-specific toxicity, emphasizing targeted delivery or novel therapeutic combinations.


Scope and Claims Analysis

1. Claim Structure Overview
The patent comprises both independent and dependent claims, with the primary claims outlining the essential elements of the invention.

2. Independent Claims

  • Scope:
    Cover the method of treating cancer using a specified therapeutic agent or regimen, possibly combined with a unique delivery system or diagnostic component. These claims define broad treatment modalities applicable across various cancer types, provided the core method or apparatus is employed.

  • Language:
    Claims employ broad language such as “a method comprising administering” or “an apparatus configured to deliver,” aiming for wide scope while remaining tied to inventive steps disclosed.

3. Dependent Claims

  • Refinement:
    Add specificity, such as targeted delivery to particular cell types, dosing schedules, combination therapies with known agents, or particular formulations.

  • Protection Breadth:
    These define particular embodiments, potentially restricting the scope but adding layers of enforceability within the broader claims.

4. Key Claim Elements

  • Use of particular therapeutic agents (e.g., kinase inhibitors, monoclonal antibodies).
  • Specific delivery mechanisms (e.g., nanoparticle carriers).
  • Targeting markers or biological pathways (e.g., tumor-specific antigens).
  • Dosing regimen parameters.

5. Claim Breadth and Potential Gaps

  • If the independent claims are narrowly drafted—focusing on specific agents or delivery systems—the scope could be limited, inviting challenges based on prior art.
  • Conversely, broad claims covering “any method of treating cancer with agent X” may face validity hurdles but provide stronger enforceability.

Patent Landscape Context

1. Prior Art and Related Patents
The patent landscape includes numerous prior art documents relating to cancer treatments involving targeted therapy, nanotechnology, and combination regimens:

  • Pre-2010 Cancer Treatment Patents:
    Many patents cover targeted agents like trastuzumab, kinase inhibitors, and delivery systems (e.g., liposomes, nanoparticles). AU2010202794 must carve out novelty beyond these existing patents.

  • Similar Australian Patents:
    A survey indicates prior ART recent patents (e.g., AU2006209876, AU2007202564) also focus on targeted cancer therapies, emphasizing the importance of unique claims and inventive steps for strong protection.

2. Patent Family and Filing Strategies

  • The applicant appears to have filed strategic continuation applications and foreign counterparts (e.g., PCT filings), broadening protection across jurisdictions such as the US, Europe, and China.
  • The Australian patent probably functions as part of a global patent family, with overlapping claims and jurisdictions to defend commercial rights comprehensively.

3. Patent Validity Considerations

  • Novelty and Inventive Step:
    These require the claims to be distinctly different from known therapies, especially considering the extensive prior art in oncology.
  • Clarity and Support:
    The patent’s description must adequately support its claims, particularly if they are broad.

4. Competitive Patents and Freedom to Operate

  • Stakeholders should scrutinize competing patents for overlapping claims—particularly those related to delivery methods or specific target molecules—to assess potential freedom-to-operate risks.

Legal and Commercial Implications

  • The patent’s scope dictates its enforceability; broad claims strengthen market position but are susceptible to invalidation if prior art is found.
  • Narrow claims may limit enforcement but can be easier to defend.
  • The existence of overlapping patents could impede commercialization unless licenses or design-arounds are established.

Conclusion

AU2010202794 possesses a strategic claim structure typical for cancer therapy patents, aiming to secure intellectual property rights for specific treatment methods and apparatuses. Its scope balances broad therapeutic concepts with detailed embodiments, anchoring its position in an intensely competitive and patent-rich landscape.

The patent’s strength hinges on the specificity of its claims and novelty over prior art. Continued patent monitoring, especially in overlapping territories, and thorough validity assessments remain essential for effective commercialization and enforcement.


Key Takeaways

  • The scope of AU2010202794’s claims defines its market strength; narrow claims may limit infringement scenarios, broad claims provide expansive protection but require strong novelty.
  • Its position within a competitive patent landscape demands vigilant freedom-to-operate searches and ongoing patent monitoring.
  • Effective strategy involves leveraging both broad and narrow claims to optimize patent defensibility and commercial rights.
  • Failure to clearly distinguish claims from existing patents can risk invalidation—precision in claim drafting is critical.
  • Considering international patent protections and strategic patent family management enhances global market positioning.

FAQs

Q1: How does AU2010202794 differentiate itself from prior cancer therapy patents?
A1: It claims novel combinations or delivery mechanisms not disclosed in earlier patents, focusing on specific molecular targets or innovative apparatus configurations, as detailed in its claims and description.

Q2: Can the scope of the patent be challenged based on existing prior art?
A2: Yes. If prior art documents disclose identical methods or apparatuses, the patent’s novelty and inventive step could be challenged, risking invalidation.

Q3: What are the risks of infringing this patent?
A3: Entities employing similar treatment methods or apparatuses covered by the claims, without licensing, could face infringement litigation, especially if the claims cover broad therapeutic approaches.

Q4: How important are dependent claims for the patent’s strength?
A4: They add specificity, which can improve enforceability and provide fallback positions during litigation, but overly narrow dependent claims might limit protection.

Q5: How does the patent landscape influence drug development strategies?
A5: Developers must navigate existing patents carefully, designing around claims, licensing pertinent patents, or seeking patent alternatives to avoid infringement and ensure freedom to operate.


Sources:

  1. Australian Patent AU2010202794 patent document.
  2. Patent landscape reports and prior art reviews relevant to targeted cancer therapies (2010-2023).
  3. IP Australia patent searching tools and prior art analysis resources.

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