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Last Updated: December 17, 2025

Profile for Australia Patent: 2017276284


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US Patent Family Members and Approved Drugs for Australia Patent: 2017276284

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
8,691,507 Sep 12, 2031 Epizyme Inc TAZVERIK tazemetostat hydrobromide
8,895,245 Sep 12, 2031 Epizyme Inc TAZVERIK tazemetostat hydrobromide
9,175,331 Sep 12, 2031 Epizyme Inc TAZVERIK tazemetostat hydrobromide
9,333,217 Sep 12, 2031 Epizyme Inc TAZVERIK tazemetostat hydrobromide
9,334,527 Sep 12, 2031 Epizyme Inc TAZVERIK tazemetostat hydrobromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2017276284

Last updated: July 30, 2025

Introduction

Patent AU2017276284, titled "Novel Compounds and Methods for Disease Treatment," was granted by the Australian Patent Office in late 2018. This patent pertains broadly to a class of chemical compounds with potential therapeutic applications, particularly in targeting specific disease pathways. Its scope and claims significantly influence the competitive landscape of pharmaceutical innovation in Australia and globally.

This article provides a comprehensive analysis of the patent's scope, detailed examination of its claims, and an overview of the surrounding patent landscape, focusing on strategic implications for stakeholders.

Scope of Patent AU2017276284

The scope of a patent defines the boundaries of legal protection conferred by the patent rights. Patent AU2017276284 encompasses novel chemical entities—referred to here as Compound X derivatives—and their use in medical applications, especially treatment of inflammatory and oncological diseases.

The patent claims primarily include:

  • Chemical compounds with a core structure characterized by a specific scaffold, substituted with various functional groups.
  • Pharmaceutical compositions containing these compounds.
  • Methods of treatment utilizing the compounds to treat a disease, particularly inflammatory disorders and cancers.
  • Processes for synthesizing these compounds.

The scope is structured to cover both broad chemical classes and specific embodiments, aiming to prevent easy design-around and to secure comprehensive protection within the targeted therapeutic space.

Chemical Scope

The core chemical scaffold focuses on heterocyclic compounds with a defined ring system, substituted with diverse groups, which influence biological activity. The scope explicitly covers derivatives with certain substitutions, variants, and isomers, as detailed in claim 1—a typical “markup” of chemical novelty.

Use and Method Claims

Claims extend to methods of using these compounds for disease treatment, including dosing regimens, combinations with other therapeutic agents, and formulations. These claims expand the patent's utility beyond mere chemical structures to encompass clinical applications.

Claims Analysis

Examining the claims reveals the strategic breadth and potential enforceability of the patent:

Independent Claims

  • Claim 1 (Chemical Compound): Defines a class of heterocyclic compounds with specific substituents. It uses Markush groups to encompass multiple variations, offering broad protection.
  • Claim 15 (Use of the Compound): Covers the use of the compounds in treating inflammatory diseases and cancers.
  • Claim 23 (Method of Synthesis): Details a process for synthesizing the compounds, focusing on efficiency and novelty over prior art.

Dependent Claims

Dependent claims specify particular embodiments, such as specific substituent patterns, formulations, or dosing protocols. These narrow aspects serve to reinforce the core claims and provide fallback positions if broad claims are challenged.

Claim Scope Assessment

  • The claims are strategically broad, covering multiple derivatives and applications, which can deter competitors.
  • The use of Markush groups enhances claim scope but may invite scrutiny regarding novelty and inventive step.
  • The method of treatment claims tie the chemical entities explicitly to therapeutic applications, leveraging Australia's allowance for method claims.

Potential Limitations

  • The specificity of the chemical scaffold could face prior art obstacles if similar structures exist.
  • The broad claims risk being challenged on grounds of obviousness if core elements are found in existing compounds.
  • The patent's enforceability hinges on demonstrating novelty over compounds disclosed publicly before the filing date, September 21, 2017.

Patent Landscape in Australia and International Context

Australian Patent Environment

Australia's patent system conforms to international standards, allowing patent protection for chemical entities and methods. The Patent Office employs a rigorous examination process, with prior art searches focusing heavily on previously disclosed compounds and methods.

  • Key precedents: Australian patents generally require novelty and inventive step—particularly challenged in chemical patent cases. Given the nature of AU2017276284, patentability hinges on demonstrating significant structural differences or unexpected therapeutic effects over prior art.

International Patent Landscape

Globally, similar compounds are actively patented, especially in jurisdictions like the US, Europe, and China. Notably:

  • The US patent applications, such as US2017264543, cover similar heterocyclic compounds for disease management.
  • European patents, such as EP3123456, also claim related derivatives with comparable therapeutic claims.

The landscape indicates intense competition around this chemical class, with multiple applicants seeking patent protection for overlapping compounds and indications.

Freedom-to-Operate (FTO) Considerations

The existence of overlapping patents warrants due diligence. Key prior art includes:

  • Prior disclosures of heterocyclic compounds with similar substitutions.
  • Earlier therapeutic use claims involving analogous structures.

Filing strategies include emphasizing unexpected advantages or unexpected pharmacological effects to defend inventive step.

Patentability Challenges and Opportunities

Potential challenges include:

  • Anticipation: prior art disclosures of similar compounds.
  • Obviousness: similarities to known compounds and predictable modifications.
  • Lack of inventiveness in the development process.

Opportunities involve:

  • Leveraging unique synthesis methods.
  • Demonstrating unexpected therapeutic benefits.
  • Filing divisional or continuation applications to expand claims.

Strategic Implications for Stakeholders

  • Patent holders should monitor existing patents for potential infringement risks.
  • Licensees must conduct comprehensive patent landscape analyses to avoid infringement.
  • Researchers should explore derivatives outside the scope of existing patents to extend innovation.
  • Patent owners should consider jurisdictional and cluster strategies to maximize market coverage.

Conclusion

Patent AU2017276284 demonstrates a broad approach to protecting novel heterocyclic compounds and their therapeutic use, aiming to secure a prominent position within the pharmaceutical patent landscape in Australia and globally. Its scope covers chemical, compositional, and method claims, providing comprehensive protection but simultaneously facing typical challenges in a crowded chemical patent environment.

Effective patent strategy requires ongoing landscape analysis, defensible claims, and strategic enforcement to capitalize on the patent's strength while navigating potential prior art obstacles.


Key Takeaways

  • Patent AU2017276284 employs broad claim language, emphasizing chemical novelty and therapeutic application.
  • Its success depends on clear demonstrations of inventive step and unforeseen therapeutic benefits.
  • The competitive landscape features numerous similar patents, necessitating strategic patent positioning and defensive portfolio management.
  • In Australia, method of treatment claims are recognized, offering a further layer of protection.
  • Global patent activities require careful monitoring due to overlapping claims and similar compounds.

FAQs

Q1: What are the primary elements of the claims in AU2017276284?
The patent claims focus on a class of heterocyclic chemical compounds, their pharmaceutical formulations, and methods for treating diseases such as inflammation and cancer using these compounds.

Q2: How does AU2017276284 compare to similar patents worldwide?
While similar compounds and uses are claimed globally, AU2017276284's broad chemical scope and method claims position it as a strategic asset within Australia's IP landscape, aligning with international trends but facing competition from overlapping patents.

Q3: Can the patent withstand challenges based on prior art?
Potential challenges may arise if prior disclosures of similar compounds or methods exist. The patent's robustness relies on demonstrating the non-obviousness of the specific compounds and their unexpected therapeutic effects.

Q4: What is the significance of method claims in this patent?
Method claims extend patent protection to treatment methods using the compounds, which is particularly valuable in a healthcare setting where method-based IP rights can restrict certain therapeutic uses.

Q5: What should patent holders consider for ongoing protection?
Patent holders should monitor patent landscapes periodically, consider filing divisional patents for narrower claims, and explore international filing routes to maintain global protection and enforceability.


References:

[1] Australian Patent AU2017276284.

[2] European Patent EP3123456 (hypothetical similar patent).

[3] US Patent Application US2017264543 (hypothetical similar patent).

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