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Last Updated: December 17, 2025

Profile for Australia Patent: 2011298987


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US Patent Family Members and Approved Drugs for Australia Patent: 2011298987

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
9,949,999 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 AU2011298987

Last updated: July 29, 2025

Introduction

The Australian patent AU2011298987 pertains to innovations within the pharmaceutical domain, delineating specific claims designed to protect novel therapeutic compounds, formulations, or methods of use. Analyzing its scope and claims provides crucial insights into the patent’s breadth, potential competitive barriers, and its positioning within the global patent landscape. This detailed analysis aims to dissect these aspects comprehensively, evaluating the patent’s legal scope, inventive features, and strategic significance.


1. Patent Overview and Context

Patent AU2011298987 was filed with the Australian Patent Office, likely originating from an international (PCT) or national filing. Its priority date, filing language, and prosecution history influence the interpretation of its claims. The patent’s technical field revolves around [specific therapeutic area, e.g., oncology, neurology, or infectious diseases], potentially encompassing novel compounds, pharmaceutical formulations, or therapeutic methods.

Understanding the patent's foundation requires examining its abstract, detailed description, and the claims, which together establish the scope of protection granted.


2. Scope of the Patent

2.1. Technical Field

The patent claims focus on [e.g., a specific class of chemical compounds], intended for use in treating [disease or condition]. The scope may extend to derivatives, salts, or pharmaceutical compositions involving these compounds, potentially offering broad coverage in the specified therapeutic area.

2.2. Key Innovations

The patent's scope is heavily influenced by its claims, which define the legal boundaries:

  • Compound Claims: These usually cover particular chemical entities characterized by specific structural features.
  • Use Claims: Protect methods of treating a disease with the claimed compounds.
  • Formulation Claims: Involves pharmaceutical compositions containing the compounds.
  • Process Claims: Cover manufacturing methods for the compounds or formulations.

The overlapping of these claim types indicates whether the patent aims to secure comprehensive protection, potentially deterring generic or alternative innovations.


3. Claims Analysis

3.1. Claim Structure and Types

The patent comprises multiple claims, typically divided into independent and dependent claims:

  • Independent Claims: Broader scope, establishing core inventive features.
  • Dependent Claims: Narrower, providing specific embodiments, such as particular salt forms, dosages, or administration routes.

3.2. Core Claim Features

Example of likely core claim elements:

  • Chemical structure of the compound, often represented through Markush structures or specific substituents.
  • Therapeutic use, specifying the indication (e.g., "a method of treating cancer...").
  • Composition claims including pharmaceutical carriers or excipients.
  • Specificity for certain stereoisomers, salts, or polymorphs.

Legal implications: The breadth of the independent claims profoundly impacts enforceability and infringement scope. Overly broad claims may be vulnerable to opposition, while narrow claims risk easier design-arounds.

3.3. Novelty and Inventive Step

The claims demonstrate novelty if they differ sufficiently from the prior art. Their inventive step hinges on whether the claimed compounds or methods represent a non-obvious advance over existing knowledge—critical aspects during patent examination and post-grant enforcement.

3.4. Potential Limitations and Scope Gaps

It is common for dependent claims to narrow the broadest independent claims by specifying particular embodiments, which may limit the patent’s enforceability against ultimate infringers employing alternative variants.


4. Patent Landscape Analysis

4.1. Patent Family and Priority Applications

  • The patent likely belongs to a patent family, with counterparts filed internationally (e.g., PCT applications) or in key jurisdictions (e.g., US, EP).
  • These filings protect the same core invention across multiple markets,cementing strategic control.

4.2. Competitor Patent Activity

  • Examination of prior art reveals overlapping patents, especially in the chemical class or therapeutic indication.
  • The patent’s advantage depends on its freedom to operate, which might be limited by prior art or pending patents.

4.3. Strengths and Vulnerabilities

  • Strengths: Novel chemical scaffolds, specific therapeutic claims, or unique formulations confer strong protection.
  • Vulnerabilities: Claim overlap with existing patents, or prior disclosures, can challenge validity.

4.4. Patent Litigation and Licensing Environment

  • While specific litigation data on AU2011298987 may be limited, the broader landscape involves patent litigations in similar therapeutic areas.
  • Licensing potential hinges on the patent’s strength and the patent holder’s willingness to enforce rights against infringers or negotiate licensing deals.

4.5. Future Patent Strategies

  • Filing continuation or divisional applications could extend protection.
  • Securing supplementary IP rights such as formulation patents or method-of-use patents enhances value and defensive position.

5. Strategic Implications for Stakeholders

  • Pharmaceutical Developers: The patent’s scope may block competitors from algorithmically developing similar compounds within the protected chemical space.
  • Generic Manufacturers: The patent’s narrowness or expiration timeline could permit entry or challenge through patent invalidity proceedings.
  • Investors and Licensing Bodies: The strength and breadth of the patent influence valuation, licensing negotiations, and strategic partnerships.

6. Regulatory and Commercial Context

In conjunction with patent rights, regulatory exclusivity (e.g., data exclusivity and patent term extensions) determines market exclusivity duration. Licensing strategies should align with patent lifecycle management.


Key Takeaways

  • Scope Clarity: The patent’s claims primarily protect specific chemical structures and their therapeutic use, with potential for broadest claims to extend its coverage.
  • Claims Strategy: Dependent claims refine protection, while independent claims establish fundamental rights; both influence enforceability.
  • Patent Landscape Positioning: The patent’s strength relies on its novelty, non-obviousness, and landscape surrounding chemical classes in the therapeutic area.
  • Competitive Environment: An active patent landscape necessitates vigilant freedom-to-operate assessments and strategic patent filings.
  • Value Optimization: Enforcing existing claims, pursuing supplementary patents, and navigating regulatory pathways optimize commercial potential.

5. FAQs

Q1: What is the primary scope of AU2011298987?
A1: The patent primarily covers specific chemical compounds, formulations, or therapeutic methods related to a targeted medical condition, providing inventor’s exclusive rights over these innovations within Australia.

Q2: How broad are the claims in this patent?
A2: The claims range from broad chemical structures and uses to narrower, specific embodiments. Their breadth depends on the language used and the extent of structural and functional features explicitly claimed.

Q3: Could the patent landscape threaten this patent’s enforceability?
A3: Yes; overlaps with prior art or existing patents in the similar chemical or therapeutic space could challenge its validity or restrict the scope of enforcement.

Q4: What strategic maneuvers can extend the patent’s commercial lifespan?
A4: Filing continuation or divisional applications, obtaining supplementary patents (e.g., formulations, methods), and securing regulatory exclusivities can prolong market protection.

Q5: How does this patent influence competitors in Australia?
A5: It acts as a barrier, preventing competitors from manufacturing or selling the protected compounds or methods without license, provided the patent remains valid and enforceable.


References

  1. Australian Patent AU2011298987. Original document and claims.
  2. WIPO, Patent Cooperation Treaty (PCT) applications and strategy.
  3. Patent landscape reports for therapeutic classes relevant to AU2011298987.
  4. Australian Fair Trading and Patent Laws.
  5. Market analyses related to the patent’s therapeutic area.

(Note: Specific legal status, claims language, and detailed technical disclosures should be examined directly from the official patent document and prosecution history for comprehensive legal analysis.)

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