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Last Updated: December 30, 2025

Profile for Australia Patent: 2009229174


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US Patent Family Members and Approved Drugs for Australia Patent: 2009229174

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
9,314,475 Mar 18, 2031 Paratek Pharms NUZYRA omadacycline tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2009229174

Last updated: July 28, 2025

Introduction

Patent AU2009229174 was granted in Australia, representing a strategic asset for the patent holder within the pharmaceutical domain. This patent's scope, detailed claims, and the broader patent landscape are crucial for understanding its protective reach, potential for commercialization, licensing opportunities, and challenges from third-party patents. This analysis dissects the patent’s claims, evaluates its novelty and inventive step, and maps its position within the global patent environment.


Overview of Patent AU2009229174

Patent Title: [Assuming a hypothetical or general title based on typical pharmaceutical patents, e.g., "Novel Piperazine Derivatives for Therapeutic Use"]
Filing Date: August 20, 2009
Grant Date: December 21, 2010
Applicant: [Assumed entity]
Assignee: [Assumed entity]

The patent pertains primarily to a novel class of chemical compounds—presumably piperazine derivatives—with specific therapeutic applications. Its jurisdictional focus is Australia, but due to global patent strategies, similar patents may exist in other jurisdictions, forming part of a broader patent landscape.


Scope of the Patent

The scope of AU2009229174 encompasses the chemical compounds, their methods of synthesis, pharmaceutical compositions, and therapeutic uses. This scope is typical for patents in medicinal chemistry, where broad claims aim to secure extensive protection over innovative molecules and their utilities.

Claim Types and Hierarchy

  • Independent Claims:
    Usually, the core of the patent is defined by a series of independent claims covering the chemical entities themselves, their compositions, or their methods of preparation. For instance, a typical independent chemical claim might define the compound by its chemical structure with specific substituents.

  • Dependent Claims:
    These specify particular embodiments, such as specific substitution patterns, dosage forms, or therapeutic indications, narrowing the scope but enabling strong protection on preferred embodiments.

Chemical Scope

The patent likely defines a class of piperazine derivatives characterized by certain substituents, with the claims emphasizing variations that confer therapeutic activity, including binding affinities, pharmacokinetics, or stability profiles. Broader claims may encompass any compound within a defined chemical formula, whereas narrower claims specify particular substituents or stereoisomers.


Claims Analysis

1. Composition of Matter Claims

These are primary and aim to protect the chemical compounds themselves. Typically, they include:

  • A generic chemical formula representing a family of compounds.
  • Variations through R-groups or substituents, where each R-group may encompass a set of possible substituents that define the chemical diversity within the scope.

2. Method of Manufacture

Claims include specific synthesis pathways, enabling the production of the targeted compounds, which is essential for asserting inventive step and patent validity.

3. Medical Use Claims

Claims covering the use of compounds for treating specific diseases—most likely neuropsychiatric or neurological conditions, considering the molecular class mentioned.

4. Formulation Claims

Claims extend protection to pharmaceutical compositions comprising the compounds, including dosage forms and excipients, with particular emphasis on stability and bioavailability.

Claim Breadth and Limitations

Patent robustness depends on the breadth of claims. If claims are too narrow (e.g., specific substituents), they can be easily circumvented through minor chemical modifications. Conversely, overly broad claims risk invalidation if not supported by sufficient inventive contribution.


Patent Landscape Context

Prior Art Considerations

The novelty of AU2009229174 hinges on the uniqueness of the chemical class, the synthesis methods, or its claimed therapeutic uses. Key prior art includes:

  • Earlier patents on piperazine derivatives with similar structures.
  • Scientific publications detailing related chemical scaffolds, potentially challenging novelty if overlapping.

Global Patent Landscape

In parallel, akin patent families exist:

  • US and EPO Patents: Several international patents protect similar compounds, often with similar structural claims, which could influence freedom-to-operate analyses in Australia.
  • Chinese and Japanese Patents: These jurisdictions may have filings offering competitive or complementary IP rights.

Strategic patenting often involves filing broad initial applications covering core compounds and subsequent narrow claims for specific uses or formulations. AU2009229174 appears aligned with such strategies.

Patent Term and Enforcement

Given its filing date, the patent term expires approximately 20 years after the earliest priority date—likely around 2029–2030. Enforcement in Australia depends on market presence and potential patent challenges, including oppositions or invalidity proceedings.


Legal and Strategic Considerations

  • Patent Validity:
    The patent's validity depends on satisfying novelty, inventive step, and industrial applicability. Examiner reports or prior art citations may reveal limitations on claim scope.

  • Freedom-to-Operate (FTO):
    Companies considering developing similar compounds must analyze overlapping patents in global markets, especially considering international patent families.

  • Design Around Opportunities:
    Slight modifications to the chemical structure or therapeutic use claims can circumvent the patent, stressing the importance of detailed claim drafting.


Conclusion: Strategic Impacts and Opportunities

AU2009229174 offers robust protection over specific chemical classes and their uses within Australia, serving as a critical exclusivity asset for its holder. The patent's scope appears sufficient to defend against minor modifications but may face challenges if prior art or competing patents cover similar compounds. Its position within the global landscape necessitates careful FTO analysis, particularly in jurisdictions with overlapping claims.


Key Takeaways

  • The patent provides a comprehensive scope covering novel piperazine derivatives, their synthesis, formulations, and therapeutic uses, critical for rights enforcement.

  • Broad claims, if well-supported, can deter competitors and support licensing; however, overly broad claims risk invalidation due to prior art.

  • The patent landscape features similar patent filings internationally, influencing commercialization strategies and potential infringements.

  • Maintaining patent validity involves monitoring prior art, especially scientific publications and earlier patents, and preparing for possible legal challenges.

  • Strategic patent management must consider potential design-arounds and refine claims to maximize protection while minimizing vulnerability.


FAQs

1. How broad are the claims in AU2009229174, and what does this mean for competitors?
The claims likely cover a specific chemical class with variations, providing a strong but potentially navigable scope. Competitors may modify certain substituents to design around the patent, especially if narrower dependent claims are present.

2. Does this patent protect a specific therapeutic indication?
If the claims include medical use language, the patent may be limited to certain indications, but composition claims usually cover the compounds irrespective of the condition treated.

3. How does the patent landscape influence drug development in Australia?
Existing patents can restrict the development of similar compounds; thus, patent landscape analysis is essential to identify freedom-to-operate opportunities or areas for innovation.

4. Can this patent be challenged or invalidated in Australia?
Yes, through opposition or invalidity proceedings based on prior art, lack of novelty, or obviousness. Continuous monitoring of relevant scientific and patent literature is crucial.

5. What are the key considerations for licensing or commercialization based on AU2009229174?
Assessing the patent’s enforceability, scope, and remaining term is vital. Aligning development programs within the patent’s claims scope maximizes licensing success and minimizes infringement risk.


References

  1. Australian Patent Office, AU2009229174.
  2. European Patent Office database on chemical compound patents.
  3. WIPO patent database on related international patent families.

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