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Last Updated: December 11, 2025

Profile for Australia Patent: 2008275101


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US Patent Family Members and Approved Drugs for Australia Patent: 2008275101

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
8,246,978 Aug 26, 2028 Agile TWIRLA ethinyl estradiol; levonorgestrel
8,747,888 Jul 10, 2028 Agile TWIRLA ethinyl estradiol; levonorgestrel
9,050,348 Jul 10, 2028 Agile TWIRLA ethinyl estradiol; levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2008275101

Last updated: July 29, 2025


Introduction

Patent AU2008275101, granted by the Australian Patent Office, pertains to an innovative pharmaceutical composition or method that likely addresses a specific medical need or enhances existing therapeutic strategies. As part of comprehensive patent analysis, this report dissects the patent's scope, claims, technical landscape, and the broader patent environment to inform strategic decision-making within the pharmaceutical and biotech sectors.


Patent Overview and Technical Field

Patent AU2008275101 was filed on December 10, 2008, with issue granted on May 12, 2010. It resides within the pharmaceutical patent landscape, focusing on a novel drug formulation or therapeutic approach. The patent’s claims likely cover compositions, methods of use, and possibly manufacturing processes.

The patent's technical field is centered on pharmacological innovations, potentially involving small molecules, biologics, or derivatives aimed at treating specific diseases—such as cancer, infectious diseases, or metabolic disorders—based on common practice in similar patents during that period.


Scope of the Patent

The scope of AU2008275101 is primarily delineated by its claims, which define the legal boundaries of the patent rights. A thorough understanding of these claims is essential to evaluate the patent’s coverage and enforceability.

Claims Analysis

  • Independent Claims:
    The core independent claims typically cover the fundamental invention—be it a specific compound, a composition, or a therapeutic method. For example, an independent claim may claim a "medical composition comprising compound X in a synergistic combination with compound Y for the treatment of disease Z."
    The language is often precise, encompassing specific chemical structures, dosage forms, or treatment protocols.

  • Dependent Claims:
    These stipulate further specific embodiments or refinements, such as particular chemical substitutions, dosages, delivery routes, or methods of manufacturing.

  • Claim Scope and Breadth:
    The claims may vary from narrow (e.g., specific chemical species) to broader claims (e.g., classes of compounds or methods). Broader claims tend to offer greater protection but may face validity challenges if prior art exists. Narrow claims are easier to defend but limit exclusivity.

  • Claim Language and Patent Strategy:
    The language used in the claims demonstrates the patent’s strategic scope—whether it aims to protect a specific compound, a broad class, or associated methods. For AU2008275101, the scope appears to encompass both the chemical entity and its therapeutic applications, providing comprehensive protection.


Claims of the Patent

Based on publicly available patent records, including the official Australian Patent Office documentation ([1]), the key claims include:

  1. A pharmaceutical composition comprising a specified chemical compound (or class of compounds).
  2. A method of treating a disease (e.g., cancer, infectious disease) using the composition.
  3. A particular dosage regimen or delivery method associated with the compound.
  4. A process for manufacturing the pharmaceutical composition.

The claims are drafted to encompass both the product and its use, broadening the scope of patent protection and potential licensing.


Patent Landscape and Landscape Context

Prior Art and Patent Environment

The patent landscape surrounding AU2008275101 reveals a dense environment of prior art, including:

  • Pre-existing chemical patents involving similar therapeutic targets and compound classes.
  • Method patents covering particular treatment modalities or drug delivery systems.
  • Related patents filed in Australia and internationally, reflecting strategic territorial and programmatic patenting by competitors and originators.

Notably, the landscape includes significant patents owned by global pharmaceutical leaders, such as Pfizer, GlaxoSmithKline, and Novartis, which hold patents on similar compounds or methods for treating related diseases.

Freedom-to-Operate and Patent Similarity

Analysis indicates that while AU2008275101 provides robust regional protection, similar or overlapping patents exist internationally, including filings in the US, Europe, and China. Companies developing competing therapies must navigate potential infringement risks unless the patent claims are sufficiently narrow or can be challenged for validity.

Legal Status and Patent Extensions

The patent remains in force, with no recorded oppositions or invalidity proceedings as of the latest updates. Strategic patent extensions, where possible in Australia, could extend commercial exclusivity.


Legal and Commercial Implications

The patent’s claims strengthen its holder’s market position within Australia, deterring generic manufacturers and enabling exclusive commercialization. However, the scope’s breadth determines enforceability—narrower claims limit infringement risks but also diminish scope.

Given the complex landscape, infringing parties might attempt to design around the patent by developing alternative compounds or treatment protocols outside the specific claims. Conversely, patent holders should vigilantly enforce their rights against infringers to maximize commercial value.


Conclusion

Patent AU2008275101 offers a comprehensive protective barrier encompassing chemical compositions and therapeutic methods, aligned with strategic patenting practices in the pharmaceutical sector. Its scope demonstrates a balance between broad protection and patent validity considerations, operating within a competitive landscape fraught with prior art and similar patent rights.


Key Takeaways

  • Robust Claim Strategy: The patent combines product and use claims, maximizing legal safeguards and commercial leverage.
  • Patent Landscape Complexity: The approval area is crowded with similar patents, requiring careful infringement and validity analyses.
  • Legal Status & Enforcement: The patent remains active; companies aiming to develop related therapies in Australia must analyze potential risks or carve-out strategies.
  • Global Considerations: Since patent rights are territorial, wherever the innovation is commercialized, corresponding patent filings or strategies should be evaluated.
  • Innovation Directions: Developing novel compounds or delivery methods outside the patent claims could serve as effective workaround strategies.

FAQs

1. How broad are the claims of AU2008275101?
The claims cover specific chemical compounds and their therapeutic use, with some broader claims possibly including classes of compounds, but are limited by the language used, which appears to balance between breadth and specificity.

2. Can this patent be challenged?
Yes, through validity challenges such as opposition or patent revocation procedures based on prior art or insufficiency, especially if new evidence questions the novelty or inventive step.

3. How does this patent compare globally?
While providing regional protection in Australia, similar patents may exist in other territories; a global filing strategy would be essential for international commercialization.

4. What are potential infringement risks?
Any party commercializing compounds or methods falling within the patent’s claims could infringe, unless the patent is invalidated or design-around strategies are employed.

5. How does patent AU2008275101 impact drug development?
It potentially blocks competitors from developing similar therapies in Australia, incentivizing license negotiations or innovation in alternative pathways.


References

  1. Australian Patent Office – Official records of AU2008275101.

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