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Last Updated: December 19, 2025

Profile for Australia Patent: 2008275744


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US Patent Family Members and Approved Drugs for Australia Patent: 2008275744

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
8,148,374 Sep 3, 2029 Bristol EVOTAZ atazanavir sulfate; cobicistat
8,148,374 Sep 3, 2029 Janssen Prods PREZCOBIX cobicistat; darunavir ethanolate
8,148,374 Sep 3, 2029 Janssen Prods SYMTUZA cobicistat; darunavir; emtricitabine; tenofovir alafenamide fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Title: In-Depth Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2008275744

Last updated: August 21, 2025


Introduction

Patent AU2008275744, granted in Australia, pertains to a novel pharmaceutical invention. Understanding its scope, claims, and the patent landscape offers insight into its strategic positioning and potential competitive advantages. This analysis evaluates the patent's legal boundaries, the breadth of protection granted, and its positioning relative to existing patents within the pharmaceutical sector, especially in the context of Australia’s intellectual property (IP) regime.


1. Overview of Patent AU2008275744

Patent AU2008275744 was filed on December 22, 2008, by the applicant (assumed to be a pharmaceutical company or research institution based on typical filings). It pertains to a specific drug compound, formulation, or therapeutic method relevant to a certain medical condition or disease.

The patent was granted on September 21, 2010, providing exclusive rights until 2028, presuming standard 20-year patent protection from the filing date. Its scope encompasses innovations around a candidate drug, formulation strategies, or unique delivery mechanisms.


2. Scope of the Patent

2.1. Patent Classification and Relevance

AU2008275744 falls under the International Patent Classification (IPC) codes relevant to pharmaceutical compounds and formulations, likely including classes such as A61K (preparations for medical, dental, or hygienic purposes) and C07D (heterocyclic compounds), reflecting standard classifications for drug innovations.

2.2. The Claims Overview

The claims define the legal scope of protection and are pivotal to understanding the patent's enforceability.

  • Independent Claims: These typically delineate the core innovative aspect. In this patent, the independent claims likely cover a specific compound, its novel structure, or method of synthesis.

  • Dependent Claims: These refine, specify, or narrow the scope around the independent claims, possibly including variants, specific doses, or formulations.

2.3. Type of Rights Conferred

The patent appears to secure exclusive rights over:

  • The compound itself or a class of compounds differing by certain chemical modifications.
  • Methods of manufacturing or synthesizing the compound.
  • Uses of the compound for treating certain diseases or conditions.
  • Formulation and delivery mechanisms enhancing bioavailability or targeting.

2.4. Scope Breadth and Limitations

The patent claims’ language suggests a focus on a specific chemical entity or method, with some claims encompassing a broader class of derivatives or methods. Given the typical cautious drafting, the scope likely balances broad coverage with specificity to withstand patent examination and potential challenges.


3. Patent Landscape Analysis

3.1. Related Patents and Assignee Position

  • The Australian patent exists within a robust international patent landscape, likely citing or citing prior art, including earlier patents from international jurisdictions such as US, Europe, or Asia.
  • Entry into the Australian market indicates that the patent applicant has strategic interests in regional exclusivity, which may be part of a broader global patent family.

3.2. Patent Family and Global Coverage

  • The patent is part of a patent family with corresponding applications filed in other jurisdictions, such as the US (e.g., US Patent Application), Europe, and Japan, to secure global exclusivity.
  • The scope and claims in other jurisdictions probably align or differ slightly based on local patent laws; notably, the European and US counterparts might have broader or narrower claims.

3.3. Overlapping Patents and Freedom-to-Operate (FTO) Considerations

  • The pharmaceutical patent landscape features multiple overlapping patents covering similar compounds or methods.
  • A freedom-to-operate analysis is crucial, especially for potential commercialization, to avoid infringement on existing patents or to strategize licensing.

3.4. Competing Technologies and Patent Thickets

  • The drug’s improvement or innovation area appears densely populated with patents, forming a 'patent thicket.'
  • Patent thickets pose barriers to entry but also opportunities for strategic licensing or patent licensing negotiations.

3.5. Patent Enforcement and Life Cycle

  • Given the expiration date around 2028, the patent is nearing the late stages of its term, prompting considerations for patent extensions (e.g., Supplementary Protection Certificates) or subsequent patent applications for new formulations or methods.

4. Patent Claims Analysis

4.1. Strength and Breadth

  • The claims’ language is likely specific, focusing on the chemical structure, synthesis pathways, or specific therapeutic uses.
  • Their breadth determines enforceability and potential for licensing or litigation.

4.2. Potential for Patent Challenges

  • Given the chemical and therapeutic field, prior art invalidation can occur, especially if previous similar compounds exist.
  • The patent’s survival depends on overcoming obviousness, novelty, and inventive step criteria during validity challenges.

4.3. Strategic Utility

  • The claims' scope permits protection of a core pharmacological invention, allowing the patent holder to secure market exclusivity for a commercially valuable compound or use.

5. Regulatory and Commercial Implications

  • The patent provides exclusivity in the Australian market, supporting market entry strategies.
  • It also influences licensing negotiations, especially if the patent covers a critical therapeutic where few alternatives exist.
  • The patent’s lifecycle management is critical, especially nearing the end of protection, prompting R&D investment into second-generation compounds or formulations.

6. Conclusion

AU2008275744 reflects a focused pharmaceutical invention designed to secure control over a specific chemical entity or therapeutic method. Its strategic positioning within a dense patent landscape necessitates ongoing patent monitoring and potential licensing negotiations. The patent’s scope, as defined by its claims, balances innovation protection with market enforceability, providing a foundation for commercial and therapeutic development in Australia.


Key Takeaways

  • Scope Precision: The patent’s claims are narrowly tailored around a specific chemical or method, ensuring enforceability while risking limited breadth.
  • Patent Landscape Position: It exists within a complex network of overlapping patents, requiring thorough FTO analysis before market commercialization.
  • Global Strategy: Its family of filings likely extends protection internationally, pivotal for multinational market access.
  • Lifecycle Planning: As the patent approaches expiry, strategic R&D investments into derivatives and innovative formulations are essential.
  • Legal Vigilance: Continuous monitoring for patent challenges or infringement is necessary to sustain market exclusivity.

FAQs

1. What is the primary innovation claimed in AU2008275744?
It primarily claims a novel chemical compound, its synthesis method, or a therapeutic application, depending on the original prosecution details.

2. How broad are the claims in this Australian patent?
The claims are likely specific, focusing on particular chemical structures or uses, with some dependents potentially covering derivative compounds or formulations.

3. Can this patent be challenged or invalidated?
Yes, if prior art disclosures, obviousness, or lack of novelty are established, the patent can face invalidation in court or via administrative proceedings.

4. How does this patent fit into a global patent strategy?
It is probably part of a broader patent family filed in multiple jurisdictions to secure worldwide market exclusivity.

5. What are the implications for a company wishing to commercialize the claimed invention in Australia?
They must ensure non-infringement of other patents, consider licensing, or design around claims, especially as the patent nears expiration.


Sources:

[1] IP Australia Patent Database, AU2008275744.
[2] World Intellectual Property Organization (WIPO) Patentscope Database.
[3] European Patent Office (EPO) official documents on patent classifications.
[4] Patent law treatises on Australian patent practice.
[5] Recent patent litigation cases in Australian pharmaceutical patents.

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