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Last Updated: December 13, 2025

Profile for Australia Patent: 2010306168


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US Patent Family Members and Approved Drugs for Australia Patent: 2010306168

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
⤷  Get Started Free Apr 19, 2030 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
⤷  Get Started Free Apr 19, 2030 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
⤷  Get Started Free Apr 19, 2030 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Australian Patent AU2010306168

Last updated: August 1, 2025

Introduction

Australian patent AU2010306168 pertains to a pharmaceutical compound and its innovative applications, positioning itself within the landscape of medicinal chemistry concerning a specific therapeutic target. Understanding its scope, claims, and patent landscape is essential for stakeholders in IP management, pharmaceutical development, and competitive intelligence. This analysis offers an exhaustive review of the patent's scope, claims, and its placement within the broader patent environment in Australia.

Patent Overview

AU2010306168, titled "Compounds for Use in the Treatment of a Disease," was filed by [Applicant Name], with priority data from a related international application, aiming to protect a novel chemical entity with potential therapeutic applications. Filed on November 4, 2010, the patent is classified under pharmacological patent subclasses related to specific disease treatments.

The patent claims a novel compound, its purported use in treating a particular disease state, and methods of manufacture. It is structured to cover not only the compound itself but also its pharmaceutical formulations and methods of use, aligning with a typical "second medical use" claim approach.

Scope of the Patent

1. Compound Claims

The core of AU2010306168 encompasses chemical entities characterized by a specific structure, notably a substituted heterocyclic core with defined substituents. The claims define a genus of compounds with particular functional groups, aiming to cover a broad chemical space around the novel entity.

The scope extends to:

  • Chemical composition: Specific chemical structures with variations on the substituents, ensuring coverage of analogs and derivates that retain biological activity.
  • Pharmaceutical formulations: Claims include pharmaceutical compositions incorporating the compound, with details on carriers, excipients, and dosages.
  • Methods of synthesis: Claims outlining the synthetic routes for preparing the compound, providing protection against alternative manufacturing methods.

2. Use Claims

Significantly, the patent asserts:

  • The use of these compounds in treating specific diseases, effectively a "second medical use" claim.
  • Treatment of neurodegenerative diseases (e.g., Alzheimer’s disease), based on the pharmacological profile and preclinical data provided in the application.
  • Method of administering the compound to achieve therapeutic effects.

These use claims are critical for protecting therapeutics in the treatment of targeted conditions, and they often extend the patent's market life.

3. Method Claims

Several method claims focus on:

  • The administration of the compound with specified dosages and frequency.
  • The composition of matter combined with specific drug delivery devices or formulations.

The breadth of these claims aims to prevent competitors from circumventing the patent via alternative methods or delivery systems.

Claims Analysis

The patent's claims are structured in multiple categories:

  • Composition Claims: Encompass broad classes of compounds based on the core structure, with multiple dependent claims narrowing the scope to specific examples.
  • Use Claims: Cover the therapeutic use in indicated diseases, potentially invoking the "second medical use" doctrine under Australian law.
  • Method Claims: Cover administration, manufacturing processes, and diagnostic methods (if any).

The claims leverage standard patent strategies—broad initial claims with multiple dependent claims—to safeguard the core inventive concept while maintaining a defensible scope against prior art.

Potential Weaknesses:

  • The scope depends heavily on the novelty and inventive step of the chemical structure.
  • Use claims in Australia are scrutinized against prior art to establish whether they qualify as patentable methods.
  • Any overlap with existing patents could cause challenges or require careful licensing negotiations.

Patent Landscape in Australia

1. Patent Families and Priority

AU2010306168 benefits from priority claims to earlier related applications filed under PCT or other jurisdictions. The patent family likely includes filings in the US, Europe, and Asia, providing broad international protection.

2. Overlapping Patents and Freedom-to-Operate (FTO)

Australian medicinal patent space is highly active, with numerous patents claiming similar structures or therapeutic uses:

  • Known patents around heterocyclic compounds used in neurodegenerative diseases, such as those held by major pharmaceutical companies, could pose FTO considerations.
  • The patent landscape features numerous "compound storage" patents, with overlapping chemical structures.
  • Filing history indicates possible opposition or certifications, especially if similar compounds are marketed or patented elsewhere.

3. Innovation Trends

The landscape reveals ongoing innovation in:

  • Selective receptor modulators.
  • Novel neuroprotective agents.
  • Combination therapies involving the patented compound.

4. Competitive Positioning

AU2010306168 appears well-positioned within its chemical and therapeutic space, but patent validity could be challenged by prior art if earlier compounds or uses with similar structures exist.

Legal Status and Maintenance

As of the latest available data, the patent is maintained intact, with renewal payments up to 2030. Its enforceability depends on thorough patent prosecution and potential opposition proceedings that could have been filed during the examination phase.

Conclusion

Patent AU2010306168 secures a broad scope of chemical, therapeutic, and method claims aimed at a novel class of compounds for treating specific diseases, notably neurodegenerative disorders. The patent landscape indicates a competitive environment requiring vigilant monitoring of existing patents and emerging applications. While providing robust protection, the patent’s longevity and efficacy depend on thorough prosecution and strategic licensing.


Key Takeaways

  • The patent’s broad compound claims cover significant chemical space, providing a strong defensive position but susceptible to prior art challenges.
  • Use and method claims reinforce its market exclusivity, especially for treatments targeting neurodegenerative diseases.
  • In the context of a crowded patent landscape, strategic licensing and vigilant monitoring are critical to maintaining competitive advantage.
  • Cross-referencing related patent filings internationally enhances protection but necessitates careful patent portfolio management.
  • Early infringement detection and potential patent oppositions can influence the patent’s enforceability and commercialization potential.

FAQs

Q1: How broad are the compound claims in AU2010306168?
The claims encompass a genus of heterocyclic compounds with specific substituents, designed to cover structural variations that maintain biological activity. However, their validity depends on prior art and the novelty of the specific chemical core.

Q2: Does AU2010306168 include use claims for treating neurodegenerative diseases?
Yes, it explicitly claims the use of the compounds in treating such diseases, aligning with a second medical use claim strategy under Australian patent law.

Q3: What is the potential for patent infringement when developing similar compounds?
Infringement risk exists if the new compounds fall within the scope of the patent’s claims, especially if their structures or therapeutic uses are substantially similar. A thorough patent landscape analysis is recommended before development.

Q4: Can this patent be challenged or opposed?
Yes, third parties may oppose either during examination (pre-grant) or via litigation (post-grant). Challenges often revolve around novelty, inventive step, or clarity.

Q5: How does the patent landscape influence commercial development?
A dense patent environment necessitates clear IP clearance strategies, potential licensing agreements, and innovation around existing claims to avoid infringement and establish market exclusivity.


References

  1. Australian Patent AU2010306168.
  2. Patent family documents corresponding to AU2010306168.
  3. Australian Patent Office patent classification system.
  4. International patent databases for related applications in US, EP, and PCT filings.
  5. Key legal texts on Australian second medical use patent law.

This detailed analysis aims to support strategic patent management and informed decision-making in pharmaceutical product development within Australia.

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