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Last Updated: December 29, 2025

Profile for Australia Patent: 2005256512


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US Patent Family Members and Approved Drugs for Australia Patent: 2005256512

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
7,994,364 Dec 27, 2025 Collegium Pharm Inc NUCYNTA tapentadol hydrochloride
7,994,364 Dec 27, 2025 Collegium Pharm Inc NUCYNTA ER tapentadol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2005256512: Scope, Claims, and Patent Landscape

Last updated: August 10, 2025

Introduction

Patent AU2005256512, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention. Understanding its scope, claims, and broader patent landscape is essential for stakeholders involved in drug development, licensing, and competition analysis. This report provides a comprehensive review of Patent AU2005256512, scrutinizing its claims, technological scope, and the surrounding patent environment in Australia and globally.

Patent Overview

Filed on December 9, 2005, and granted on July 19, 2007, AU2005256512 is titled "Pharmaceutical Compositions and Methods for Treatment." It focuses on specific chemical entities and methods for their therapeutic use, originally attributed to a class of compounds with potential utility in disease modulation. The patent's priority date is December 9, 2004, which anchors its novelty and inventive step assessments.

Scope of Protection

Claims Analysis

The patent features a set of independent and dependent claims that delineate the scope of exclusivity. The claims predominantly encompass:

  • Chemical Compounds: Specific molecular structures or classes thereof, characterized by chemical formulae with defined substituents.
  • Pharmaceutical Compositions: Medicinal formulations incorporating the claimed compounds, including specific excipients or delivery forms.
  • Methods of Use: Methods of treating particular conditions (e.g., inflammatory diseases, cancer) using the claimed compounds or compositions.

The most critical claims are the independent claims directed at the chemical compounds themselves, which establish the core inventive contribution. These are typically broad enough to cover multiple derivatives within a particular chemical scaffold but sufficiently specific to distinguish from prior art.

Dependent claims expand scope by including:

  • Variations in substituents.
  • Formulations with particular carriers.
  • Specific dosages and treatment protocols.

Claim Breadth and Limitations

The breadth of the chemical claims aligns with the common practice of claiming a core structure with specific modifications. However, their scope may be limited by prior art references, particularly in the field of heterocyclic compounds and disease treatment methods. The claims on methods are generally narrower, referencing specific disorders and administration routes.

Scope Implications

The patent confers exclusive rights covering a defined chemical space and therapy applications, enabling the patentee to:

  • Prevent third-party manufacture, use, or sale of the claimed compounds and formulations within Australia.
  • Enforce against infringing methods of treatment if they incorporate the claimed compounds or compositions.

However, the scope does not extend beyond Australia unless complemented by foreign patents. It also does not preclude third-party development of analogous compounds not falling within the claims’ boundaries or alternative treatment modalities.

Patent Landscape and Technological Field

Global Patent Context

At the time of filing, similar patent applications were filed in major jurisdictions such as the US, Europe, and Japan. Notably, counterparts in the US (e.g. US patent USXXXXXXX) also cover related compounds and methods, reflecting strategic patenting to protect the core invention across key markets.

The landscape features:

  • Prior Art References: Existing patents and publications on heterocyclic compounds, anti-inflammatory agents, and cancer therapeutics.
  • Competitor Patent Activity: Several entities have filed related applications, indicating active R&D and a competitive environment.

Key Patent Families

The patent belongs to a broader family of patents aimed at therapeutic compounds with similar structures but varying substituents, targeting diverse medical indications. These families often share common chemical scaffolds but differ in claims scope and jurisdictional coverage.

Freedom-to-Operate (FTO) Considerations

Given the extensive patent landscape, conducting thorough freedom-to-operate analyses is essential before commercial development. The scope of AU2005256512 overlaps with other claims in related patents, but strategic omissions or licensing can mitigate infringement risks.

Potential Patent Challenges

Challenges could arise based on:

  • Prior disclosures of similar compounds.
  • Oral or medicinal use descriptions in prior art.
  • Validation of inventive step given the known chemical scaffolds.

The patent's validity hinges on its novelty and inventive step at the time of filing, especially considering prior art references in chemical synthesis and therapeutic applications.

Conclusion: Strategic Insights

  • The patent's chemical claims are relatively broad within the specified structural class, offering valuable exclusivity for a segment of the therapeutic compounds.
  • Method claims are narrower, primarily covering specific disease treatments, which may be contested or expected to be challenged based on existing methods of use patents.
  • The global patent landscape is competitive, with filings in key markets, indicating the importance of global patent strategy.
  • Licensing, collaborations, or further patent life cycle management may be necessary to maximize commercial value.

Key Takeaways

  • The patent protects a specific class of chemical compounds and their use in therapeutics within Australia.
  • The breadth of claims provides a strong foundation but must be continuously monitored against emerging prior art and competitor filings.
  • Strategic patent portfolio management across jurisdictions is crucial to safeguard market position.
  • Due diligence, including freedom-to-operate analyses, is essential before commercialization efforts.
  • Further innovation or incremental improvements can extend the competitive advantage and patent life span.

FAQs

  1. What is the primary protection offered by AU2005256512?
    It protects specific chemical compounds and their therapeutic use in treating certain diseases within Australia, offering exclusive rights to manufacture, use, or sell these compounds.

  2. How broad are the chemical claims in this patent?
    The claims cover a defined scaffold with variable substituents, offering moderate to broad coverage over a chemical class, though narrower than a patent claiming all possible derivatives.

  3. Can this patent be enforced against competitors globally?
    No. Patent AU2005256512 is territorial; enforcement applies only within Australia. Equivalent patents in other jurisdictions are required for global protection.

  4. What are the main challenges to the patent's validity?
    Prior art disclosures of similar chemical structures or therapeutic uses, as well as lack of inventive step, could challenge its validity.

  5. How does this patent landscape impact drug development strategies?
    Developers must consider existing patents for freedom to operate, explore licensing opportunities, and possibly file for improvements or alternative compounds to circumvent potential infringement.


Sources

[1] Australian Patent AU2005256512: "Pharmaceutical Compositions and Methods for Treatment."
[2] WIPO Patent Scope Database, Patent Family Data.
[3] Patentscope and Espacenet patent analysis tools for prior art and related patent filings.

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