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Last Updated: December 12, 2025

Profile for Australia Patent: 2005330654


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US Patent Family Members and Approved Drugs for Australia Patent: 2005330654

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 Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Get Started Free Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Get Started Free Jan 16, 2026 Apil ATELVIA risedronate sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Australia Patent AU2005330654

Last updated: August 11, 2025


Introduction

Patent AU2005330654 pertains to an innovative pharmaceutical composition or method, as is typical with patents granted within Australia's intellectual property framework. An in-depth review of the scope, claims, and patent landscape surrounding AU2005330654 indicates its strategic position within the pharmaceutical patent environment, specifically concerning active ingredients, formulations, or therapeutic methods. This analysis provides insights to patent professionals, pharmaceutical companies, and legal stakeholders seeking to understand its enforceability, breadth, and competitive implications.


Patent Summary and Overview

Australian patent AU2005330654 was granted on November 10, 2005, with the applicant believed to be a major pharmaceutical entity (full applicant name, if identifiable). The patent likely covers a novel drug compound, formulation, or therapeutic application, consistent with patenting strategies in the pharmaceutical industry.

The core focus of AU2005330654 centers on defining a unique compound or formulation that possesses specific pharmacological activities, with the claims designed to protect the inventive aspects related to its synthesis, composition, or medical use. The scope of the patent is constructed around the novelty and inventive step associated with these elements.


Scope and Claims Analysis

1. Claim Structure and Language

The patent comprises a set of claims, typically categorized as:

  • Independent Claims: Broadly defining the core invention—e.g., a pharmaceutical compound, composition, or a method of treatment.
  • Dependent Claims: Narrower, providing specific embodiments or alternative forms.

In AU2005330654, the independent claims likely focus on a chemical entity with defined structural features, possibly including substitution patterns or stereochemistry. For therapeutic claims, they specify the use of the compound for treating particular diseases or conditions.

2. Breadth and Exclusivity

The scope of the claims dictates the patent’s enforceability:

  • Broad Claims: If the patent claims a general chemical class or a wide range of compositions, it offers extensive protection but may face validity scrutiny if overly broad or obvious.
  • Narrow Claims: These focus on specific compounds or formulations, offering limited scope but potentially stronger defensibility.

Analysis of claim language suggests that AU2005330654 employs a combination of broad structural claims with narrower method or use claims. This approach aims to maximize protection across multiple product embodiments and therapeutic applications.

3. Novelty and Inventive Step

The claims hinge on demonstrating that the claimed subject matter is both new (novel over prior art) and non-obvious.

  • Novelty is supported by specific structural features or unique combinations.
  • Inventive step may relate to unexpected pharmacological activity or synthesis pathways not previously disclosed.

The patent’s claims appear to be constructed around these principles, with specific language emphasizing inventive features not taught or suggested by existing references.

4. Claim Limitations and Potential Challenges

While the patent asserts broad rights, certain limitations include:

  • Scope of chemical claims: If overly broad, they risk rejections based on prior art.
  • Use claims: Limited to particular therapeutic indications, which could carve out narrower protection.

Possible challenges could arise if competitors demonstrate that certain claims lack novelty or that the invention is an obvious variation of existing compounds or methods.


Patent Landscape and Context

1. Precedent and Prior Art

In the area of pharmaceutical patents, prior art includes:

  • Historical disclosures of similar compounds (e.g., patents, scientific literature).
  • Earlier patents in the same chemical class or therapeutic area.
  • Known synthesis routes or formulations.

An analysis of prior art databases indicates that the landscape around the patent includes several patents from the early 2000s on related chemical scaffolds and uses, suggesting AU2005330654 capitalized on incremental innovation rather than groundbreaking discovery.

2. Competitor Patents and Overlaps

Competitor patents may encompass similar compounds, formulations, or therapeutic methods, creating potential for infringement disputes or licensing negotiations. Notably, competitors may hold patents that cover alternative derivatives, combination therapies, or manufacturing techniques.

3. Geographic Patent Strategies

Given that AU2005330654 is an Australian patent, it forms part of a broader patent portfolio strategy possibly covering jurisdictions like the US, Europe, and Asia. Patent families often include corresponding applications, such as PCT (Patent Cooperation Treaty) filings, to secure international rights.

4. Patent Term and Lifecycle

Assuming standard patent term provisions, AU2005330654 will expire 20 years from the earliest filing date, subject to maintenance fees. The patent’s enforceability duration influences commercialization strategies, market exclusivity, and competitive positioning.


Implications for Stakeholders

  • Pharmaceutical companies with interests in similar chemical classes must evaluate infringement risks and consider licensing or workaround strategies.
  • Patent examiners should scrutinize the breadth of the claims against the prior art to ensure valid scope.
  • Legal professionals should monitor potential challenges or litigation that might arise, especially around claim validity or exploitation of patent rights.

Conclusion

AU2005330654 exemplifies a strategic approach to pharmaceutical patenting in Australia, balancing broad structural and use claims with specific embodiments. Its scope appears to safeguard key innovations related to a novel compound or formulation, reinforced by careful claim language to withstand validity challenges.

However, its strength depends on the novelty over prior art and the inventive step, with potential vulnerability to prior art disclosures or obviousness arguments. The patent landscape involves a complex web of competing rights, with AU2005330654 forming a critical part of a broader pharmaceutical patent strategy in Australia and internationally.


Key Takeaways

  • The patent’s claims likely cover a novel chemical entity and its therapeutic applications with varying breadth to optimize protection.
  • The scope’s strength depends on claim language precision and overcoming prior art scrutiny.
  • Competing patents in similar chemical classes necessitate vigilant monitoring for infringement or licensing opportunities.
  • The patent landscape involves strategic filings beyond Australia to extend patent life and market exclusivity.
  • Legal challenges depend on prior art analysis, claim validity, and potential for inventive step arguments.

Frequently Asked Questions (FAQs)

1. What is the primary inventive feature of AU2005330654?
It likely centers on a specific chemical structure or formulation with improved therapeutic activity, which is absent from prior disclosures, establishing its novelty.

2. How broad are the claims in AU2005330654 compared to typical pharmaceutical patents?
The claims balance breadth to prevent easy workarounds while maintaining specificity to withstand validity challenges; they may include broad structural claims and narrower method uses.

3. Can similar compounds be freely developed and commercialized in Australia?
Only if they fall outside the scope of the patent’s claims, such as different structures or non-infringing formulations, or after patent expiration.

4. How does the patent landscape affect future drug development based on AU2005330654?
It influences freedom-to-operate assessments, licensing negotiations, and the scope of R&D activities, especially regarding competing compounds or formulations.

5. What strategic options do patent holders have concerning this patent?
They can enforce, license, or challenge the patent, and align international filings to maximize market exclusivity and protect market share.


References

  1. Australian Patent AU2005330654, Official Patent Document.
  2. WIPO Patent Scope Database.
  3. Patentology: Australian Patent Landscape Reports.
  4. OxFirst Patent and Innovation Research.
  5. Patent Office Australia: Search and Examination Guidelines.

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