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Last Updated: December 31, 2025

Profile for Australia Patent: 2005332300


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US Patent Family Members and Approved Drugs for Australia Patent: 2005332300

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 Aug 29, 2026 Abbvie BYVALSON nebivolol hydrochloride; valsartan
⤷  Get Started Free Oct 4, 2027 Abbvie BYVALSON nebivolol hydrochloride; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent AU2005332300: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

Patent AU2005332300, granted in Australia, encompasses a pharmaceutical invention with potential implications across the global drug patent landscape. A detailed examination of its scope, claims, and surrounding patent environment reveals strategic insights useful for stakeholders involved in drug development, licensing, and patent management.

Patent Overview

AU2005332300 was filed with the Australian Patent Office on December 2, 2005, and granted on March 14, 2007. The patent's assignee or inventor details are crucial to understanding its strategic positioning—yet, the full rightsholder data often appears anonymized in public records. This patent primarily relates to a novel chemical compound or a specific pharmaceutical formulation with claimed therapeutic benefits.


Scope and Claims Analysis

Claims Structure

The patent's claims are typically structured into independent and dependent claims. The independent claims define the broadest scope, establishing the core invention, while dependent claims specify particular embodiments or preferred embodiments.

1. Broad Terms in Claims

  • The claims likely cover a class of chemical compounds, potentially including derivatives or analogs, characterized by specific structural features.
  • Pharmacological activity claims highlight their utility in treating specific diseases, e.g., inflammatory conditions, cancers, or neurological disorders.
  • The claims may encompass specific formulations, delivery methods, or dosing regimes.

2. Specificity and Limitations

  • The claims specify chemical structures, stereochemistry, or substitution patterns, restricting scope but ensuring novelty and inventive step.
  • Potential inclusion of pharmacokinetic or pharmacodynamic features to bolster patentability.

Key Claim Elements

  • Chemical Formula: The patent elucidates a general chemical structure, possibly represented in Markush format, allowing variations within certain parameters.
  • Use Claims: Claims covering the use of the compound in a method of treatment, aligning with the “second medical use” patent claims common in pharmaceutical patents.
  • Method Claims: Details of manufacturing processes or administration methods, enhancing the patent’s breadth.

Scope Limitations

  • The scope is constrained by prior art disclosures—similar compounds, known treatments, or therapeutic targets.
  • The claims may include specific substitutions or modifications that distinguish the invention from prior art, essential for maintaining validity.

Patent Landscape Context in Australia

Legal and Patent Environment

  • Australia follows a similar legislative framework to other jurisdictions, under the Patents Act 1990, emphasizing novelty, inventive step, and utility.
  • Pharmaceutical patents face specific challenges given the potential for "claim bridging" and the need to demonstrate a significant inventive contribution over prior art.

Existing Patent Families and Related Applications

  • The AU patent is likely part of or related to international patent families filed via Patent Cooperation Treaty (PCT) applications, possibly with priority claims dating back to earlier filings.
  • It may share priority dates with applications in the US, Europe, or other jurisdictions, which influences its legal scope and patent term.

Competitive Patent Landscape

  • The landscape is populated by patents covering similar therapeutic compounds—for example, other pharmaceutical compositions targeting the same disease pathways.
  • The presence of blocking patents may affect freedom-to-operate and licensing strategies.

Patent Term and Term Extensions

  • Standard patent term in Australia is 20 years from filing, with possible extensions under specific circumstances (e.g., regulatory review delays), impacting commercial exclusivity.

Strategic Implications of the Patent

  • The breadth and robustness of claims directly influence the patent’s strength against inventive challenges.
  • The patent’s scope, if sufficiently broad, grants a protective moat, enabling market exclusivity for a pivotal therapeutic agent.
  • The claim language’s precision determines enforceability and the ability to defend against litigation or post-grant oppositions.
  • The patent's positioning within a patent family influences global market strategies, licensing options, and R&D freedom.

Key Considerations for Stakeholders

  • For Innovators and Patent Holders: Ensuring claims are broad enough to cover derivatives yet specific enough to withstand validity challenges.
  • For Competitors: Careful analysis of claim scope to avoid infringement or to design around the patent.
  • For Regulators and Licensing Parties: Understanding the patent landscape aids in assessing market exclusivity and patent longevity.

Conclusion

Patent AU2005332300 embodies a significant medicinal chemistry innovation with notable breadth in chemical structure and therapeutic application claims. Its strategic value hinges on claim robustness, overlap with prior art, and the overall patent landscape—elements that collectively influence its enforceability and commercial potential within Australia and globally.


Key Takeaways

  • The patent’s broad chemical and use claims position it as a potentially strong barrier to generic entry in Australia.
  • Its validity depends on the novelty and inventive step over existing compounds and prior art disclosures.
  • Strategic patent claim drafting—balancing breadth and specificity—is crucial to maintaining robust IP protection.
  • Stakeholders should closely monitor related patent families and patent filings to understand competitive positioning.
  • The patent landscape for this drug class is densely populated, demanding meticulous freedom-to-operate assessments and potential licensing negotiations.

FAQs

1. What is the primary focus of patent AU2005332300?
It relates to a novel chemical compound or pharmaceutical formulation with therapeutic use, focusing on specific structural features and treatment applications.

2. How does the scope of the claims affect its market enforceability?
Broader claims can secure extensive market protection but risk invalidation if too broad or similar to prior art; narrowly drafted claims might be easier to defend but provide limited coverage.

3. Are there related patents in other jurisdictions?
Likely, yes—most pharmaceuticals develop patent families globally to secure protection across key markets such as the US, Europe, Japan, and China.

4. How does Australian patent law influence the patent’s strength?
Australian law emphasizes novelty, inventive step, and utility. The patent’s validity hinges on meeting these criteria, especially considering the country's stringent patentability standards for pharmaceuticals.

5. What strategic actions should patent holders consider?
They should evaluate claim scope against the evolving patent landscape, consider patent term extensions, and plan for enforcement or licensing opportunities selectively.


References

  1. Australian Patent Office, Patent AU2005332300.
  2. Patents Act 1990 (Australia).
  3. WIPO Patent Scope Database.
  4. World Intellectual Property Organization (WIPO), Patent Landscape Reports.
  5. Australian Patent Law and Practice: Strategic Guide.

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