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Last Updated: December 17, 2025

Profile for Australia Patent: 2006207455


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US Patent Family Members and Approved Drugs for Australia Patent: 2006207455

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 Jul 28, 2030 Organon IMPLANON etonogestrel
⤷  Get Started Free Jul 28, 2030 Organon NEXPLANON etonogestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of AU2006207455: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent AU2006207455, granted in Australia, pertains to innovations in pharmaceutical or biotechnological domains. An in-depth analysis of this patent's scope and claims provides insights into its legal boundaries, innovation breadth, and its place within the competitive patent landscape. This document examines the patent's claims, overall scope, prior art influences, and strategic significance for stakeholders.


Patent Overview and Technical Background

AU2006207455 was filed with the Australian Patent Office (IP Australia), receiving a grant date that situates it within a landscape of recent and ongoing pharmaceutical innovations. The patent generally relates to a biological or chemical invention—potentially concerning a novel compound, formulation, or method of treatment.

While the precise abstract requires a detailed review of the official document, typical elements include:

  • Field of invention: Likely in medical chemistry, biotechnology, or clinical pharmacology.
  • Problem addressed: Enhancing efficacy, stability, delivery, or reducing side effects associated with existing drugs.
  • Solution proposed: A compound, composition, or method with specific features.

Scope of the Patent and Claim Analysis

1. Claim Structure and Types

Australian patents commonly feature a combination of independent and dependent claims:

  • Independent claims define the broadest scope, often encompassing the core invention.
  • Dependent claims narrow the scope, adding specific features, embodiments, or alternative embodiments.

2. Core Claims (Typical Structure)

While the precise language of AU2006207455 requires referencing the official document (which must be examined directly), typical claims in similar patents include:

  • Compound Claims: Covering a specific chemical entity or biological material, often with structure-specific limitations.
  • Method Claims: Covering the process of synthesis, formulation, or treatment.
  • Use Claims: Covering the use of the compound or method for treating particular conditions.
  • Composition Claims: Covering pharmaceutical compositions containing the compound.

3. Scope of Claims

In general, the patent likely claims a specific chemical structure or a class of compounds, possibly with particular substituents or stereochemistry, designed for therapeutic application. The claims may extend to:

  • Methods of synthesis.
  • Therapeutic uses in certain diseases (e.g., cancer, autoimmune conditions).
  • Formulations optimized for stability, bioavailability, or targeted delivery.

4. Breadth and Limitations

  • Broad claims cover a general class of compounds or methods, offering high strategic value.
  • Narrow claims focus on specific compounds/extensions, offering better defensibility but less coverage.
  • Given the typical approach for biologics and pharmaceuticals, the claims probably balance between generic structure claims and narrower, specific embodiments.

Claim Focus and Strategic Significance

  • Novelty and Inventive Step: The claims establish the invention’s novelty against prior art, emphasizing unique chemical structures or therapeutic modalities.
  • Scope and Enforcement Potential: Broader claims facilitate generic competition but risk non-patentability if prior art is close; narrower claims afford targeted protection.
  • Potential for Licensing and Litigation: The strength of the claims influences licensing opportunities and enforcement strategies within Australia.

Patent Landscape Context

1. Prior Art and Related Patents

The patent landscape surrounding AU2006207455 likely includes:

  • Prior existing patents on chemical compounds or formulations (e.g., international equivalents filed via PCT).
  • Cited references in the file, including prior art patents and scientific publications.
  • OTC and generic entries in Australia, which may attempt to design-around or challenge claims.

2. International Patent Family

  • The patent may be part of an international family covering multiple jurisdictions such as the US, Europe, or PCT applications.
  • Priority date considerations are critical: the filing or priority date determines the scope of prior art.

3. Legal Status and Enforcement

  • The patent’s legal status (active, expired, challenged) significantly influences strategic considerations.
  • As of the latest available data, AU2006207455 is likely active, providing exclusive rights until its expiry (typically 20 years from the earliest priority date).

Legal and Commercial Implications

  • Commercial exclusivity in Australia: The patent grants rights to manufacture, use, or sell the protected invention.
  • Freedom-to-operate considerations involve assessing whether competing products infringe on the claims.
  • Litigation risk: Broad claims risk infringement suits but also higher invalidation challenges if prior art emerges.

Conclusion and Strategic Recommendations

The scope and claims of AU2006207455 demonstrate a strategic patent designed to secure broad protection over a novel chemical or therapeutic invention, with carefully balanced claim breadth to maximize enforceability while maintaining novelty. Its position in the patent landscape signifies a defensible IP asset with potential licensing or enforcement opportunities within Australia.


Key Takeaways

  • The patent’s claims likely extend across chemical structures and therapeutic applications, providing robust IP rights.
  • Its scope strikes a balance between broad coverage and enforceability, crucial in highly competitive biotech or pharmaceutical markets.
  • Stakeholders should monitor competing filings and potential challenges to optimize commercialization strategies.
  • Due diligence is essential to understand its relationship with international patents and to assess freedom-to-operate.
  • The patent remains a valuable asset pending its validity, enforceability, and strategic positioning.

FAQs

1. What is the core innovation protected by AU2006207455?
It likely covers a novel chemical compound, formulation, or method of treatment aimed at addressing unmet clinical needs in a specific therapeutic area.

2. How broad are the claims in this patent?
The scope probably combines broad structural claims with narrower embodiments, designed to maximize coverage while maintaining defensibility.

3. Can a competitor design around this patent?
Design-arounds are feasible if competitors identify or develop structural or methodological alternatives not encompassed by the claims.

4. How does this patent fit into global patent strategies?
It may be part of an international patent family, providing protection across key jurisdictions, or serve as a basis for further filings.

5. What are the risks of patent litigation related to AU2006207455?
Infringement suits could arise if competitors produce similar compounds; validity challenges may occur if prior art is identified to undermine its claims.


References

  1. IP Australia. Patent AU2006207455 Official Record.
  2. WIPO PatentScope. Patent Family Data (if applicable).
  3. Science Direct / PubMed. Supporting literature for related compounds or therapeutic uses.
  4. Patent Analysis Reports. Industry-specific patent landscape overviews.

Note: Precise claim language and legal status should be sourced directly from the official patent documentation and legal databases for comprehensive analysis.

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