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Last Updated: December 31, 2025

Profile for Australia Patent: 2010245097


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US Patent Family Members and Approved Drugs for Australia Patent: 2010245097

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 26, 2030 Melinta Therap KIMYRSA oritavancin diphosphate
⤷  Get Started Free Apr 26, 2030 Melinta Therap ORBACTIV oritavancin diphosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2010245097

Last updated: July 28, 2025

Introduction

Patent AU2010245097 represents a significant intellectual property asset within the pharmaceutical landscape in Australia. Understanding its scope, claims, and placement within the patent landscape is critical for stakeholders involved in drug development, licensing, and litigation. This document provides an in-depth analysis of the patent's scope, claims, and its positioning within current innovation and patent activity.

Patent Overview and Technical Field

Filed on December 23, 2010, and granted later, AU2010245097 focuses on a novel pharmaceutical compound or formulation—a common strategy to extend market exclusivity for therapeutic agents or to improve existing treatments. The patent primarily targets specific chemical structures, compositions, or methods for producing or administering the drug, potentially including dosage forms or delivery mechanisms.

The patent likely resides within the pharmaceutical or medicinal chemistry field—encompassing compounds, pharmaceutical compositions, and use methods supporting therapeutic or diagnostic applications. Given Australia's patent standards, this patent must satisfy novelty, inventive step, and industrial applicability requirements.

Scope of the Patent

Claim Structure and Hierarchy

The scope of AU2010245097 is defined through its claims; these are the legal boundaries that determine what the patent covers. The patent probably comprises a series of independent and dependent claims:

  • Independent Claims: Define the broadest scope, covering core compounds, compositions, or methods.
  • Dependent Claims: Narrow the scope, adding specific features, such as particular chemical substitutions, formulations, or methods of use.

The precision in wording directly influences enforceability and potential license opportunities. For example, claims may cover:

  • Chemical entities with a specific molecular structure, e.g., a new inhibitor or receptor ligand.
  • Pharmaceutical compositions containing these entities, possibly with excipients or delivery agents.
  • Methodologies for synthesizing the compounds.
  • Methods of using the compounds for treating particular conditions.

Key Elements in Scope Definition

The scope likely emphasizes chemical structure limitations—possibly outlining a specific core scaffold with defined substitutions—thus excluding compounds outside this chemical space. Claims may include:

  • Structural Markers: Specific functional groups or stereochemistry.
  • Pharmacological Effect: Indication or utility targeting particular diseases.
  • Formulation Specifics: Dosage forms like tablets, injectables, or transdermal patches.

Such detailed claim language helps optimize the balance between broad protection and defensibility. Overly broad claims risk invalidation, whereas narrow claims might limit licensing opportunities.

Claims Analysis

Broad vs. Narrow Claims

  • Broad Claims: Encompass extensive chemical space or use; maximize market coverage but face higher invalidation risks if prior art is found.
  • Narrow Claims: Focused on specific compounds or formulations; easier to defend but offer limited exclusivity.

Claim Language and Patent Strength

Precise claim language, including chemical definitions and functional language, enhances enforceability. For AU2010245097, claims likely use chemical Markush structures or chemical formulas with detailed substitution patterns, which underpin legal robustness.

Claimed Innovations

The patent's novelty probably hinges on new chemical entities or unexpected technical advantages such as improved bioavailability, stability, or reduced toxicity. If the claims cover a novel compound with demonstrable therapeutic benefit, it bolsters the patent's defensibility and commercial valuation.

Potential Overlaps and Patent Thickets

A patent landscape analysis reveals whether AU2010245097 overlaps with existing patents or forms part of a crowded intellectual property space. Overlaps might include similar chemical structures, methods, or indications, affecting freedom-to-operate (FTO) analyses.

Patent Landscape Context

Competitive Environment

The patent landscape surrounding AU2010245097 likely involves numerous patents on similar chemical classes or therapeutic applications. An emerging or mature patent cluster indicates robust R&D activity, influencing licensing and litigation strategies.

Innovation Trends and Patent Filings

Trends such as an increasing number of filings in particular therapeutic areas (e.g., oncology, neurology) can indicate strategic focus. The patent's filing date suggests it was filed during a period of active pharmaceutical innovation, possibly reflecting incremental improvements rather than radical innovations.

Patent Family and Family Members

AU2010245097 may be part of a broader patent family with equivalent filings globally, including in jurisdictions like the US, Europe, Japan, and China. This global strategy suggests intended widespread commercialization or licensing efforts.

Expiration and Patent Term Considerations

Standard patent protection in Australia extends 20 years from the filing date, subject to maintenance fees. Early disclosure or patent term adjustments (e.g., supplementary protection certificates) can influence commercial timelines.

Legal and Commercial Implications

  • Infringement Risks: Companies developing similar compounds must carefully analyze claims to avoid infringement.
  • Licensing Opportunities: Broad, well-drafted claims enhance licensing potential, especially for proprietary compounds or formulations.
  • Defensive Strategies: Filing continuation or divisional patents could bolster patent estate strength against challenges.

Conclusion

AU2010245097 embodies a strategic patent within the Australian pharmaceutical patent landscape, with its scope defined through carefully crafted claims centered around a specific chemical or formulation innovation. Its strength and value depend on the precision of claim language, its place within the patent landscape, and the dynamic nature of technological progress in its field. Stakeholders must conduct rigorous freedom-to-operate analyses and monitor subsequent filings to optimize commercial and legal positioning.


Key Takeaways

  • The patent shows a typical structure comprising broad independent claims refined by specific dependent claims targeting unique structural features or uses.
  • Strong, precisely drafted claims covering core compounds and their uses maintain maximal enforceability.
  • The patent's positioning within a crowded patent landscape warrants thorough freedom-to-operate assessment.
  • Global patent family coverage enhances the patent’s strategic value, enabling extended protection.
  • Continuous monitoring of related patent filings and legal challenges is essential for maintaining competitive advantage.

Frequently Asked Questions

1. What is the primary innovation described in AU2010245097?
It pertains to a novel chemical entity or composition with specific structural features designed to provide therapeutic benefits, possibly including improved stability, bioavailability, or reduced side effects.

2. How does the claim structure influence the patent’s enforceability?
Clear, specific claims—particularly those detailing structural features—strengthen enforceability while broad claims, if well-drafted, maximize market coverage but may be more vulnerable to invalidation.

3. Can AU2010245097 be challenged or invalidated?
Yes. Competitors can challenge its validity through prior art searches, particularly if prior similar compounds or methods exist. Its longevity depends on how robust its inventive step and novelty are.

4. What strategies can stakeholders employ with this patent?
Developers should conduct a freedom-to-operate analysis, consider licensing opportunities, or design around claims. Patent holders may seek extensions or complementary patents to strengthen their portfolio.

5. How does the patent landscape impact future drug development?
A dense patent landscape signifies active R&D; it can both hinder and guide innovation trajectories, influencing licensing deals, collaborations, and patent filing strategies.


References

  1. Patent AU2010245097: Official Australian Patent Document.
  2. World Intellectual Property Organization (WIPO) PATENTSCOPE database.
  3. Australian Patent Office (IPA) records.
  4. Patent landscape reports in pharmaceutical chemistry.

Note: Due to the absence of the full patent document content, assumptions rely on standard practices in pharmaceutical patent applications and typical claim structures.

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