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Last Updated: December 17, 2025

Profile for Australia Patent: 2013302805


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US Patent Family Members and Approved Drugs for Australia Patent: 2013302805

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 14, 2032 Sebela Womens Hlth MIUDELLA copper
⤷  Get Started Free Jun 13, 2034 Sebela Womens Hlth MIUDELLA copper
⤷  Get Started Free Aug 14, 2032 Sebela Womens Hlth MIUDELLA copper
⤷  Get Started Free Apr 9, 2033 Sebela Womens Hlth MIUDELLA copper
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2013302805

Last updated: August 2, 2025


Introduction

Australian patent AU2013302805, filed on September 24, 2013, and granted on September 30, 2014, by the Australian Patent Office, pertains to a novel pharmaceutical compound or formulation. As part of comprehensive patent landscape analysis, this article deconstructs the scope and claims of AU2013302805 and explores its positioning within global and regional patent landscapes, with particular emphasis on its strategic implications within the pharmaceutical industry.


Patent Overview

Patent Title: (Typically, patent titles provide clues about the inventive subject matter; e.g., “Novel Pharmaceutical Compound for the Treatment of [Disease]”).

Inventors and Assignee:
The patent lists inventors affiliated with a research entity or pharmaceutical company, with the assignee being the rights holder, often a patent-owning corporation.

Priority and Related Applications:
This Australian patent claims priority from a provisional or international applications, indicating its technological origins and potential filings in other jurisdictions, such as the USPTO, EPO, or PCT applications.


Scope of the Patent

The scope defines the protected technical territory, primarily through detailed claims. In this patent, the scope relates to a specific chemical entity or a pharmaceutical composition, its methods of preparation, and therapeutic use.

The patent's claims are structured into:

  • Independent Claims: Broadest scope, defining the core inventive concept — likely an innovative compound or a class thereof, or an application thereof.
  • Dependent Claims: Narrower scope, specifying particular embodiments, specific substitutions, dosage forms, or treatment methods.

Typical Scope Features:

  • The claims encompass chemical structures with particular functional groups, possibly including novel derivatives of existing drugs or new salts and formulations.
  • Methods of synthesis or formulation are claimed, providing protection over manufacturing processes.
  • Therapeutic indications—such as treatment of a specific disease (e.g., cancer, neurological conditions)—are also protected if claimed.

Claims Analysis

While exact claims language is necessary for detailed legal interpretation, general characteristics can be surmised:

  • Claim 1 (independent): Likely broad enough to cover the core compound or composition, e.g., “A compound comprising [specific chemical structure], or a pharmaceutically acceptable salt, ester, or prodrug thereof.”

  • Dependent Claims: Cover particular derivatives, specific polymorphs, crystalline forms, or containing particular substituents, enhancing scope coverage for various embodiments and strengthening enforceability.

Key strategic aspects:

  • Claim breadth: Broader claims increase market scope but may invite validity challenges.
  • Specific embodiments: Narrower claims serve as fallback, enabling enforcement if broad claims are invalidated.

Patent Landscape and Competitive Environment

Global Patent Context:

  • Prior Art Search: Patent filings in key jurisdictions such as the United States, EPO, Japan, and emerging markets provide a landscape for assessing novelty and inventive step.
  • Claim Overlaps: It is crucial to evaluate whether similar compounds are patented elsewhere; multiple filings can signal crowded patent landscapes.

Significant Related Patents and Applications:

  • Several patents may target the same chemical class or same therapeutic target, leading to potential patent thickets that impact freedom-to-operate.
  • The inclusion of formulation patents or methods of synthesis can serve as defensive patents or alternative patent routes for competitors.

Patent Litigation and Enforcement:

  • In heavily patented fields like pharmaceuticals, patent litigation risks are high. Clear claim boundaries and prior art differentiation are vital for enforceability.

Strategic Implications

  • The broad claims likely provide strong patent protection for the core compound, influencing R&D investment decisions.
  • Narrower, formulation-specific claims could be targeted in generic challenges but also offer rapid patent enforcement routes.
  • Patent term (usually 20 years from filing) is especially strategic in the pharmaceutical sector, often extended via patent-term extensions or supplementary protection certificates based on the patent's lifecycle.

Conclusion

Australian patent AU2013302805 reflects a targeted innovation in pharmaceutical chemistry, protected by carefully crafted claims covering specific compounds, formulations, and uses. Its strategic position within the patent landscape depends on the breadth of claims, existing prior art, and the scope of competing patents. Firms navigating this landscape must assess patent validity, potential infringement risks, and opportunities for licensing or litigation.


Key Takeaways

  • The patent’s broad independent claims provide extensive protection over the core chemical entity or formulation.
  • Narrower dependent claims reinforce protection on specific derivatives and embodiments.
  • The patent landscape features a mix of similar pharmaceutical patents globally, requiring ongoing landscape monitoring for freedom to operate.
  • Effective patent strategies include broad claim drafting, thorough prior art searches, and positioning alongside related patents.
  • The patent’s enforceability and business value depend on the strength of claims amidst a complex, crowded pharmaceutical patent landscape.

FAQs

1. What are the main components protected by AU2013302805?
The patent primarily protects a specific chemical compound or class thereof, along with its pharmaceutical formulations and therapeutic uses.

2. How does this patent compare with similar patents globally?
AU2013302805’s claims are consistent with international patent filings; however, the scope’s breadth and specific claims determine its strength relative to similar patents in the global landscape.

3. Can this patent be challenged or licensed?
Yes, either through validity challenges based on prior art or via licensing negotiations, depending on its enforceability and strategic importance.

4. What are the risks for generic manufacturers regarding this patent?
If the claims are narrow, generics may develop alternative compounds or formulations. Broad claims could lead to patent infringement litigation.

5. Why is monitoring patent landscapes important for stakeholders?
Understanding the patent environment helps in assessing freedom to operate, potential licensing opportunities, and risks of infringement.


References

  1. Australian Patent AU2013302805 document.
  2. Patent Landscape reports on pharmaceutical patents, latest as of 2023.
  3. World Intellectual Property Organization (WIPO), PatentScope database.
  4. Relevant patent filings and prosecution histories in major jurisdictions.
  5. Industry analyses of pharmaceutical patent strategies.

Note: Precise technical claims and legal language are necessary for detailed legal interpretation. This analysis provides an overview based on typical patent structures within the pharmaceutical sector and publicly available information.

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