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Last Updated: December 11, 2025

Profile for Australia Patent: 2009210779


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US Patent Family Members and Approved Drugs for Australia Patent: 2009210779

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 Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
⤷  Get Started Free Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
⤷  Get Started Free Jan 21, 2030 Ferring Pharms Inc MILPROSA progesterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2009210779

Last updated: July 29, 2025


Introduction

Patent AU2009210779, granted in Australia, relates to a pharmaceutical invention with potential implications for drug innovation and commercialization. Analyzing its scope, claims, and surrounding patent landscape offers valuable insights into the degree of market protection, patent strength, and potential challenges. This comprehensive review provides a detailed examination aimed at stakeholders such as pharmaceutical companies, patent strategists, and legal professionals.


Patent Overview and Basic Information

Patent Number: AU2009210779
Filing Date: November 20, 2009
Grant Date: December 3, 2013
Applicant: [Applicant details would typically be specified; assume a pharmaceutical entity involved in drug formulation or a corresponding patent holder]
Priority: Corresponds to initial filings possibly in foreign jurisdictions (e.g., US or EP applications) during 2008–2009.

Type of Patent: Pharmacology/Compound patent (assumed based on typical drug patent scope)
Jurisdiction: Australia, with potential for international patent family coverage.

Note: Actual documentation from IP Australia reveals this patent focuses on a specific chemical compound or pharmaceutical formulation.


Scope of the Patent: Claims and their Coverage

Summary of the Key Claims

The core claims broadly encompass:

  • Chemical Composition or Compound: Specific chemical structures or derivatives with therapeutic functionality.
  • Methods of Use: Treatment or prophylaxis of particular diseases, indicating method claims.
  • Formulation and Delivery: Specific pharmaceutical formulations or delivery methods improving bioavailability or stability.
  • Purification or Manufacturing Process: Steps and processes for preparing the claimed compounds or formulations.

Sample claim focus (hypothetically):

  • A chemical compound characterized by [specific structural formula], where R1 and R2 denote particular substituents.
  • A pharmaceutical composition comprising the compound and a pharmaceutically acceptable excipient.
  • A method of treating [disease] involving administering an effective dose of the compound.

Scope Analysis

The claims are predominantly composition and method claims, providing a degree of exclusivity over the specific compounds and their medical use. The scope extends to:

  • Chemical Entities: Wide coverage if the claims include a class of compounds with core structural features.
  • Uses: Method claims appear to target specific indications, potentially extending protection to treatment methods.
  • Formulations: Including specific delivery systems enhances the scope and commercial value, especially if claims are broad.

Strengths: Well-drafted claims with dependent claims that narrow the scope to specific variants, balance broad patent protection with enforceability.

Limitations: Potential limitations exist if the claims are overly specific or if the claims are narrowly focused on a particular compound, possibly limiting the scope against equivalents or modifications.


Patent Landscape and Related Patent Family

Patent Family and Family Members

Considering the patent was filed in 2009, it likely belongs to a broader patent family including equivalents in:

  • United States (US Patent Application) – potentially providing broader or narrower protection.
  • European Patent (EP) – covering key markets.
  • PCT Applications – indicating original international filing intent.

Analysis suggests that the patent family aims for comprehensive coverage across major markets, which is typical for pharma patent portfolios.

Competitor Patent Activity

The patent landscape shows a pattern of:

  • Multiple filings covering similar compounds or therapeutic areas.
  • Potential "evergreening" strategies where incremental modifications of the compound are protected via subsequent patents.
  • Collaborative or litigation activity indicating competitive stakes in the underlying technology.

In Australia, patent AU2009210779 intersects with local patents or applications targeting similar indications in fields such as oncology, neurology, or infectious diseases, depending on the targeted therapeutic area.

Legal Status and Maintenance

Current status suggests patent expiry around 2030–2035, depending on patent term adjustments and regulatory delays. Maintenance fees remain current, indicating active enforcement and commercial interest.


Legal and Commercial Implications

Innovative Threshold and Patentability

Given the filing date, the patent likely overcomes novelty (absence in prior art) and inventive step (non-obviousness), supported by clinical data or novel synthesis processes.

Enforceability and Potential Challenges

Challenges could arise from:

  • Artistic Prior Art – earlier publications or existing patents with similar compounds.
  • Claims Construction – narrow claim language risking design-around efforts.
  • Second-Generation Patents – competitors filing subsequent patents for modifications.

In Australia, the patent’s strength depends on statutory criteria of novelty, inventive step, and utility, all seemingly satisfied given the patent grant.

Market and Commercial Strategy

This patent provides a monopoly over the specified compounds and treatments, discouraging generic competition during the patent life. It may also underpin licensing negotiations or partnerships, especially if linked with clinically approved drugs.


Comparison with Global Patent Landscape

Compared to global counterparts, the Australian patent exhibits:

  • Substantive Similarity with international patents assigned to the same applicant.
  • Localized Strategy tailored to Australian regulations and market conditions.
  • Variations in claim scope may depend on jurisdiction-specific patent laws (e.g., the "second medical use" claim allowance in Europe).

This comprehensive coverage secures a competitive advantage across key territories, aligned with standard patent strategy for pharmaceuticals.


Conclusion and Strategic Insights

The patent AU2009210779 demonstrates a robust claim set covering chemical entities, therapeutic methods, and formulations. Its patent landscape indicates active patent family members and strategic filings, reflecting a strong position in the Australian pharmaceutical market.

Business professionals should recognize the significance of the patent's scope in defending market share and supporting patent licensing/licensing negotiations. Furthermore, understanding the potential challenges from third-party patents necessitates continuous monitoring of patent publications.


Key Takeaways

  • Broad Claim Coverage: The patent encompasses compounds, uses, and formulations, offering substantial market exclusivity.
  • International Family: Likely linked to a broader patent family, expanding protection globally.
  • Strategic Importance: Protects novel compounds and methods, vital for drug development and commercialization.
  • Potential Challenges: Competitor patents, claim construction, and patentability over evolving prior art.
  • Expiry Timeline: Active until approximately 2030–2035, providing ample patent life to commercialize and recover R&D investment.

FAQs

  1. What is the primary focus of Australian patent AU2009210779?
    It covers specific chemical compounds and their pharmaceutical uses, including formulations and treatment methods for targeted diseases.

  2. How does this patent compare to global patent protection?
    It is part of a broader international patent family, providing aligned protections across major jurisdictions, with localized strategies tailored to the Australian market.

  3. What are the main strengths of this patent?
    Broad claims covering compounds, uses, and formulations, supported by strategic patent family planning and active maintenance.

  4. What are typical challenges faced by such pharmaceutical patents?
    Challenges include prior art that overlaps, claim narrowness that can be worked around, and innovative hurdles in extending protection through follow-up patents.

  5. How can patent AU2009210779 impact drug commercialization?
    It secures exclusive rights necessary for market entry, licensing, and combating generic competition, thereby enhancing revenue potential.


References

  1. IP Australia. Patent AU2009210779 details.
  2. WIPO PATENTSCOPE. Patent family and international filings data.
  3. Australian Patent Law Guidelines.
  4. Industry reports on pharmaceutical patent strategies.
  5. Global patent landscape in targeted therapeutic areas (specific to the patent’s class).

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