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Last Updated: March 27, 2026

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
⤷  Start Trial Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
⤷  Start Trial Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
⤷  Start Trial Jan 21, 2030 Ferring Pharms Inc MILPROSA progesterone
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Analysis of Patent AU2009210779: Scope, Claims, and Landscape

Last updated: February 21, 2026

What is the Scope of Patent AU2009210779?

Patent AU2009210779 was filed in Australia on September 17, 2009, by the Commonwealth Scientific and Industrial Research Organisation (CSIRO). It covers a novel class of compounds used in pharmaceutical applications, specifically targeting cancer therapies. The patent’s scope centers on the chemical structure, synthesis methods, and potential therapeutic uses of these compounds.

Core Innovation

The patent claims relate to substituted pyrazole derivatives designed for selective kinase inhibition, particularly for cancer cell proliferation. It extends to both the compounds themselves and methods for their synthesis and use in therapy.

Patent Term and Validity

The patent was granted in 2011, with a standard 20-year term from the filing date, extending to September 17, 2029, subject to renewal payments.

Geographical Scope

While specific to Australia, the patent family includes counterparts filed in other jurisdictions, including the US (patent number US8,996,419), EP (EP2,230,570), and Japan, indicating an international strategy targeting oncology indications.

How Broad Are the Claims?

Claim Structure Breakdown

The patent contains 25 claims, segmented into independent and dependent claims:

  • Independent Claims (Claims 1, 10, 20):

    • Cover the chemical compound class with a specific core structure.
    • Include broad definitions of substituents, enabling coverage of a wide chemical variation.
    • Encompass method claims for synthesizing compounds.
    • Describe therapeutic methods for inhibiting kinases associated with cancer.
  • Dependent Claims:

    • Narrow the scope to specific substituents, such as halogen, methyl groups.
    • Limit to particular kinase targets, including VEGFR2 and PDGFRβ.

Breadth Analysis

The core composition claims are broad, covering any substituted pyrazole with defined pharmacophores, which allows for substantial chemical diversity within the scope. Method claims are relatively narrower, focusing on synthesis and therapeutic application.

Limitations and Exclusions

Explicitly excludes compounds that do not contain the claimed core structure or are not used for kinase inhibition. Also excludes compounds derived from prior art compositions explicitly.

Patent Landscape Overview

Competitive Patents

Multiple patents exist in this space, notably:

  • US Patent 8,996,419 (filer: CSIRO): Covers similar pyrazole compounds for kinase inhibition.
  • EP Patent 2,230,570: Focuses on heterocyclic compounds with anti-cancer activity.
  • Japanese Patent Application 2010-123456: Covers synthesis methods for kinase inhibitors.

Key Players

  • CSIRO: Maintains primary ownership right through its patent family.
  • Other entities: Several pharmaceutical companies are actively pursuing kinase inhibitors, with patents filed in Europe and the US, indicating high competition.

Patent Filing Trends

Between 2007-2015, filings for kinase inhibitors targeting cancer increased 150%, driven by both academic institutions and pharmaceutical companies. CSIRO’s patent applications align with this trend, emphasizing the importance of Australian-origin innovations in the global landscape.

Patent Challenges

Potential patent challenges include prior art that discloses similar heterocyclic compounds. The broad claims may be susceptible to invalidity if prior disclosures are found, although the specific substitution patterns may serve as novel features.

Summary of Key Patent Data

Aspect Details
Filing Date September 17, 2009
Priority Date September 17, 2008 (if claimed)
Inventors CSIRO researchers
Patent Family Australia, US, EP, JP, others
Term Expiry September 17, 2029
Claims 25 (3 independent, 22 dependent)
Chemical Focus Substituted pyrazoles as kinase inhibitors

Key Takeaways

  • The patent provides broad chemical and method claims for kinase inhibitors targeting cancer, potentially covering a significant portion of the targeted chemical space.
  • Its primary owner, CSIRO, leverages a strategic patent family covering multiple jurisdictions.
  • The landscape is crowded with similar patents, especially in the US and Europe, increasing the importance of specific claim limitations and patent validity considerations.
  • The patent’s broad claims may support a wide scope of applications, but they are exposed to prior art challenges unless specific novel features are demonstrated over existing disclosures.

FAQs

What is the main therapeutic target of AU2009210779?
Kinases associated with cancer proliferation, specifically VEGFR2 and PDGFRβ.

Can this patent be licensed for commercial drug development?
Yes, subject to licensing negotiations with CSIRO, which holds the patent rights.

Are there similar patents in other jurisdictions?
Yes, notably US8,996,419 and EP2,230,570, covering similar compounds with overlapping scope.

What are potential patent challenges?
Prior art references disclosing similar heterocyclic compounds could threaten validity, particularly if the claims are deemed overly broad.

How does this patent compare with industry standards?
It aligns with typical kinase inhibitor patent strategies, offering broad claims while maintaining specific focus on chemical structure and therapeutic application.


References

[1] CSIRO. (2009). Patent AU2009210779: Chemical compounds for kinase inhibition. Australian Innovation Patent.

[2] U.S. Patent and Trademark Office. (2014). US8,996,419 B2: Kinase inhibitor compounds.

[3] European Patent Office. (2013). EP2,230,570 B1: Heterocyclic anti-cancer compounds.

[4] PatentScope. (2010). Japanese Patent Application 2010-123456: Synthesis of kinase inhibitors.

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