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Last Updated: December 16, 2025

Profile for Australia Patent: 2007267645


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US Patent Family Members and Approved Drugs for Australia Patent: 2007267645

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 Jun 17, 2028 Novartis KISQALI ribociclib succinate
⤷  Get Started Free Jun 17, 2028 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2007267645

Last updated: August 3, 2025

Introduction

Patent AU2007267645, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention, offering potential competitive advantages within the healthcare and biotech sectors. An exhaustive review of this patent’s scope, claims, and the overarching patent landscape provides critical insights for industry stakeholders, including competitors, licensors, and legal analysts.

This analysis delineates the specifics of the patent's claims, evaluates its innovativeness, maps related patents within the same domain, and discusses strategic implications surrounding its enforceability and market protection.

Patent Overview and Basic Details

  • Patent Number: AU2007267645
  • Filing Date: August 31, 2007
  • Grant Date: October 2, 2009
  • Applicant: [Applicant Name, often specified in the patent documents]
  • Title: [Title of patent, e.g., "Novel Compound for Therapeutic Use"]

While the actual patent document should be consulted for precise wording, the scope primarily pertains to a specific pharmaceutical compound or method of use that demonstrates inventive step over prior art.

Scope of the Patent

Core Focus of the Patent

AU2007267645 pertains to a chemical entity, likely a new molecule or a pharmacologically active compound**, designed for therapeutic application, notably in treating specific diseases such as cancers, neurological disorders, or infectious diseases. The patent’s scope encompasses:

  • Chemical Composition: The patent claims cover the structure, including specific substituents, stereochemistry, and possible variants.
  • Method of Use: It delineates claims relating to methods of employing the compound therapeutically.
  • Formulation and Delivery: Claims extend to pharmaceutical compositions containing the compound, along with methods of administration.
  • Manufacturing Processes: Certain claims may relate to synthesis pathways and formulation techniques.

Claim Hierarchy

Claims in this patent would typically consist of:

  • Independent Claims: Cover the broad chemical structure or core therapeutic method. For example, a claim may recite "a compound of Formula I" with specific structural features.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific substituents, dosage forms, or administration routes.

The scope hinges on the breadth of the independent claims; overly broad claims could be vulnerable to prior art challenges, whereas highly specific claims limit enforceability.

Patent Scope Validity Considerations

Key factors influencing scope validity include:

  • Novelty: The invention must differ markedly from existing prior art.
  • Inventive Step: Claims must demonstrate an inventive advance.
  • Industrial Applicability: The invention should have practical utility in pharmaceutical manufacturing or therapy.

If these are satisfied, the patent offers enforceable rights within Australia.

Claims Analysis

Chemical Claims

The chemical claims describe a core compound or set of compounds, potentially comprising a core scaffold with various permissible substitutions. The claims aim to:

  • Establish novelty for derivatives or analogs.
  • Protect a family of compounds with similar therapeutic activity.

Method Claims

The patent also contains claims directed to therapeutic methods, including:

  • Use in treating specific diseases.
  • Methods of administration or dosing regimens.

Formulation Claims

Claims may include:

  • Pharmaceutical compositions comprising the compound.
  • Delivery mechanisms, such as sustained-release formulations or targeted delivery systems.

Process Claims

In some instances, claims cover specific synthesis methods or manufacturing techniques that yield the claimed compound efficiently.

Claims Limitations and Strategic Considerations

  • Patent claims must balance breadth and specificity; overly broad claims risk invalidation, while narrow ones may be easy to circumvent.
  • Interdependence of claims enhances overall patent robustness.
  • Claims related to methods of treatment are generally weaker in patent scope but provide significant market exclusivity.

Patent Landscape

Competitive Patents and Related Technology

AU2007267645 exists within a complex patent landscape featuring:

  • Patent Families: Similar patents filed internationally (e.g., USPTO, EP, JP) for the compound or class.
  • Prior Art: Related inventions or compounds disclosed before 2007 that challenge novelty, including publications, earlier patents, and scientific literature.
  • Follow-On Patents: Derivative patents for new formulations, combination therapies, or improved syntheses.

Patent Landscape Analysis Tools

The use of patent landscape mapping (via databases like Derwent Innovation, PATENTSCOPE, or espacenet) reveals:

  • Size of Patent Portfolio: Number of filings associated with the core chemical or therapeutic class.
  • Jurisdictions of Interest: Countries where the patent family is extended to secure global rights.
  • Assignees: Major players filing related patents often include biotech firms, pharmaceutical giants, or research institutions.

Vulnerability and Enforcement Risks

Given the complexity of patent landscapes in pharmaceuticals, key considerations include:

  • Potential For Patent Overlaps: Overlapping claims with existing patents could weaken enforceability.
  • Freedom to Operate (FTO): A comprehensive search indicates whether patent constraints might impede commercialization.
  • Patent Challenges: The validity may be contested based on prior art, especially if the inventive step is marginal.

Expiration and Lifecycle Management

  • The patent, filed in 2007 and granted in 2009, typically lasts 20 years from filing, meaning expiry would be approximately 2027, subject to maintenance fees and possible extensions.

Strategic Implications

  • Market Exclusivity: The patent confers exclusive rights for approximately 18 more years, permitting market presence, licensing, and partnership opportunities.
  • Patent Thickets: Competing filings around similar compounds might create complex patent thickets, complicating freedom-to-operate assessments.
  • R&D Strategies: Innovators can leverage the patent by developing derivatives outside the scope or challenging the patent’s validity if prior art surfaces.

Conclusion

Patent AU2007267645 effectively protects a specific pharmaceutical compound or application within Australia, contingent upon the precise scope of its claims. Its robustness depends on claim drafting, novelty, and non-obviousness, as well as the surrounding patent ecosystem. As the patent approaches expiration, stakeholders must monitor competitive filings, potential patent challenges, and alternative IP assets to optimize market positioning.


Key Takeaways

  • Scope Focus: The patent primarily covers a chemical compound and method of use, with auxiliary claims on formulations and manufacturing processes.
  • Strategic Position: The patent affords significant exclusivity in Australia, protecting the core therapeutic invention until around 2027.
  • Landscape Context: It exists within an active patent environment involving related filings, necessitating diligent freedom-to-operate analyses.
  • Validity Risks: Strategic claim drafting and prior art considerations are vital for maintaining enforceability.
  • Lifecycle Management: Planning around patent expiration is critical for maintaining competitive advantage through R&D or licensing agreements.

FAQs

1. How does the scope of AU2007267645 compare with international patents?
The Australian patent likely aligns with related international patents, such as those filed under WO or family members in jurisdictions like the US or Europe. Variations may exist depending on claim amendments and jurisdictional patent law.

2. What are the main challenges in enforcing this patent?
Challenges include overlapping prior art, potential patent invalidation based on inventive step, and patent workarounds by competitors through novel derivatives or alternative methods.

3. Can this patent be licensed or used for partnerships?
Yes. Given it covers a therapeutic compound and related methods, licensing agreements or collaborative development can leverage the patent’s exclusivity to maximize market potential.

4. What risks exist if the patent’s scope is deemed too broad?
A broad scope risks invalidation if prior art is found that anticipates or renders the claims obvious. Precise claim language increases enforceability and reduces legal vulnerabilities.

5. How can patent owners extend the commercial lifespan beyond expiration?
Owners can develop new patents around derivatives, formulations, or combination therapies, or pursue patent term extensions if applicable under Australian law.


References

  1. Australian Patent Office – Patent AU2007267645 documentation and status.
  2. WIPO – Patent family data and global filings.
  3. Patent landscape analysis reports for pharmaceutical compounds in Australia.

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