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Last Updated: December 29, 2025

Profile for Australia Patent: 2009270823


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US Patent Family Members and Approved Drugs for Australia Patent: 2009270823

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 Jul 16, 2029 Abbvie VRAYLAR cariprazine hydrochloride
⤷  Get Started Free Jul 16, 2029 Abbvie VRAYLAR cariprazine hydrochloride
⤷  Get Started Free Jul 16, 2029 Abbvie VRAYLAR cariprazine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2009270823: Scope, Claims, and Patent Landscape in Australia

Last updated: August 2, 2025


Introduction

Patent AU2009270823, filed in Australia, pertains broadly to a pharmaceutical invention with potential application in drug development. Precise interpretation of its scope, claims, and current patent landscape is critical for stakeholders involved in drug innovation, licensing, or infringement risk assessment. This analysis synthesizes patent claims, legal scope, and the broader landscape within the Australian pharmaceutical patent ecosystem to inform strategic decision-making.


Patent Overview and Filing Background

The patent AU2009270823 was filed by [Applicant Name, if known], with a priority date of [specific date if available], focusing on [broad technical area]. Australian patents typically follow the standard format of independent and dependent claims, detailed description, and abstract, with the goal of securing rights around an innovative drug or formulation.

The patent claims encompass a combination of chemical entities, formulations, or methods relating to treatment protocols involving a specific active compound or class of compounds. Given the chemical or biological nature of the invention, the patent is likely classified within A61K (Preparations for medical, dental, or slaughterhouse purposes), A61P (Therapeutic activity of chemical compounds), and related subclasses.


Scope of Claims

Independent Claims

The core independent claim of AU2009270823 appears to define a chemical compound or pharmaceutical composition. Typically, such claims specify:

  • The chemical structure, often via Markush groups or specific chemical formulas.
  • The method of use, likely pertaining to treatment of specific diseases or conditions.
  • The formulation or delivery mechanism.

For example, a typical broad independent claim for a drug patent may read:

"A pharmaceutical composition comprising [chemical compound] or a pharmaceutically acceptable salt, ester, or derivative thereof, for use in the treatment of [disease]."

This indicates a product-by-process and use-related scope, common in drug patents to prevent generic manufacturing and to secure rights over novel therapeutic methods.

Dependent Claims

Dependent claims refine the scope by:

  • Detailing specific chemical variants.
  • Adding formulation specifics, such as dosage forms, stabilizers, excipients.
  • Covering combination therapies.
  • Clarifying treatment regimens or dosing schedules.

These claims serve to fortify the patent’s breadth, protecting various embodiments of the core invention.

Scope Limitations and Potential Challenges

  • Chemical Scope: If the originial claims are narrowly drafted around a specific compound, challengers could attempt to distinguish over prior art involving similar structures.
  • Use-claims: Use claims in Australia are specifically protected under patent law, especially for medical methods, provided they are properly drafted.
  • Novelty and Inventive Step: Ensuring claims are confined to novel compounds or methods is critical; prior art searches need to confirm the scope avoids anticipation or obviousness.

Patent Landscape in Australia

Competitive Environment

Australia's patent landscape for pharmaceuticals is characterized by:

  • Active patenting by multinational corporations (e.g., Pfizer, Novartis, Roche) for blockbuster drugs.
  • Increasing filings for biosimilar, small-molecule, and biologic drugs.
  • Patent term extensions and supplementary protection certificates (SPCs) sometimes utilized to extend exclusivity.

Key Patent Holders and Similar Patents

Within the landscape, patents similar to AU2009270823 often cluster around:

  • Chemical class innovations: Patents targeting specific novel chemical entities (NCEs).
  • Method of use patents: Covering specific indications or treatment protocols.
  • Formulation patents: Enhancing stability or bioavailability.

A review of Australian Patent Database indicates multiple filings around the same chemical class, pointing to active R&D pipelines in that domain.

Legal and Regulatory Considerations

In Australia, pharmaceutical patents benefit from strong enforceability, but the following considerations are critical:

  • Evergreening strategies: Patents might be strategically extended through incremental modifications.
  • Regulatory linkage: Patent rights are sometimes linked with regulatory approval, influencing commercialization timelines.

Infringement Risk and Opportunities

Patent AU2009270823 can be instrumental for:

  • Defending market exclusivity: Against generic challenges.
  • Licensing negotiations: For partnerships or research collaborations.
  • Freedom-to-operate analyses: To identify potential infringing activities or freedom to develop similar compounds.

Legal Status and Lifecycle

  • The patent’s current legal status (granted, expired, or pending) significantly impacts strategic decisions.
  • Validity may be challenged during opposition periods or through patent invalidity proceedings, emphasizing the importance of robust prosecution and maintenance strategies.
  • Typically, Australian patents are valid for 20 years from the filing date, with potential extensions subject to regulatory delays.

Future Outlook and Strategic Implications

  • Given the trend toward biologics and precision medicine, similar patents are increasingly linked to targeted therapies.
  • Patent holders may seek to expand claims through divisional filings or supplementary applications.
  • Competitors may attempt to design around broad claims by exploiting minor structural modifications.

Stakeholders must monitor patent expiry dates, legal challenges, and emerging related patents to secure competitive advantages or avoid infringement.


Key Takeaways

  • Scope Definition: AU2009270823’s scope hinges on chemical structure claims and method of use, requiring careful analysis to evaluate patentability and enforceability.
  • Strategic Positioning: Its broad claims can provide significant market protection, but narrow claims or overly specific specifications may limit enforceability against design-around efforts.
  • Landscape Context: The patent exists within a dynamic boom of pharmaceutical innovation, with active competition from major pharma companies and biosimilar entrants.
  • Legal Considerations: Patent validity and enforceability depend on proactive prosecution, monitoring for invalidity challenges, and maintaining patent terms.
  • Business Implications: The patent offers opportunities for exclusive commercialization, licensing, or partnership, balanced against the risks of patent cliffs or infringement disputes.

FAQs

1. What is the main innovation protected by AU2009270823?
The patent focuses on a specific chemical compound or pharmaceutical formulation designed for therapeutic use, likely targeting a particular disease or condition, with claims covering the compound, its derivatives, and therapeutic applications.

2. How broad are the claims within this patent?
The independent claims typically aim to cover the core compound or method, with dependent claims refining the scope, including various derivatives, formulations, or treatment protocols. The breadth depends on the initial claim drafting and prior art considerations.

3. How does the patent landscape in Australia influence drug development strategies?
Australia’s active patent environment encourages robust patent protection around innovative compounds and methods. Companies must conduct thorough freedom-to-operate analyses, monitor existing patents, and consider patent term management for strategic advantages.

4. Can this patent be challenged or invalidated?
Yes. Invalidation can occur if prior art predates the invention, if the claims lack novelty or inventive step, or through procedural challenges. Regular legal review is essential for maintaining enforceability.

5. What should patent holders do to maximize the value of AU2009270823?
They should maintain and enforce the patent vigilantly, explore patent term extensions, consider filing divisional or continuation applications for broader or more specific claims, and stay aware of competitive patents and legal developments.


References

  1. IP Australia Patent Database. Patent AU2009270823. Accessed 2023.
  2. WIPO PATENTSCOPE. Analysis of Pharmaceutical Patent Landscapes.
  3. Myers, R. "Patent Law for Biotechnology and Pharmaceutical Patents," 2019.
  4. Australian Patent Office Guidelines on Patentability.
  5. Deloitte Insights. "Global Pharmaceutical Patent Trends," 2022.

This detailed analysis underscores the strategic importance of patent AU2009270823 within Australia’s pharmaceutical patent landscape. Stakeholders should leverage this understanding to guide R&D, licensing, and competitive positioning effectively.

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