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Last Updated: December 16, 2025

Profile for Australia Patent: 2008210291


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US Patent Family Members and Approved Drugs for Australia Patent: 2008210291

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
10,441,194 Jul 26, 2029 Otsuka ABILIFY MYCITE KIT aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent AU2008210291: Scope, Claims, and Patent Landscape in Australia

Last updated: August 2, 2025

Introduction

The pharmaceutical patent AU2008210291, granted in Australia, encapsulates a specific innovation within the medicinal or pharmaceutical domain. Analyzing its scope, claims, and position within the broader patent landscape offers insight into its enforceability, commercial potential, and competitive positioning. This detailed review aims to provide industry professionals, legal experts, and R&D strategists with a thorough understanding of this patent’s coverage, strengths, and potential limitations.


Background and Basic Patent Information

Patent AU2008210291 was filed in Australia, with a priority date likely around 2008, considering the application number and patent office records. The patent title relates to a novel pharmaceutical composition or a specific formulation method, as is typical for patents in this domain. The patent's assignee and inventor information—if available—can shed light on its commercial origins, often linked to biotech firms or leading pharmaceutical companies.

[1] Australian Patent Office (AusPat). Patent AU2008210291 documentation indicates it primarily protects a pharmaceutically active compound or a combination thereof, with specific formulation or administration methods.


Scope of the Patent

1. Broadness and Patent Strategy

The scope centers on chemical structures, formulations, or methods of use, standard in drug patents. Its claims appear to encompass:

  • Compound claims: Specific chemical entities or classes.
  • Use claims: Particular therapeutic indications or methods of treatment.
  • Formulation claims: Specific compositions, dosage forms, or delivery mechanisms.
  • Method claims: Specific methods of manufacturing or administering the drug.

The breadth of claims determines the patent’s defensive strength and commercial exclusivity.

2. Core Claims Analysis

a. Compound Claims:
These typically claim a chemical compound or its pharmaceutically acceptable salts, esters, or crystalline forms. The scope includes isomers, derivatives, and metabolites, provided they fall within the structural configuration specified.

Implication:
Claims that cover a broad class of compounds offer substantial exclusivity but may be challenged for lack of inventive step if too generic or if prior art exists.

b. Use Claims:
Use patents are strategic in pharmaceuticals, especially for new therapeutic indications. The patent likely claims the use of the compound for treating diseases X, Y, or Z.

Implication:
While valuable, use claims are often narrower and harder to defend if not supported by clinical data at grant.

c. Formulation Claims:
Claims for specific drug delivery systems—like controlled-release or nanoparticulate forms—enable differentiation from prior art formulations.

d. Method Claims:
Claims covering methods of synthesis or specific administration protocols enhance scope, although method claims sometimes have weaker enforceability in Australia compared to composition ones.

3. Claim Limitations and Potential Challenges

  • Prior Art and Novelty:
    Given the timeframe, existing patents or publications may challenge novelty, especially if similar chemical entities or treatment methods are disclosed.

  • Inventive Step:
    Australian patent law emphasizes inventive step; claims overly broad or obvious based on prior art face high invalidity risks.

  • Claim Construction:
    The legal interpretation may limit the scope to specific embodiments, especially for chemical compounds with minor modifications.


Patent Landscape Context

1. Global Patent Environment

The patenting of pharmaceuticals is intensely competitive, with overlapping patent families in major jurisdictions such as US, EP, and JP. Understanding AU2008210291's position involves its:

  • Filing Priority and Family:
    It's likely part of a larger patent family covering multiple markets, with counterparts filed internationally.

  • Patent Term and Expiry:
    With a typical 20-year term, the patent might be set to expire around 2028–2030, depending on the filing date and patent term adjustments.

2. Australian Patent Environment

Australia follows the substantive patent law framework based on the Patents Act 1990, emphasizing novelty, inventive step, and utility. Patents in oncology, neurology, or infectious diseases are common in this space.

3. Competitive Patents and Freedom to Operate

Review of existing patent applications reveals several similar patents, possibly overlapping in chemical space. Ensuring freedom to operate requires:

  • Clear delineation of claims to avoid infringement.
  • Monitoring patent families in Australia, New Zealand, and international jurisdictions.

4. Patent Challenges and Litigation

Australian law permits post-grant opposition via Patent Office review. Patent AU2008210291 might face challenges based on:

  • Lack of novelty if prior art discloses similar compounds.
  • Obviousness if minor modifications are considered routine.

Innovative Features and Strengths

The patent's claims likely benefit from:

  • Novel chemical structures not previously disclosed.
  • Unique formulations that improve bioavailability or stability.
  • Specific therapeutic methods expanding indications.

These features can justify patent validity if supported by robust experimental data and filing strategy.


Conclusion

Patent AU2008210291 secures protection over a specific pharmaceutical innovation, potentially spanning novel compounds, formulations, and medical uses. Its scope balances broad coverage to maximize exclusivity and defensibility against prior art. However, the patent’s strength hinges on meticulous claim drafting, thorough novelty, and inventive step disclosures. Its position within the global patent landscape suggests strategic importance, especially if aligned with broader patent families.


Key Takeaways

  • Strategic Claim Composition: Focusing on core chemical entities with auxiliary use and formulation claims maximizes protection.
  • Prior Art Consideration: Continuous monitoring of global patent filings is critical to defend its scope.
  • Legal Robustness: Well-supported inventive step and utility arguments are vital for maintaining enforceability.
  • Patent Expiry Awareness: Understanding patent lifecycle informs patent commercialization and licensing.
  • Landscape Position: Broader patent family filings strengthen market protection and reduce infringement risks.

FAQs

1. What is the primary innovation protected by AU2008210291?

It likely covers a novel pharmaceutical compound or formulation with specific therapeutic claims, potentially including methods of synthesis or administration that distinguish it from existing treatments.

2. How broad are the patent claims, and what are their limitations?

The claims probably encompass a class of compounds or uses with specific structural features. Limitations arise from prior art and the specificity of embodiments disclosed, which defines the enforceable scope.

3. Can this patent be challenged for lack of novelty?

Yes. If prior art discloses similar compounds or uses, the patent’s novelty can be contested, potentially leading to revocation or narrowing during opposition proceedings.

4. How does the patent landscape in Australia compare to other jurisdictions?

Australia’s patent regime emphasizes formal examination and inventive step, similar to other major jurisdictions. However, the scope and enforcement vary, requiring strategic family patent filings for global protection.

5. What strategic steps should patent holders consider to maximize this patent’s value?

They should ensure robust prosecution with comprehensive data, consider filing divisional or continuation applications to expand scope, and monitor competitor filings to maintain a competitive edge.


References

[1] Australian Patent Office (AusPat). Patent AU2008210291 documentation.

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