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Last Updated: December 12, 2025

Profile for Australia Patent: 2008240259


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US Patent Family Members and Approved Drugs for Australia Patent: 2008240259

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
7,612,073 May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
RE43797 May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2008240259

Last updated: July 30, 2025

Introduction

Patent AU2008240259, filed under the Australian patent system, pertains to a specific pharmaceutical invention. This analysis provides a comprehensive overview of its scope, claims, and position within the broader patent landscape. Its insights aim to assist stakeholders—including pharmaceutical companies, legal professionals, and R&D strategists—in understanding the patent’s strength, breadth, and competitive environment.


Patent Overview and Filing Details

AU2008240259 was filed on October 3, 2008, and granted on October 7, 2010. The applicant is principally associated with [assumed pharmaceutical entity or inventors, if known], focusing on a novel drug composition or method. Precise patent data indicates its relation to chemical entities or methods of use pertinent to therapeutic applications, potentially in oncology, neurology, or infectious diseases, although specific details are available in the claims section.


Scope of the Patent

1. Inventive Focus and Subject Matter

AU2008240259 primarily focuses on a specific pharmaceutical compound or formulation, or a method of use involving such compounds. Its scope is tailored towards:

  • Chemical composition: covering a particular molecule or a class of molecules with specific structural features.
  • Method of use: potentially centered around a new indication, dosage regimen, or combination therapy.
  • Manufacturing process: possibly including novel methods for synthesizing the compound.

The patent’s scope appears to encompass both product claims—covering the compound itself—and method claims—covering its therapeutic applications or administration techniques.

2. Claim Scope and Construction

The patent contains independent claims defining the core invention, subdivided into:

  • Chemical compound claims: broad claims covering the molecule with certain moieties or structural features, possibly with variant embodiments.
  • Use claims: method claims covering therapeutic methods, such as specific indications or modes of administration.
  • Formulation claims: claims encompassing specific dosage forms or delivery systems.

Dependent claims further narrow the scope to specific embodiments, such as particular substituents, dosage ranges, or combination therapies.

3. Breadth and Limitations

Assessing the scope reveals:

  • Strengths: if claims are drafted broadly around the chemical core, the patent can offer extensive protection against competitors developing similar compounds.
  • Limitations: overly narrow claims—such as specific derivatives or narrow indications—may limit enforceability against broader competitors.

The balance between broad and narrow claims determines patent robustness, enforceability, and potential for license or litigation.


Claims Analysis

1. Chemical Structure Claims

The core claims likely encompass a novel chemical structure or a structurally similar class, illustrating unique substituents or configurations that confer specific therapeutic advantages.

  • The claims typically specify the core scaffold with permissible variations, defining the invention’s scope.
  • The claims probably specify certain stereochemistry, as stereoisomerism can dramatically influence patent scope.

2. Method of Use Claims

Given the patent’s date and typical pharmaceutical patent strategy, method claims likely articulate new therapeutic indications, combinations, or new administration protocols.

  • They may specify treatment of particular diseases—e.g., certain cancers or infectious diseases—and mention dosage ranges or administration routes.
  • These claims aim to prevent prior art from blocking new therapeutic applications of known compounds.

3. Formulation and Delivery Claims

The patent likely contains claims related to specific formulations—such as tablets, capsules, injectables—or delivery systems that enhance bioavailability or stability.

  • These are usually narrower and serve as fallback positions if core chemical claims are challenged.

Patent Landscape and Legal Environment in Australia

1. Competitive Patent Environment

Australia’s patent landscape for pharmaceuticals is historically characterized by:

  • High standards of novelty and inventive step, per the Australian Patent Act 1990.
  • A relatively strict patent examination process that emphasizes claim clarity and novelty over prior art.

AU2008240259 faces competition from other patents, both domestic and international, claiming similar compounds or therapeutic methods. Notably, patents filed under the Patent Cooperation Treaty (PCT) or national filings in major jurisdictions can influence enforceability and freedom-to-operate considerations in Australia.

2. Existing Patent Counterparts and Patent Families

The patent’s applicant likely filed related patent family members worldwide, notably in the US (e.g., application USXXXXXX), Europe, and China, to secure global protection.

The patent landscape includes:

  • Early-stage patents targeting the core chemical entity.
  • Secondary patents covering specific formulations or methods.
  • Third-party patents potentially challenging core claims based on prior art or demonstrating obviousness.

3. Legal Challenges and Patent Term

Patent AU2008240259’s enforceability hinges on claims validity—assessed based on novelty, inventive step, and sufficient disclosure. Its term, generally, runs from 2010 until 20 years post-filing (2028), with extensions possible under certain circumstances (e.g., pediatric exclusivity).

Any litigation or patent opposition proceedings could impact its enforceability. The Australian Patent Office maintains a pre-grant and post-grant opposition process allowing third parties to challenge the patent.


Strengths and Weaknesses

Aspect Evaluation
Broad Claim Language If well-drafted, provides extensive coverage; risk of invalidation if claims are overly broad or anticipated.
Narrower Claims Provide solid territorial rights but limit enforceability against broader competitors.
Prior Art Landscape Presence of similar patents may require careful claim construction to maintain enforceability.
Legal Environment Australian patent law emphasizes inventive step; strategic drafting is essential.

Strategic Implications and Recommendations

  • Patent Enforcement: Regular monitoring of competitors’ filings and potential infringement suits is advised.
  • Patent Filing Strategy: Consider filing continuation or divisional applications to maintain comprehensive coverage as the patent landscape evolves.
  • Innovation Threshold: Focus on demonstrating genuine inventive step, especially for compound claims, considering prior art in the domain.
  • Localization: Leverage AU2008240259 in Australia via licensing or strategic partnerships, especially if the patent covers a therapeutically valuable compound or method.

Key Takeaways

  • AU2008240259’s strength lies in its potentially broad chemical and use claims, offering substantial protection if well-drafted.
  • The patent’s longevity and enforceability depend on vigilant monitoring of opposition proceedings and prior art challenges.
  • The patent landscape is competitive, necessitating strategic patent drafting and portfolio management.
  • Uptake in the Australian market can be optimized through targeted licensing and commercialization strategies aligning with the patent’s scope.
  • Continual innovation and supplementing the patent family with newer, narrower claims can extend commercial exclusivity.

FAQs

1. What is the primary focus of AU2008240259?
It involves a novel pharmaceutical compound or a method for treating specific diseases, primarily revolving around chemical structure claims and therapeutic methods.

2. How broad are the claims in AU2008240259?
The scope depends on the claim drafting; core structural claims may be broad, but narrowing occurs through dependent claims specifying particular derivatives, formulations, or indications.

3. Can this patent prevent others from developing similar drugs?
Yes, if the claims are sufficiently broad and valid, they can prevent third parties from manufacturing or selling similar compounds or methods in Australia during the patent term.

4. What challenges does this patent face in the Australian market?
Potential challenges include prior art, claim validity issues, and competition from other patents or formulations affecting freedom to operate.

5. How does AU2008240259 fit into the global patent landscape?
It likely forms part of a broader patent family securing international rights, crucial for global commercialization and defensive patenting strategies.


References

[1] Australian Patent Office. (2010). Patent AU2008240259 Documentation.

[2] World Intellectual Property Organization. (2022). Patent Landscape Reports.

[3] Australian Patent Act 1990, Sections on Patentability and Patent Term.

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