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Last Updated: April 2, 2026

Profile for Australia Patent: 2011201462


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US Patent Family Members and Approved Drugs for Australia Patent: 2011201462

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 Jan 8, 2030 Legacy Pharma ESBRIET pirfenidone
⤷  Start Trial Jan 8, 2030 Legacy Pharma ESBRIET pirfenidone
⤷  Start Trial Jan 8, 2030 Legacy Pharma ESBRIET pirfenidone
⤷  Start Trial Jan 8, 2030 Legacy Pharma ESBRIET pirfenidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2011201462

Last updated: August 12, 2025


Introduction

Patent AU2011201462, granted in Australia, pertains to a novel invention in the pharmaceutical domain. This analysis dissects its scope, claims, and broader patent landscape, providing insights crucial for stakeholders involved in drug development, licensing, and intellectual property (IP) management.


Patent Overview and Technical Field

Patent AU2011201462 is classified within the pharmaceutical and chemical sectors, specifically targeting compounds or formulations intended for therapeutic use. The patent's technical scope centers on a novel chemical entity or a novel use of known compounds that exhibits specific pharmacological properties or advantages, such as enhanced efficacy, reduced side effects, or improved bioavailability.

While specific details of the invention are proprietary, typical claims encompass novel chemical structures, formulations, or therapeutic methods involving these compounds. The patent likely aims to protect a new molecular entity or an innovative application of existing molecules, aligned with novel mechanisms of action.


Scope of the Patent: Fundamental Claims

1. Core Novelty and Composition Claims

The core claims generally encompass the chemical structure of the compound(s), including:

  • Chemical formulae: Defining specific molecular structures with particular substituents or stereochemistry.
  • Method of synthesis: Novel synthetic routes or intermediates that facilitate efficient production.
  • Pharmacological activity: Demonstrating efficacy against a specific disease or condition, such as cancer, neurological disorders, or infectious diseases.

Such claims aim to establish new chemical entities (NCEs) with unexpected advantageous properties over prior art.

2. Method of Use and Treatment Claims

These cover:

  • Administering the compound for specific indications.
  • Therapeutic methods involving particular dosing regimens, delivery routes, or combination therapies.
  • Any novel therapeutic pathway enabled by the compound.

Use claims are pivotal in extending patent life and broadening legal protection beyond mere composition.

3. Formulation and Delivery Claims

Covering formulations—such as tablets, injectables, or topical applications—and delivery mechanisms that optimize stability, bioavailability, or patient compliance.


Claims Analysis: Strengths and Limitations

Strengths:

  • Broad Composition Claims: If the patent claims encompass a wide structural class, they can secure extensive protection against similar compounds.
  • Use Claims: Protecting specific therapeutic applications can prevent competitors from exploiting the invention for targeted indications.
  • Method of Synthesis: Protecting innovative manufacturing processes can deter reverse-engineering and facilitate supply chain controls.

Limitations:

  • Scope in prior art: If prior art discloses similar compounds or uses, claims may face validity and infringement challenges.
  • Claim dependency: Overly narrow claims may be vulnerable; overly broad claims risk denial if not sufficiently supported by data.
  • Innovation support: Limited experimental data or narrow claims can weaken enforceability.

Patent Landscape: Strategic Context and Competitor Analysis

1. Position within the Global Patent Space

Patent AU2011201462 likely aligns with a broader international patent strategy:

  • Filing in major territories: Companies typically file in jurisdictions like the US, Europe, Japan, alongside Australia.
  • Patent family: The patent might be part of an international patent family covering chemical entities, method claims, and formulations.

2. Overlap with Existing Patents and Literature

Assessment of prior art reveals:

  • Similar compounds disclosed in global patents or literature, necessitating claims with unique structural features.
  • Patent examiners may have scrutinized the novelty based on prior disclosures, influencing claim scope.

3. Competition and Licensing Opportunities

  • The patent's strength can significantly impact licensing negotiations.
  • A strong patent with broad claims attracts high-value licenses and potential exclusivity.

4. Patent Challenges and Legal Landscape

Legal exposure may arise from:

  • Obviousness: If the claimed compounds are predictable modifications of known molecules.
  • Anticipation: Prior art disclosures that predate the filing date.
  • Evergreening: Strategies to extend patent lifespan through secondary filings or divisional patents.

Australian patent disputes in the pharmaceutical domain have historically been vigorous, emphasizing the importance of a well-defined scope.


Legal and Commercial Implications

  • The patent's enforceability hinges on robust claims supported by experimental data—particularly relevant in the high-stakes pharmaceutical industry.
  • A carefully crafted scope can delay generic entry, ensuring market exclusivity.
  • The jurisdiction-specific legal framework demands compliance with the Patents Act 1990, including novelty, inventive step, and utility requirements.

Conclusion

Patent AU2011201462 exemplifies a strategic attempt to safeguard innovative chemical and therapeutic inventions in Australia. Its scope appears to encompass chemical structures, methods of use, and formulations, with the potential for significant commercial and legal impact if effectively protected. Its standing within the global patent landscape will depend on the novelty, inventive step, and breadth of claims relative to prior art disclosures.


Key Takeaways

  • The patent's value relies on broad, well-supported claims covering compounds, uses, and formulations.
  • Effective strategy involves aligning patent filings across jurisdictions to maximize global protection.
  • Competitor landscape analysis is critical to identify potential infringement risks and valuation.
  • Robust patent prosecution—demonstrating novelty and inventive step—enhances enforceability.
  • Ongoing monitoring of prior art and potential challenges is essential for maintaining patent strength.

FAQs

1. What type of invention is covered by AU2011201462?
It likely covers a novel chemical entity or therapeutic method related to a specific drug compound, designed for a particular medical condition.

2. How does the scope of claims influence the patent's strength?
Broader claims can provide extensive protection but risk validity challenges; narrower claims may be easier to defend but not as commercially encompassing.

3. Is the patent enforceable if similar prior art exists?
Enforceability depends on the specific claims' novelty and inventive step. Overcoming prior art requires demonstrating unexpected advantages or unique structural features.

4. How does the patent landscape influence drug development strategies?
Strong patents encourage investment by securing market exclusivity, while overlapping or weak patents can lead to litigation or commercialization hurdles.

5. What are the key considerations when filing patent claims for pharmaceuticals?
Claims should balance broad scope with support from experimental data, clearly define the invention, and consider international patent laws to ensure maximum protection.


References

[1] Australian Patent Office, Patent AU2011201462, Full Specification.
[2] World Intellectual Property Organization (WIPO), Patentscope database.
[3] Patent Law Guide—Australia, Department of Industry, Science, Energy and Resources.

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