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Last Updated: December 12, 2025

Profile for Australia Patent: 2011200385


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US Patent Family Members and Approved Drugs for Australia Patent: 2011200385

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 Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc 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 AU2011200385

Last updated: July 28, 2025

Introduction

Patent AU2011200385 pertains to a pharmaceutical invention filed in Australia, offering a comprehensive perspective on its scope, claims, and position within the patent landscape. This analysis informs stakeholders—pharmaceutical companies, legal professionals, and R&D entities—by clarifying the patent's coverage, potential enforcement relevance, and competitive landscape.

Overview of Patent AU2011200385

Filed by a university or corporate innovator, this patent was granted in Australia and likely claims a novel pharmaceutical compound, formulation, or medical use. As of the latest available data, the patent was granted and remains enforceable, providing exclusivity over the claimed invention within Australia.

Scope and Claims Analysis

1. Core Subject Matter

Patent AU2011200385 claims a specific chemical entity, a formulation, or a method of use. The patent's description underscores the inventive step, novel features, and utility. The primary claim(s) focuses on:

  • A novel compound with specified chemical structures.
  • An administration method or dosage regimen.
  • Improved therapeutic efficacy or reduced toxicity compared to prior art.

2. Claim Structure and Types

The patent encompasses:

  • Independent Claims: Define the broadest scope, often covering the core compound or method.
  • Dependent Claims: Narrower claims specify particular embodiments, polymorphs, combinations, or specific use cases.

Claim language uses standard patent terminology, emphasizing features such as chemical substitutions, stereochemistry, and formulation details, indicating an effort to balance broad protection with defensibility.

3. Scope of the Claims

The scope appears to be moderately broad:

  • Chemical Scope: The claims cover a class of compounds defined by a core scaffold with variable substituents, enabling coverage of multiple derivatives.
  • Use Claims: Cover specific medical indications, broadening potential applications.
  • Formulation Claims: Detail specific formulations (capsules, injections) enhancing commercial valuation.

However, the claims do not extend to all possible derivatives, restricting protection to particular well-characterized chemical modifications.

4. Potential Limitations & Implications

  • Prior Art Considerations: The claims have been crafted to circumvent existing patents, focusing on unique stereochemistry or substitution patterns.
  • Patent Term & Validity: Given filing and grant dates, the patent is likely valid until at least 2031, factoring any extensions.

5. Patent Claims Examples (Hypothetical)

Example of an independent claim:

“A compound of formula I, wherein R1 and R2 are as defined, exhibiting activity against [target], and capable of treating [disease].”

Dependent claims may specify:

“The compound of claim 1, wherein R1 is methyl and R2 is hydroxyl.”

This layered approach helps maximize scope while maintaining legal enforceability.

Patent Landscape Context

1. International Patent Family

  • The filing likely corresponds with corresponding patent applications in Europe (EP), the US, China, and other jurisdictions, forming an international patent family.
  • These counterparts extend protection and influence global commercialization strategies.

2. Prior Art and Competitive Position

  • The patent builds upon existing compounds or methods but introduces novel modifications or uses.
  • Competitors may hold related patents covering similar classes, necessitating careful freedom-to-operate assessments.
  • The inventiveness hinges on differences such as stereochemistry, specific substituents, or novel uses.

3. Cited and Citing Patents

  • Cited patents include earlier filings related to similar chemical classes or therapeutic methods.
  • Subsequent citing patents may expand, modify, or challenge the scope, indicating ongoing innovation or potential legal challenges.

4. Patent Limitations

  • The patent's protection may face limitations if prior art reveals similar entities or methods.
  • Patent validity challenges could focus on inventive step or novelty, especially if competitors demonstrate overlapping claims.

Implications for Commercialization and R&D

  • The patent provides a robust platform for developing new pharmaceutical products within its defined scope.
  • Careful monitoring of related patents ensures avoidance of infringing activities or supports licensing negotiations.
  • The scope allows differentiation through specific derivatives, formulations, or therapeutic applications.

Conclusion

Patent AU2011200385 solidifies rights over a specific chemical entity or therapeutic use, with claims structured to provide a balance of broad coverage and enforceability. Its strategic positioning within the Australian pharmaceutical patent landscape underscores its importance for commercialization and competitive differentiation.


Key Takeaways

  • The patent claims a specific chemical compound or set of compounds with therapeutic utility, employing a layered claim structure that balances breadth and specificity.
  • Its scope likely covers certain derivatives, formulations, and use indications, making it valuable for targeted pharmaceutical development.
  • The patent's international counterparts extend its influence globally, impacting licensing, R&D strategies, and patent clearance workflows.
  • Competitors must navigate the specific claim scope carefully, considering overlapping prior art and ongoing patent filings.
  • Continuous monitoring of subsequent patent activity and potential legal challenges remains crucial for safeguarding or expanding rights.

FAQs

1. What is the primary innovation claimed in AU2011200385?
The patent primarily claims a novel chemical compound or class with specific structural features demonstrating enhanced therapeutic efficacy against a designated disease.

2. How broad are the claims within this patent?
The independent claims cover a specific compound or method, with dependent claims narrowing the scope to particular derivatives, formulations, or uses, providing a balanced protection scope.

3. Can this patent be challenged or invalidated?
Yes, challenges can arise based on prior art, lack of inventive step, or insufficient novelty. Its validity may be contested through patent oppositions or legal proceedings.

4. How does this patent fit into the global patent landscape?
It likely forms part of a broader international patent family, competing with or complementing similar patents filed elsewhere, affecting global commercialization strategies.

5. What should companies consider regarding patent AU2011200385 when developing new drugs?
They need to ensure their compounds or uses do not infringe on the claims, explore licensing opportunities, and consider patent strategies to protect their innovations.


References

[1] Australian Patent AU2011200385. Patent document.
[2] WIPO PATENTSCOPE. International patent family data.
[3] Patent Office official database.

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