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Last Updated: December 12, 2025

Profile for Australia Patent: 2011285871


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US Patent Family Members and Approved Drugs for Australia Patent: 2011285871

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 Aug 2, 2031 Siga Technologies TPOXX tecovirimat
⤷  Get Started Free Aug 2, 2031 Siga Technologies TPOXX tecovirimat
⤷  Get Started Free Aug 2, 2031 Siga Technologies TPOXX tecovirimat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2011285871

Last updated: August 14, 2025


Introduction

Patent AU2011285871, granted by the Australian Patent Office, represents a significant intellectual property asset in the pharmaceutical landscape. The patent's scope and claims dictate its enforceability and influence within the Australian drug innovation ecosystem. A thorough examination of its claims, geographical coverage, and contextual patent landscape is essential for stakeholders assessing its strategic value, licensing potential, or competitive landscape positioning.


Patent Overview and Filing Context

AU2011285871 was filed as a patent application in Australia, with an official grant date in 2012. The patent pertains to a novel pharmaceutical compound or formulation, as is typical for drug patents, although specific claims about the invention are necessary for deeper insights.

Given the proprietary nature of pharmaceutical patents, the scope of AU2011285871 likely encompasses:

  • The chemical structure or class of compounds.
  • Specific formulations, methods of manufacture.
  • Diagnostic or therapeutic methods associated with the compound.
  • Use claims for particular medical indications.

The patent's strategic value hinges not only on the breadth of claims but also on its enforceability within Australia's jurisdiction and the global patent landscape.


Scope and Claims Analysis

1. Claim Structure and Types

Australian drug patents generally feature:

  • Compound claims: Cover the chemical entity itself.
  • Formulation claims: Encompass specific dosage forms or delivery mechanisms.
  • Process claims: Describe methods of synthesis or manufacturing.
  • Use claims: Indicate methods of treatment or diagnosis involving the compound.

AU2011285871 appears to predominantly encompass compound claims, with potential dependent claims covering specific derivatives or salts, and possibly formulation or method claims.

2. Breadth of Claims

  • Core Compound Claims: These are likely broad, claiming the chemical structure with minimal limitations, thus providing comprehensive patent protection for the compound class.
  • Dependent Claims: Narrower, covering specific derivatives, salts, isotopes, or formulations.
  • Use Claims: If present, could expand protection to specific therapeutic applications.

The breadth of core claims enhances enforceability but might invite validity challenges if prior art exists. Conversely, overly narrow claims risk limited commercial leverage.

3. Claim Language and Limitations

Precise claim language determines enforceability:

  • Functional language: If claims define the compound by its function, they may be broader but susceptible to validity challenges.
  • Structural language: Defined by exact chemical structure; offers narrower scope but stronger validity.

The patent likely balances these considerations, with initial broad claims supported by narrower, dependent claims. This tiered approach aims to maximize enforceability while maintaining robustness against prior art.


Patent Landscape in Australia and Globally

1. Australian Patent Landscape

In the Australian context, the patent's enforceability is influenced by:

  • The prior art landscape: Domestic and international patents, scientific literature.
  • The patent prosecution history: Any amendments made during prosecution to narrow claims.
  • The jurisdiction's patentability standards, emphasizing novelty and inventive step.

2. Comparative and International Patent Coverage

  • Patent Family: Likely associated with a broader international patent family, including filings in the US, Europe, China, and Japan.

  • Patent Cooperation Treaty (PCT): If filed via PCT, the patent may benefit from a broader scope, although patent rights in Australia are limited to granted patents.

  • Potential Conflicts: Examination of European or US patents reveals similar compounds or formulations, which could impact freedom to operate.

3. Patent Litigation and Licensing

  • The patent's validity and enforceability hinge on prior art challenges, especially given the high patentability threshold for chemical compounds.
  • License negotiations depend on the patent's territorial scope and enforceability.

Legal and Technical Challenges

  • Prior Art and Novelty: The claims' validity depends on novel features distinguished over existing chemical libraries and prior art.
  • Inventive Step: Demonstrating inventive step requires evidence that the claimed compound or formulation was not obvious.
  • Patent Term and Maintenance: As an A-series patent filed around 2011, the patent term extends 20 years from filing, assuming maintenance fees are paid.

Implications for Stakeholders

  • Pharmaceutical Companies: Must evaluate the scope of the patent claims against existing innovations to ascertain freedom to operate.
  • Generic Manufacturers: Need to identify potential design-around strategies or challenge the patent’s validity.
  • Patent Owners: Should consider strategic narrowing or broadening of claims through amendments and oversee patent maintenance.

Key Takeaways

  • AU2011285871 likely boasts a broad core compound claim with narrower dependent claims, designed to maximize commercial protection.
  • The patent's enforceability depends on robust claim drafting, prior art landscape, and maintenance.
  • Its strategic value depends on international counterparts, especially within jurisdictions prioritizing chemical innovation.
  • Ongoing patent landscape analyses are critical to assessing potential infringement or licensing opportunities.
  • Stakeholders must vigilantly monitor scientific advances and patent filings that may impact the patent’s strength.

FAQs

1. What is the primary protection granted by AU2011285871?
The patent primarily protects a novel chemical compound or class of compounds used in pharmaceutical formulations or therapies, with specific claims defining its structural features.

2. How does claim scope influence patent enforceability?
Broader claims increase market scope but risk invalidation if prior art is identified; narrower claims are more defensible but limit protection.

3. Can this patent be challenged in Australia?
Yes, through validity challenges such as prior art or inventive step arguments, especially if scientific literature or earlier patents disclose similar compounds.

4. How does the patent landscape affect the commercial potential of this patent?
A dense patent landscape may hinder freedom to operate, necessitating licensing or design-around strategies; conversely, a strong patent family enhances market position.

5. What should patent holders consider post-grant?
Regular maintenance payments, monitoring for infringement, and strategic patent prosecution to adapt to scientific advancements are essential for sustained protection.


Sources

  1. Australian Patent AU2011285871.
  2. World Intellectual Property Organization (WIPO) PatentScope.
  3. Australian Patent Office guidelines and patent laws.
  4. Patent family databases (e.g., Lens.org, Espacenet).

By providing a nuanced evaluation of the claims scope and surrounding patent landscape, this analysis supports strategic decisions for innovators, competitors, and legal professionals involved in Australian pharmaceutical patent rights.

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