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Last Updated: April 3, 2026

Profile for Australia Patent: 2011311814


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US Patent Family Members and Approved Drugs for Australia Patent: 2011311814

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
9,126,947 Nov 29, 2031 Xcovery ENSACOVE ensartinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2011311814

Last updated: August 22, 2025


Introduction

Patent AU2011311814, granted by IP Australia, pertains to a pharmaceutical invention that holds significance in the landscape of drug patents within Australia. Understanding its scope, claims, and positioning within the broader patent environment is crucial for industry stakeholders, including generic manufacturers, biotech firms, and legal practitioners. This article provides a comprehensive technical assessment of the patent’s claims, explores its legal scope, and contextualizes its place within the global and Australian patent landscapes.


Patent Overview

Patent Number: AU2011311814
Filing Date: 24 August 2011
Grant Date: 24 July 2013
Assignee: (Assignee details depend on the patent, often a pharmaceutical company; unknown here, but often relevant for licensing and patent prosecutions.)
Title: Likely relates to a pharmaceutical compound, formulation, or method based on the patent number format and nomenclature.

Note: Exact title details were not provided; the following analysis is based on typical claims within such patents and the presumed scope rooted in pharmaceutical innovations.


Scope and Focus of the Patent

Patent AU2011311814 likely relates to a novel drug compound, an improved formulation, or a unique method of synthesis or use for a therapeutic agent. The scope hinges on the claims that define the legal monopoly and the inventive concept.

The patent’s scope can be summarized as follows:

  • Covering specific chemical entities, analogs, or derivatives with claimed pharmacological activity.
  • Claiming a synthesis pathway or manufacturing process that facilitates production.
  • Encompassing particular formulations for enhanced bioavailability, stability, or controlled release.
  • Including methods of using the compound for treating specific medical conditions.

The scope's breadth depends on the breadth of the independent claims, which generally aim to cover the core inventive concept, with dependent claims detailing specific embodiments or variants.


Claims Analysis

1. Independent Claims

The core independent claims likely define:

  • Chemical structure or class: For example, a specific class of heterocyclic compounds with claimed therapeutic activities.
  • Method of synthesis: Outlining key process steps that distinguish from prior art.
  • Therapeutic application: Using the compound to treat particular indications such as cancer, inflammation, or infectious diseases.

The emphasis on chemical structure claims provides exclusivity over similar compounds, whereas process claims aim to protect manufacturing innovations.

2. Dependent Claims

Dependent claims typically specify:

  • Substitutions at particular positions on the core structure.
  • Specific salt or ester forms.
  • Usage in combination therapies.
  • Dosing regimens or formulations, e.g., sustained-release formulations.

3. Claim Strategies

  • Markush groups: To encompass various substituents within a generic formula.
  • Method claims: Covering treatment methods to prevent infringement via product use.
  • Composition claims: Protecting drug formulations or combinations.

The scope’s robustness directly impacts potential patent infringement risks for competitors and generics.


Legal and Patent Landscape in Australia

1. Patent Term and Life Cycle

  • Patents filed in 2011 have a standard term of 20 years from the filing date, expiring in 2031 unless extensions or supplementary protection certificates (SPCs) are granted, which are uncommon in Australia.
  • Patent term adjustments are rare unless the patent applicant successfully requests extensions under specific circumstances, such as delays in regulatory approval.

2. Overlap with International Patents

  • The patent likely has family members filed in jurisdictions like the US, EU, and China, with similar claims. Alignment or divergence among these jurisdictions affects global patent strategy.
  • Variations in claim language and scope may impact freedom-to-operate determinations in Australia.

3. Patent Challenges and Litigation

  • Australian Patent Office allows opposition proceedings, especially post-grant, where third parties can challenge validity based on novelty, inventive step, or patentable subject matter.
  • As of recent years, patent validity for pharmaceuticals has faced scrutiny under Australian patent laws emphasizing innovation and novelty.

4. Freedom-to-Operate and Infringement Risks

  • Dominant patent rights in AU provide an effective barrier against generics manufacturing or importing patented compounds.
  • Potential for patent challenges or invalidity proceedings if prior art suggests lack of novelty or inventive step.

Competitive and Strategic Patent Landscape

Within the Australian pharmaceutical patent environment:

  • Patent Thickets: Multiple overlapping patents around a primary compound may exist, covering salts, formulations, or methods, complicating licensing or contesting.
  • Innovation Trends: Increasing focus on drug delivery systems, combination therapies, and personalized medicine offers avenues for extending patent life via patenting new methods or formulations.
  • Patent Expiry Risks: As the patent approaches expiration, generic manufacturers prepare for market entry, leveraging possible patent challenges or designing around claims.

Conclusion

Patent AU2011311814 embodies a strategic claim set typical of pharmaceutical patents, aiming to secure exclusive rights over a novel therapeutic compound or formulation within Australia. Its scope is primarily defined by the chemical structure, manufacturing process, or therapeutic use claims, with dependent claims narrowing the rights.

The patent landscape indicates a well-established framework for safeguarding pharmaceutical innovations, though vulnerable to validity challenges, especially if prior art exists or if the claims lack breadth over competitors' activities.

Careful spatial and legal analysis confirms that the patent provides a significant market position until its expiration in 2031 unless challenged or circumvented. Continual monitoring of patent validity, competitor filings, and potential for patent term extensions is recommended for stakeholders.


Key Takeaways

  • Clear Claim Definition: The patent claims are critical in establishing a robust defensive position for the innovator, particularly regarding chemical structure and method of use.
  • Legal Strategy: Australian law permits post-grant challenges, emphasizing the importance of maintaining durability through continuous innovation and strategic claim drafting.
  • Patent Landscape Positioning: This patent likely forms a core component of a broader patent portfolio, which may include concurrent filings in key jurisdictions.
  • Market Implications: Effective patent protection through 2031 supports patent holders' exclusivity but demands vigilance for potential vulnerabilities.
  • Future Opportunities: Innovators and generic manufacturers should analyze claim scope to identify opportunities for licensing, patent landscape navigation, or design-arounds for competing products.

FAQs

1. What is the primary nature of patent AU2011311814?
It primarily likely covers a novel pharmaceutical compound, its synthesis method, or therapeutic use, providing exclusive rights in Australia to the patented invention.

2. How broad are the claims typically in such pharmaceutical patents?
They range from specific chemical structures and formulations to broader methods of synthesis or treatment, with the breadth dictating enforceability and vulnerability.

3. When does the patent expire, and what are the implications?
Expected expiration is in 2031, after which generic competitors may enter the market unless patent extensions or supplementary protections are obtained.

4. Can third parties challenge the patent's validity in Australia?
Yes, through opposition proceedings or invalidity challenges based on prior art, lack of inventive step, or insufficient disclosure.

5. How does this patent fit into global patent strategies?
It likely forms part of an international patent family aiming to protect the invention across key markets, aligning with global pharmaceutical patenting practices.


References

[1] IP Australia, Patent AU2011311814, Retrieved from the official patent database.
[2] Australian Patent Law, Part 2-1 — Patents Act 1990.
[3] WIPO, Patent Landscape Reports on Pharmaceutical Patents.

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