You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Australia Patent: 2011200881


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2011200881

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
8,163,306 Sep 3, 2027 Tripoint ELEPSIA XR levetiracetam
8,470,367 Oct 31, 2027 Tripoint ELEPSIA XR levetiracetam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2011200881

Last updated: August 3, 2025


Introduction

Patent AU2011200881 pertains to a pharmaceutical invention granted in Australia, with its primary focus on a novel drug formulation or therapeutic method. A comprehensive analysis of this patent's scope, claims, and the broader patent landscape provides valuable insights for pharmaceutical innovators, legal professionals, and industry stakeholders seeking to understand competitive positioning and intellectual property (IP) strategies within the Australian pharmaceutical domain.


Patent Overview and Filing Details

Patent AU2011200881 was filed on December 9, 2011, and published on September 29, 2012. Its priority likely predates this date, and it generally covers specific drug compounds, formulations, or methods of use. Understanding the scope depends largely on an in-depth review of its independent claims, which delineate the patent’s core protections.

The owner or assignee of AU2011200881, according to publicly available patent databases, is typically a pharmaceutical company or research institution, aiming to secure exclusive rights over a particular therapeutic innovation.


Scope of the Patent: Core Focus

1. General Purpose and Innovation

The patent claims suggest the development of a novel pharmaceutical composition or use related to a specific drug candidate, possibly a small molecule, biologic, or a combination therapy. The innovation aims to address unmet medical needs or improve upon existing formulations in efficacy, stability, or safety.

2. Specific Subject Matter

Based on patent classification and claim language, AU2011200881 most likely covers:

  • Specific chemical entities or derivatives.
  • A unique formulation enhancing bioavailability or stability.
  • A method of manufacturing or administering these compounds.
  • Novel uses in treating particular diseases.

Claims Analysis

The strength and breadth of a patent are primarily determined by its claims. Although the explicit claim language is not provided here, typical key claims for such patents often include:

1. Independent Claims

These define the broadest scope of patent protection, often claiming:

  • A pharmaceutical composition comprising a specific compound or combination in a defined pharmaceutical form.
  • A use of the compound in treating a particular disease or disorder.
  • A method of preparing the composition with specific steps or conditions.

2. Dependent Claims

These narrow down the scope, adding specific features or embodiments, such as:

  • Dosage ranges.
  • Formulation details (e.g., extended-release, transdermal).
  • Selection of excipients or delivery devices.
  • Specific patient populations or treatment regimens.

3. Interpretation and Limitations

The claims likely focus on the novelty of the compound or use, with limitations fixed to the chemical structure, specific therapeutic indications, or manufacturing process parameters. These parameters serve to carve out a protective envelope around the invention, balancing breadth with enforceability.


Patent Landscape in Australia

1. Competitor Patentability and Patent Landscape

The Australian patent landscape surrounding this patent involves:

  • Prior Art Search Results: Similar formulations or methods disclosed prior to 2011 may limit claim breadth or enforceability.
  • Regional Patent Filings: Similar patents filed across jurisdictions such as Europe, the US, or other Asia-Pacific countries suggest strategic patenting to block competitors or establish market exclusivity.
  • Crown or Governmental Patents: If the invention stems from publicly funded research, licensing and commercial rights could be affected.

2. Patent Family and Related Applications

AU2011200881 may be part of a broader patent family, complementing applications in other jurisdictions. Such family members can provide global coverage and define the scope of protection beyond Australia. Examination of family members can reveal the variation in claims, scope, and strategic intent.

3. Patent Term and Lifecycle

The patent, filed in 2011, typically has a term expiring around 2031, contingent on patent term adjustments or potential extensions granted in Australia. This delineates the window of market exclusivity and guides R&D and commercialization strategies.


Legal and Commercial Implications

1. Patent Validity and Enforceability

Patent validity depends on novelty, inventive step, and sufficient disclosure. Given the aggressive patenting in the pharmaceutical field, AU2011200881 is likely defensible if it addresses specific chemical modifications or uses not disclosed previously.

2. Potential for Infringement and Licensing

Competitors operating in Australia must carefully analyze whether their products fall within the claims' scope. The patent’s enforceability enables its owner to pursue infringement actions, while licensing negotiations could generate revenue or strategic alliances.

3. Freedom-to-Operate (FTO) Analysis

Prior to commercial launch, companies need to conduct FTO assessments considering AU2011200881 and other relevant patents, especially if involving similar compounds or formulations. Overlap with prior art or claims’ narrow scope may reduce infringement risks.


Strategic Considerations

1. Patent Enforcement and Defense

Regular patent monitoring and legal preparedness are crucial. Should competitors develop similar compounds within the scope of AU2011200881, the patent holder can enforce exclusivity or negotiate licensing arrangements.

2. Competitive Positioning

The strength of the claims and the scope of patent protection influence market strategies. Narrow claims may motivate competitors to Design Around; broad claims provide stronger moat but may face validity challenges.

3. Future Patent Filings

Filing continuation or divisional applications, or pursuing patents on derivatives and new uses, can extend coverage and maintain market dominance.


Conclusion

AU2011200881 embodies a strategic pharmaceutical patent with a scope centered on specific drug formulations, compounds, or methods of use. Its claims, likely meticulously drafted to balance breadth and validity, form a crucial part of the owner’s IP portfolio within Australia's legal framework. Ensuring alignment with patent landscape dynamics, competitor activity, and evolving therapeutic targets remains essential for leveraging the patent’s full value.


Key Takeaways

  • The scope of AU2011200881 primarily hinges on detailed chemical or therapeutic claims—scrutinizing claim language reveals enforceable rights.
  • The patent landscape includes prior art considerations and related family applications, which shape strategic protections.
  • Maintaining enforceability involves vigilant patent monitoring, particularly against potential infringers or workarounds.
  • Broader regional patent strategies through family applications can extend protection but require careful alignment with local statutes.
  • Future patent filings, including continuations or improvements, can sustain competitive advantages and market exclusivity.

FAQs

1. What is the main therapeutic focus of AU2011200881?
While specific claims are needed for full clarity, the patent appears to cover novel drug compounds or formulations targeting particular diseases, likely within the oncology, neurology, or metabolic disorder domains, based on typical patent trends.

2. How broad are the patent claims in AU2011200881?
The claims’ breadth depends on how the independent claims are drafted. Broad claims protect a wide scope of similar compounds or uses, but may face validity issues if challenged, whereas narrow claims are easier to defend but limit coverage.

3. Can this patent be challenged or invalidated?
Yes. Grounds for invalidation include lack of novelty, inventive step, or insufficient disclosure. Prior art searches can identify vulnerabilities or overlaps.

4. How does AU2011200881 compare to patents filed elsewhere?
Its strategic value increases if it is part of an international patent family. Comparing claims and scope across jurisdictions can reveal differences and opportunities for global protection.

5. What is the significance of patent landscaping in this context?
Patent landscaping helps identify overlaps, potential infringers, and innovation gaps, informing R&D, licensing, and litigation strategies.


Sources

  1. Australian Patent Office (AusPat).
  2. World Intellectual Property Organization (WIPO) PATENTSCOPE.
  3. Espacenet Patent Database.
  4. Patent Analytics Reports.
  5. Literature on pharmaceutical patent strategy and law.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.