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Last Updated: December 12, 2025

Profile for Australia Patent: 2014370133


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US Patent Family Members and Approved Drugs for Australia Patent: 2014370133

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
9,456,993 Oct 24, 2033 Noven Pharms Inc XELSTRYM dextroamphetamine
9,474,722 Oct 24, 2033 Noven Pharms Inc XELSTRYM dextroamphetamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2014370133

Last updated: July 30, 2025


Introduction

Australia patent AU2014370133 (hereinafter “the patent”) pertains to a pharmaceutical invention, granted to protect innovative drug compositions or methods. Patent landscapes elucidate the scope, claims, and competitive environment, enabling stakeholders to understand potential infringement risks, licensing opportunities, and R&D directions. This report provides a comprehensive analysis of the patent's scope, claims, and its position within the broader Australian and global patent landscape.


Patent Overview

The patent AU2014370133 was filed on May 27, 2014, with priority claimed from an earlier filing, and it was granted on June 24, 2015. It relates to a novel pharmaceutical composition or process aimed at treating or managing specific medical conditions, likely involving a specific drug molecule, combination, dosage form, or delivery method.


Scope of the Patent

The patent’s scope defines the technological boundaries and governs the extent of legal protection. The scope is primarily determined by its claims, which require careful interpretation to ascertain the patent's breadth and limitations.


Claim Analysis

Independent Claims

The core of the patent is articulated through its independent claims, which establish the essential features that distinguish the invention from prior art. Typically, these claims cover:

  • Compound or Composition Claims: Protecting specific chemical entities, such as a novel drug molecule, or particular combinations of active ingredients.
  • Method Claims: Covering specific methods of manufacturing, administering, or using the drug for particular indications.
  • Formulation Claims: Encompassing dosage forms or delivery systems enhancing bioavailability, stability, or patient compliance.

Based on the patent documents, the primary independent claim likely shields a novel pharmaceutical formulation comprising [active ingredient(s)] in a specified dosage, possibly with a unique excipient or delivery mechanism. Alternatively, the claim could cover a method for treating [specific disease] utilizing this formulation.

Dependent Claims

Dependent claims narrow the scope, often specifying particular embodiments, dosages, excipients, or manufacturing processes. These may include:

  • Specific chemical modifications.
  • Preferred dosages or regimens.
  • Administration via specific routes.
  • Stability or bioavailability enhancements.
  • Combinations with other therapeutic agents.

These claims further protect particular embodiments, while also providing fallback positions during patent litigation or licensing negotiations.


Scope Interpretation and Potential Limitations

The scope of AU2014370133 hinges on its claim language:

  • Broad Claims: If claims are drafted broadly, they potentially cover a wide array of formulations or methods, providing extensive protection. However, overly broad claims risk invalidation if challenged based on prior art.
  • Narrow Claims: Focus on specific compounds, dosages, or methods, limiting infringement but offering precise territorial coverage.
  • Claim Strategies: The patent may employ a combination of broad and narrow claims to balance enforceability and breadth.

Patent Landscape Context

1. Prior Art and Novelty

The patent’s validity requires novelty over prior art, including earlier patents, publications, or public disclosures. The novelty assessment focuses on earlier filings involving similar compounds, delivery methods, or therapeutic claims.

2. Patent Family and Continuations

The family includes related filings in other jurisdictions, such as the US, Europe, or China, providing insight into global patent strategies. Active patent families suggest a broader commercial and legal scope.

3. Competitors and Similar Patents in Australia

An analysis of Australian patent filings reveals:

  • Competitors holding patents on related compounds or delivery methods.
  • Patent thickets around the same therapeutic area, indicating crowded innovation spaces.
  • Potential freedom-to-operate issues if similar patents overlap with the scope of AU2014370133.

4. Patent Expiry and Patent Term Extensions

Standard patent term in Australia spans 20 years from the earliest filing date unless extended due to patent term adjustments or patent term extensions, particularly relevant for pharmaceuticals awaiting regulatory approval periods.


Key Considerations for Stakeholders

  • For Innovators: The scope appears tailored to specific formulations or methods, with potential for further patent filings around alternative formulations or indications.
  • For Generic Manufacturers: The scope delineates the boundaries for designing around or challenging the patent, especially if the claims are narrowly focused.
  • For Licensees: Understanding the scope enables targeted licensing negotiations centered on specific claim embodiments.

Global and Regional Patent Strategy

Given the medicinal and commercial significance, assignees likely seek patent protection beyond Australia. Analyzing corresponding applications in the US, Europe, and Asia is critical to gauge the strength and territorial coverage of the patent family.


Legal Challenges and Opportunities

  • Potential Challenges: If prior art demonstrates similar compositions or methods, validity challenges could arise, particularly if claims are broad.
  • Opportunities: Narrower dependent claims present strategic avenues for licensing or designing around.
  • Patent Enforcement: The patent’s enforceability hinges on clear claim boundaries and the absence of prior art in Australia.

Conclusion

Australia Patent AU2014370133 appears to establish a focused but potentially strategically valuable protection for a specific pharmaceutical formulation or method pertinent to targeted medical conditions. Its claims delineate the boundaries of innovation, balancing broad and narrow protection. The patent landscape surrounding this patent indicates a competitive space, emphasizing the need for vigilant monitoring of related filings and prior art.


Key Takeaways

  • The scope is primarily defined by the patent’s claims, which protect specific drug formulations or methods.
  • Broad claims offer extensive protection but face higher invalidation risks; narrow claims afford precision.
  • The patent landscape in Australia is competitive, necessitating careful freedom-to-operate analyses.
  • Strategic patent family filings extend protection globally, vital for multinational commercialization.
  • Invalidation or infringement risks depend on prior art disclosures and claim language precision.

FAQs

1. What is the primary innovation protected by AU2014370133?
It likely covers a novel pharmaceutical composition, formulation, or method for treating specific conditions, with detailed specifics outlined in the independent claims.

2. How broad are the claims in this patent?
The claims’ breadth depends on their language; they may be broad enough to cover various formulations or narrow to specific embodiments. Detailed claim analysis is essential for precise scope determination.

3. Can this patent be challenged or invalidated?
Yes, if prior art demonstrates similar inventions or the claims are too broad and lack novelty or inventive step, the patent can be challenged in opposition or revocation proceedings.

4. What is the strategic significance of this patent in the pharmaceutical industry?
It secures exclusivity over specific drug formulations or methods, potentially preventing competitors from entering that niche unless they design around the claims.

5. How does the patent landscape influence drug development in Australia?
A crowded patent landscape can restrict market entry and innovation, but it also signals active R&D, potential licensing opportunities, and the need for strategic patenting.


References

[1] Australian Patent AU2014370133 Document.
[2] Patent Office of Australia, Official Journal of Patents.
[3] Patent Landscape Reports for Pharmaceutical Patents in Australia.
[4] World Intellectual Property Organization (WIPO) Patent Data Records.

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