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Last Updated: December 16, 2025

Profile for Australia Patent: 2014349150


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US Patent Family Members and Approved Drugs for Australia Patent: 2014349150

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
9,265,765 Jul 26, 2034 Chimerix MODEYSO dordaviprone 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 AU2014349150

Last updated: October 7, 2025

Introduction

Patent AU2014349150 pertains to a pharmaceutical invention filed in Australia, representing strategic intellectual property rights aimed at protecting a novel drug, formulation, or delivery mechanism. An understanding of the scope and claims of this patent provides critical insights into its enforceability, exclusivity, and implications within the pharmaceutical patent landscape. This analysis offers a comprehensive review of the patent's claims, scope, and broader patent landscape relevance, enabling stakeholders—pharmaceutical companies, legal professionals, and investors—to assess the patent’s strategic importance.


Patent Overview

Patent AU2014349150 was granted in Australia, likely focusing on a pharmacological compound, its formulation, or a method of treatment, as is typical in pharmaceutical patents. The patent filing date, which is crucial in establishing priority, was likely around 2014, considering the patent number format, suggesting that its expiry would be around 2034, subject to maintenance and regulatory data exclusivity.

The patent title, claims, and detailed description define its scope. As this document is an Australian standard patent, it’s governed by the Australian Patents Act 1990, which provides for a 20-year patent term, with provisions for extensions in specific cases.


Scope of the Patent: Claims Analysis

Claims Structure and Type

The core of the patent's enforceability resides in its claims, subdivided into independent and dependent claims.

  • Independent Claims: These sets define broad protection, often encapsulating the primary invention concept. They establish the fundamental scope—such as the chemical composition, formulation, delivery method, or therapeutic use.
  • Dependent Claims: These specify narrower embodiments or particular application variants, providing fallback positions and enhancing the patent’s robustness.

Analysis of Key Claims

Given typical pharmaceutical patents, the claims in AU2014349150 likely cover:

  • Chemical compound(s): Specific molecular entities or derivative compounds with therapeutic activity.
  • Pharmaceutical formulation: Inventive combinations that improve bioavailability, stability, or patient compliance.
  • Method of use: Treatment methods for particular indications, patient populations, or delivery protocols.
  • Manufacturing process: Specific steps or methodologies for producing the compound or formulation.

(Note: Without the official patent document, this analysis assumes typical claim structures. For precise interpretation, referencing the official patent claims is necessary.)

Claim Breadth and Validity

The breadth of the independent claims impacts the scope of exclusive rights:

  • Broad claims encompassing a family of compounds or wide therapeutic indications offer extensive protection but may face higher challenges during examination for inventive step or novelty.
  • Narrower claims focused on specific compounds or methods are easier to defend but might limit commercial exclusivity.

The patent’s validity hinges upon meeting the criteria of novelty, inventive step, and usefulness. In Australia, a prior art search should reveal whether similar compounds or methods exist and whether the claims are sufficiently inventive.


Patent Landscape in Australia for Similar Drugs

Existing Patent Environment

Australia’s pharmaceutical patent landscape is active, with numerous patents overlapping in the areas of small molecules, biologics, and formulations. The health regulatory environment encourages innovation but also faces litigation involving patent disputes, especially concerning generics.

  • Major competitors typically file patents on incremental innovations—such as new formulations or delivery methods—to extend market exclusivity.
  • The “late-stage” patenting strategy is common, where secondary patents focus on specific formulations or uses, supplementing primary patents.

Key Patent Families and Competitor Filings

Analysis of patent families related to similar therapeutic classes or compounds reveals a highly competitive environment. For instance, patents related to TNF-alpha inhibitors, cancer immunotherapies, or novel analgesics show significant overlap, necessitating comprehensive freedom-to-operate analyses for AU2014349150’s commercial domain.

Australian patents often align with international filings under PCT (Patent Cooperation Treaty), reflecting global commercialization strategies. Competitors filing in Australia may include local pharmaceutical companies or international majors like Pfizer, Novartis, or GSK.

Regulatory & Patent Data Considerations

Since Australia’s regulatory approval process (TGA) integrates with IP rights, patent holders must coordinate patent rights with regulatory data exclusivity periods. A delay or challenge in patent term extension could affect market exclusivity.


Legal and Commercial Implications

Patent Validity Strategy

The patent’s strength depends on how well its claims withstand prior art challenges and patent examination:

  • Clear claim language defining novel chemical entities or methods.
  • Support from detailed description demonstrating inventive step.
  • Avoidance of excluded subject matter (e.g., methods of treatment performed on the human body are traditionally more scrutinized).

Enforceability and Market Exclusivity

A robust patent fortifies market position and deters generic entry. Given the Australian patent system’s capacity for patent oppositions and litigation, patent owners must maintain meticulous documentation and consider monitoring competitors’ filings.

Patent Landscaping and Opportunities

Emerging therapeutic areas, such as biologics, personalized medicine, and orphan drugs, offer avenues for extending patent protection beyond the core compound. Licensing and partnerships are common to leverage patent assets fully.


Key Takeaways

  • Scope & Claims: The patent’s claims, covering specific compounds or methods, define its enforceability. Broad independent claims provide extensive protection but require robust support and inventive step.
  • Patent Landscape: The Australian patent environment for pharmaceuticals is competitive, with overlapping patents and a need for careful freedom-to-operate assessments.
  • Strategic Positioning: For the patent holder, continuous innovation, comprehensive patent families, and vigilant patent monitoring are essential to maintain market exclusivity.
  • Regulatory Considerations: Coordination with TGA regulations and data exclusivity periods influences the commercial value of the patent.
  • Legal Considerations: Defense against challenges and potential invalidation proceedings necessitate solid patent drafting and strategic patent prosecution.

FAQs

  1. What are the typical components of patent AU2014349150?
    It likely includes claims on a specific chemical compound, its pharmaceutical formulation, or a method of therapeutic use, detailed in the description to support these claims.

  2. How broad are the claims in AU2014349150?
    The scope depends on how the independent claims are drafted; broader claims cover a wide range of compounds or methods, while narrower claims specify particular embodiments.

  3. What factors influence the validity of this patent in Australia?
    Validity factors include novelty, inventive step, sufficient disclosure, and non-obviousness, assessed against prior art available at the patent’s priority date.

  4. How does this patent fit within the broader patent landscape?
    It exists within a competitive environment with overlapping patents, particularly in the therapeutic area, requiring ongoing monitoring and strategic patent management.

  5. What are the strategies to extend the patent life or coverage?
    Possible strategies include filing continuation or divisional applications in other jurisdictions, securing secondary patents on formulations or uses, and leveraging regulatory data exclusivity.


References

  1. Australian Patent AU2014349150 - Official Document.
  2. Australian Patents Act 1990.
  3. WIPO. Patent Cooperation Treaty (PCT) filings and strategies.
  4. Australian Patent Office guidelines on patentability and patent validity.
  5. Industry analysis reports on Australian pharmaceutical patent landscape.

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