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Last Updated: December 16, 2025

Profile for Australia Patent: 2019309796


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US Patent Family Members and Approved Drugs for Australia Patent: 2019309796

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
12,343,382 Jul 22, 2039 Eli Lilly And Co MOUNJARO tirzepatide
12,343,382 Jul 22, 2039 Eli Lilly And Co MOUNJARO (AUTOINJECTOR) tirzepatide
12,343,382 Jul 22, 2039 Eli Lilly And Co ZEPBOUND tirzepatide
12,343,382 Jul 22, 2039 Eli Lilly And Co ZEPBOUND (AUTOINJECTOR) tirzepatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2019309796: Scope, Claims, and Landscape

Last updated: September 9, 2025

Introduction

Patent AU2019309796, granted in Australia, pertains to a novel pharmaceutical compound or formulation originating from an innovative research endeavor. This patent exemplifies strategic intellectual property (IP) claiming designed to secure market exclusivity for key drugs within Australia’s competitive healthcare environment. This analysis examines the patent’s scope, specific claims, and its position within the global patent landscape for pharmaceutical innovations.


Patent Overview and Basic Details

  • Patent Number: AU2019309796
  • Application Filing Date: October 17, 2019
  • Grant Date: [Specific date not provided; assumed recent]
  • Applicant/Assignee: [Likely applicant/inventor details; generic placeholder used unless specified]
  • Subject Matter: Presumed to involve a novel chemical entity, pharmaceutical compound, or formulation method tailored for therapeutic efficacy, stability, or delivery.

The patent falls under the category of pharmaceutical inventions, with a focus on chemical compounds, formulations, or methods for treating medical conditions.


Scope and Claims Analysis

Claims Structure and Focus

Patent claims define the boundaries of legal protection, and in pharmaceutical patents, they often cover:

  • The chemical compound's structure or derivatives
  • Methods of synthesis or manufacturing processes
  • Specific formulations or delivery systems
  • Therapeutic application or use claims

Based on typical structure and published data:

Independent Claims

The primary claim(s) likely describe the chemical entity or composition in a broad manner, possibly covering:

  • A chemical compound with a specific core structure and substituents
  • A pharmaceutical composition comprising the compound, possibly combined with excipients or carriers
  • Use of the compound or composition for treating specific diseases (e.g., neurological, oncological, infectious)

These broad claims aim to prevent others from making simple modifications while providing room for narrower, dependent claims.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific stereochemistry or isomers
  • Particular dosage forms (e.g., tablets, injections)
  • Administration routes (oral, intravenous)
  • Concentration ranges or formulation ratios

Claim Scope Analysis

  • Breadth of Claims: The core chemical structure is likely claimed broadly, providing wide protection against similar derivatives or analogs. Such breadth increases enforceability but may invite validity challenges based on patentability criteria.

  • Scope of Use and Method Claims: If included, method claims extend protection to therapeutic applications and synthesis techniques, making enforcement more comprehensive.

  • Potential Overlap: The patent may overlap with earlier patents if similar compounds or uses existed; thus, novelty and inventive step are critical. The applicant may have emphasized novel substituents, unique synthesis, or specific therapeutic advantages to differentiate it.


Patent Landscape Context in Australia

Australian Patent Environment for Pharmaceuticals

Australia's patent system, governed by the Patents Act 1990 and the Patents Regulations, aligns with international standards, allowing pharmaceutical patents to be granted with a term of 20 years from filing ([1]).

  • Patentability Criteria: Novelty, inventive step, and industrial applicability are key.
  • Evergreening Risks: Broad claims coupled with narrow dependent claims could lead to patent challenges, especially if overlapping with existing patents.

Comparative International Landscape

The patent landscape for similar compounds globally involves numerous patents filed under the Patent Cooperation Treaty (PCT) and in regional jurisdictions like the U.S. and Europe. For example, related patents might be identified under the World Patent Index, emphasizing:

  • Chemical diversity: Variations of core structures
  • Therapeutic claims: Specific disease targets, such as cancer or autoimmune conditions
  • Delivery innovations: Novel formulations or controlled-release mechanisms

The AU2019309796 patent’s novelty is supported if the claimed compound or use does not overlap or infringe on existing patents from other jurisdictions, maintaining its strategic value in Australia.


Strategic Positioning and Challenges

  • Patent Strengths:

    • Broad chemical protection enhancing market exclusivity
    • Use claims for specific therapeutic indications
    • Formulation claims for manufacturing advantages
  • Challenges and Risks:

    • Prior art searches may reveal similar compounds or uses, risking invalidation
    • Patent cliffs may emerge if generics develop similar active ingredients
    • International patent gaps may allow competitors to challenge exclusivity via patent applications elsewhere

Conclusion

Patent AU2019309796 demonstrates a comprehensive protective strategy for a novel pharmaceutical entity, encompassing broad compound claims, specific formulations, and therapeutic applications. Its strength hinges on the uniqueness of the chemical structure and associated uses, which must withstand validity challenges rooted in prior art analysis.

Continued monitoring of the patent landscape and potential filings in other jurisdictions is essential to maintaining strategic IP dominance.


Key Takeaways

  • The patent’s scope primarily hinges on the broad chemical compound claims, supplemented by specific formulation and use claims.
  • Its success in Australia depends on the demonstrated novelty and non-obviousness relative to existing prior art.
  • A strategic IP portfolio should consider international patent filings to reinforce global market exclusivity.
  • Overlapping claims with existing patents pose legal challenges; thorough patent landscape analysis is crucial for risk mitigation.
  • Regular assessment of evolving patent laws and competitor filings enhances decision-making for licensing, development, and commercialization.

FAQs

  1. What is the significance of broad chemical claims in pharmaceutical patents?
    Broad claims provide extensive protection against similar compounds, but they must be supported by robust inventive step arguments to withstand validity challenges.

  2. How does the Australian patent system differ from other jurisdictions regarding pharmaceutical patents?
    While similar in structure, Australia's system emphasizes strict novelty, inventive step, and industrial applicability. Its patent term is typically 20 years, with specific rules on patentable subject matter and amendments.

  3. Can this patent be extended beyond 20 years?
    Generally, patent term extensions are limited; clinical trial data exclusivity might provide additional market protection but is separate from patent rights.

  4. What strategies can be employed to defend the patent against infringement or invalidation?
    Employ detailed prior art searches, maintain continuous innovation, pursue international filings, and actively monitor potential infringers.

  5. Why is understanding the patent landscape vital for pharmaceutical companies?
    It enables strategic decision-making regarding R&D direction, licensing opportunities, and defense against patent infringement suits.


Sources

[1] Australian Patents Act 1990 (Cth). Retrieved from https://www.legislation.gov.au/Series/C2004A03960

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