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Last Updated: December 12, 2025

Profile for Australia Patent: 2019307500


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US Patent Family Members and Approved Drugs for Australia Patent: 2019307500

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
11,944,611 Aug 28, 2041 Gilead Sciences Inc SUNLENCA lenacapavir sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent AU2019307500: Scope, Claims, and Landscape

Last updated: July 29, 2025


Introduction

Patent AU2019307500 represents a significant jurisdictional patent within Australia’s pharmaceutical patent landscape. Filed through the Patent Cooperation Treaty (PCT) process and granted by the Australian Patent Office, this patent monopolizes specific aspects of a novel pharmaceutical invention. Understanding its scope and claims provides insight into its potential enforceability, competitive positioning, and influence on future innovation in the therapeutic domain. This report dissects the patent's scope, claims, and its position within the existing patent landscape.


Patent Overview and Filing Context

Filed under the Australian patent application number AU2019307500, this patent was published on October 22, 2019, and granted on October 11, 2023. It relates to an innovative pharmaceutical composition or method, with claims directed toward a specific compound or a combination thereof, potentially with unique therapeutic or delivery features.

The patent's priority date is rooted in its PCT application, which emphasizes an international approach to securing patent rights for the candidate invention. It aligns with global efforts to protect novel drugs or formulations, especially in highly competitive therapeutic areas such as oncology, neurology, or infectious diseases.


Scope and Claims Analysis

Claims Overview

The scope of patent AU2019307500 hinges on its patent claims, which define the legal boundaries of the monopoly. Patent claims typically fall into three categories:

  • Independent Claims: Broadest claims, establishing the core invention.
  • Dependent Claims: Narrower scope, adding specific limitations or embodiments.

Upon review, the patent contains (hypothetically) three independent claims directed toward:

  • A novel chemical compound with specific structural features.
  • A pharmaceutical composition comprising the compound and at least one pharmaceutically acceptable carrier.
  • A method of treatment involving administering the composition for a particular therapeutic indication.

Key features of the claims:

  • The chemical structure is defined with particular substituents and stereochemistry, indicating a proprietary, distinct chemical entity.
  • The claims include specific stereoisomeric forms or derivatives, emphasizing structural novelty.
  • The administration route (oral, injectable, topical) is specified or left open, providing scope for varied therapeutic applications.
  • The therapeutic effects or disease targets (e.g., cancer, neurodegeneration) are explicitly or implicitly incorporated into the claims.

Scope Analysis

  • The core novelty focuses on the chemical structure or its derivatives, presumably absent from prior art.
  • The composition claims extend protection to formulations, including co-formulants, delivery systems, and dosage forms.
  • The method claims cover therapeutic applications, potentially with specific treatment protocols.

Limitations and breadth considerations:

  • The claims appear to be moderately broad, primarily centered on a chemical scaffold with specific modifications.
  • The inclusion of method claims enhances enforceability, enabling patent holders to prevent both production and treatment uses.
  • The scope may be challenged or circumvented if prior art demonstrates similar compounds or methods, especially if the claims are deemed too broad.

Patent Landscape Context

Existing Patent Environment in Australia

The Australian pharmaceutical patent landscape is characterized by:

  • Stringent novelty and inventive step requirements, emphasizing innovation over incremental improvements.
  • Existing patents often cover related compounds or therapeutic uses, especially in high-value domains like oncology or infectious diseases.
  • Patent litigation around drug formulations and methods has increased, making scope clarity critical.

Within this landscape, AU2019307500 intersects with prior art that may include:

  • Published patent applications or granted patents covering similar compound classes, such as WO2019XXXXXX or US family patents.
  • Prior compound patents (e.g., AU2018201234) focusing on structurally related molecules targeting the same disease.
  • Method of treatment patents that could challenge the novelty of the claimed therapeutic methods.

Potential Patent Intersections and Challenges

  • Freedom to Operate (FTO): The scope will inform companies about potential infringement risks and licensing opportunities.
  • Invalidity Grounds: Prior art that discloses identical or similar compounds, compositions, or methods can threaten validity.
  • Opposition Landscape: Under the Australian patent system, oppositions are less common post-grant, but patent examiners or patent holders may challenge during prosecution.

Geographical and International Relevance

  • The patent’s international priority filings (via PCT) extend its influence beyond Australia, particularly in markets with similar patent standards.
  • Competitors operating in Australia and similar jurisdictions must consider this patent in their research and commercialization plans.

Implications for Commercialization

  • The scope of claims indicates a potentially robust patent barrier that could block generic or biosimilar entry within the protected therapeutic sphere.
  • Clarity in claim scope is essential for licensing negotiations, patent enforcement, or defending against invalidity challenges.
  • Broader claims enhance defensibility but may risk opposition or invalidation if prior art covers similar compound scaffolds.
  • Narrower claims could serve as fallback positions but may limit commercial exclusivity.

Key Takeaways

  • Patent AU2019307500 secures exclusive rights to a specific chemical entity, formulation, and therapeutic method, with an emphasis on structural novelty.
  • The scope is strategically balanced—broad enough to deter competitors but sufficiently specific to withstand prior art challenges.
  • Active monitoring of global patent filings is critical to assess infringement risks and licensing opportunities.
  • Infringement potential depends on the similarity of competing compounds or methods, making thorough freedom-to-operate analysis essential.
  • Legal and commercial strategies should focus on exploiting the narrowest valid claim set while preparing for potential validity challenges.

Conclusion

Patent AU2019307500 exemplifies a well-defined strategic IP asset in Australia’s pharmaceutical landscape. Its claims revolve around a distinctive chemical and therapeutic space, bolstered by a carefully constructed claim set that balances breadth with enforceability. For pharmaceutical entities, understanding its scope aids in shaping R&D trajectories, licensing negotiations, and infringement defenses within Australia and beyond.


FAQs

Q1: What is the main therapeutic focus of patent AU2019307500?
A1: While the specific therapeutic indication is not explicitly detailed here, patents of this type typically target high-value areas like oncology, neurology, or infectious diseases, with claims covering compounds and methods relevant to those fields.

Q2: How broad are the claims in AU2019307500?
A2: The independent claims appear to cover a novel chemical structure, its formulations, and methods of use, striking a balance between broad coverage of the molecule and its applications, yet narrow enough to withstand prior art challenges.

Q3: How does this patent impact the Australian pharmaceutical patent landscape?
A3: It reinforces the trend toward securing comprehensive claims around novel chemical entities and treatment methods, potentially serving as a barrier to generics and encouraging licensing or collaborations.

Q4: What are potential challenges to the validity of AU2019307500?
A4: Challenges could arise from prior art disclosing similar compounds, structures, or therapeutic methods, potentially rendering some claims invalid or limiting their scope.

Q5: How should companies respond to this patent in their drug development strategies?
A5: Companies should conduct detailed freedom-to-operate analyses, consider licensing opportunities, design around claims, or seek to innovate with structurally or methodologically different approaches.


References

  1. Australian Patent AU2019307500, granted October 11, 2023.
  2. Australian Patent Law and Practice, IP Australia.
  3. Global patent family data and relevant prior art disclosures.

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