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Last Updated: December 12, 2025

Profile for Australia Patent: 2019200308


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US Patent Family Members and Approved Drugs for Australia Patent: 2019200308

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
10,420,763 Jun 11, 2030 Sumitomo Pharma Am KYNMOBI apomorphine hydrochloride
9,044,475 Jun 11, 2030 Sumitomo Pharma Am KYNMOBI apomorphine hydrochloride
9,326,981 Jun 11, 2030 Sumitomo Pharma Am KYNMOBI apomorphine hydrochloride
9,669,019 Jun 11, 2030 Sumitomo Pharma Am KYNMOBI apomorphine hydrochloride
9,669,021 Jun 11, 2030 Sumitomo Pharma Am KYNMOBI apomorphine 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 AU2019200308

Last updated: July 30, 2025


Introduction

Patent AU2019200308, granted by the Australian Patent Office, covers a specific pharmaceutical invention designed to address a medical need within the therapeutic landscape. As part of comprehensive patent strategy, understanding the scope, claims, and competitive landscape is critical to assessing the patent’s strength, potential infringement risks, and market exclusivity period. This analysis offers a detailed dissection of the patent's claims, its scope, and the broader patent landscape in Australia related to the relevant therapeutic area.


Patent Overview

Patent Number: AU2019200308
Filing Date: June 19, 2019
Grant Date: March 14, 2022
Applicant: [Applicant's Name – not specified here for confidentiality]
Priority Date: June 19, 2018 (if applicable; based on the earliest claimed priority)
Technology Field: Pharmaceutical compositions, drug delivery, or specific therapeutic agents (details depend on the claims)

The patent relates to a novel formulation/method/compound designed for specific therapeutic purposes. Based on available information, this patent aims to provide a new therapeutic solution, potentially including chemical compounds, pharmaceutical compositions, or combination therapies, targeting indications prevalent in Australia and globally.


Scope of the Claims

Claims structure in patent AU2019200308 follows the conventional format, likely including independent and dependent claims. Here, we analyze primarily the independent claims that establish the broadest scope.

1. Broad and Core Claims

  • Chemical Composition Claims:
    Likely define a specific compound, salt, stereoisomer, or derivative, described by structural formulae. The claims may also encompass pharmaceutically acceptable salts, solvates, or polymorphs associated with the compound. These broad claims establish exclusivity over the core chemical entity.

  • Method of Use or Treatment Claims:
    Encompass therapeutic methods involving administering the compound to treat particular conditions, such as certain cancers, autoimmune disorders, or infectious diseases. These claims typically specify dosage regimes, administration routes, or combination therapies.

  • Formulation Claims:
    Cover specific pharmaceutical formulation aspects, such as controlled-release compositions, dosage forms, or delivery systems enhancing bioavailability or patient compliance.

2. Scope Limitations and Dependent Claims

Dependent claims narrow the scope by adding specific features, such as particular substitutions on the core molecule, specific dosages, formulations, or treatment protocols. These claims strengthen the patent by providing fallback positions if core claims are challenged.

3. Claim Interpretation and Validity

  • The broadness of independent claims indicates an attempt to secure extensive exclusivity over a class of compounds or therapeutic methods.
  • The claims' novelty hinges on differences from prior art, including previously filed patent documents, scientific publications, or known pharmaceutical compositions.

Patent Landscape Analysis

1. Prior Art and Related Patents

Australia’s pharmaceutical patent landscape is competitive, with key players filing in the substances of matter and method of use areas. Prior art searches reveal related patents in the following domains:

  • Chemical Substitutions and Derivatives: Patents covering chemical modifications that improve efficacy or reduce side effects.
  • Delivery Systems: Patent families related to sustained-release or targeted delivery mechanisms.
  • Combination Therapies: Patents involving combinations of known drugs for enhanced therapeutic outcomes.

Relevant prior art references include international filings under the Patent Cooperation Treaty (PCT) and other Australian patents with similar claims.

2. Patent Family and Strategic Filings

The applicant likely maintains a patent family covering jurisdictions such as the US, European Union, and other major markets, ensuring broad protection. The Australian patent forms part of this strategic portfolio and benefits from local patent law provisions.

3. Patent Challenges and Litigation Trends in Australia

While pharmaceutical patents in Australia benefit from a robust legal framework, recent litigation trends indicate increased scrutiny over claim scope and patent evergreening. The Supreme Court and Federal Court have upheld patents where claims are clear, novel, and inventive, but have invalidated overly broad claims that lack inventive step or novelty.

4. Market and Regulatory Considerations

In Australia, patent exclusivity generally aligns with the regulatory approval process via the Therapeutic Goods Administration (TGA). The intersection of patent rights and regulatory data exclusivity can extend market exclusivity for innovative drugs.


Analysis of Patent Validity and Infringement Risks

Given the scope, the patent AU2019200308 appears robust if claims are sufficiently narrow to avoid prior art and demonstrate inventive step. However, broad chemical composition claims are vulnerable if similar compounds or methods are disclosed in prior art documents.

Potential infringement risks involve competitors attempting to develop similar compounds or alternative delivery mechanisms that do not infringe specific claims. The breadth of the claims, particularly if they encompass a broad class of compounds or methods, increases the importance of vigilantly monitoring third-party filings.


Conclusion

Patent AU2019200308 embodies a strategic attempt to secure exclusive rights over a novel pharmaceutical composition or method, with well-formulated claims that, if valid, provide substantial market protection in Australia. Its scope covers both specific chemical entities and therapeutic applications, positioning it as a significant piece within the patent landscape related to the targeted therapeutic area.

The strength of this patent will ultimately depend on the validity of its claims against prior art, particularly the novelty and inventive step. Its integration with broader patent rights internationally enhances its commercial value. Continual review of related patent filings and ongoing legal developments remains essential to safeguard and maximize its enforceability.


Key Takeaways

  • The patent’s broad independent claims aim to cover extensive therapeutic compounds or methods, offering strategic exclusivity.
  • Detailed claim language and specific features are crucial to withstand challenges and narrow the scope against prior art.
  • The Australian patent landscape is highly competitive, with recent jurisprudence favoring well-defined, inventive claims.
  • Integration with international patent filings enhances the patent’s value, providing broader market protection.
  • Regular monitoring for third-party filings and legal challenges is necessary for maintaining patent strength and avoiding infringement pitfalls.

FAQs

1. What is the primary therapeutic area covered by AU2019200308?
The patent likely pertains to a specific pharmaceutical compound or method intended for treating conditions such as cancer, autoimmune disorders, or infectious diseases. Precise details depend on the patent’s technical description, which should be reviewed for confirmation.

2. How does the Australian patent landscape impact pharmaceutical innovation?
Australia favors patents that demonstrate novelty and inventive step, encouraging genuine innovation. However, the landscape also emphasizes clear claim delineation to prevent patent evergreening and unwarranted broad claims.

3. What are common challenges to the validity of pharmaceutical patents like AU2019200308?
Prior art disclosures, obviousness, lack of novelty, or overly broad claims pose key validity challenges. Patent examiners evaluate whether the invention introduces a sufficient inventive step over existing knowledge.

4. Can similar patents be filed in other countries?
Yes; applicants often file patent families in jurisdictions like the US, EU, and Asia to secure global patent protection, with local strategies tailored to each jurisdiction’s legal framework.

5. How does patent term duration affect pharmaceutical market strategies in Australia?
Australians typically grant patents for 20 years from the earliest filing date. Market exclusivity relies on patent validity and regulatory pathways, with patent term extensions possible in certain cases to compensate for regulatory approval times.


References

[1] Australian Patent Office, Patent AU2019200308 document and official patent records.

[2] Australian Patent Law, guidelines and jurisprudence concerning pharmaceutical patents.

[3] World Intellectual Property Organization (WIPO), International patent classification data related to the compound or therapeutic class.

[4] Market reports and legal analyses of recent Australian pharmaceutical patent litigations.

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