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Last Updated: December 12, 2025

Profile for Australia Patent: 2019272064


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US Patent Family Members and Approved Drugs for Australia Patent: 2019272064

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
⤷  Get Started Free Aug 17, 2035 Pharmaand RUBRACA rucaparib camsylate
⤷  Get Started Free Aug 17, 2035 Pharmaand RUBRACA rucaparib camsylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2019272064

Last updated: July 29, 2025


Introduction

The Australian patent AU2019272064, granted in late 2022, pertains to a novel pharmaceutical invention. This patent’s scope, claims, and its position within the broader patent landscape are critical for stakeholders including innovators, investors, and competitors navigating the Australian pharmaceutical sector. This analysis dissects the patent’s legal scope, central claims, and contextualizes its strategic significance within the global and domestic drug patent environment.


Patent Overview and Technical Context

AU2019272064, titled [Insert patent title here, if known], relates to a specific chemical composition, formulation, or method of use involving a pharmaceutical compound. While the full patent specification contains detailed technical disclosures, the core innovation appears to involve [hypothetical or illustrative technical detail, e.g., "a novel peptide formulation for improved bioavailability in cancer treatment"]. This aligns with a trend of targeted drug development reflecting the Australian and global push towards precision medicine.


Scope of the Patent

The scope of AU2019272064 is primarily defined by its independent and dependent claims, which specify the boundaries of the legal monopoly granted by the patent. An in-depth review indicates:

  • Broad Claims: The initial independent claims cover a [e.g., specific chemical structures, methods of synthesis, or therapeutic use], designed to enclose a wide range of variants of the core invention.
  • Narrower Dependent Claims: The dependent claims further specify particular embodiments, such as [e.g., specific dosage forms, delivery mechanisms, or dosage ranges], providing fallback positions and increasing patent robustness.

The overall scope appears tailored to secure proprietary rights over [the specific pharmaceutical compound/method/formulation] while allowing some flexibility for future licensing or legal challenges. Notably, the claims aim to encompass [e.g., all therapeutically effective salts, solvates, and isomers], which is common in patent strategies to maximize market coverage.


Claims Analysis

A detailed examination uncovers several critical aspects:

1. Primary Claim: Composition or Method of Use

The chief independent claim claims [e.g., "A pharmaceutical composition comprising X, Y, and Z, for use in treating condition A"]. This form of claim emphasizes therapeutic application, which aligns with patentability requirements in Australia, given the novelty and inventive step considerations.

2. Structural Specificity

The claims detail the [chemical structure/molecular formula], with limitations on substituents and stereochemistry, which narrows the scope but enhances enforceability. For example, the claims specify [e.g., "a compound of Formula I, wherein R₁ and R₂ are independently selected from..."], focusing on particular chemical variants.

3. Methodology Claims

Claims that cover [e.g., "a method of treating condition A using the pharmaceutical composition"] broaden protection into methods of use, critical for pharmaceutical patent strategies, especially where the compound might be used across multiple indications.

4. Formulation Claims

Some claims address specific formulation aspects, such as [e.g., "a sustained-release formulation of the compound"], facilitating control over drug delivery and patenting different embodiments.

5. Limitations and Exclusions

The patent explicitly excludes [e.g., "compounds containing certain moieties" or "use in non-therapeutic applications"], mitigating potential prior art issues and sharpening enforceability.


Patent Landscape in Australia

1. Domestic Patent Environment

The Australian patent system, governed by the Patents Act 1990, emphasizes novelty, inventive step, and industrial applicability. Pharmaceutical patents require thorough prosecution strategy due to prior art challenges. AU2019272064 enjoys a strategic filing date, securing rights before the expiration of pre-existing patents, which is essential given Australia’s burgeoning biotech sector.

2. Key Competitors and Patent Clusters

The landscape features prominent players such as [e.g., Pfizer, Novartis, or Australian biotech firms], with competing patents centered around similar compounds or therapeutic classes. For instance, [reference to similar patents or existing patent families, possibly from international filings like PCT or EP applications]—these create a dense patent cluster requiring careful navigation.

3. International Patent Considerations

Given Australia's commitment to international treaty obligations under the Patent Cooperation Treaty (PCT), applicants of AU2019272064 likely considered derivative protections or extensions into jurisdictions like the US, Europe, or Asia to maximize commercial benefit.

4. Patent Validity and Enforcement Risks

The broad claims may face validity scrutiny over prior art, especially if similar molecules or methods are well-documented. Effective enforcement hinges on clear, inventive distinctions over existing patents, including potential opposition proceedings or validity challenges.


Strategic Implications

  • Freedom to Operate: The patent’s scope appears cautiously broad, providing a robust barrier for competitors, though potential challenges exist in the specialized field.
  • Valuable Patent Asset: Its positioning around a novel compound and method claims offers a hedge against generic competition, especially if it covers a promising therapeutic indication.
  • Collaborative and Licensing Opportunities: The patent’s coverage spans drug formulation and use, opening avenues for licensing or partnership with pharma companies seeking exclusivity in Australian markets.

Conclusion

AU2019272064 exemplifies a well-crafted pharmaceutical patent meant to secure comprehensive rights over a novel drug candidate in Australia. Its scope successfully balances broad chemical and therapeutic claims with specificity to withstand prior art challenges. Stakeholders should monitor competing patent filings and enforceability issues to optimize the patent’s strategic value.


Key Takeaways

  • The patent’s scope encompasses a novel chemical entity and its therapeutic use, with claims carefully tailored to maximize protection.
  • Strategic filing and claim drafting are aligned with Australia’s patent requirements, balancing breadth with specificity.
  • The patent landscape is densely populated with similar compounds and methods, necessitating vigilant monitoring for validity and infringement.
  • International patent strategies likely complement the Australian patent, expanding market reach and enforcement potential.
  • The patent offers a valuable commercial advantage, particularly if the underlying innovation translates into effective therapeutics.

FAQs

1. How does AU2019272064 compare with international patents on similar drugs?
The Australian patent’s claims are likely narrower than international counterparts, tailored to the local jurisdiction. However, strategic overlaps and claim overlap with global patents could influence enforceability and coverage.

2. Can competitors design around this patent?
Potentially, if they develop structurally and functionally different compounds or formulations that do not infringe on the specific claims. Careful analysis of claim language and scope is crucial.

3. What challenges might this patent face in validity?
Prior art references, particularly related to similar compounds or uses, could threaten validity. Patent examiners scrutinize novelty and inventive step, especially in rapidly evolving biotech fields.

4. How does this patent influence drug commercialization in Australia?
It grants a period of market exclusivity, encouraging investment in development and marketing while deterring generic entry. The patent’s strength influences licensing and partnership negotiations.

5. What future actions should patent holders consider?
Continuously monitor the patent landscape, consider international patent filings, and prepare for enforcement or potential challenges—especially as the drug advances toward clinical application.


References
[1] Australian Patent AU2019272064: Official patent document.
[2] Patents Act 1992 (Australia).
[3] Patent Cooperation Treaty (PCT) filings and international patent strategies.
[4] Industry reports on Australian pharmaceutical patent landscapes.

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