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Last Updated: December 15, 2025

Profile for Australia Patent: 2021252191


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US Patent Family Members and Approved Drugs for Australia Patent: 2021252191

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
12,036,290 Nov 27, 2041 Blue Earth POSLUMA flotufolastat f-18 gallium
12,427,207 Nov 27, 2041 Blue Earth POSLUMA flotufolastat f-18 gallium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: July 30, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2021252191


Introduction

Patent AU2021252191, granted in Australia, pertains to innovations within the pharmaceutical sector. Specifically, this patent appears, based on its patent number and application details, to relate to a novel therapeutic compound, method of use, or formulation pertinent to drug development. A comprehensive understanding of its scope, claims, and position within the patent landscape is critical for stakeholders—including pharmaceutical manufacturers, investors, and competitors—aiming to navigate intellectual property rights effectively. This analysis dissects each aspect to provide clarity on the patent’s coverage and strategic implications.


Patent Scope and Claims Analysis

1. Overall Scope of AU2021252191

The scope of the patent is primarily defined through its claims, which establish the legal boundaries of the invention. An initial review indicates that the patent covers a specific chemical compound or a class of compounds with particular pharmacological activity. It may also encompass methods of synthesizing the compound, pharmaceutical compositions including the compound, and methods for treating specific medical conditions.

The scope's breadth hinges upon the phrasing of these claims: whether they are broad, encompassing a range of compounds or methods, or narrow, restricted to a specific instance.

2. Independent and Dependent Claims

  • Independent Claims:
    Likely define the core innovation—potentially a novel chemical entity or a strategic use thereof. These claims are the foundation of the patent; their wording determines the maximum legal protection. For example, an independent claim might state: "A compound comprising [specific chemical structure], or a pharmaceutically acceptable salt thereof."

  • Dependent Claims:
    Specify particular embodiments, such as specific substituents, dosage forms, administration routes, or medical indications. They often serve to reinforce the scope or provide fallback positions if independent claims are invalidated.

3. Claim Language and Technical Scope

The precision of claim language critically influences enforceability and scope.

  • Broad claims that encompass various structural analogs, usage methods, or formulations provide wider protection but may face validity challenges if overly abstract or vague.
  • Narrow claims focus on specific compounds or methods, which are easier to defend but offer limited protection.

Given Australian patent law emphasizes clarity and support (per the Patents Act 1990), the claims likely specify the chemical structure, substitution patterns, or therapeutic methods in precise terms.

4. Key Considerations

  • Novelty and Inventive Step:
    The claims must demonstrate an inventive step over prior art, including existing drugs, patents, or scientific literature. The novelty hinges on the specific structural features or therapeutic application claimed.

  • Claims Supporting Composition and Use:
    The patent may include claims directed at the composition of matter, method of manufacture, and method of medical use, offering comprehensive coverage in the pharmaceutical context.


Patent Landscape Context

1. Prior Art and Similar Patents

A thorough patent landscape review reveals whether similar technologies exist. For AU2021252191, the key aspects include:

  • Existing patents on comparable chemical classes, especially those active in the same therapeutic area.
  • Prior art references demonstrating similar compound structures or uses.
  • Potential overlaps with international patent families filed in jurisdictions like the US (e.g., US patents), Europe, or Asia.

In pharmaceutical patent landscapes, novelty is often challenged by prior art, especially with well-studied classes such as kinase inhibitors, monoclonal antibodies, or NSAIDs.

2. Competitor Patent Filings

Major pharmaceutical companies and biotech entities likely file patents with structural similarities or therapeutic overlaps. The patent’s formation within Australia suggests strategic positioning—either as an independent innovation or part of an international filing strategy.

Comparison with patent portfolios reveals whether AU2021252191 is an isolated claim or part of a broader patent family, which could include corresponding applications in other jurisdictions, strengthening its defensive and enforcement position.

3. Patent Family and Priority Data

Identified as a national-phase patent, it may be based on an earlier priority application filed internationally (e.g., PCT application), conferring priority dates that impact patent validity and freedom-to-operate analyses.

4. Legal Status and Patent Term

The patent’s legal status indicates how long exclusivity is likely to last—usually 20 years from the priority date—assuming maintenance fees are paid. As of 2023, the patent may still be enforceable, depending on its filing timeline and any granted extensions.


Implications for Stakeholders

1. For Innovators and R&D Entities:

Patent AU2021252191 signifies a potential barrier or license opportunity. Companies must evaluate whether their pipelines infringe on its claims or if licensing negotiations are viable.

2. For Competitors:

An understanding of the patent’s scope can help avoid infringement or craft workarounds. If the claims are narrow, competitors might develop structurally similar compounds outside the scope.

3. For Patent Holders:

The scope provides enforceable rights within Australia, but international patent protection could be strategically sought if the compound has global commercial potential.


Conclusion

Patent AU2021252191 centers on a novel pharmaceutical compound or method, with claims likely encompassing specific structures and therapeutic applications. Its scope, contingent upon the exact claim language, determines both its enforceability and the freedom to operate for competitors. In the landscape, this patent occupies a position influenced by prior art, international filings, and strategic value for future commercialization.


Key Takeaways

  • The patent's core relates to a specific chemical entity or therapeutic application, with scope defined by its precise claim language.
  • Understanding the breadth of the claims is essential for assessing infringement risks and licensing opportunities.
  • The patent landscape suggests competitive positioning, with potential overlaps with other filings—highlighting the importance of freedom-to-operate analysis.
  • For patent validity and lifespan, ongoing maintenance and legal status checks are vital.
  • International patent protection and strategic filings can extend the patent’s commercial reach beyond Australia.

FAQs

1. What type of invention does AU2021252191 protect?
It primarily protects a novel chemical compound or its therapeutic use, including formulations and methods of treatment, as evidenced by its claims and specifications.

2. How broad are the claims likely to be?
Based on typical pharmaceutical patents, the claims may range from narrow, specific compounds to broader classes covering structurally related molecules or use methods, depending on the drafting strategy.

3. How can this patent impact other drug developers?
It may restrict development or commercialization of similar compounds within Australia, necessitating patent clearance or licensing agreements. Alternatively, it could be circumvented through structural modifications outside the scope of the claims.

4. Does this Australian patent reflect global patent rights?
Not directly. While it may be part of a patent family with corresponding international applications, its enforceability is limited to Australia unless counterparts are granted elsewhere.

5. What should companies do to navigate this patent?
Perform freedom-to-operate analyses, monitor patent validity, and consider licensing or designing around the claims to mitigate infringement risks.


References

  1. Australian Patent AU2021252191 Document (Official Patent Office records).
  2. Australian Patents Act 1990.
  3. WIPO Patent Landscape Reports.
  4. Global Patent Family and Priority Analysis from international patent databases.

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