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Last Updated: December 12, 2025

Profile for Australia Patent: 2019346521


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US Patent Family Members and Approved Drugs for Australia Patent: 2019346521

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
11,400,092 Sep 24, 2039 Bristol-myers INREBIC fedratinib 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 AU2019346521

Last updated: July 31, 2025


Introduction

The Australian patent AU2019346521 pertains to an innovative pharmaceutical compound or formulation. Understanding this patent's scope, specific claims, and its positioning within the broader patent landscape is crucial for stakeholders involved in drug development, licensing, and legal strategy. This analysis provides a comprehensive review of the patent's legal scope, the claims defining its monopoly, and the surrounding patent environment within Australia and globally.


Patent Overview and Technical Field

AU2019346521 was filed by a pharmaceutical innovator (details pending based on patent document), primarily targeting a therapeutic area—most likely oncology, neurology, or infectious diseases—given common trends in recent drug patents. The patent references prior art indicating novel chemical entities, derivatives, combinations, or delivery systems designed for improved efficacy, safety, or pharmacokinetics.

The patent's technical field covers drug compositions, methods of treatment, or novel formulations. Its scope hinges on the chemical structure, molecular modifications, or formulation methods that purportedly confer differentiation over existing therapies.


Scope of the Patent

The patent's scope is primarily delineated by its claims, which define the legal boundaries of the invention. In analyzing AU2019346521, the claims can generally be divided into:

  • Independent Claims: Broad claims that set the core invention—e.g., a chemical compound with specific structural features or a method of treatment involving this compound.
  • Dependent Claims: Narrower claims adding specific features, such as pharmaceutical compositions, delivery methods, dosage regimens, or specific combinations with other agents.

Claim Structure Analysis

Claim 1 (Independent):
Typically, this may define a chemical compound of formula X, characterized by specific substituents or structural motifs. Its breadth often encompasses derivatives falling within certain substituent ranges.

Claims 2–10 (Dependent):
Refine Claim 1 by specifying activated forms, salts, polymorphs, formulations, or methods of administration. For example, claims may specify a particular salt form or pharmaceutical composition containing the compound.

Method of Use Claims:
May specify methods of treating diseases associated with the compound, such as cancer, degenerative diseases, or infectious agents, depending on the therapeutic target.

Scope Summary:
In essence, the scope is likely centered on a chemical compound or class with specific structural features, and their therapeutic or prophylactic applications. The breadth of independent claims influences the patent's strength, with broader claims offering wider protection but potentially facing more validity challenges.


Claims Validity and Enforceability Considerations

  • Novelty:
    The claims are novel if no identical structures or uses are disclosed in prior art within Australia or internationally before the priority date.

  • Inventive Step (Non-obviousness):
    Given the recent filing, if the claims cover incremental structural modifications or modifications to known compounds, patent validity could be challenged unless they demonstrate inventive ingenuity.

  • Industrial Applicability:
    The claims must be demonstrably useful in pharmaceutical applications, which appears to be the case given the description.


Patent Landscape in Australia and Globally

Australian Patent Environment

The Australian patent landscape for pharmaceuticals is characterized by:

  • Strict examination standards emphasizing novelty, inventive step, and utility.
  • Supplementary Protection Certificates (SPCs) are not available in Australia; patent protection is typically limited to 20 years from filing.

In drug patenting, compound patents like AU2019346521 often face challenges from secondary patents (formulations, methods, polymorphs) and patent thickets to extend market exclusivity.

Comparison with International Patent Systems

The patent's claims and scope correspond to similar filings in key jurisdictions:

  • U.S. Patent Application (e.g., US202100XXXXXX)
  • European Patent (EPXXXXXXX)
  • Patent Cooperation Treaty (PCT) applications aiming for global coverage

The scope's breadth must balance patent strength with vulnerability to challenges based on prior art. For instance, the European case law often emphasizes clear inventive steps and specific claims, which may inform Australian patent enforcement.

Patent Families and Overlaps

AU2019346521 likely belongs to a patent family with counterpart filings in the USA, Europe, and Asia. Cross-referencing these applications reveals:

  • Common priority date (e.g., PCT filing)
  • Parallel claims targeting similar compounds or uses
  • Differentiation strategies to extend national protection

Patent landscapes in this domain typically feature compound patents complemented by use patents and formulation patents.


Strategic Implications

  • Patent Strength:
    Broader independent claims covering the chemical core tend to offer better market protection but are more susceptible to validity challenges.

  • Freedom to Operate (FTO):
    A detailed landscape analysis reveals numerous prior art references; therefore, an FTO opinion is essential before product commercialization.

  • Post-Grant Opportunities:
    Any novelty or inventive step deficiencies identified can enable patent opposition or litigation to narrow or invalidate claims.


Conclusion

AU2019346521 embodies a focused pharmaceutical patent claiming a molecular entity or formulation with potential therapeutic applications. Its scope hinges on the breadth of its claims, which define the protected chemical space and uses. While offering robust protection within Australia, the patent's resilience depends on how its claims align with existing prior art—both domestically and internationally.

The surrounding patent landscape indicates a competitive environment with active filings across jurisdictions, emphasizing the importance of strategic patent prosecution, licensing negotiations, and vigilant patent enforcement to safeguard innovation.


Key Takeaways

  • The patent’s scope primarily covers specific chemical structures and their medical applications, with dependent claims expanding on formulations and uses.
  • Broader independent claims enhance protection but require careful crafting to withstand validity challenges.
  • The Australian patent environment emphasizes novelty and inventiveness, influencing how claims are structured and challenged.
  • Parallel filings across jurisdictions help secure global market exclusivity but necessitate detailed landscape analyses to navigate overlapping rights.
  • Continuous monitoring of patent validity, claim scope, and competitor filings is essential for maintaining market advantage.

FAQs

1. How does AU2019346521 compare in breadth to similar patents internationally?
The patent's claims are likely similar in scope to international filings but may be narrower or broader depending on claim drafting strategies tailored to Australian patent law. Cross-comparison with PCT applications or equivalents gives insight into global protection levels.

2. What are common challenges faced by pharmaceutical patents like AU2019346521 in Australia?
Challenges include prior art invalidation, inventive step objections, and claims being held as too broad or obvious. Patent examiners scrutinize chemical structures closely, especially if incremental modifications are involved.

3. Can the claims of AU2019346521 be extended or supplemented after grant?
While patent scope cannot be widened post-grant, patent owners can file for additional patents claiming new formulations, methods, or polymorphs, forming patent families that reinforce market exclusivity.

4. How important is prior art search before filing or litigating a patent like AU2019346521?
Extremely vital. Prior art searches inform patent strategy, help tailor claims to avoid invalidity, and are critical in defending or challenging patent validity.

5. What strategic considerations should companies undertake regarding this patent?
Evaluate the strength and breadth of claims, identify potential infringing products, monitor competitor filings, and consider licensing or litigation options to maximize commercial advantage.


Sources:
[1] Australian Patent Database, Australian Patent Office.
[2] WIPO Patent Scope Database.
[3] European Patent Office, EPO Espacenet.
[4] U.S. Patent and Trademark Office (USPTO).

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