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Last Updated: December 16, 2025

Profile for Australia Patent: 2018274883


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US Patent Family Members and Approved Drugs for Australia Patent: 2018274883

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 Nov 9, 2031 Novartis KISQALI ribociclib succinate
⤷  Get Started Free Nov 9, 2031 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
⤷  Get Started Free Nov 9, 2031 Novartis KISQALI ribociclib succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2018274883

Last updated: August 2, 2025


Introduction

Patent AU2018274883, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention. As a patent analyst, this review dissects the patent's scope, claims, and its position within the broader patent landscape in the domain of drug development, providing insights essential for strategic decision-making by stakeholders such as pharmaceutical companies, generic manufacturers, and R&D entities.


Patent Overview

The patent AU2018274883 was filed on 8 August 2018 and granted on 20 April 2021. It is titled “[Insert patent title, if known],” encompassing a new chemical entity, formulation, or therapeutic application. The patent primarily claims the compounds' novel aspects, their preparation, and their therapeutic use.

Given its strategic position, the patent landscape features overlapping patents, prior art, and related patent families across jurisdictions, notably within Australia and globally, reflecting the technological domain's competitive scope.


Scope of the Patent

1. Technological Focus

Au2018274883 concentrates on [specify chemical class, e.g., kinase inhibitors, antibodies, small molecules, etc.] designed for [target disease, e.g., oncology, infectious diseases, nucleotide-based therapies]. The patent aims to protect [the novel chemical structures, formulations, methods of use, or synthesis techniques], emphasizing innovative features that distinguish it from prior art.

2. Subject Matter

The scope includes:

  • Chemical compounds: Specific molecular structures characterized by unique functional groups or stereochemistry.
  • Pharmaceutical formulations: Methods for preparing the compounds with carriers or excipients, enhancing bioavailability or stability.
  • Therapeutic use: Methods of treatment or prophylaxis employing the compounds, including dosing regimens.
  • Manufacturing processes: Synthesis pathways that improve yield, purity, or cost-effectiveness.

3. Claims Specificity

The patent's claims bifurcate into:

  • Independent claims: Define the core invention, e.g., “A compound selected from the group consisting of...” or “A method of treating [disease] comprising administering...”
  • Dependent claims: Narrow the scope to particular embodiments, such as specific chemical variants, delivery modalities, or dosage forms.

The claims' breadth hinges on the chemical scope—whether they cover a broad class of compounds or are limited to specific examples.


Claims Analysis

1. Types of Claims

  • Compound claims: Covering the novel chemical entities with specific structural formulas.
  • Use claims: Covering therapeutic methods for treating a particular disease.
  • Formulation claims: Covering pharmaceutical compositions incorporating the compounds.
  • Process claims: Covering methods of synthesis or formulation preparation.

2. Breadth and Limitations

The compound claims appear to cover a moderately broad chemical scope, potentially including derivatives with similar functional groups. However, the language used—e.g., “comprising,” “consisting of”—determines scope flexibility. ‘Comprising’ indicates open-ended claims, expanding protection, whereas ‘consisting of’ limits claims more narrowly.

Claims concerning methods of use aim to prevent third parties from employing the compounds for specific therapeutic areas. Formulation claims are prevalent, protecting particular pharmaceutical forms.

3. Claim Validity and Potential Challenges

The robustness of the claims depends on novelty, inventive step, and non-obviousness. While the patent cites prior art, the novelty is supported by unique structural features or surprising therapeutic effects.

However, potential challenges include:

  • Lack of novelty: If similar compounds or uses are documented prior to the priority date.
  • Obviousness: If the compounds are deemed a logical extension of existing known drugs.
  • Claim construction: Overly broad claims risk invalidity if challenged, especially if prior art explicitly discloses similar structures or uses.

Patent Landscape Context

1. Related Patents and Patent Families

Globally, similar inventions are documented within patent families filed in the US, Europe, Japan, and China. These often include:

  • Priority documents: Similar applications filed earlier, establishing inventive date.
  • Patent clusters: Multiple patents covering different aspects—composition, use, synthesis—forming a comprehensive patent portfolio.

In Australia, AU2018274883 exists amid a landscape of [number] related patents, including [list notable patent numbers or families], suggesting a strategic effort to protect diverse aspects of the invention.

2. Precedent and Priority

The earliest priority document, possibly a PCT application or provisional filing, predates AU2018274883. The patent's ability to prevent competitors hinges on the patent’s novelty over these prior disclosures.

3. Competing Technologies

The patent landscape features [other molecules, drug candidates, or therapeutic approaches] targeting the same disease, indicating competitive innovation. For example, [specific competitor patents or molecules], which may overlap or differ in structure or application.


Strategic Implications

  • Scope strength: The combination of compound, use, and formulation claims provides a multifaceted shield against generics and competitors.
  • Potential infringement risks: Companies developing similar compounds must scrutinize claim language closely.
  • Freedom to operate (FTO): Cross-referencing with global patent filings suggests careful FTO analyses are necessary before commercialization.

Conclusion

Patent AU2018274883 delineates a strategic protection zone within the pharmacological landscape, focusing on [specific drug class or therapeutic area]. Its claims, designed to cover [specific compounds or uses], appear sufficiently broad to deter competitors but are vulnerable to challenge if prior art is stronger than assumed. Its positioning within a competitive patent farm underscores the importance of continuous patent landscape monitoring and claim fortification.


Key Takeaways

  • Broad yet precise: The patent's claims target specific chemical structures and therapeutic methods, balancing scope and defensibility.
  • Landscape competition: Multiple patents exist covering similar compounds, requiring vigilance for potential infringement or invalidity challenges.
  • Strategic importance: This patent adds valuable proprietary weight in Australia’s pharmaceutical market and possibly beyond, considering global patent family filings.
  • Innovation complementarity: It complements existing patents, creating a robust IP portfolio supporting market exclusivity.
  • Due diligence necessity: Stakeholders should conduct comprehensive freedom-to-operate analyses considering overlapping patents worldwide.

FAQs

1. Does AU2018274883 cover all derivatives of the disclosed compound?
The broadness of the claims depends on claim language. If the claims specify “comprising” or use Markush groups, they may encompass a wide range of derivatives. However, specific structural limitations could narrow protection.

2. How does this patent compare with similar patents in Europe or the US?
While filings often parallel each other within a patent family, differences in claim scope, claim language, and legal standards can result in varying levels of protection. An in-depth analysis of related patent claims is necessary to assess similarities.

3. Can generic drug manufacturers design around this patent?
Potentially, by developing compounds outside the scope of the claims, such as structural modifications not covered, or targeting different mechanisms of action, but this depends on claim breadth and prior art.

4. What are the main legal challenges this patent might face?
Challenges may revolve around allegations of lack of novelty, obviousness, or insufficient disclosure. Prior art disclosures in the same chemical class can threaten validity.

5. How does patent family strategy influence this patent’s protection?
A comprehensive patent family across jurisdictions can strengthen territorial rights, prevent workarounds, and support global commercialization strategies.


References

  1. Australian Patent AU2018274883.
  2. Patent landscape reports and patent databases (e.g., WIPO PATENTSCOPE, Espacenet).
  3. Prior art disclosures cited during prosecution, if publicly available.

(Note: Specific patent family references or prior art disclosures should be appended following detailed searches.)

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