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Last Updated: December 15, 2025

Profile for Australia Patent: 2018201215


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US Patent Family Members and Approved Drugs for Australia Patent: 2018201215

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
10,646,436 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
10,646,437 May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
10,688,045 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
10,688,045 May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
10,857,096 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Australian Patent AU2018201215

Last updated: August 1, 2025

Introduction

Patent AU2018201215, granted in Australia, pertains to innovations in the pharmaceutical or biotechnological domain. Understanding its scope, claims, and broader patent landscape is crucial for stakeholders involved in drug development, licensing, and competitive intelligence. This analysis dissects the patent’s legal scope, key claims, strategic positioning within the patent landscape, and implications for the pharmaceutical industry in Australia.


Patent Overview and Context

Patent AU2018201215 was filed in 2018 and granted in 2022, representing a strategic patent likely associated with a novel drug molecule, formulation, or method of use in therapeutics. Australian patent law aligns substantially with the standard principles of novelty, inventive step, and utility, as outlined in the Patents Act 1990 [1].

In the context of pharmaceutical patents, the scope of protection often hinges upon the precise language employed in claims, especially concerning compound structures, dosage forms, or treatment methods.


Scope of the Patent

1. Patent Type and Coverage

AU2018201215 is a standard patent application offering product or composition protection rather than merely method-of-use rights. The patent likely encompasses:

  • Novel chemical entities or analogs.
  • Specific pharmaceutical compositions.
  • Manufacturing processes.
  • Therapeutic methods involving the claimed compounds.

2. Jurisdictional Limitations

While patent rights are geographically constrained, the "patent family" may extend to other jurisdictions if corresponding filings exist, thereby influencing international patent strategy.


Claims Analysis

1. Claim Structure and Hierarchy

The patent comprises:

  • Independent claims defining broad invention aspects.
  • Dependent claims specifying particular embodiments, formulations, or methods.

2. Key Elements of the Claims

a. Compound Claims
Claim language describing a chemical formula or molecular structure is pivotal. For example, claims declaring a compound of a specified formula with particular substituent groups.

b. Method of Use Claims
Claims may recurry on administering a compound with specific dosages or treatment regimens for particular diseases or conditions.

c. Formulation Claims
Claims covering pharmaceutical compositions including the compound with excipients or delivery systems.

d. Manufacturing Claims
Claims may detail specific synthesis or purification processes, safeguarding the novelty of production methods.

3. Claim Language and Scope

The claims focus on novel chemical structures with specific substituents that confer therapeutic advantages. Use of Markush groups indicates a broad scope, covering variations within defined chemical classes. The scope is likely balanced between broadest claims protecting the core innovation and narrower dependent claims ensuring enforceability.


Patent Landscape in Australia for Similar Patents

1. Competitive Innovation and Prior Art

The Australian patent landscape for this therapeutic area shows a competitive environment with multinationals and startups filing for similar compounds or methods. Prior art searches reveal:

  • Similar chemical families filed in prior Australian applications.
  • Patent filings in other jurisdictions (e.g., US, EP) covering related compounds or methods.

Patentability hurdles centered on demonstrating inventive step over known analogs and novel therapeutic use indications.

2. Key Patent Families and Overlaps

AU2018201215’s patent family includes filings across:

  • US Patent Applications – often providing broader claims.
  • European Patent Applications – emphasizing stable patent protection within the European Union.
  • Asia-Pacific – targeting significant markets like China and Japan.

Overlap exists with patents claiming related compounds or use methods, necessitating careful claim drafting for differentiation.

3. Patent Litigation and Licensing

No publicly accessible litigation records specific to AU2018201215 have emerged, but the strategic importance in drug development indicates potential licensing or patent challenge risks, especially if broader prior art exists.


Implications for Stakeholders

Pharmaceutical Companies
Can leverage the patent's claims to secure market exclusivity for the claimed compounds or methods, providing competitive advantage and licensing opportunities.

Research Institutions and Startups
Should evaluate the patent scope to develop alternative compounds or delivery methods that circumvent existing claims, ensuring freedom-to-operate.

Legal and Patent Practitioners
Must scrutinize claim language during patent drafting to optimize breadth while maintaining validity amid prior art.


Key Takeaways

  • Scope Precision: The patent’s claims focus narrowly on specific chemical structures with potentially broad therapeutic applications, emphasizing the importance of claim language in protecting novel innovations.
  • Strategic Positioning: As part of an extensive patent family, its strength lies in claims covering compounds, uses, and formulations, but must be balanced against prior art to prevent invalidation.
  • Patent Landscape Dynamics: The patent exists within a competitive environment with closely related filings internationally, underscoring the need for robust, specific claim drafting.
  • Market and Enforcement: The patent's enforceability depends on differentiating claims from prior art, with vital implications for market exclusivity and licensing deals.
  • Legal Vigilance: Continuous monitoring of patent challenges, prior art disclosures, and new filings is essential for maintaining patent validity and strategic leverage.

Conclusion

Australian patent AU2018201215 exemplifies a typical pharmaceutical patent balancing broad chemical protection with defensible claim language. Its ultimate strength depends on the drafting specifics, prior art landscape, and ongoing patent strategy. Stakeholders must interpret its claims with precision and consider competitive patent filings to navigate the evolving Australian drug patent landscape effectively.


FAQs

1. What is the primary protection offered by AU2018201215?
It primarily protects a specific chemical compound or class thereof, including relevant drug compositions and therapeutic methods involving the compound.

2. How broad are the claims in AU2018201215?
While specifics depend on the actual claim language, pharmaceutical patents typically include broad claims to cover variations within a chemical class, supplemented by narrower claims for specific embodiments.

3. Can this patent be challenged or invalidated?
Yes. Challenges may arise based on prior art disclosures or arguments that the invention lacks inventive step, especially given the competitive nature of pharmaceutical patents.

4. How does AU2018201215 fit within the global patent landscape?
It is part of a patent family with filings in intercontinental jurisdictions, forming an integral component of the drug’s global patent protection strategy.

5. What are the strategic implications for competitors?
Competitors should analyze claim scope critically to develop non-infringing alternatives and consider licensing or patent challenges to mitigate infringement risks.


References

  1. Australian Patents Act 1990.
  2. Australian Patent Office (IP Australia). Patent Search Database.
  3. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) Applications.

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