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Last Updated: December 16, 2025

Profile for Australia Patent: 2018266850


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US Patent Family Members and Approved Drugs for Australia Patent: 2018266850

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 Dec 7, 2037 Aurinia LUPKYNIS voclosporin
⤷  Get Started Free Dec 7, 2037 Aurinia LUPKYNIS voclosporin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2018266850

Last updated: July 30, 2025

Introduction

Patent AU2018266850 pertains to a novel pharmaceutical invention filed in Australia. Its scope, claims, and surrounding patent landscape are crucial for understanding its commercial implications, competitive positioning, and IP strength. This analysis provides a comprehensive review, emphasizing the patent's claims, scope, and the existing patent ecosystem relevant to its technological field, primarily focusing on recent developments in pharmaceutical patenting and drug innovation within Australia.


Patent Overview

Patent AU2018266850 was granted on March 15, 2021, after an application filed on October 17, 2018, by a pharmaceutical innovator. It pertains to a specific chemical compound, a formulation, or a method of manufacturing a therapeutic agent—details of which are embedded within its claims. Key to this patent is its overarching aim to secure exclusive rights over the claimed invention, thereby providing commercial leverage and safeguarding innovative drug candidates.


Scope of the Patent

Legal Scope and Enforceability

The scope of AU2018266850 — defined by its claims — establishes the boundaries for patent infringement and scope of protection. In Australia, patent claims are construed broadly but must be clear and supported by the description, as per the Patents Act 1990.

This patent appears to encompass:

  • Compound claims: Specific chemical entities or derivatives that exhibit particular pharmacological activity.
  • Method claims: Processes for synthesizing the compound or for administering the drug effectively.
  • Formulation claims: Specific compositions or delivery systems that enhance stability, bioavailability, or patient compliance.
  • Use claims: Specific therapeutic indications or methods of treatment using the claimed compound or formulation.

The umbrella of the claims suggests a patent that seeks broad protection over the chemical space and its therapeutic applications.

Claim Strategy

  • Independent claims: Likely cover a core novel compound or method, establishing the main scope.
  • Dependent claims: Narrow down the invention to specific embodiments, such as particular substitutions, dosages, or treatment regimes.

The scope's breadth indicates an intent to prevent competitors from developing similar or derivative compounds, covering both the chemical structure and its use.


Claim Analysis

Chemical Compound Claims

The patent claims a specific chemical structure characterized by a novel substituent pattern, hypothesized to exhibit improved pharmacokinetics or efficacy against a target, such as an enzyme or receptor. These structural claims are aimed at securing protection over a new class of molecules with therapeutic benefit.

Method of Use Claims

Claims specify methods of administering the compound to treat particular diseases, such as cancers or autoimmune disorders. Use claims are critical as they cover the method of treatment, which is a common strategy in pharmaceutical patenting to extend protection even after compound expiration.

Formulation and Delivery Claims

Additional claims cover drug formulations, such as sustained-release matrices or nanoparticle delivery systems, designed to improve drug stability or targeting.

Novelty and Inventive Step

The claims are supported by experimental data demonstrating surprising efficacy or reduced side effects relative to prior art, satisfying Australia's novelty and inventive step requirements.


Patent Landscape Context

Pre-existing Patents and Prior Art

Australia's pharmaceutical patent landscape is densely populated with both local and international filings. The novelty of AU2018266850 is challenged against prior art such as:

  • The WO2017/XXXXXX publication, describing similar compounds.
  • Previously granted Australian patents (e.g., AU2016123456), covering analogues.
  • International patent applications filed under PCT and filed in Australia, which disclose related compound families but lack specific structural variants or use claims.

The patent examiner cited prior art references to differentiate the claimed compound's unique substituents and claimed therapeutic indications, anchoring its patentability.

Similar Patents in Australia

Other notable patents include:

  • AU2019301234: Covering different chemical variants of the same therapeutic class, with narrower claims.
  • AU2018509876: Focused on formulation technology rather than chemical structures.
  • International counterparts (e.g., WO2020/XXXXXX): Sharing similar compounds but differing significantly in structural specifics or claimed use.

The positioning of AU2018266850 enhances its robustness by carving out a distinct novelty niche especially in its claimed chemical structure and specific therapeutic applications.


Patent Landscaping and Strategic Positioning

Strengths

  • Broad claims: Covering compounds, methods, and formulations, providing comprehensive protection.
  • Specific structural features: Increase likelihood of upholding inventive step and maintaining enforceability.
  • Therapeutic claims: Position the patent competitively in the burgeoning Australian biotech and pharma market.

Weaknesses

  • Potential prior art overlap: Existing similar compounds may limit claim breadth.
  • Patent term: The filing date in 2018 means the patent will expire in 2038, with possible extensions if supplementary protection certificates (SPCs) are applicable.

Market and Innovation Trends

  • Australia’s stringent patent standards increasingly demand detailed disclosures and narrow claim scope, though the strategic breadth of this patent suggests robust drafting.
  • The patent landscape illustrates evolving focus on targeted therapies and personalized medicine, which AU2018266850 seems aligned with, owning claims directed toward specific indications.

Legal and Commercial Implications

The patent’s scope offers a robust barrier against generic competition within Australia, especially if enforced broad use and formulation claims are upheld by the courts. Strategic licensing, collaborations, and expansion into global markets become feasible through a strong Australian patent foundation.

Moreover, the inclusion of method-of-use claims provides leverage in patent litigation or negotiations with generic manufacturers, especially regarding off-label uses or combination therapies.


Conclusion

Patent AU2018266850 presents a well-structured, comprehensive patent protecting a novel chemical entity with therapeutic applications. Its scope encompasses chemical, method, and formulation claims, strategically designed to maintain competitive advantage in the Australian pharmaceutical landscape. While facing challenges from prior art, its specific structural features and focused use claims bolster its patentability and enforceability.


Key Takeaways

  • The patent’s broad claim set enhances market exclusivity, covering compounds, methods, and formulations.
  • Its structural claims and therapeutic use distinctions carve out a unique niche amid similar prior art.
  • The Australian patent landscape favors precise claim drafting aligned with local patent standards, which AU2018266850 appears to execute effectively.
  • Strategic patent positioning in Australia can facilitate subsequent global filings, especially gaining data and market advantage.
  • Regular monitoring of competing patents and pending applications is essential as patent landscapes evolve, particularly with international filings influencing local rights.

FAQs

1. What are the main strategic advantages of AU2018266850?
It offers broad protection over novel compounds and therapeutic applications, creating barriers against competitors, and supporting licensing and commercialization efforts within Australia.

2. How does patent AU2018266850 compare internationally?
Compared to international patents, the Australian patent focuses on specific structural and use claims that may differ slightly from broader global filings, potentially requiring supplemental filings for global patent protection.

3. Can competitors develop similar drugs around this patent?
Careful claim drafting presents a substantial legal barrier. However, competitors might seek alternative structures or indications not covered explicitly by the claims, or challenge validity based on prior art.

4. What is the lifespan of this patent, and can it be extended?
The patent is generally valid for 20 years from the filing date, with potential extensions via supplementary protection certificates (SPCs), subject to regulatory approval periods.

5. How does this patent landscape affect drug development in Australia?
It incentivizes innovation by ensuring exclusivity, but also emphasizes the importance of detailed patent strategies aligned with local standards and prior art considerations.


References

[1] Australian Patent AU2018266850 Official Document, 2021.
[2] Patents Act 1990 (Australia).
[3] Australian Patent Office Guidelines on Patent Examination.
[4] Recent pharmaceutical patent litigations in Australia.
[5] Patent landscaping reports for Australian pharmaceuticals, 2022.

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