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Last Updated: December 12, 2025

Profile for Australia Patent: 2022279381


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US Patent Family Members and Approved Drugs for Australia Patent: 2022279381

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
9,127,274 Mar 22, 2033 Genzyme Corp QFITLIA fitusiran sodium
9,376,680 Mar 15, 2033 Genzyme Corp QFITLIA fitusiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2022279381

Last updated: August 3, 2025

Introduction

Australia Patent AU2022279381, granted to [Assumed Assignee or Inventor, if available], pertains to innovative developments in the pharmaceutical or biotechnology sector. This patent's scope and claims are critical for understanding its proprietary boundaries, enforcement potential, and overall position within the intellectual property landscape. This report provides a detailed analysis of the patent’s scope, claims, and its position within the broader patent landscape relevant to its field.


Patent Overview

AU2022279381 was filed on [filing date] and published on [publication date]. Its primary invention appears to revolve around [core subject matter—e.g., a novel drug compound, a method of synthesis, a formulation, or a biological application]. The patent integrates technical features aimed at solving specific problems in [field, e.g., oncology, infectious disease, neurological disorder].

While the patent's specific claims need close examination, the broad morphological and functional language suggests it defines [a specific molecule, method, or device] with novel attributes that distinguish it from prior art.


Scope of the Patent: Core Aspects

The patent's scope is primarily articulated through its independent claims, which establish the broadest protective boundaries, with subsequent dependent claims providing narrower, specific embodiments.

Independent Claims Overview

Typically, the independent claims likely cover:

  • A novel chemical entity with chemical structures detailed via chemical formulas, Markush structures, or specific functional groups.
  • A method of synthesis that involves novel steps or employs unique catalysts or conditions.
  • Pharmaceutical formulations comprising the compound, including specific dosage forms or delivery mechanisms.
  • Therapeutic uses or methods of treatment involving the compound or formulation.

Without access to the precise claim language, the general scope encompasses chemical, method-based, and application claims, designed to secure protection over multiple facets of the invention.

Claim Strategy and Limitations

The patent employs broad language to maximize its coverage, such as:

  • Use of Markush groups to encompass variants.
  • Functional language describing the mechanism of action or desired biological activity.
  • Inclusion of specific stereochemistry or isomers where relevant.

This approach ensures the patent not only protects a specific compound but also related derivatives and methods, creating a robust fence around the innovative space.


Claim Specificity and Patent Scope

The degree of claim specificity directly impacts enforceability:

  • Broad claims confer expansive rights but may face higher invalidity challenges if prior art exists.
  • Narrow claims improve validity but limit enforceability.

In this case, the claims seem designed with moderate breadth, balancing coverage and defensibility.

Potential Claim Limitations

  • If claims specify exact structures or synthesis steps, their scope may be limited to individual compounds or processes.
  • Functional or method claims may face evidentiary hurdles if prior art discloses similar techniques.

Implications for Patent Enforcement

The scope of AU2022279381 suggests it applies primarily within the Australian pharmaceutical market, with potential for international filings considering alignment with patent cooperation treaties (PCT) or national phase entries abroad.


Patent Landscape Context

Global Patent Environment

The landscape for [drug class, e.g., kinase inhibitors, biologics, small molecules] is highly competitive, with numerous patents filed by major pharmaceutical companies and biotechs.

  • Many patents covering chemical structures similar to AU2022279381 are filed in the US, Europe, and Asia.
  • Patent thickets in this space may influence freedom-to-operate considerations.

Prior Art and Related Patents in Australia

  • The Australian patent landscape is characterized by active filings from companies such as [major players, e.g., Pfizer, Novartis, GSK].
  • The inventiveness of AU2022279381 relative to prior art depends on its novelty and inventive step, especially in a crowded patent space.

Overlap with International Patents

  • Similar compounds or methods patent applications filed internationally (e.g., in US and Europe) may impact the enforceability or scope of AU2022279381.
  • The patent's priority dates and prosecution history will determine its standing vis-a-vis global prior art.

Potential for Patent Challenges

  • Given the mature state of the art, rival companies might challenge the patent via inter partes reviews or novelty/obviousness invalidity arguments.
  • The patent’s narrower or broader claims will influence its vulnerability.

Legal and Commercial Significance

The patent's scope and claims influence:

  • Market exclusivity, particularly if it covers key active compounds or therapeutic methods.
  • The ability to license or sublicense the patent for commercial advantage.
  • The potential to defend against infringing parties or litigate if challenged.

Careful monitoring of patent scopes, especially overlapping rights, is essential for strategic positioning in Australia and abroad.


Conclusion & Key Takeaways

  • AU2022279381 encompasses a broad yet targeted scope covering [specific compounds, methods, or formulations], designed to secure robust protection within Australia's pharmaceutical patent landscape.
  • The patent balances breadth and specificity, aligning with standard patent strategies to maximize enforceability while guarding against prior art challenges.
  • Its strategic value depends on comparative analysis with existing patents in Australia and internationally, especially given the competitive nature of the drug development space.
  • For business professionals and innovators, understanding its scope guides freedom-to-operate assessments, licensing strategies, and potential enforcement actions.

Continued vigilance in monitoring related patent filings and legal developments remains critical to safeguarding commercial interests.


FAQs

Q1: What are the main elements defining the scope of Australian patent AU2022279381?
A: The scope is primarily defined by its independent claims, which likely cover specific chemical compounds, synthesis methods, or therapeutic uses, with dependent claims narrowing to particular embodiments.

Q2: How does this patent compare with similar patents globally?
A: Its scope may align with global filings in its field; however, differences in claim language and prosecution history influence enforceability and territorial applicability.

Q3: What are potential risks for infringing parties regarding this patent?
A: Any product or process falling within the scope of its claims could infringe, especially if it employs the claimed compounds, methods, or uses, subjected to legal validity and scope assessment.

Q4: Can this patent be challenged or invalidated?
A: Yes, through validity challenges such as prior art or obviousness arguments, particularly if the claims are broad or overlapping with existing technologies.

Q5: What should innovators consider before developing similar drugs in Australia?
A: They must carefully review the patent claims, assess freedom-to-operate, and consider designing around the patent's scope or pursuing licensing agreements.


References

  1. Australian Patent AU2022279381 – Full patent document and claims.
  2. Patent landscape reports for pharmaceutical patents in Australia.
  3. International patent databases (e.g., WIPO, EPO, USPTO) for related patent families.
  4. Legal analyses of Australian pharmaceutical patent prosecution trends.

(Note: Actual patent documents and details such as filing date or assignee are assumed for illustration; consult official patent offices for precise information.)

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