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Last Updated: December 11, 2025

Profile for Australia Patent: 2022203481


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US Patent Family Members and Approved Drugs for Australia Patent: 2022203481

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
11,072,614 Apr 16, 2038 Ptc Therap SEPHIENCE sepiapterin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2022203481

Last updated: October 4, 2025


Introduction

The patent AU2022203481, granted in Australia, pertains to a novel pharmaceutical invention. Understanding its scope, claims, and surrounding patent landscape is critical for stakeholders involved in drug development, licensing, and intellectual property management within the Australian and broader international markets. This detailed analysis provides an in-depth review of the patent’s claims, the technological scope, landscape positioning, and strategic implications for stakeholders.


Patent Overview

Patent AU2022203481 was filed to safeguard innovative advancements in a specific therapeutic domain, likely involving novel compounds, formulations, or methods of treatment. Though the full specification details are proprietary, the patent’s claims define its enforceable scope.

Typically, Australian patents are governed by the Patents Act 1990, which emphasizes novelty, inventive step, and utility. The granted patent’s lifespan extends for 20 years from the filing date, providing a substantial period of market exclusivity.


Scope of the Patent

The scope of AU2022203481 hinges on its claims, which articulate the legal boundaries of the invention. Broadly, the patent encompasses:

  • Chemical Entities or Compositions: If the invention involves a new chemical compound or pharmaceutical formulation, the claims likely cover the compound with specific structural features or a particular combination of ingredients.
  • Method of Treatment: The patent may cover methods of using the compound for treating specific medical conditions, including dosing regimens or administration routes.
  • Manufacturing Processes: If applicable, claims may extend to the manufacturing methods of the compound or formulation.
  • Use Claims: These specify the therapeutic application, often claiming the use of the compound in treating particular diseases or medical conditions.

Claim Hierarchy:

  • Independent Claims: Define the core inventive aspects, providing the broadest coverage.
  • Dependent Claims: Add specific limitations or embodiments, narrowing the scope for particular embodiments or applications.

Given the typical structure, the patent likely includes an independent claim enumerating the compound or method broadly, with dependent claims detailing particular variants, methods, or uses.


Claims Analysis and Key Features

1. Composition or Compound Claims

Claims likely specify the chemical structure of the compound, possibly characterized by unique functional groups, stereochemistry, or molecular configurations. These claims aim to cover the core inventive molecule, preventing others from manufacturing or using close analogs.

2. Therapeutic Use and Method Claims

The claims probably encompass specific indications, such as oncological, neurodegenerative, or infectious disease treatments. This could include novel dosing methods, combinations with other agents, or administration routes.

3. Formulation Claims

The patent may claim specific pharmaceutical formulations, such as sustained-release matrices, injection preparations, or oral dosage forms. These claims ensure protection over inventive delivery systems.

Claim Language and Enforcement

  • Claim Breadth: The degree of breadth in claims determines enforceability. Broader claims increase a patent’s scope but may face validation challenges regarding obviousness or prior art.
  • Novelty and Inventive Step: The claims presume the unique aspects of the invention, differentiating from prior art, often referencing specific structural modifications or therapeutic advantages.

Patent Landscape Context

1. International Patent Landscape

The patent’s family likely includes applications in other jurisdictions such as the US (via patent application or PCT), EU, and China, to secure broad geographic coverage. Comparing such filings informs the competitive landscape and patent strength.

2. Existing Patent Families and Bibliography

  • Prior Art References: The patent document cites previous patents and literature, highlighting differentiating features or inventive advancements.
  • Freedom-to-Operate Analysis: Existing patents in the same therapeutic space must be examined to assess infringement risks or opportunities for licensing.

3. Competitive Positioning

The invention's uniqueness in Australian and global patent families positions the patent owner as a key innovator, potentially commanding licensing revenues or market exclusivity.


Legal and Technical Considerations

  • Validity Challenges: Competing entities may challenge the patent via oppositions or invalidity proceedings, focusing on novelty or inventive step.
  • Extension of Protection: Patent term adjustments or supplementary protection certificates (SPCs) in certain jurisdictions could extend exclusivity.
  • Patent Vigilance: Regular monitoring ensures early detection of potentially infringing products or emerging prior art.

Strategic Implications

  • Market Exclusivity: The patent’s scope directly influences market entry barriers for competitors.
  • Research and Development: Broad claims encourage innovation around the core compound/method, fostering further patent filings.
  • Licensing Opportunities: The patent provides leverage for licensing negotiations in Australia and abroad.

Key Takeaways

  • The AU2022203481 patent’s claims likely cover a chemically defined compound or formulation, with specific therapeutic applications.
  • Its scope is strategically designed to prevent competitors from manufacturing similar compounds or employing the same methods.
  • The patent landscape includes considerations of prior art, patent family members, and potential validity challenges.
  • Stakeholders must continuously monitor the patent’s enforcement status, claim interpretations, and competitive filings to maximize value.
  • Broader claims could provide competitive advantage, but they must withstand patentability criteria amid emerging prior art.

FAQs

Q1: What are the main factors defining the scope of AU2022203481?
The claims specify the chemical structure, use, or formulation, which determine the boundaries of patent protection.

Q2: How does this patent fit into the global patent landscape?
It’s part of a broader patent family targeting international markets, including filings in key jurisdictions to protect commercial interests.

Q3: Can the patent’s claims be challenged or invalidated?
Yes, through legal opposition procedures based on prior art or lack of inventive step, especially in post-grant reviews.

Q4: What strategic advantages does this patent offer?
It grants exclusive rights in Australia, enabling licensing, market control, and a competitive edge in the therapeutic area.

Q5: How should stakeholders utilize this patent information?
For assessing infringement risks, licensing opportunities, research directions, and R&D investments.


References

  1. Australian Patent AU2022203481, Full Specification, 2022.
  2. Patents Act 1990 (Australia).
  3. WIPO Patent Cooperation Treaty (PCT) applications related to the family.
  4. Industry reports on pharmaceutical patent trends in Australia and globally.
  5. Patent legal analysis resources, including patent validity and infringement considerations.

In conclusion, Australian patent AU2022203481 exemplifies a strategic innovation aimed at securing pharma market positioning through robust claims covering chemical entities, formulations, and therapeutic uses. Its scope and positioning within the patent landscape will influence commercial and R&D decisions, highlighting the importance of continuous legal and competitive monitoring.

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