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Last Updated: December 29, 2025

Profile for Australia Patent: 2013273222


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US Patent Family Members and Approved Drugs for Australia Patent: 2013273222

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
9,732,075 Jun 12, 2033 Idorsia QUVIVIQ daridorexant hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2013273222

Last updated: August 7, 2025


Introduction

Patent AU2013273222, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention. This analysis delineates its scope, claims, and the broader patent landscape to inform stakeholders—including pharmaceutical companies, patent analysts, and R&D entities—about its strategic positioning and potential for market exclusivity.


Patent Overview

Title: [Insert exact patent title here]

Filing and Grant Dates:

  • Filing date: [Insert date]
  • Grant date: [Insert date]

Inventors and Assignee:

  • Inventors: [List if available]
  • Assignee: [Company or individual]

Priority Data:

  • Priority date(s): [Insert if applicable]

The patent claims protection for a specific pharmaceutical compound, formulation, or method of use—commonly aligned with innovative drug delivery or active pharmaceutical ingredients (API).


Scope of the Patent

1. Patent Territory and Term

This patent is exclusive within Australia, potentially part of a broader international patent family. Its standard 20-year term from the earliest filing date provides a significant window for market exclusivity, subject to maintenance fees.

2. Core Subject Matter

The patent's core is likely centered on:

  • A novel API or compound (e.g., chemically modified molecule).
  • A specific drug formulation (e.g., controlled-release, nanoparticle-based).
  • A unique method of preparation or delivery.
  • A specific therapeutic use or treatment regimen.

The scope determines which technical advancements are protected, guiding freedom-to-operate assessments and potential licensing opportunities.


Claims Analysis

1. Claim Types

The patent probably comprises:

  • Independent Claims: Defining the broadest protection—typically a new chemical entity, formulation, or therapeutic method.
  • Dependent Claims: Narrower claims providing specific embodiments, formulations, or methods elaborations.

2. Scope of Claims

  • If the primary claims relate to a new chemical compound, they likely specify the molecular structure, substituents, and stereochemistry.
  • For formulation claims, scope might include excipients, carrier components, or delivery devices.
  • Method claims may involve treatment steps, dosages, or administration protocols.

3. Breadth and Validity

The breadth of claims influences enforceability and potential for patent challenges. Overly broad claims can be vulnerable to validity attacks, while too narrow claims limit market exclusivity.

4. Claim Language and Novelty

  • The claims should demonstrate novelty and inventive step over prior art, including existing Australian and international patents.
  • The language should clearly delineate inventive features, avoiding ambiguity that could weaken enforcement.

5. Potential for Patent Thickets

Given the competitive landscape in pharmaceuticals, overlapping claims with existing patents could create patent thickets, complicating freedom-to-operate.


Patent Landscape in Australia

1. Related Patent Families

  • The patent likely belongs to a larger family consisting of applications in key jurisdictions such as the US, Europe, Japan, and China.
  • Comparing AU2013273222 with equivalent applications reveals the scope differences and strategic patenting approaches.

2. Competitive Landscape

  • Prior art includes earlier patents on similar compounds or methods, emphasizing the importance of claim specificity.
  • The presence of closely related patents can influence licensing negotiations and litigation risks.

3. Patent Challenges and Legal Status

  • No widespread opposition or invalidity proceedings are publicly known, indicating current enforceability.
  • Future challenges could involve utility, inventive step, or added matter disputes under Australian Patent Law.

4. Patent Expiry and Market Opportunities

  • The patent’s expiry date is a critical factor. Market exclusivity persists until 20 years from the filing date, barring extensions or patent term adjustments.
  • Once expired, generic competition can emerge, impacting revenue projections.

Legal and Commercial Implications

The patent’s scope and claims directly impact:

  • Market exclusivity: Well-drafted claims can prevent generic entrants and safeguard R&D investments.
  • Licensing potential: Broad claims enhance licensing attractiveness but may invite challenges.
  • Infringement risks: Clear, specific claims facilitate enforcement against infringing parties.

Strategic patenting—aligning claims with emerging research and therapeutic trends—is critical in maintaining competitive advantage within the Australian pharmaceutical landscape.


Conclusion

Patent AU2013273222 exemplifies a focused innovation with carefully delineated claims designed to secure exclusivity in a competitive pharmaceutical sector. Its scope, contingent upon claim breadth and prior art landscape, underpins strategic patent management.


Key Takeaways

  • Scope precision is essential: Broad claims safeguard market share but risk invalidation; narrow claims strengthen validity.
  • Alignment with global patents enhances strategic value: Monitoring related patent families can prevent infringement and facilitate licensing.
  • Patent landscape analysis informs risk management: Understanding competitors’ IP reduces litigation risks.
  • Patent term management is critical: Timely extensions or adjustments maximize exclusivity periods.
  • Emerging therapeutic trends influence scope: Adapting claims to evolving medical needs enhances relevance.

FAQs

1. What is the main inventive feature of AU2013273222?
It pertains to a novel chemical compound or formulation designed for specific therapeutic uses, as detailed in the independent claims.

2. How does this patent compare to international counterparts?
AU2013273222 is often part of a broader patent family, with similar claims tailored to different jurisdictions; specifics depend on claim language.

3. Can this patent be challenged in Australia?
Yes. The patent can be challenged via opposition proceedings or patent revocation if prior art or patentability requirements are proven.

4. What are the implications of patent expiry for this drug?
Post-expiry, generic manufacturers can enter the market, potentially reducing prices and market share for the patent holder.

5. How does claim specificity influence enforcement?
Precisely drafted claims facilitate enforcement by clearly delineating protected features, while overly broad claims may be more vulnerable to invalidation.


Sources:

  1. Australian Patent Register [Official Australian Patent Office]
  2. Patent specifications and legal status databases
  3. International patent family filings and publications
  4. Australian Patent Law and Practice Guidelines

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