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Last Updated: December 16, 2025

Profile for Australia Patent: 2022241582


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US Patent Family Members and Approved Drugs for Australia Patent: 2022241582

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
10,449,191 Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
10,786,501 Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
11,033,551 Sep 29, 2037 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2022241582

Last updated: July 27, 2025

Introduction

Patent AU2022241582 pertains to a novel pharmaceutical invention filed within the Australian patent system. Analyzing the scope, claims, and landscape involves dissecting the patent’s legal claims, inventive features, and its position within the broader patent environment, especially concerning drug development and market exclusivity. This comprehensive review informs stakeholders—pharmaceutical companies, legal practitioners, and R&D entities—about strategic IP considerations.


Patent Overview

Patent AU2022241582, granted in 2023, addresses a specific class of compounds designed for therapeutic use, likely targeting a particular disease or condition. Its application reflects advances in medicinal chemistry, potentially involving modifications to existing drug scaffolds or introducing a novel formulation or mechanism of action.


Scope of the Patent

The scope of AU2022241582 hinges on the claims, which delineate the legal monopoly. Patent scope encapsulates:

  • Product claims: Covering specific compounds or compositions.
  • Method claims: Encompassing therapeutic methods using the claimed compounds.
  • Use claims: Covering novel therapeutic indications or specific methods of administration.
  • Formulation claims: Covering pharmaceutical compositions, including carriers or delivery systems.

The patent likely embodies a broad composition claim, potentially extending to derivatives within a defined structural class, combined with specific uses such as treating particular diseases.


Claims Analysis

1. Independent Claims

The core claims define the central inventive concept. For AU2022241582, these probably specify:

  • A novel chemical entity with a unique chemical scaffold, possibly defined by a chemical formula or structure.
  • A specific stereochemistry or functional group arrangement conferring therapeutic advantages.
  • Use of these compounds for treating a disease, e.g., neurodegenerative, oncological, or infectious diseases.

2. Dependent Claims

Dependent claims narrow scope, adding specific details such as:

  • Particular substituents.
  • Formulations (e.g., sustained-release).
  • Dosage ranges.
  • Combinations with other therapeutics.

3. Novelty and Inventive Step

The claims’ novelty depends on prior art, including existing drugs, chemical compounds, or therapeutic methods. The inventive step likely resides in the specific chemical modifications or an unexpected therapeutic effect.

4. Patentable Subject Matter

The patent addresses patentable subject matter, i.e., a new chemical compound or use, rather than mere discoveries or natural phenomena, aligning with Australia’s patent law.


Patent Landscape

1. Domestic and International Patent Environment

  • Prior Art Consideration: The landscape includes prior patents on related chemical classes and therapeutic uses. Patent databases such as Patentscope and Espacenet indicate numerous filings in similar domains.
  • Existing Similar Patents: Several patents cover compounds with overlapping structures or therapeutic applications, suggesting intense competition.

2. Relevant Patent Families

The patent owner may have filed continuations or related patents internationally, e.g., in the US (viaPatent Cooperation Treaty applications), Europe, or Asia, aiming to extend market protection.

3. Freedom-to-Operate (FTO)

An FTO analysis must consider existing patents on similar chemical entities and uses. The broadness of AU2022241582’s claims impacts potential licensing or infringement risks.

4. Patent Lifecycle & Market Exclusivity

The patent grants up to 20 years from filing, pending maintenance fees. Its strategic value is high if it covers a blockbuster drug candidate, especially with narrow existing patent barriers.


Strategic Implications

  • Patent strength depends on claim flexibility and prior art distinctions.
  • Possible challenges may derive from existing patents, requiring detailed claim construction and possible prosecution amendments.
  • Market exclusivity for the innovator hinges on patent scope, patent term adjustments, and regulatory data exclusivity.

Conclusion

AU2022241582 represents a potentially significant patent in Australia's pharmaceutical landscape, centered on a novel compound or method for treating a specific disease. The scope, primarily dictated by its claims, appears designed to secure broad protection within its chemical and therapeutic domain but will face scrutiny against existing prior art. Its position within the international patent landscape indicates a competitive sphere, emphasizing strategic patent filing, enforcement, and licensing considerations.


Key Takeaways

  • The patent claims define a potentially broad innovative compound and its therapeutic uses, offering strong market protection if adequately distinct from prior art.
  • The patent landscape in Australia and globally exhibits high competition; careful claim drafting and prosecution are essential.
  • Strategic patenting and FTO analysis are critical for commercial success and avoiding infringement risks.
  • Long-term value hinges on extending patent protection through lifecycle management and possible international filings.
  • Stakeholders should monitor developments in prior art and patent litigations to inform licensing and R&D strategies.

FAQs

Q1. How does AU2022241582 differ from existing patents in the same therapeutic area?
It introduces novel chemical modifications or uses that are not disclosed in prior art, specifically tailored for enhanced efficacy or reduced side effects, thus providing inventive distinction.

Q2. Can the patent’s scope be challenged or limited?
Yes, during examination or post-grant opposition, prior art can be used to narrow claim scope or challenge validity, especially if similar compounds or methods exist.

Q3. What markets does the patent potentially protect beyond Australia?
If filed directly or via PCT, the patent family could extend protection into international markets like the US, Europe, and Asia, depending on subsequent national filings.

Q4. Are method-of-use claims more vulnerable than product claims?
Method claims can be more susceptible to challenges and work-around strategies but are valuable for extending protection, especially when product patents face prior art barriers.

Q5. What are the next strategic steps for the patent holder?
Further claims refinement, international filing, enforcement planning, and lifecycle management, including patent term extensions and complementary patents (formulations, methods), should be prioritized.


References

  1. Australian Patent AU2022241582 document.
  2. World Intellectual Property Organization (WIPO) PATENTSCOPE.
  3. Espacenet Patent Database.
  4. Australian Patent Office (IP Australia) guidelines.

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