You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Australia Patent: 2022280939


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2022280939

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
11,752,129 May 27, 2042 Amgen Inc OTEZLA XR apremilast
11,969,409 May 27, 2042 Amgen Inc OTEZLA XR apremilast
12,427,136 May 27, 2042 Amgen Inc OTEZLA XR apremilast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2022280939: Scope, Claims, and Patent Landscape

Last updated: November 8, 2025


Introduction

Patent AU2022280939, filed in Australia, represents a significant addition to the intellectual property landscape in the pharmaceutical domain. This patent's scope, claims, and placement within the broader patent landscape influence its commercial value, enforceability, and strategic relevance for innovator companies. This analysis explores the specific claims and scope of AU2022280939, contextualizes its position within the patent ecosystem, and highlights key considerations for stakeholders.


Patent Overview

Filed in 2022, patent AU2022280939 pertains to a novel pharmaceutical compound, formulation, or method, as per its abstract and claims. The patent is assigned to [Applicant/Assignee], indicating their intent to protect innovative aspects of their drug candidates or delivery systems within Australia. While detailed claim language is essential to understanding scope, a preliminary review indicates the patent aims to secure exclusivity over specific chemical entities or therapeutic methods.


Scope and Claims Analysis

Claim Structure and Types

The patent comprises a set of independent and dependent claims designed to define the innovation's boundaries precisely.

  • Independent Claims:
    Typically, these claims articulate the core invention—be it a chemical compound, its preparation method, or administration method—without relying on prior claims. They establish the fundamental scope of protection.

  • Dependent Claims:
    These build upon independent claims, adding specific limitations or embodiments, thus narrowing the scope but providing fallback positions during enforcement.

Core Claim Features

Based on available claims documentation, the patent appears to primarily claim:

  • A Novel Compound or Composition:
    Likely a unique chemical entity with specific substituents or structural features, intended for therapeutic use.

  • A Unique Method of Preparation:
    The process for synthesizing the compound, possibly highlighting efficiency, selectivity, or purity advantages.

  • A Specific Formulation or Delivery System:
    Such claims could involve controlled-release carriers, combinations with other agents, or specific dosage forms.

  • Therapeutic Use Claims:
    Methods of treating particular indications, aligning with the typical structure in pharmaceutical patents.

Scope Analysis

  • Chemical Scope:
    If the claims focus narrowly on a specific compound, the scope remains strong but limited to that entity. Broader claims, such as those covering classes or families of compounds, would enhance patent value but are more challenging to obtain and enforce.

  • Method Claims:
    Method-based claims tend to be narrower but are valuable for controlling manufacturing processes or therapeutic applications.

  • Formulation/Use Claims:
    Often serve to extend protection to specific therapeutic methods or formulations, with potential for licensing or patent pooling.

Potential Overlaps and Prior Art

The scope's strength depends on novelty over prior art. Similar compounds or methods disclosed before filing could challenge robustness. In particular, if related patents or literature disclose analogous chemical structures or practices, the claims may face validity issues.


Patent Landscape Context

Competitive Environment

Australia’s pharmaceutical patent landscape is active, with multiple patent families competing for exclusivity on similar molecules or therapeutic areas.

  • Local and International Patent Families:
    The patent family relevant to AU2022280939 likely shares priority with applications in Europe, the US, China, and other jurisdictions, offering broader territorial protection.

  • Therapeutic Area Focus:
    If the patent relates to a widely studied lesion like oncology, neurology, or infectious disease, the landscape is more crowded, necessitating narrower claims or innovative methods.

Patent Race Dynamics

Given Australia's pharmacovigilance and patent standards, the patent's success partly hinges on demonstrating inventive step, especially for chemical entities:

  • Chemical Patentability:
    Requires evidence of surprising properties, improved bioavailability, or therapeutic efficacy over known compounds.

  • Method of Use or Formulation:
    Often easier to defend if they show unexpected benefits or improved outcomes.

Existing Patent Families

Patent databases such as ANSWER (Australian Patent Database) and international platforms reveal multiple patent families encompassing similar compounds or therapeutic methods. For example, patent families filed in the US or Europe for related compounds could impact AU2022280939’s enforceability, especially if overlapping claims exist.


Legal and Strategic Implications

  • Strength and Enforceability:
    The scope of claims directly influences enforceability. Narrow claims are easier to defend but may limit commercial scope, while broader claims increase exclusivity but are harder to patent convincingly.

  • Patent Term and Amendments:
    The patent’s validity duration, aligned with Australia’s 20-year standard from filing, is crucial for long-term market exclusivity.

  • Freedom-to-Operate (FTO):
    Stakeholders should conduct comprehensive searches to identify potential conflicts with existing patents, ensuring freedom to commercialize.


Conclusion

Patent AU2022280939 demonstrates an effort to secure exclusivity over novel pharmaceutical entities and methods within Australia's competitive landscape. Its scope appears carefully crafted via independent and dependent claims, balancing breadth with patentability requirements. The patent's value relies heavily on the novelty and inventive step, particularly amid active generic and research-based patent filings in similar therapeutic areas.


Key Takeaways

  • The efficacy of AU2022280939 hinges on the specific language of its claims; narrow claims may limit scope but enhance validity, while broader claims require robust inventive support.
  • Patents in this domain must carefully navigate prior art—especially given global patent filings covering similar compounds or therapeutic methods.
  • The strategic positioning of AU2022280939 can benefit from aligning claim scope with international patent families, ensuring comprehensive territorial coverage.
  • Ongoing patent landscape monitoring is essential to detect potential conflicts or opportunities for patent strengthening.
  • Stakeholders should consider complementary patent strategies, including data exclusivity and formulation patents, to maximize market protection.

FAQs

Q1: What is the primary focus of patent AU2022280939?
A: The patent primarily claims a novel pharmaceutical compound or composition, along with methods of preparation or therapeutic use, aiming to secure exclusive rights in Australia.

Q2: How does the scope of claims affect patent enforceability?
A: Broader claims can provide extensive protection but may be more vulnerable to validity challenges, whereas narrower claims are easier to defend but limit the extent of exclusivity.

Q3: Are there risks of patent infringement from existing patents?
A: Yes; stakeholders should conduct thorough patent landscape analyses to assess potential overlaps or conflicts with existing patents, particularly in similar therapeutic areas.

Q4: How does the patent landscape influence commercialization strategies?
A: A crowded landscape requires strategic claim drafting, possibly seeking extensions via international filings, and developing complementary patents to strengthen market position.

Q5: What are the next steps after securing patent AU2022280939?
A: Ensuring patent maintenance, monitoring for infringement, evaluating opportunities for licensing, and potentially filing corresponding patents in other jurisdictions to maximize protection.


References

  1. Australian Patent Office, Official Patent Document AU2022280939.
  2. WIPO PATENTSCOPE, Patent Family Data.
  3. European Patent Office, Patent Search Reports.
  4. Google Patents, Related Patent Applications and Literature.
  5. Australian Patent Law and Guidelines, 2022 Edition.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.