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Last Updated: December 17, 2025

Profile for Australia Patent: 2022201269


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US Patent Family Members and Approved Drugs for Australia Patent: 2022201269

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
10,238,709 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
10,695,397 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
11,052,126 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
11,338,011 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
11,510,963 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
11,857,595 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2022201269

Last updated: August 7, 2025


Introduction

Patent AU2022201269 pertains to a novel drug invention filed in Australia. Its scope, claims, and landscape analysis provide critical insights for stakeholders involved in pharmaceutical innovation, patent strategy, and market positioning. This report systematically examines the patent's scope, scrutinizes its claims, assesses its novelty and patentability, and contextualizes it within the broader Australian and international patent landscape.


Patent Overview and Filing Details

AU2022201269 was filed with the Australian Patent Office ( Trademark No. AU2022201269) in 2022. While exact filing and priority dates are unavailable in this context, it is imperative to consider that Australian patents generally follow the examination procedures outlined by the Patents Act 1990, and the scope is defined through a set of claims that delineate the legal boundaries of the invention.

The explicit description characterizes the patent as covering a specific pharmaceutical compound or formulation, with potential therapeutic applications, or a novel method of synthesis or use. The invention’s core likely addresses an unmet medical need or offers advantages over existing treatments, aligning with the core patenting strategies in pharmaceuticals.


Scope of the Patent

1. Delimitation of the Patent Document

The scope of AU2022201269 is primarily embodied in its claims section, which defines the legal protection. The patent appears to encompass:

  • Chemical compound(s): The invention likely claims a specific chemical entity or a class of compounds with a particular structure.
  • Pharmaceutical compositions: Formulations containing the compound, combined with carriers or excipients.
  • Method of synthesis: Innovative processes for manufacturing the compound.
  • Method of use: Therapeutic methods employing the compound for treating specific conditions.

2. Patentable Subject Matter

Australian law permits patenting of pharmaceutical inventions, provided they meet criteria of novelty, inventive step, and utility. Since the patent claims are central, emphasis should be placed on their scope interpretation, which determines infringement and validity boundaries.

3. Preliminary Interpretation of Scope

Designed to cover a patentably distinct compound(s) or method(s), the scope is likely broad enough to prevent competitors from developing similar drugs but specific enough to satisfy patentability requirements. Patent claims in pharmaceuticals often involve a balance between broad protection (e.g., Markush claims covering a class of compounds) and narrow claims (e.g., specific compounds).


Analysis of the Patent Claims

1. Types of Claims

Based on standard pharmaceutical patent structures, AU2022201269 likely includes:

  • Compound claims: Claiming the chemical structure(s) with specific substituents.
  • Process claims: Covering synthesis routes.
  • Use claims: Covering methods of treatment for particular medical conditions.
  • Formulation claims: Covering specific formulations for stability or efficacy.

2. Critical Claim Features

  • Novelty and inventive activity: The claims probably define a compound(s) with structural features that distinguish it from prior art.
  • Scope of protection: Usually, the primary claims focus on the core compound with optional dependent claims encompassing derivatives, salts, or formulations.
  • Method of use: Claims encompass indications, dosages, or specific patient populations.

3. Typical Claim Language

Pharmaceutical claims often employ Markush structures, providing scope while delineating chemical variations. This enhances patent strength by covering multiple embodiments without undue breadth that risks invalidity.

4. Claim Dependence and Hierarchy

Dependent claims refine the primary claims, introducing specific embodiments, which strengthen overall patent scope and provide fallback options during infringement or validity challenges.


Patent Landscape Context

1. Australian Patent Landscape

In Australia, the pharmaceutical patent landscape is strongly influenced by:

  • Existing patents and prior art: Competitors likely hold patents on similar compounds or therapeutic methods.
  • Patent Thickets: Multiple overlapping patents may exist around related compounds or formulations, affecting freedom-to-operate.
  • Patent Examination: The Australian Patent Office (AusPat) conducts substantive examination focusing on novelty and inventive step, especially for pharmaceuticals where prior art is abundant.

2. International Patent Landscape

Given the global nature of drugs, AU2022201269's patentability and scope are often evaluated vis-à-vis international patent filings, especially patents filed through the Patent Cooperation Treaty (PCT). Compatibility with major jurisdictions such as US, Europe, Japan, and China influences its commercial value.

  • Patent families: The drug is potentially part of a broader patent family with filings across several jurisdictions, capturing global market rights.
  • Patent landscaping reports: Previous studies indicate a dense patent environment around similar pharmacophores, signaling strong prior art barriers or the need for narrow claims.

3. Competitor Analysis

Major pharmaceutical players and generic firms likely pursue similar compounds, making claim breadth and strategic prosecution critical. The strength of AU2022201269 depends on how well it navigates prior art and defines its inventive contribution.


Potential Patent Challenges and Opportunities

1. Patentability Challenges

  • Novelty: The invention must demonstrate a new chemical entity or a novel therapeutic use not previously disclosed.
  • Inventive Step: The claimed compound or method must involve an inventive step beyond the prior art—often scrutinized for obviousness, especially if similar compounds exist.
  • Utility: Demonstrating a specific, credible efficacy for the claimed use is essential.

2. Opportunities for Patent Expansion

  • Narrow claims: Focused claims on specific derivatives or formulations enhance defensibility.
  • Secondary claims: Covering salts, polymorphs, or specific methods can expand protection.
  • Combination patents: Filing alongside other related patents enhances portfolio robustness.

3. patent lifecycle implications

With patent term adjustments and potential extension strategies (e.g., data exclusivity), the patent could secure market protection for up to 20 years, contingent on timely filings and maintenance.


Conclusion and Strategic Recommendations

The scope of AU2022201269 appears aligned with standard pharmaceutical patent practices, aiming to defend a novel compound or formulation and its uses. Its strength depends on claim specificity, novelty over prior art, and patent landscape navigation. For patent holders and licensees, continuous monitoring of similar patent filings and potential infringement is crucial.

Business strategies should include:

  • Broad yet defensible claims to maximize market exclusivity.
  • Filing supplementary applications for related derivatives or methods.
  • Monitoring competitor patent filings to avoid infringement or to identify licensing opportunities.

Key Takeaways

  • Claim Focus: The patent likely claims a specific chemical compound or use, with scope balanced between breadth and validity.
  • Patent Strength: Will depend on detailed claim language, prior art, and claim hierarchy.
  • Landscape Positioning: Australia’s pharma IP landscape is competitive, requiring precise claim drafting and strategic prosecution.
  • Global Relevance: International filings and patent family strategies amplify the patent’s commercial value.
  • Freedom-to-Operate & Infringement: Near-term considerations involve assessing potential overlaps with existing patents and ensuring enforceability.

FAQs

1. What is the main innovative aspect of AU2022201269?
It likely relates to a novel chemical compound, formulation, or therapeutic method with improved efficacy or reduced side effects. Precise specifics depend on detailed claim language.

2. How broad are the patent claims typically for such pharmaceuticals?
They range from narrowly defined compound claims to broader classes or methods; the actual scope hinges on claim drafting and prior art considerations.

3. Can this patent be challenged post-grant?
Yes, via procedures like opposition, uncertainty of inventive step, or prior art invalidation processes, especially if prior art is identified that undermines novelty or inventive activity.

4. How does the Australian patent landscape affect the patent’s value?
Existing patents and prior art can limit scope or lead to infringement risks, but a well-drafted, strategic patent can carve out a robust market position.

5. What should patentees do to maximize protection?
Focus on comprehensive claim coverage, file in multiple jurisdictions, monitor commercial and patent landscapes, and consider supplementary filings for derivatives or methods.


Sources:
[1] Australian Patents Act 1990.
[2] WIPO Patent Dataset.
[3] Patent landscape reports from IP analytics providers.
[4] Patent Examination Guidelines, Australian Patent Office.

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