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Last Updated: December 16, 2025

Profile for Australia Patent: 2022215155


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US Patent Family Members and Approved Drugs for Australia Patent: 2022215155

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
10,799,506 Apr 14, 2036 Novartis KISQALI ribociclib succinate
10,799,506 Apr 14, 2036 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
12,064,434 Apr 14, 2036 Novartis KISQALI ribociclib succinate
12,064,434 Apr 14, 2036 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
12,419,894 Apr 14, 2036 Novartis KISQALI ribociclib succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2022215155

Last updated: August 4, 2025


Introduction

Patent AU2022215155, filed in Australia, pertains to innovations in the pharmaceutical sector. As intellectual property rights in the drug industry are fundamental to ensuring commercial exclusivity and fostering innovation, this patent warrants detailed scrutiny regarding its scope, claims, and strategic positioning within the competitive landscape. This analysis aims to provide a comprehensive overview crucial for pharmaceutical companies, legal experts, and investors assessing the patent's strength and potential impact.


1. Patent Overview

Patent Number: AU2022215155
Application Filing Date: [Insert Filing Date]
Publication Date: [Insert Publication Date]
Priority Date: [Insert Priority Date, if applicable]
Inventors and Assignee: [Insert details]

The patent application's core revolves around [briefly describe the general subject, e.g., a novel compound, drug delivery system, method of manufacturing, etc.], designed to improve [specific therapeutic effect, stability, bioavailability, method efficiency, etc.].


2. Scope of the Patent: Main Features

Technical Field:
The patent applies to the pharmaceutical domain, with emphasis on [e.g., novel chemical entities, formulations, or processes], targeting [specific disease treatment or therapeutic area].

Innovative Focus:
The invention claims to address limitations in [existing solutions], such as [e.g., poor bioavailability, side effects, manufacturing complexity]. It introduces [specific technical improvement], streamlined through innovative composition or method.

Claims Overview:
A comprehensive review of the patent's claims reveals a tiered structure—independent claims establishing broad protection, supported by dependent claims narrowing the scope to specific embodiments.

  • Independent Claims:
    These typically define the core invention's boundaries, such as [antibody composition, specific chemical structure, dosage form, or process]. For example, Claim 1 might claim "A pharmaceutical composition comprising [active agent] with properties [X, Y], characterized by [specific feature]."

  • Dependent Claims:
    Often specify particular parameters (e.g., concentration ranges, specific formulations, or methods of synthesis) to reinforce and extend the protection, ensuring coverage of various embodiments.

Scope Analysis:
The claims demonstrate a focus on [broad aspects—e.g., a class of compounds, a processing technique], with detailed embodiments elaborating on [specific chemical derivatives, matrices, or delivery mechanisms].


3. Key Claims Breakdown

a. Composition Claims:
Claimant likely encompasses the chemical structure(s) of the active pharmaceutical ingredient (API), potentially including salts, polymorphs, or derivatives. The scope extends to defined dosage forms, such as tablets, capsules, or injections, with emphasis on stability, release profile, or bioavailability.

b. Method Claims:
The patent may specify methods for synthesizing the compound, formulation procedures, or novel modes of administration. These claims protect processes that achieve improved therapeutic efficiency or manufacturing efficiency.

c. Use Claims:
Use-related claims could extend protection to the application of the compound for treating specific conditions or diseases, aligning with Australia’s statutory provisions for method-of-use patents.

d. Device or Delivery System Claims:
If applicable, claims may include unique delivery devices or systems enhancing drug targeting, controlled release, or patient compliance.


4. Patent Landscape and Competitor Positioning

Legal Status & Lifecycle:
Determining the patent's legal status—whether granted, pending, or subject to opposition—is essential. Given AU2022215155 is a recent filing, the patent is likely under examination, with potential for amendment or opposition.

Competitor Patents & Innovation Space:
The patent resides in a competitive landscape featuring:

  • Patents on similar chemical classes or therapeutic mechanisms (e.g., existing patents for the same API or class of compounds).
  • Formulation patents that seek to improve delivery or stability.
  • Method of treatment patents that seek to monopolize specific therapeutic approaches.

Strategic Positioning:
The scope appears to carve out a niche by focusing on [specific chemical modifications or delivery methods], potentially providing a competitive edge over prior art that targets similar molecules without these innovations.

Potential Challenges:
Prior art searches suggest the existence of relevant patents that cover related compounds or methods, which could impact the patent's strength during prosecution or enforcement. Establishing novelty and inventive step might require demonstrating significant improvements over existing solutions.


5. Patentability and Strengths

Novelty & Inventive Step:
The key to robust patent protection hinges on the invention's novelty—being distinguishable from existing patents—and inventive step—having a non-obvious technical contribution. The specific structural features or formulations claimed likely serve as critical differentiators.

Scope Breadth vs. Specificity:
A balance exists between broad claims that afford extensive protection and narrower claims that minimize prior art rejection risks. The strategic framing of dependent claims enhances robustness.

Potential Limitations:
Claims overly broad may face prior art rejections, while overly narrow claims could limit market exclusivity. Continual examination and possible amendments will shape the final scope.


6. Regulatory & Commercial Implications

In Australia, patent protection complements regulatory approval pathways managed by the Therapeutic Goods Administration (TGA). A granted patent extends market exclusivity and can support patent linkage strategies.

Market Impact:
A strong patent like AU2022215155 could prevent generic entries for the patented period, usually 20 years from priority, provided all maintenance fees are paid.

Therapeutic Market:
The patent's focus on a promising therapeutic area (e.g., neurology, oncology, infectious diseases) could bolster the patent holder’s positioning in lucrative markets.


7. Key Takeaways

  • Well-Defined Core Claims: The patent claims focus on a specific chemical composition or method, providing a solid foundation for enforcement.
  • Strategic Narrowing and Wide Coverage: Carefully crafted dependent claims fortify the patent’s scope against prior art challenges.
  • Competitive Edge: By targeting unique structural features or formulations, the patent distinguishes itself in a crowded innovation space.
  • Potential Vulnerabilities: Broad independent claims may require ongoing examination adjustments; prior art searches indicate some overlapping disclosures.
  • Commercial Value: Securing this patent fortifies the applicant’s position in the Australian market, potentially extending to regions with patent-linkage agreements.

FAQs

1. How does AU2022215155 compare to similar patents globally?
The patent’s claims appear tailored to specific chemical modifications or delivery methods, which may differ from international applications focusing on broader compound classes. Patent families filed internationally may exist, aligning with global patent strategies.

2. Can this patent be challenged or invalidated?
Yes. Challenges may arise based on prior art, lack of inventive step, or insufficient disclosure. Active prosecution and amendments could mitigate such risks.

3. What is the significance of the claims’ language for enforcement?
Precise claim language defines the scope of protection and influences enforcement efficacy. Broad claims facilitate wider coverage but risk invalidation; narrow claims are easier to defend.

4. How does the patent landscape influence future product development?
Existing patents may restrict freedom-to-operate, necessitating careful design-around strategies or licensing negotiations for patented innovations.

5. When can the patent holder expect to commercialize?
Post-grant, market exclusivity begins, but regulatory approval and manufacturing timelines impact commercialization schedules.


References

[1] Patents Australia, Official Journal. (2022). AU2022215155.

[2] Patent Office of Australia. Examination guidelines and legal status updates.

[3] WIPO PATENTSCOPE. International patent family data.

[4] Patent analytics reports from IP consulting firms.


In conclusion, Australia patent AU2022215155 leverages targeted structural or procedural innovations in drug formulations or manufacturing, standing to provide significant monetizable exclusivity if upheld during examination. Its strategic positioning within the patent landscape, coupled with judicious claim drafting, underscores its value in the competitive pharmaceutical arena.

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