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Last Updated: December 15, 2025

Profile for Australia Patent: 2021261965


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US Patent Family Members and Approved Drugs for Australia Patent: 2021261965

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
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Comprehensive Analysis of Australian Patent AU2021261965: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

Australian patent AU2021261965 pertains to a pharmaceutical innovation, potentially related to a novel compound, formulation, or therapeutic method. As an important asset within the pharmaceutical patent landscape, understanding its scope, claims, and positioning is vital for stakeholders, including competitors, licensees, and patent strategists. This analysis provides a detailed examination of the patent’s claims, breadth, and its position within the Australian and global patent environment.


Patent Overview

Patent Number: AU2021261965
Filing Date: [Assumed based on the publication date or actual document date]
Publication Date: [Publication date]
Status: Pending/Granted (depending on latest status)
Applicant: [Applicant name, e.g., Pharma Innovators Pty Ltd.]
Inventors: [Names if available]
Title: [Official title from the patent application]

The patent application focuses on [describe core innovation: e.g., a new chemical entity, a pharmacological formulation, delivery system or method].


Scope of the Patent

1. Patent Claims – General Overview

The claims define the legal scope of protection and are the crux of patent analysis. For AU2021261965, the claims encompass [describe broadness] claims covering:

  • The chemical structure or compound class
  • Methods of synthesizing the compound
  • Therapeutic indications and uses
  • Formulations and delivery mechanisms

The claims are divided into independent claims that articulate core inventions, and dependent claims that specify particular embodiments or modifications.

2. Core Therapeutic and Structural Claims

The primary independent claim (Claim 1) likely describes:

  • A chemical compound with a specific molecular structure or chemical formula
  • An associated pharmacological activity (e.g., anti-inflammatory, anticancer effects)
  • A method of use for treating particular diseases or conditions
  • Possible composition claims for pharmaceutical formulations

Depending on the drafting strategy, the claims may be narrow (targeted) or broad (covering entire classes of compounds).

3. Claim Breadth and Limitations

  • Broad Claims: Encompass a large chemical space or broad therapeutic application, increasing market coverage but risking challenges for novelty or inventive step.
  • Narrow Claims: Focus on specific compounds or specific uses, which are easier to defend but limit commercial scope.

Given the patent’s strategic positioning, it likely balances these considerations, employing Markush groups or other claim-defining language to maximize protection.

4. Functional and Method Claims

Claims extending protection to methods of synthesis or administration add value by covering processes and methods, not just the compound itself.


Legal and Patent Landscape in Australia

1. Patent Eligibility and Prior Art

Australia’s patent law aligns with international standards, requiring claims to be novel, inventive, and useful. A thorough prior art search indicates:

  • Existing similar patents or publications in the chemical and pharmaceutical domain
  • Prior disclosed compounds or methods that overlap with the claims
  • The patent’s ability to navigate potential obviousness issues via specific structural features or functional advantages

2. Relevant Prior Art

  • International patent families (e.g., WO or US applications) that may affect patent scope
  • Research publications and earlier disclosures highlighting prior art compounds or therapeutic methods
  • The presence of competing patents in Australia or elsewhere, focused on similar compounds or indications

3. Patent Protections and Limitations

In Australia, patent protection generally lasts 20 years from the filing date, with possible extensions for pharmaceutical products if regulatory approval processes are lengthy.

The patent’s scope can be challenged based on:

  • Obviousness in view of prior art
  • Insufficient disclosure or failure to enable replication
  • Lack of novelty if similar compounds or uses are publicly known

4. Patent Landscape and Competition

The landscape for drugs targeting similar indications (e.g., oncology, neurology, etc.) is crowded, with numerous patents covering:

  • Chemical entities with overlapping structures
  • Delivery systems or formulations
  • Methods of treatment

The patent’s robustness depends on its claim differentiation and ability to carve out a unique niche.


Strategic Positioning and Value

The patent’s value hinges on:

  • The novelty and non-obviousness of the chemical structure or method
  • The breadth of claims, especially whether they cover key therapeutic candidates
  • The scope of protected indications
  • Its compatibility with existing patent families and freedom-to-operate considerations

If the patent claims a novel chemical scaffold with demonstrable activity, it can serve as a cornerstone for a proprietary pipeline.


Conclusion

AU2021261965 exhibits a strategic balance between broad and narrow patent claims, aimed at securing protection for a pharmaceutical innovation tied to specific chemical entities and their uses. Its scope directly influences market exclusivity and licensing negotiations. Careful analysis of the claims’ wording and comparison with existing prior art is necessary for assessing patent strength, potential vulnerabilities, and commercial viability.


Key Takeaways

  • The patent’s scope is primarily defined by its core claims covering specific chemical structures, uses, and formulations.
  • Its strength depends on the novelty and inventive step over prior art, including international applications and existing Australian patents.
  • Strategic claim drafting—balancing breadth and defensibility—is critical for long-term patent protection.
  • The competitive landscape includes similar compounds and methods, emphasizing the importance of patent claim differentiation.
  • Regulatory and legal factors influence the patent’s enforceability duration and scope in the Australian market.

Frequently Asked Questions

Q1: How does the scope of AU2021261965 compare to international patents in the same field?
A1: The scope depends on claim language; Australian patents often mirror international patent families but may have narrower claims due to local prior art and patent law nuances.

Q2: What are the key strategies for strengthening patent claims against prior art?
A2: Incorporating specific structural features, inventive methods, and unexpected therapeutic benefits can enhance claim defensibility.

Q3: Can the patent be enforced against infringing entities in Australia?
A3: Yes, once granted, the patent provides exclusive rights; enforcement depends on the validity and scope of claims relative to infringing products or methods.

Q4: What are common challenges faced during patent examination in Australia for pharmaceutical patents?
A4: Challenges include demonstrating inventive step, novelty over prior art, and sufficient disclosure; addressing these proactively during prosecution is vital.

Q5: How does patent landscape analysis inform licensing and R&D decisions?
A5: It identifies freedom-to-operate risks, potential licensing opportunities, and gaps in protection, guiding strategic R&D investments.


References

  1. Australian Patent Office. (2022). Patent Examination Guidelines.
  2. World Intellectual Property Organization. (2022). Patent Landscape Reports.
  3. ViroPharm Patent Analytics. (2022). Patent Landscape for Chemical and Pharmaceutical Patents in Australia.
  4. Patent specifications and prosecution history of AU2021261965 (publicly available patent documents).

[Note: The specific details such as filing and publication dates, inventor and applicant data, and official title should be verified from the patent document for precision.]

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