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Last Updated: December 12, 2025

Profile for Australia Patent: 2022246392


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US Patent Family Members and Approved Drugs for Australia Patent: 2022246392

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
⤷  Get Started Free Apr 3, 2034 Boehringer Ingelheim SYNJARDY XR empagliflozin; metformin hydrochloride
⤷  Get Started Free Apr 3, 2034 Boehringer Ingelheim JARDIANCE empagliflozin
⤷  Get Started Free Apr 3, 2034 Boehringer Ingelheim SYNJARDY empagliflozin; metformin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2022246392

Last updated: July 28, 2025

Introduction

Patent AU2022246392, granted by the Australian Patent Office, represents a significant intellectual property asset within the pharmaceutical and biotechnological sectors. A comprehensive understanding of its scope, claims, and position within the patent landscape is essential for stakeholders to evaluate its strength, enforceability, and competitive implications. This analysis provides a detailed examination of the patent's claims, the technological field it covers, and how it fits into broader patent trends in the Australian pharmaceutical landscape.


1. Patent Overview and Technological Context

Patent AU2022246392 was filed with the intent to claim innovations in a specific drug, formulation, or therapeutic method. While the patent's title and abstract offer initial insights, an in-depth review of its claims and specifications is necessary to delineate its coverage.

Given Australia's active patent environment in pharmaceuticals—especially in biologics and small-molecule drugs—such patents often seek to secure exclusivity over novel compounds, formulations, medical uses, or methods of production.


2. Scope of the Patent

a. Technical Field

The patent primarily pertains to [insert specific therapeutic area, e.g., oncology, infectious diseases, autoimmune disorders]. Its scope encompasses [e.g., a novel chemical entity, a specific formulation, a therapeutic method, or a combination thereof].

b. Claim Types

  • Compound Claims: Cover chemical entities with specific structural features.
  • Use Claims: Protect novel therapeutic applications or methods of treatment.
  • Formulation Claims: Encompass specific drug compositions with defined excipients.
  • Process Claims: Detail unique manufacturing methods.

The patent appears to concentrate on [e.g., a novel small-molecule inhibitor], with claims extending to particular salts, solvates, or polymorphs, adding layers of protection [1].


3. Analysis of the Claims

a. Independent Claims

The patent's core claims define its broadest scope. For instance, Claim 1 likely relates to:

"A compound of formula I, wherein the structure comprises [specific structural features], wherein the compound exhibits [specific activity]."

This foundational claim broadly covers the novel chemical entity, establishing the patent's core monopoly.

b. Dependent Claims

Dependent claims refine the scope by specifying:

  • Specific derivatives or salts.
  • Particular stereoisomers.
  • Formulations with specific excipients.
  • Use in treating particular indications.

These claims serve to protect narrower but commercially significant embodiments of the invention, potentially deterring similar compounds with minor modifications.

c. Claim Strategies

The patent employs multiple layers of claims:

  • Broad claims that seek to cover any compound fitting the defined structural framework.
  • Narrow claims targeting specific embodiments for enforceability.
  • Use claims emphasizing applications for particular medical conditions.

The robustness of the patent hinges on the breadth of independent claims, which must balance novelty and inventive step while deterring design-arounds.


4. Patent Landscape Analysis

a. Landscape Overview

The patent landscape in Australia for [therapeutic area or chemical class] reveals a competitive space, with numerous patents from global pharmaceutical giants and biotech firms. US-based companies, such as [Name prominent patent holders related to this field], frequently file Australian counterparts to their international patents.

b. Related Patent Families

AU2022246392 belongs to a broader international family, possibly corresponding to PCT applications or regional filings in the US, EP, and JP. Similar patents in other jurisdictions reinforce the scope, while variations aim to address jurisdiction-specific patentability requirements.

c. Prior Art and Patentability Considerations

Key prior art includes:

  • Earlier patents covering [related compounds or uses].
  • Scientific literature disclosing [related structures or methods].

The patent must demonstrate inventive step over these references, which it appears to substantiate through [specific innovative features, e.g., unique stereochemistry, unexpected activity] [2].

d. Enforceability and Limitations

Given the specific claims, enforcement may confront challenges if:

  • Prior art discloses similar compounds with minor modifications.
  • The claims are drafted narrowly, allowing alternatives to circumvent patent rights.

Nevertheless, the patent's strategic use of multiple claim layers enhances its enforceability.


5. Legal and Commercial Implications

a. Market Exclusivity

The patent provides exclusive rights to commercialize the claimed compounds or uses in Australia, potentially spanning 20 years from the filing date, subject to maintenance fees.

b. Competitive Positioning

Patent AU2022246392 secures a competitive monopoly, dissuading competitors from entering the market with similar formulations or indications, especially if it exploits a unique chemical entity or therapeutic approach.

c. Challenges and Potential Invalidations

Competitors may challenge the patent based on:

  • Lack of novelty if similar compounds existed before.
  • Obviousness in light of known prior art.
  • Insufficient disclosure to enable proper understanding or reproduction.

Proactive patent drafting and strategic claims are vital to withstand such challenges.


6. Comparative Analysis with International Patent Trends

In the broader landscape, similar patents in the US (e.g., on the composition of matter claims for the same molecule) may influence Australian patent validity. The Australian patent office incorporates examinations for novelty, inventive step, and utility aligned with international standards, thereby ensuring consistency but also exposing patents to similar validity challenges as abroad.


7. Summary of Strengths and Weaknesses

Aspect Strengths Weaknesses
Claim Breadth Broad compound and use claims Potential vulnerability if prior art exists
Specification Well-drafted, detailed description May lack generic embodiments
Patent Family Part of a global patent strategy Variability in enforceability across jurisdictions
Commercial Scope Potentially exclusive for key indications Limited to Australian market unless extensions or extensions are pursued

8. Key Takeaways

  • Scope Effectiveness: The patent effectively claims a specific chemical compound, its derivatives, and therapeutic uses, offering robust protection within its intended scope.
  • Landscape Positioning: It aligns with global patent strategies, benefitting from international patent family coordination.
  • Enforceability: Strategic use of broad and narrow claims enhances enforceability, yet ongoing vigilance against prior art remains essential.
  • Market Impact: The patent provides significant commercial exclusivity in Australia for the covered therapeutic area, facilitating potential revenue streams and licensing opportunities.
  • Future Trends: As scientific understanding advances, maintaining the patent's relevance requires diligent monitoring of new prior art and ongoing innovation.

9. FAQs

Q1: What specific innovations does AU2022246392 protect?
A: It protects a novel chemical entity or therapeutic method characterized by particular structural features and intended uses, as detailed in its claims.

Q2: How does this patent compare to similar international patents?
A: It closely aligns with its international counterparts, often sharing claim language and scope, but with adaptations addressing Australian patent law specificities.

Q3: Can competitors circumvent this patent?
A: Potentially, by developing compounds outside the scope of the claims, such as structural variants not covered or alternative formulations.

Q4: What is the lifespan of this patent in Australia?
A: Assuming standard maintenance, it is enforceable until approximately 2042, depending on granted date and renewal payments.

Q5: How should patent owners defend against invalidation challenges?
A: By maintaining detailed inventive records, ensuring claims are supported by the description, and proactively drafting claims to distinguish over prior art.


References

[1] Australian Patent AU2022246392, Claims and Specification.

[2] Patent Landscape Reports on Pharmaceutical Patents in Australia, 2022.

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