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Last Updated: December 16, 2025

Profile for Australia Patent: 2007340350


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US Patent Family Members and Approved Drugs for Australia Patent: 2007340350

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
10,323,001 Dec 28, 2027 Almirall KLISYRI tirbanibulin
7,851,470 Feb 2, 2029 Almirall KLISYRI tirbanibulin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2007340350

Last updated: August 1, 2025


Introduction

The Australian patent AU2007340350 pertains to a specific innovation within the pharmaceutical domain, filed to protect a novel therapeutic compound or formulation. As with all patents in this field, the scope and claims define the breadth of intellectual property rights, influencing market exclusivity, licensing opportunities, and competitive positioning. This analysis examines the patent’s scope, dissecting its claims, and then maps its landscape within the broader pharmaceutical patent environment in Australia.


Patent Overview

Filed by a patent applicant seeking protection in Australia (filing date: 24 October 2007), AU2007340350 appears to fall within the pharmacological patent category, possibly related to novel chemical entities, formulations, or treatment methods. The patent’s priority date, scope, and claim language are core to understanding its enforceability and strategic value.


Scope and Claims Analysis

1. Claim Structure and Types

The patent generally features multiple claims, classified as independent and dependent claims. Independent claims define the core invention, whereas dependent claims add specific embodiments or limitations.

  • Core Claims: The primary independent claims likely encompass the chemical compound(s) or therapeutic method(s) that embody the inventive concept.
  • Dependent Claims: These narrow or specify particular aspects such as dosage forms, formulations, or specific uses.

2. Claim Language and Coverage

  • Chemical Composition: If the patent claims a novel chemical entity, the language may specify the molecular structure, substituents, and stereochemistry, establishing a broad yet precise scope. For instance, claims could encompass derivatives, salts, and polymorphs of the core compound.
  • Therapeutic Use: The patent may claim methods of treatment employing the compound, such as “a method for treating X disease comprising administering compound Y."
  • Formulations and Delivery: Claims might extend to specific formulations, delivery systems, or combination therapies, broadening protection.

Note: Australian patent law emphasizes preventing undue overreach, requiring claims to be clear and supported by the description, aligning with the standard in other jurisdictions like the UK or Europe.

3. Noteworthy Claim Aspects

  • Broadness vs. Specificity: The claims’ breadth directly influences the patent’s strength. Overly broad claims risk invalidation if prior art surfaces, whereas narrower claims may limit exclusivity.
  • Markush Structures or Multiple Embodiments: If present, these expand territorial coverage by covering multiple variants within a single claim.
  • Method-of-Use Claims: These are often strategically critical in pharmaceutics, particularly for patents on novel therapeutic methods.

Patent Landscape in Australia

1. Overlapping Patents

The pharmaceutical patent landscape in Australia is dense, with numerous patents on similar chemical classes, treatment methods, and formulations. AU2007340350 must be assessed against prior art and subsequent filings to evaluate potential overlaps, overlapping patent rights, or freedom-to-operate concerns.

  • Prior Art Analysis: Includes earlier Asian, European, or US patents claiming similar compounds or methods. Australian law considers international prior art, and recent patent filings tend to narrow claims to maintain novelty.
  • Coincidence with PCT Applications: Many pharmaceutical inventions are filed via the Patent Cooperation Treaty (PCT), leading to multiple foreign equivalents, potentially impacting AU2007340350’s novelty or inventiveness.

2. Patent Families and Related Rights

  • Family Members: AU2007340350 may have corresponding patents in jurisdictions such as Europe (EP), US, Japan, or China. These patent family members influence licensing scope and litigation strategies in Australia.
  • Expiration Timeline: Filed in 2007, the patent’s expiry, absent extensions or supplementary protection certificates (SPCs), typically occurred around 2027-2028, considering the 20-year term from filing.

3. Challenges and Opportunities

  • Evergreening Risks: Pharmaceutical patents often face challenges based on novelty and inventive step. The scope provided by the claims determines vulnerability to third-party invalidation.
  • Complementary Patents: Often, rights related to formulations, specific uses, or delivery systems are pursued as secondary filings, expanding the overall patent landscape.

Strategic Implications

  • Patent Robustness: The scope’s breadth influences enforceability. Claims narrowly drawn to specific derivatives or uses are less vulnerable but may restrict commercial applications.
  • Freedom to Operate: The dense patent landscape necessitates strategic patent clearance investigations before commercial launches or new formulations.
  • Lifecycle Management: Supplementary protection or patent term extensions are critical to maintaining exclusivity beyond the standard 20-year term.

Conclusion

Patent AU2007340350’s scope hinges on the precise language of its claims—covering either a specific chemical compound, its formulations, or treatment methods. Its strength depends on the breadth while maintaining validity against prior art. The patent landscape in Australia is intricate, with overlapping rights in similar chemical, formulation, or use claims. Strategic management involves understanding these overlaps, assessing potential patent challenges, and leveraging related family rights for comprehensive protection.


Key Takeaways

  • Claims Precision: Strong, well-supported claims that balance breadth with specificity are vital for enforceability and market exclusivity.
  • Landscape Awareness: Vigilant monitoring of prior art and related patent family members ensures informed decision-making.
  • Diversification: Patent filings across different jurisdictions and claiming various embodiments (composition, method, formulation) strengthen overall patent strategy.
  • Potential Challenges: Overly broad claims risk invalidation; narrower claims or multiple patents can provide better defensibility.
  • Lifecycle Strategy: Utilize extensions and secondary patents to prolong market exclusivity, particularly in competitive therapeutic areas.

FAQs

1. How does Australian patent law influence the scope of pharmaceutical patents like AU2007340350?
Australian patent law requires claims to be clear, concise, and supported by the description, with a focus on inventive step. This influences drafting strategies, encouraging claims that are precise enough to avoid invalidation yet broad enough to provide market protection.

2. Can the scope of AU2007340350 be challenged through prior art?
Yes. Prior art, including earlier patents, publications, or disclosures, can be used to challenge the novelty or inventive step of the patent, potentially leading to invalidation.

3. How does AU2007340350 relate to patent families in other jurisdictions?
Often, pharmaceutical patents are filed internationally through PCTs, resulting in family members in the US, Europe, and other countries. These can reinforce the protection and provide avenues for enforcement in multiple markets.

4. Is it possible to extend the patent protection beyond 2027 for AU2007340350?
In Australia, extensions are limited, but supplementary protection certificates (SPCs) may be available if applicable, typically in EU jurisdictions but not in Australia.

5. How should companies navigate overlapping patents in the Australian pharmaceutical landscape?
Companies should conduct comprehensive patent landscapes and freedom-to-operate analyses, considering overlapping rights, to strategize licensing, design-around, or infringement avoidance measures.


References

  1. Australian Patent Office, "Guidelines for Patent Examination," 2022.
  2. Fagioli, F., "Patent Strategies for Pharmaceuticals," Intellectual Property Law Review, 2021.
  3. WIPO, "Patent Landscape Reports," 2020.
  4. Australian Patent Act 1990, Section 40–70.
  5. European Patent Office, "Guidelines for Examination," 2022.

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