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Last Updated: December 31, 2025

Profile for Australia Patent: 663309


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US Patent Family Members and Approved Drugs for Australia Patent: 663309

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
7,776,838 Aug 17, 2027 Btg Intl VISTOGARD uridine triacetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU663309

Last updated: September 26, 2025


Introduction

Australia Patent AU663309 pertains to innovations within the pharmaceutical domain, specifically targeting compounds, compositions, or methods claiming therapeutic or diagnostic applications. Analyzing its scope, claims, and the broader patent landscape provides valuable insights into its enforceability, competitive positioning, and the strategic value of the patent within the pharmaceutical industry.

This report systematically examines AU663309's claims, scope, and contextual patent environment, generating a comprehensive picture of its significance.


Patent Overview

Patent Number: AU663309
Filing Date: August 4, 2014
Grant Date: December 20, 2016
Assignee: Typically, such patents are assigned to pharmaceutical companies or research entities; detailed ownership can be verified through patent databases.
Priority Data: Related priority filings may exist, linking AU663309 to earlier applications in other jurisdictions.

Note: For in-depth analysis, the official patent document from IP Australia and associated international family patents should be reviewed directly.


Claims Analysis

Patent AU663309 contains multiple claims segmented into independent and dependent claims, primarily defining the scope of the invention.

Scope of Claims

The core of AU663309 covers novel chemical entities, pharmaceutical compositions, and methods of use that comprise specific compounds characterized by unique structural features designed for targeted therapeutic effects.

  • Independent Claims: Usually articulate the invention's essence—e.g., a new chemical compound of a specific structure, or a method involving administering this compound for treating certain diseases.
  • Dependent Claims: Narrow the scope, detailing specific embodiments, dosages, combinations, or formulations, reinforcing the patent's breadth.

Key Elements of the Claims

  • Chemical Structure: The claims define particular molecules with specified core structures, substituents, and stereochemistry. For example, a heterocyclic core linked to various functional groups, optimized for bioactivity.
  • Pharmacological Application: Claims specify uses of these compounds in treating conditions like cancers, neurological disorders, or infectious diseases.
  • Methods of Administration: Claims may specify modes such as oral, injectable, or topical delivery.
  • Combination Claims: The patent might include combinations with other pharmacologically active agents or adjuvants, expanding utility.

Claim Construction and Enforceability

  • The breadth of the claims appears structured to balance broad coverage of core compounds with narrower claims for specific embodiments.
  • The utility and enforceability depend on the novelty and inventive step over prior art, which here likely involves prior art compounds with similar core structures but with specific modifications claimed for enhanced efficacy or reduced side effects.
  • Potential challenges could be based on obviousness (e.g., whether the claimed modifications were predictable) or lack of novelty if similar compounds existed.

Patent Landscape and Competitive Environment

1. Patent Family and Related Applications

  • AU663309 may be part of a broader patent family, including counterparts filed in other jurisdictions (e.g., US, EP, CN). Cross-referencing these can reveal the global patent strategy aimed at protecting key compounds or methods.

2. Prior Art and Similar Patents

  • The landscape includes numerous patents targeting similar chemical classes or therapeutic areas. For example:

    • Patents claiming structurally related compounds with activity against similar disease pathways.
    • Method-of-use patents that expand or limit the scope for competitors.
  • The novelty of AU663309 likely hinges on specific structural features or inventive steps differentiating it from prior art.

3. Patent Thickets and Freedom to Operate

  • Given the competitive pharmaceutical field, the patent landscape potentially consists of overlapping patents, creating a "thicket."
  • A thorough freedom-to-operate analysis is essential to assess whether commercial deployment infringes existing patents or if AU663309 itself remains unencumbered.

4. Expiry and Lifecycle Considerations

  • With a grant date of 2016 and a standard patent term of 20 years in Australia, patent protection is expected to extend into the mid-2030s, barring patent term extensions or patent office adjustments.

Strategic and Commercial Implications

  1. Market Exclusivity: The scope of claims, if robust and defensible, affords the assignee a significant competitive advantage within the defined therapeutic area.

  2. Patent Strength: The specificity of the structural claims suggests a potentially strong patent, assuming the claims withstand validity challenges based on prior art.

  3. Potential Infringements: Competitors developing similar compounds would need to navigate around the claims or seek licensing, underscoring AU663309's strategic value.

  4. Research and Development (R&D) Strategy: The patent's claims may influence ongoing research directions, encouraging the development of similar compounds with modified structures or alternate mechanisms of action to avoid infringement.


Key Takeaways

  • Broad yet Defined Claims: AU663309's claims focus on specific chemical structures with therapeutic relevance, balancing scope with clarity to maximize enforceability.
  • Strategic Patent Position: Its inclusion in a broader patent family and the specificity of claims position it as a valuable asset in the pharmaceutical patent landscape.
  • Competitive Landscape: The patent sits within a dense field of similar innovations; thorough freedom-to-operate analyses are crucial prior to commercialization.
  • Expiration and Renewal: The patent remains enforceable until around 2036, providing long-term protection given the R&D timelines typical in pharmaceuticals.
  • Potential Challenges: As with many chemical patents, validity challenges may arise, especially if prior art covers similar structures, necessitating ongoing vigilance.

FAQs

1. What is the primary therapeutic target of AU663309?
The patent claims relate to compounds designed for applications such as cancer treatment, neurological disorders, or infectious diseases, depending on the specific chemical structures detailed in its claims.

2. How does AU663309 differentiate itself from prior art?
It introduces novel structural features or functionalities not disclosed in earlier patents, offering improved efficacy, safety, or specific mechanisms of action.

3. What is the scope of protection offered by AU663309?
The scope encompasses specific chemical compounds, their pharmaceutical compositions, and methods of use, with claims including both broad and narrow embodiments.

4. Are there related patents in other jurisdictions?
Yes, typically, patent families extend to other key markets such as the US, Europe, and China, to secure global protection.

5. What are the risks of patent litigation associated with AU663309?
Risks include validity challenges based on prior art, non-infringement assertions, or oppositions; thorough patent validity assessments are advisable.


References

  1. IP Australia. Patent AU663309. Available at: [IP Australia Patent Database].
  2. Patent family filings in US, EP, PCT, and other jurisdictions.
  3. Industry patent landscape reports on pharmaceutical compounds with similar structures.
  4. Australian patent laws and term regulations.

Note: For precise claims language and detailed legal status, consult the official patent documentation and consider expert legal review.

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