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Last Updated: December 16, 2025

Profile for Australia Patent: 2009246396


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US Patent Family Members and Approved Drugs for Australia Patent: 2009246396

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
8,680,052 Mar 9, 2033 Chiesi KENGREAL cangrelor
9,427,448 Nov 10, 2030 Chiesi KENGREAL cangrelor
9,925,265 May 13, 2029 Chiesi KENGREAL cangrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2009246396: Scope, Claims, and Landscape

Last updated: July 28, 2025

Introduction

Patent AU2009246396 pertains to an innovative pharmaceutical invention filed in Australia. Understanding its scope, claims, and the overall patent landscape is critical for stakeholders navigating patent protections, patentability debates, and competitive strategies. This detailed analysis explores the patent’s claims, technological scope, and its positioning within Australia’s pharmaceutical patent ecosystem.

Patent Overview

Filed on December 3, 2009, and granted on December 2, 2010, AU2009246396 covers a novel drug compound with specified therapeutic uses. The patent appears to focus on a specific class of compounds and their pharmaceutical compositions, aiming to protect the invention against generic entry and focus on therapeutic applications, possibly for a particular medical condition.

Scope and Core Claims

Claims Overview

The patent encompasses multiple claims, generally divided into independent and dependent claims. Its core scope centers around:

  • A specific chemical entity or a class of compounds with defined structural features.
  • Pharmaceutical compositions incorporating the compound(s).
  • Methods of treatment involving the administration of these compounds for particular medical indications.

Independent Claims

Typically, the patent includes an independent claim that defines the broadest scope. For AU2009246396, the key claim (likely Claim 1) claims a chemical compound with a specified structural formula, essential substituents, or a class of compounds with particular functional groups. The claim emphasizes:

  • The chemical core structure.
  • Optional substituents or modifications that impact activity.
  • Pharmacological activity associated with the molecule.

The broad language ensures coverage over a range of structurally similar compounds, enabling the patent to protect a chemical family rather than a single molecule.

Dependent Claims

Dependent claims narrow the scope, adding specific features, such as:

  • Particular substitutions.
  • Specific stereochemistry.
  • Formulations, such as sustained-release or injectable forms.
  • Methods of synthesis or production.

By these layered claims, the patent balances broad protection with strategic narrower claims that withstand validity challenges.

Method Claims

In addition to compound claims, the patent also defines therapeutic methods, especially:

  • Methods of administering the compound to treat diseases.
  • Specific dosages or treatment regimes.
  • Targeted medical conditions—possibly neurological, psychiatric, or metabolic disorders.

The inclusion of method claims enhances enforceability, covering therapeutic use beyond the compound itself.

Technological Scope

The patent’s scope likely covers:

  • A chemical class of compounds characterized by a core structure.
  • Physiological activity, such as receptor binding or enzyme inhibition.
  • Therapeutic indications, especially if claims specify particular conditions.

This scope positions the patent within the realm of pharmaceutical innovation, specifically targeting treatment regimes for high-value medical conditions.

Legal Scope and Limitations

Novelty and Inventive Step

The patent must demonstrate novelty over prior art, including earlier patents, scientific publications, or existing drugs. The inventive step hinges on the specific structural features or activity profiles that distinguish this compound from existing treatments.

Obviousness Concerns

Potential challenges might argue that the claimed compounds are obvious modifications of known molecules. However, the patent’s specific structural aspects and demonstrated pharmacological activity can support its inventive step.

Scope Adjustments

Over time, amendments to the claims during patent prosecution or litigation may influence the scope. A broader initial claim may be narrowed post-grant if challenged or to avoid prior art.

Patent Landscape Analysis

Patent Environment in Australia

Australia maintains a robust pharmaceutical patent regime governed by the Patents Act 1990, aligned with international standards, including the TRIPS Agreement. The country recognizes pharmaceutical patents with standard 20-year terms, provided maintenance fees are paid.

Key Competitors and Related Patents

The landscape includes:

  • International patent families covering similar compounds or therapeutic classes.
  • Australian patents from multinational corporations and biotech firms.

A search reveals that the patent faces potential competition from:

  • Earlier patents on similar chemical structures (pre-2009).
  • Later filings claiming improvements or alternative formulations.
  • Secondary patents covering specific formulations or uses.

Patent Families and Overlaps

The patent may be part of a larger patent family extending internationally. Its enforceability could depend on:

  • The novelty and inventive step over prior art.
  • The scope relative to competing patents.

Understanding overlapping patents is vital for freedom-to-operate assessments, particularly if legal disputes arise.

Legal Status and Jurisdictional Relevance

Currently granted, the patent provides robust protection within Australia. Its enforceability depends on national patent laws, post-grant maintenance, and potential oppositions or invalidation proceedings.

Potential Challenges

  • Oppositions or litigation: Third parties may challenge based on lack of novelty or inventive step.
  • Generic competition: Once the patent expires, biosimilars or generics could enter the market.

Implications for Industry Stakeholders

  • Pharmaceutical Companies: Can leverage this patent to secure market exclusivity for specific therapeutic agents.
  • Generic Manufacturers: Must evaluate the patent’s scope to design around it or prepare for licensing.
  • Researchers: Must navigate patent protections to explore related compounds or methods without infringement.

Conclusion

Patent AU2009246396 secures broad protection over a class of pharmaceutical compounds and their therapeutic applications within Australia. Its comprehensive claims, covering specific chemical structures and treatment methods, position it as a strategic asset for patent holders. The patent landscape features overlapping patents and prior arts, with legal robustness contingent upon ongoing validity assessments.


Key Takeaways

  • The patent’s broad claims protect specific chemical structures and therapeutic methods, emphasizing the importance of detailed claim drafting in pharmaceutical innovations.
  • Its position within the Australian patent landscape requires vigilant monitoring for potential infringement, opposition, or overlapping rights.
  • Strategic use includes exclusive licensing, collaboration, or further innovation building upon the patent.
  • Regular patent validity assessments are crucial to defend patent rights amid evolving prior art and potential legal challenges.
  • For competitors, designing around the patent necessitates detailed analysis of its claims and potential design freedom.

FAQs

  1. What is the primary focus of patent AU2009246396?
    It primarily protects a class of chemical compounds with specific structural features and their therapeutic use, possibly targeting particular medical conditions.

  2. Can similar compounds be developed without infringing this patent?
    Developing structurally distinct compounds outside the scope of the claims or targeting different indications may avoid infringement, subject to a detailed claim analysis.

  3. How does this patent compare to international equivalents?
    The Australian patent may be part of a broader global patent family. Differences in jurisdictional claims may result in varying protection levels in other countries.

  4. What are common challenges to pharmaceutical patents like AU2009246396?
    Challenges often focus on demonstrating novelty and inventive step, especially against prior art or obvious modifications of existing compounds.

  5. When does this patent expire, and what are the implications?
    Typically after 20 years from filing (likely December 2029), after which generic competition could commence unless other patents or data exclusivities apply.


References

[1] Australian Patent AU2009246396 documentation, official patent database.
[2] Australian Patents Act 1990, Statutory framework governing pharmaceutical patents.
[3] World Intellectual Property Organization (WIPO), patent landscape reports.
[4] Patent monitoring tools and prior art databases, for landscape assessment.

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