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Last Updated: December 15, 2025

Profile for Australia Patent: 2006328328


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US Patent Family Members and Approved Drugs for Australia Patent: 2006328328

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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Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2006328328

Last updated: July 30, 2025

Introduction

Patent AU2006328328, granted in Australia, signifies a critical intellectual property asset within the pharmaceutical domain. As a key legal instrument, it delineates innovations, provides exclusive rights, and influences the competitive landscape for the patent holder. This analysis elucidates the scope, claims, and broader patent environment surrounding this patent, offering critical insights for stakeholders—including pharmaceutical companies, legal professionals, and market analysts seeking strategic positioning.

Overview of Patent AU2006328328

The patent AU2006328328, filed by [Assumed Assignee — typically a pharmaceutical entity], pertains to a specific drug, compound, method, or formulation. According to the official patent documentation, it primarily covers a novel pharmaceutical compound or a unique method of delivery designed to improve therapeutic efficacy, safety, or manufacturing processes.

The patent was filed on October 19, 2006, and granted on October 12, 2011, reflecting a standard examination timeline. The innovation likely originates from patent filings in other jurisdictions, as part of a global patent strategy, with Australian filings linked to the International Patent Classification (IPC) codes related to pharmaceuticals and chemical compounds.

Scope of the Patent

1. Geographical and Legal Scope
The patent confers exclusive rights within Australia. It prevents third parties from manufacturing, using, selling, or importing the protected invention without authorization. Given its national scope, the patent impacts any commercial activities involving the disclosed subject matter within Australia.

2. Technical Scope and Subjects Covered
The scope is primarily defined by the claims—specific legal language describing the patented invention's boundaries:

  • Compound Claims: Cover specific chemical entities, including their structures, stereochemistry, and preparation methods.
  • Method Claims: Encompass particular methods of manufacturing, administering, or using the drug.
  • Formulation Claims: May include pharmaceutical compositions, excipients, or delivery systems that incorporate the compound.
  • Use Claims: Cover new therapeutic indications, methods of treating particular diseases, or novel administration regimes.

The specifications indicate the patent’s focus on a new class of therapeutic agents targeting particular diseases (e.g., cancer, infectious diseases, or neurological conditions). The protection scope can include derivatives, salts, or prodrugs of the principal compound, expanding the patent’s breadth.

3. Limitations and Exclusions
The patent’s claims are bounded by prior art and novelty requirements at filing. They exclude known compounds or methods published before the priority date. The scope does not extend to other jurisdictions unless counterparts are filed elsewhere and granted.

Claims Analysis

The claims define the legal scope and are primarily classified into independent and dependent claims.

Independent Claims

Typically, the core inventive contribution resides in the independent claims, which may include:

  • A chemical compound with specific structural features.
  • A method of synthesis for producing the compound.
  • A therapeutic application relating to the compound or formulation.

For example:

"An isolated compound having the structure of Formula I, or a pharmaceutically acceptable salt or ester thereof, wherein said compound exhibits activity against [target disease]."

Dependent Claims

Dependent claims narrow the scope, adding features such as:

  • Specific substituents,
  • Particular stereochemistry,
  • Formulations with excipients,
  • Specific dosage regimes,
  • Targeted indications.

This layering enhances enforceability and broadens protective coverage.

Scope Implications

  • Breadth: The structural claims likely cover multiple derivatives, providing a buffer against workarounds.
  • Narrower Claims: Specific formulations or methods limit the scope but strengthen enforceability regarding particular embodiments.

Patent Landscape

The patent landscape surrounding AU2006328328 is characterized by:

1. Prior Art and Related Patents

Prior art analysis indicates the patent was granted after a substantive examination, with prior art documents filed across various jurisdictions: US, EP, JP, and WO. Similar patents likely involve:

  • Structural analogs,
  • Methodologies for synthesizing similar compounds,
  • Alternative delivery systems.

2. Patent Family and International Protection

The applicant probably filed corresponding patents under the Patent Cooperation Treaty (PCT), covering numerous jurisdictions, including pending or granted patents. This multi-national strategy secures exclusivity beyond Australia, vital for commercial success in global markets.

3. Competitive Patent Filings

Other entities may have filed blocker patents or second-generation compounds to circumvent or improve upon the original patent scope. The landscape is typically competitive, with derivative patents attempting to carve out niche protections.

4. Patent Expiry and Crowding

Considering the filing date (2006), the patent's expected legal life is approximately 20 years from filing—meaning expiry around 2026. As expiration approaches, generic companies may assess patent challenges or formulate biosimilars or generics.

5. Patent Litigation and Oppositions

Australian patent law allows for opposition proceedings within months of grant, but no records indicate that AU2006328328 faced opposition or litigation. Its robustness depends on claim clarity and prosecution strategy.

Strategic Implications for Stakeholders

  • Pharmaceutical companies may explore licensing, partnerships, or patent clearance before launching similar products.
  • Generic manufacturers will monitor expiry timelines and patent challenges.
  • R&D entities could study the patent scope to identify gaps or opportunities for novel derivatives.

Conclusion

Patent AU2006328328 distinctly defines a protected chemical entity and associated methods, forming a significant part of the patent landscape for its therapeutic class within Australia. Its broad claims on the compound and uses underscore its importance in securing market exclusivity. Nevertheless, competitors and licensees must assess related patents, prior art, and expiry timelines to inform strategic decisions.


Key Takeaways

  • The patent protects a specific pharmaceutical compound, method, or formulation with broad structural claims to prevent circumvention.
  • The scope primarily hinges on the claims, which include chemical structures, methods of synthesis, and therapeutic uses.
  • The Australian patent landscape includes international patents, patent family members, and possible derivatives or second-generation inventions.
  • Expiration around 2026 presents opportunities for generic entry, contingent on successful patent challenges.
  • Stakeholders must continuously monitor related patents, legal developments, and market changes to navigate the competitive landscape.

FAQs

  1. What is the primary innovation protected by AU2006328328?
    It covers a novel chemical compound, associated synthesis methods, and therapeutic uses against specified diseases, tailored to the patent's claims.

  2. How broad are the claims within this patent?
    The claims encompass the chemical structure, salts, derivatives, synthesis methods, and specific methods of therapy, providing a wide protective scope.

  3. Does this patent cover global protection?
    No. It solely grants rights within Australia; however, equivalent filings in other jurisdictions may exist as part of an international patent strategy.

  4. When does the patent expire, and what does that mean for competitors?
    Expected expiry is around 2026, after which generic companies can legally produce similar drugs unless patent extensions or other protections are in place.

  5. Are there any legal challenges or oppositions associated with this patent?
    No public records indicate opposition. Its enforceability depends on claim scope and the validity of cited prior art.


Sources:
[1] Australian Patent Database, AU2006328328 application and granted documents.
[2] World Intellectual Property Organization (WIPO) PatentScope.
[3] Australasian Legal Information Institute (AustLII) for patent law context.

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