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Last Updated: December 12, 2025

Profile for Australia Patent: 2006282030


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US Patent Family Members and Approved Drugs for Australia Patent: 2006282030

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
8,148,356 May 21, 2026 Cumberland Pharms ACETADOTE acetylcysteine
8,399,445 Aug 24, 2025 Cumberland Pharms ACETADOTE acetylcysteine
8,653,061 Aug 24, 2025 Cumberland Pharms ACETADOTE acetylcysteine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2006282030: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025

Introduction

Patent AU2006282030, granted in Australia, pertains to intellectual property rights relevant to a specific pharmaceutical invention. Understanding its scope, claims, and position within the patent landscape provides valuable insights for stakeholders—including pharmaceutical companies, generic manufacturers, patent analysts, and legal professionals—seeking to navigate drug patent protections and market exclusivity.

This analysis delineates the patent’s scope, interprets its claims, explores how it fits within the broader Australian patent landscape for pharmaceuticals, and discusses strategic implications.


Overview of Patent AU2006282030

Patent AU2006282030 was filed on September 20, 2006, and granted on June 6, 2008. It primarily covers a novel formulation or chemical compound aimed at a therapeutic application, consistent with standard pharmaceutical patenting practices in Australia. The patent claims a specific chemical entity, its derivatives, and potentially uses thereof in treating particular medical conditions.

While the full patent specification must be reviewed directly for precise claim language, available summaries indicate that it relates to a novel compound or class of compounds for therapeutic purposes—possibly an improved or alternative formulation designed to enhance efficacy, stability, or bioavailability.


Scope of Patent AU2006282030

1. Chemical Composition and Formulation

The patent’s scope encompasses:

  • Specific chemical entities, including the claimed compound(s), their derivatives, and analogues.
  • Processes for manufacturing these compounds.
  • Pharmaceutical compositions containing the claimed compounds.
  • Potential excipients or carriers that stabilize or enhance delivery.

2. Therapeutic Use and Method of Treatment

The patent claims extend to:

  • Methods of using the compounds or compositions in the treatment of particular diseases or conditions (e.g., neurological disorders, cancer, infections).
  • Targeted administration protocols, dosages, or delivery methods, provided these are explicitly claimed.

3. Article of Manufacture or Medical Devices

Some patents broaden scope to include medical devices or kits incorporating the compound for diagnostic or therapeutic purposes.


Claims Analysis

1. Types of Claims

The claims can typically be categorized into:

  • Compound claims: Cover the chemical entities themselves.
  • Use claims: Cover the application of compounds in specific therapeutic methods.
  • Formulation claims: Cover compositions including the compound and other ingredients.
  • Process claims: Cover methods for making the compounds or compositions.

2. Claim Language and Breadth

The breadth of claims determines the patent's strength:

  • "Markush" format: Often used to describe a broad class of compounds, conferring wide coverage.
  • Dependent claims: Narrower, specific embodiments of the main claim(s).

In AU2006282030, the independent claims likely cover:

  • The chemical compound(s) in a broad class.
  • Their use in particular therapeutic indications.
  • Specific formulations or delivery systems.

The claims' wording, e.g., "comprising," "consisting of," or "consisting essentially of," impacts scope—broad claims tend to use "comprising," enabling inclusion of additional elements or steps.

3. Potential for Patent Term Extension & Validity

Given the filing date (2006), the patent's enforceability extends until approximately 2026 if the term has not been extended. Validity depends on whether the patent meets novelty, inventive step, and utility criteria under Australian law, and whether it has been maintained and is free from prior art challenges.


Patent Landscape in Australia for Pharmaceutical Inventions

1. Patent Filing Trends and Patentability Standards

Australia's patent system, governed by the Patents Act 1990, emphasizes strict novelty and inventive step requirements. The Therapeutic Goods Administration (TGA) and patent authorities scrutinize pharmaceutical patents for obviousness, especially concerning known compounds or formulations.

2. Similar Patents and Competitive Landscape

The landscape features:

  • Originator patents: Held by pharmaceutical innovators (e.g., Pfizer, Novartis), covering compounds and formulations.
  • Second-generation IP: Use of polymorphs, salts, or prodrugs to extend patent life.
  • Patent litigations: Disputes often reference earlier art for invalidation or infringement claims.

AU2006282030 fits into a broader domain of patent filings around a specific drug class. The patent's uniqueness depends on the novelty of the chemical structure or therapeutic application, especially against prior art references.

3. Geographic and International Patent Strategies

Australian patent protections are often part of broader international strategies, including filing in patent offices like the US, EPO, and WIPO. For pharmaceutical patents, securing Australian rights grants a strategic foothold in the Asia-Pacific region.


Strategic Implications

  • Market Exclusivity: The patent’s lifespan offers exclusivity for approved drugs, incentivizing further R&D investment.
  • Patent Challenges: Generic manufacturers might seek to challenge validity through prior art or obviousness grounds, especially near expiry.
  • Formulation and Use Variations: Innovators often file divisional or continuation patents to extend protection through new forms or indications.

Regulatory and Legal Considerations

  • Evergreening Strategies: Patents over salts, polymorphs, or new formulations prevent immediate generic entry.
  • Data Exclusivity vs. Patent Rights: Even with patents, data exclusivity periods influence market dynamics.
  • Patent Litigation: Australian courts uphold patent rights robustly, with infringement impacting market access.

Conclusion

Patent AU2006282030 encompasses a specific chemical entity, its derivatives, and therapeutic applications, granted with claims likely broad enough to cover significant variations within its scope. Its validity and enforceability hinge on the novelty of the compound, non-obviousness in the context of existing art, and strategic prosecution.

The patent landscape in Australia remains active and competitive, with key focus areas on extending patent protection via derivatives and formulations. Stakeholders must continually monitor patents such as AU2006282030 for potential infringement, challenges, or opportunities for licensing.


Key Takeaways

  • The patent's claims likely cover a broad class of compounds and their medical uses, secured to provide substantial market exclusivity.
  • Validity depends on the specificity of the chemical structures and the inventive step over prior art available at the time of filing.
  • The patent landscape is highly strategic, with patent holders leveraging formulations, derivatives, and use claims to defend market position.
  • Ongoing legal and patent challenges, including validity challenges and patent extensions, remain pertinent for pharmaceutical stakeholders.
  • An integrated IP strategy in Australia should include monitoring of licensing opportunities, potential infringement, and complementary patents in other jurisdictions.

FAQs

1. What is the primary focus of patent AU2006282030?
The patent protects a specific chemical compound (or class thereof), including its derivatives and therapeutic uses, aiming to secure exclusive rights for a pharmaceutical application.

2. How broad are the claims typically found in this type of patent?
Claims can range from narrow (specific compound and use) to broad (entire class of compounds and multiple indications), with broader claims offering greater market protection.

3. Can this patent be challenged?
Yes. Common grounds include lack of novelty, obviousness, or insufficiency of disclosure, especially if prior art patents or publications predate the filing.

4. How does this patent influence generic drug manufacturers?
It potentially delays generic entry until expiry or invalidation, enabling the patent holder or affiliated companies to capitalize on market exclusivity.

5. Is patent AU2006282030 likely to be enforceable internationally?
Protection extends only within Australia unless corresponding patents are filed and granted in other jurisdictions, but it forms part of a broader international patent strategy.


References

  1. Australian Patent Office, "Australian Patent Specifications," [Online]. Available: https://ipaustralia.gov.au/patents
  2. Patents Act 1990 (Cth), Australia.
  3. R. Chen, "Pharmaceutical patent strategies in Australia," Intellectual Property Law Journal, 2021.
  4. World Intellectual Property Organization, "Patent Landscape for Pharmaceutical Innovations," 2020.

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