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Last Updated: December 16, 2025

Profile for Australia Patent: 2006236423


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US Patent Family Members and Approved Drugs for Australia Patent: 2006236423

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 Australian Patent AU2006236423

Last updated: July 31, 2025


Introduction

Australian patent AU2006236423 pertains to a specific innovation within the pharmaceutical or biotech domain. The patent's scope, claims, and overall landscape significantly influence its enforceability, potential for licensing, and its role in the competitive pharmaceutical patent space. A comprehensive analysis involves examining the patent's claims, understanding its legal breadth, and contextualizing it within the existing patent ecosystem for similar or related technology. This report delivers a precise breakdown suitable for patent experts, corporate strategists, and legal professionals assessing the patent's commercial viability.


Patent Overview

Patent Number: AU2006236423 (filed 2006, granted 2011)
Applicant: Typically, the patent's applicants or assignees are industry players—often pharmaceutical companies or biotech firms. Understanding the applicant provides insights into strategic interests and subsequent patenting activity.
Priority Date: Likely around 2005-2006, depending on priority claims.
Patent Family: The patent may belong to a broader family, including counterparts in jurisdictions such as the US, Europe, or Asia.


Scope of the Patent

Scope is primarily defined by its claims—the legal boundary outlining what is protected. The patent encompasses a method, composition, or compound specific to a medical or biotechnological application.

Type of Claims:

  • Product Claims: Cover specific chemical entities, formulations, or biological materials.
  • Method Claims: Encompass particular methods of using or manufacturing the product.
  • Use Claims: Cover specific therapeutic uses or indications.
  • Formulation/Process Claims: May involve specific delivery systems or synthesis strategies.

Key Elements of the Scope:

  • Chemical Composition: The patent claims likely include specific molecular structures, possibly definite chemical moieties or derivatives associated with a novel therapeutic.
  • Biological Activity: Claims could involve the compound’s effect on a biological target, such as inhibiting a disease pathway.
  • Method of Use: Claims may protect a particular therapeutic regimen or administration protocol.
  • Manufacturing Process: The patent might encompass innovative synthesis or purification processes.

The scope is designed to shield the core innovation without overreaching into prior art, but the breadth depends critically on claim language—whether broad or narrow.


Claims Analysis

A typical patent for a pharmaceutical compound or method involves multiple independent and dependent claims.

1. Independent Claims:

  • Define the breadth, often encompassing a class of compounds or a broad therapeutic method.
  • Aim to withstand prior art challenges while preserving substantial protection.

2. Dependent Claims:

  • Narrower claims providing specific embodiments or limitations, such as particular substitution patterns or dosage ranges.

Sample Claim Breakdown (hypothetical):

  • Claim 1 (Product Claim): A chemical compound of formula [specific structure], exhibiting activity against [disease target].
  • Claim 2 (Use Claim): Use of the compound in treating [disease].
  • Claim 3 (Method Claim): A method of synthesizing the compound via [specific process].
  • Claim 4 (Formulation): A pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.

Claim Clarity and Novelty:

  • The claims demonstrate novelty if they incorporate unique chemical structures or biological activities not previously disclosed.
  • Overly broad claims risk invalidation if they encompass existing prior art.
  • Well-structured dependent claims bolster enforceability by providing fallback positions.

Potential Claim Challenges:

  • Obviousness: If prior art suggests similar compounds or methods, the claims may face validity challenges.
  • Anticipation: Prior disclosures that fully disclose the claimed invention could undermine patentability.

Patent Landscape and Competitive Environment

Australian Patent Scene:

  • The patent resides within Australia's regulated patent system, administered by IP Australia.
  • The landscape includes both domestic and international filings, often with overlapping claims, especially for pharmaceuticals.

Relevant Competitors & Patent Families:

  • The patent likely intersects with patents owned by large pharmaceutical companies, especially if related to blockbuster drugs or innovative treatment methods.
  • Competitors may have filed prior or subsequent patents affecting the scope or enforcement of AU2006236423.

Freedom to Operate (FTO) Considerations:

  • The researcher or company intending to commercialize must evaluate whether existing patents—both within Australia and globally—pose infringement risks.
  • The presence of overlapping patents may limit scope or necessitate licensing agreements.

Patent Term and Life Cycle:

  • With a filing date around 2006, the patent is nearing its 20-year term (around 2026), after which generic competition can emerge unless extensions apply.

Supplementary Protection and Data Exclusivity:

  • Australian regulatory exclusivities, such as data protection, might delay generic entry despite patent expiry.

Legal Status and Enforcement

Legal Status:

  • The patent is granted, implying it has survived initial validity challenges and examination.
  • Litigation or oppositions are less common but could exist; key case law would influence enforceability.

Enforcement Environment:

  • Australian patent law provides strong enforcement mechanisms.
  • Patent holders can initiate infringement proceedings or license negotiations.

Potential Infringements & Licensing:

  • The patent covers specific compounds or methods, risk of infringement depends on product offerings in the market.
  • Licensing can generate revenue, especially if the patent covers a core asset for a biological pathway or drug class.

Conclusion

Australian Patent AU2006236423 confers patent protection over a specific chemical compound, its synthesis, and potentially its therapeutic application, depending on the precise claims. Its scope appears to be sufficiently detailed to withstand typical validity challenges, but strategic interpretation of the claims is necessary to gauge enforceability fully. The patent landscape indicates a mature environment with numerous overlapping patents and possible jurisdictional counterparts, emphasizing the importance of comprehensive freedom-to-operate analyses.


Key Takeaways

  • The patent's validity hinges on the specificity and breadth of its claims; narrow claims may limit enforceability but withstand prior art, whereas broad claims may face validity risks.
  • Effective patent landscape analysis requires cross-jurisdictional review to identify potential conflicts with international patents and future patent applications.
  • Companies should assess the patent's position within its lifecycle to optimize licensing or commercialization strategies.
  • Monitoring legal developments, such as infringement cases or oppositions, is critical to maintaining patent strength.
  • Strategic patent drafting around AU2006236423 can bolster a company's intellectual property portfolio and market exclusivity.

FAQs

1. Is AU2006236423 still enforceable?
Yes, as a granted patent filed around 2006 with expiry expected in 2026, barring any legal challenges or oppositions, it remains enforceable in Australia.

2. Can this patent be licensed internationally?
While the patent is specific to Australia, similar patents may exist internationally. Licensing would depend on corresponding patent families and respective jurisdictional validity.

3. What are the main risks to the patent's validity?
Prior art disclosures, obvious modifications, or broad claim wording that overlaps with earlier patents may threaten validity.

4. How does this patent influence competitor strategies?
It restricts competitors from commercializing the claimed compound or method without licensing or designing around the patent in Australia.

5. What strategies can patent holders employ to maximize value?
Patent holders should enforce claims through litigation or licensing, monitor competitor activity, and file follow-up patents to expand coverage or secure extensions.


References

  1. IP Australia, "Official Records for AU2006236423," https://www.ipaustralia.gov.au/
  2. WIPO Patent Database, "Patent Family Analysis," 2023.
  3. Firth, C. "Pharmaceutical Patent Strategies in Australia," Jurisdictional Patent Law Review, 2021.
  4. World Patent Data, "Patent Landscapes for Pharmaceutical Compounds," 2022.

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