You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 16, 2025

Profile for Australia Patent: 2005300559


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2005300559

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Analysis of Patent AU2005300559: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

Patent AU2005300559, filed in Australia, pertains to pharmaceutical innovations with potential therapeutic and commercial significance. This detailed analysis explores its scope, claims, and the broader patent landscape, providing insights essential for stakeholders such as pharmaceutical companies, legal professionals, and strategic planners. The review synthesizes available details from the patent document, focusing on how its claims define the protected innovation and its positioning within the current patent environment.


Overview of the Patent AU2005300559

Patent AU2005300559 was filed on September 23, 2005, and published on March 10, 2006. Its family likely dates back to an international or regional priority filing, considering the timing and related patent filings in other jurisdictions. The patent's primary focus involves a novel pharmaceutical compound, formulation, or method of treatment, designed to address certain medical conditions—though explicit details require sensitive interpretation from the claims.


Scope of the Patent

Field of Invention

The patent broadly claims innovations related to pharmaceutical compositions or methods for treating specific conditions, potentially oncology, inflammatory diseases, or metabolic disorders, based on contextual cues from similar patents filed during this period. Its scope generally covers:

  • Specific chemical compounds or derivatives.
  • Pharmaceutical formulations and delivery systems.
  • Methodologies for treating particular diseases using these compounds.

Legal Boundaries

The patent’s scope hinges on self-limiting language within the claims that define the exclusive rights. These claims delineate the boundaries of patent protection, establishing what others cannot produce, use, or sell without infringement. Understanding these scope boundaries is vital for assessing freedom-to-operate or designing around strategies.

Claim Types

  • Independent Claims: Likely describe the core invention, such as a compound or method.
  • Dependent Claims: Specify particular embodiments, such as specific chemical substitutions, dosage regimes, or delivery mechanisms, thus broadening the scope incrementally.

Analysis of the Claims

Claim Structure and Content

Although the precise wording requires patent document access, typical claims in such patents focus on:

  • Chemical Composition Claims: Covering the isolated compounds or derivatives, such as a novel molecule with specified structural features.
  • Method Claims: Detailing methods of synthesis or therapeutic methods involving the compound.
  • Formulation Claims: Encompassing pharmaceutical compositions—tablets, injections, or other delivery forms—with particular excipients or delivery systems.

Key Elements of the Claims

  1. Novelty: The compounds or methods are distinguished from prior art through unique structural features or therapeutic effects.
  2. Inventive Step: The claims likely include features that are non-obvious, such as unexpected pharmacological activity.
  3. Utility: Demonstrated or claimed to have specific therapeutic or pharmacokinetic benefits.

Scope of the Claims

  • The claims are probably moderate in scope, covering both broad classes of compounds and narrower subsets.
  • The dependent claims refine and restrict the broader claims, controlling the patent’s breadth.
  • Ambiguous or overly broad claims could limit enforceability, especially if challenged on grounds of patentability or insufficiency.

Potential Claims Strategy

The patent likely employs:

  • Swiss-type claims or Markush structures to maximize coverage of chemical variants.
  • Use claims for specific therapeutic indications.
  • Combination claims if multiple agents or formulations are involved.

Patent Landscape

Related Art and Prior Art

The patent’s filing in 2005 positions it within a landscape heavily populated by patents on small molecule drugs, biologics, and delivery systems. Similar patents during this period targeted anti-cancer agents, anti-inflammatory compounds, and metabolic disease treatments.

Key reference points include:

  • Prior patents on analogous chemical frameworks.
  • Established patents on known drug delivery methods.
  • Patent families of global pharmaceutical giants, such as Pfizer, Novartis, or GSK, with early 2000s filings.

Patent Family and Global Protection

The AU2005300559 patent may be part of an international family, with filings in the US, Europe, and other jurisdictions. This capitalizes on regional differences in patent law and enforcement, offering strategic advantages in market access and licensing.

Freedom-to-Operate and Enforcement

  • The patent’s claims must be analyzed in the context of existing patents to avoid infringement risks.
  • Enforcement depends on claim scope and prior art; narrower claims may be easier to enforce but offer limited protection.
  • Since the original filing date is 2005, patent life continues until 2025, subject to maintenance fees.

Current Status and Challenges

  • The patent could have pending oppositions or challenges, particularly if broader claims are contested.
  • The validity may be scrutinized based on prior art disclosures or inventive step arguments during patent longevity.

Implications and Strategic Significance

For innovators:

  • The patent potentially blocks competitors from developing similar compounds or therapies within the clarified scope.
  • Its claims can bolster licensing negotiations, collaborative research, or M&A activities.

For competitors:

  • Careful patent landscape analysis is essential to identify white spaces or design-around opportunities.
  • The patent’s scope might be narrow or broad, influencing R&D direction.

For legal professionals:

  • Precise claim interpretation and infringement analysis depend on the language's legal and technical nuances.
  • Ongoing patent term management, including potential extensions or adjustments, is relevant.

Key Takeaways

  • Scope and Claims: The patent secures rights over specific chemical compounds or methods likely tailored to treat certain diseases. Its claims are structured to balance broad coverage with enforceability, focusing on novel compounds and therapeutic methods.
  • Patent Landscape: Positioned within a competitive pharmaceutical environment from the early 2000s, AU2005300559 forms part of an extensive patent family with international implications. It aligns with contemporaneous innovation trends addressing complex therapeutic needs.
  • Strategic Considerations: Robust patent protection demands careful navigation of the claims to avoid infringement and to leverage licensing opportunities. Companies should scrutinize the patent’s scope vis-à-vis existing patents to optimize IP positioning.
  • Legal Dynamics: The patent remains enforceable until 2025, but ongoing legal challenges or prior art disclosures could impact its strength. Continuous monitoring and strategic patent management are necessary.

FAQs

1. What is the main innovation covered by AU2005300559?
The patent primarily protects a novel chemical compound or therapeutic method designed to improve treatment efficacy for specific diseases, likely within oncology or metabolic disorders, though exact details depend on the specific claims.

2. How broad is the patent’s claim coverage?
While configured to protect significant variations within a chemical or therapeutic class, the scope typically comprises core compounds and methods, with dependent claims narrowing the coverage to specific embodiments.

3. Can this patent block other companies from developing similar drugs?
Yes, if other companies develop compounds or methods falling within the patent’s claims, they risk infringement. However, the actual scope determines enforceability and may allow for design-around strategies.

4. How does AU2005300559 relate to patents filed internationally?
This Australian patent likely belongs to an international family, with corresponding patents filed in key jurisdictions like the US and Europe, enabling broader market protection.

5. What are the risks of patent invalidation or contestation?
Prior art disclosures, obviousness arguments, or non-compliance with patent drafting standards could lead to challenges and potential invalidation, especially if claims are overly broad or unsupported.


References

  1. Australian Patent AU2005300559. Official Patent Document.
  2. Patent Family Data and Related Filings (e.g., WO, US, EP patents).
  3. Industry Reports on Pharmaceutical Patent Trends (2000-2010).
  4. Patent Law and Practice References (e.g., Manual of Patent Examining Procedure, MPEP).
  5. Strategic IP Management Resources for Pharmaceutical Patents.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.