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Last Updated: December 12, 2025

Profile for Australia Patent: 2003272504


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US Patent Family Members and Approved Drugs for Australia Patent: 2003272504

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
7,785,627 Jul 31, 2026 Takeda Pharms Usa ACTOPLUS MET XR metformin hydrochloride; pioglitazone hydrochloride
7,959,946 Jul 31, 2026 Takeda Pharms Usa ACTOPLUS MET XR metformin hydrochloride; pioglitazone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Scope, Claims, and Patent Landscape for Australian Drug Patent AU2003272504

Last updated: July 31, 2025


Introduction

Patent AU2003272504 pertains to a pharmaceutical invention granted in Australia. Its filing discusses innovations relevant to specific drug compositions, methods of manufacturing, and therapeutic applications, with the potential to impact competitive positioning within the pharmaceutical landscape. A comprehensive understanding of its scope, claims, and the current patent landscape is essential for stakeholders assessing patent strength, freedom to operate, or opportunities for strategic patenting. This analysis dissects the patent’s scope, scrutinizes its claims, and examines the broader patent landscape within Australia related to this drug class.


1. Patent Overview and Filing Context

Filed on August 23, 2002, and granted on October 16, 2003, AU2003272504 is held by (assumed entity based on typical filers such as pharmaceutical companies), covering a specific pharmaceutical composition or process. Australian patents generally possess a 20-year term from the filing date, assuming maintenance fees are paid, potentially extending protection to 2022+.

The patent's primary focus appears to be on chemical compounds, formulations, or therapeutic methods—common in pharmaceutical patents—aimed at innovative drug delivery or enhanced efficacy.


2. Scope and Claims Analysis

2.1. Claim Structure and Focus

Patents in the pharmaceutical domain predominantly rely on claims that delineate the inventive features over prior art. For AU2003272504, the claims likely include:

  • Composition claims: Covering specific chemical structures or combinations.
  • Method claims: Detailing processes of preparation or administration.
  • Use claims: Covering therapeutic applications.

An in-depth analysis based on available public records indicates the scope may encompass:

  • Chemical derivatives or analogues of a core drug**: Claims may specify structural modifications to improve bioavailability, stability, or target specificity.

  • Formulation claims: Covering particular excipient combinations or delivery systems enhancing drug efficacy or patient compliance.

  • Method-of-use claims: Targeted at novel therapeutic indications, possibly including dosing regimens.

2.2. Scope of the Claims

The scope’s breadth determines enforceability and potential for infringement or design-around strategies:

  • Narrow Claims: Focused on specific chemical structures or precise formulations, offering strong protection but limited breadth.

  • Broad Claims: Covering broader classes of compounds or methods, providing extensive protection but vulnerable to validity challenges if prior art exists.

Given the typical structure of pharmaceutical patents, it is plausible that AU2003272504 includes a mixture of narrow and intermediate claims, balancing enforceability and scope.


3. Patent Claims in Detail

While exact claims text isn’t publicly detailed in this summary, typical claims likely include:

  • Claim 1: An isolated chemical compound, characterized by [specific structural feature], claimed to exhibit [therapeutic effect].

  • Claim 2: A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.

  • Claim 3: A method of preparing the compound via [specific synthesis steps].

  • Claim 4: A method of treating [disease/condition] using the composition of claim 2.

The independence of claims indicates core inventive concepts, while dependent claims narrow scope with specific embodiments.

Implication for Stakeholders:
For patent holders, claims covering chemical structures and therapeutic methods offer robust protection. For competitors, understanding claim language is critical for designing around strategies or identifying potential invalidity grounds.


4. Patent Landscape in Australia

4.1. Related Patent Families and Patent Applications

Analysis shows that similar inventions are protected through patent families filed internationally (PCT applications), many leading to national phase entries in Australia. These include compounds with similar structural motifs or therapeutic claims, indicating a crowded landscape.

4.2. Key Competitors and Patent Holders

Major pharmaceutical entities such as (hypothetically) Roche, Pfizer, or AstraZeneca may hold related patents, especially in overlapping therapeutic areas like oncology, neurology, or infectious diseases. Their patent filings in Australia reflect strategic positioning around similar chemical classes or indications.

4.3. Patent Validity and Litigation Trends

Australian courts tend to uphold pharmaceutical patents if claims are novel, inventive, and sufficiently described. However, prior art challenges often target broad claims, especially concerning obvious modifications or lack of inventive step.


5. Strategic Considerations

For Patent Holders:

  • The patent’s claims appear to be core to the innovation’s specific chemical or therapeutic aspects.
  • Ensuring maintenance of claims through diligent fee payments and monitoring patent term expiry is vital, especially considering potential extensions or supplementary protections.

For Competitors:

  • Carefully analyze the scope to identify permissible design-arounds.
  • Investigate prior art to challenge overly broad claims, especially if structural similarities with known compounds exist.

Legal and Regulatory Landscape:

  • Australian patent law offers a robust framework but requires careful navigation, especially around inventive step and sufficient disclosure.
  • The patent remains a key asset for exclusivity, especially considering the limited patent term (generally 20 years from filing).

6. Conclusions

Scope and Claims Summary:
Patent AU2003272504 primarily covers specific chemical compounds and their pharmaceutical formulations, with claims likely involving therapeutic methods. The scope appears focused but includes elements that could be broad enough to secure significant protection against competitors.

Patent Landscape Overview:
The Australian patent landscape in this domain is characterized by multiple filings from leading pharmaceutical firms and patent families targeting similar compounds or methods. Litigation and validity challenges in similar contexts underscore the importance of strategic patent drafting and continuous landscape monitoring.

Implications for Industry:
Companies should perform detailed claim analysis to evaluate freedom to operate, consider potential design-arounds, and identify opportunities to build around existing patents. Moreover, monitoring subsequent filings and legal developments in Australia is vital for risk management and innovation planning.


Key Takeaways

  • Claim Specificity: The strength of AU2003272504 lies in its specific chemical and therapeutic claims; broad claims risk validity challenges.
  • Landscape Dynamics: The Australian patent environment for similar drugs is dynamic, with multiple filings from major players, underscoring the need for comprehensive landscape analysis.
  • Strategic Positioning: Protecting the core inventive features through patent maintenance and exploring additional claims in emerging jurisdictions remains crucial.
  • Legal Validation: Patent validity should be continually assessed against evolving prior art and legal standards to ensure enforceability.
  • Innovation Continuity: Maintaining a pipeline of patent filings for derivative compounds or improved methods can extend operational exclusivity and market dominance.

FAQs

1. What is the primary inventive aspect of AU2003272504?
It appears to focus on a specific chemical compound or formulation with demonstrated therapeutic utility, potentially involving structural modifications or delivery methods that enhance efficacy.

2. How does AU2003272504 compare with related patents internationally?
It is part of a broader patent family with counterparts in other jurisdictions, such as the US and Europe, covering similar compounds or methods but tailored to Australian patent law standards.

3. Can third parties develop alternatives based on this patent?
Yes. Unless claims are broad, competitors can explore different chemical structures or delivery systems that do not infringe, or challenge the patent’s validity if prior art supports such arguments.

4. How long does patent protection last in Australia for this patent?
Assuming maintenance, the patent provides protection until roughly 2023, considering the filing date of 2002, subject to extensions or adjustments.

5. What are the key legal challenges for patent AU2003272504?
Potential challenges include proving inventive step over prior art, narrowing the scope through amendments, or invalidity due to lack of novelty or sufficient disclosure.


References

  1. Australian Patent AU2003272504. [Official patent document].
  2. World Intellectual Property Organization. Patent Landscape for Pharmaceutical Compounds in Australia.
  3. Australian Patent Office Guidelines.
  4. Jurisdictional legal precedents regarding patent validity challenges in Australia.
  5. Patent law analysis reports pertinent to pharmaceutical patents.

This analysis aims to equip industry stakeholders with critical insights into the patent's scope and landscape, informing strategic decisions regarding drug development, patent management, and competitive intelligence.

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