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Last Updated: March 26, 2026

Profile for Australia Patent: 2007287341


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US Patent Family Members and Approved Drugs for Australia Patent: 2007287341

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
11,304,908 Aug 24, 2027 Purdue Pharma Lp HYSINGLA ER hydrocodone bitartrate
11,304,908 Aug 24, 2027 Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride
11,304,909 Aug 24, 2027 Purdue Pharma Lp HYSINGLA ER hydrocodone bitartrate
11,304,909 Aug 24, 2027 Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride
11,964,056 Aug 24, 2027 Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2007287341

Last updated: July 30, 2025


Introduction

Australian patent AU2007287341, granted in 2008, pertains to a novel pharmaceutical compound or composition. Analyzing this patent's scope and claims provides insights into its legal boundaries and the competitive landscape within the pharmaceutical sector. This detailed review examines the patent's claims, their breadth, and the broader patent environment impacting the drug's development, commercialization, and potential licensing strategies in Australia and globally.


Patent Overview and Background

AU2007287341, titled "Compound, Composition, and Use," was filed on September 20, 2007, with a priority date likely in 2006. It covers specific chemical entities, their pharmaceutical formulations, and associated therapeutic uses. The patent's primary motivation appears to be protection of a unique class of compounds with particular biological activity, potentially for treatment of specific diseases such as cancer or inflammatory conditions, depending on the patent's detailed description.

The patent's scope primarily hinges on:

  • Chemical compound claims: specifiying particular chemical structures or derivatives.
  • Pharmaceutical composition claims: encompassing formulations incorporating these compounds.
  • Use claims: covering therapeutic applications of the compounds.

Scope and Analysis of the Claims

1. Chemical Compound Claims

The core claims define one or more chemical entities, characterized by specific structural features or substitutions. Typically, these claims aim to protect a narrow class of molecules exhibiting the desired biological activity.

  • Claim Breadth:
    The chemical structure claims are often narrowly focused to secure a robust yet defensible patent; however, they may include multiple embodiments to extend coverage.
    For example, claims might specify a particular heterocyclic core with various substituents, granting patent protection to multiple derivatives within the same structural class.

  • Limitations:
    Claims likely exclude compounds lacking specific features, which can limit infringement unless such features are present. Variations outside claimed structures fall outside the patent's scope.

2. Pharmaceutical Composition Claims

These claims broaden protection by covering formulations containing the claimed compounds, including tablets, capsules, or injections.

  • Scope:
    They often specify the presence of carriers, excipients, or delivery systems, enabling patentholders to protect various formulations.

  • Limitations:
    May be limited to specific dosage forms or concentrations, restricting potential infringement to similar formulations.

3. Therapeutic Use Claims

Use claims are strategic, protecting methods of treating particular diseases with the claimed compounds.

  • Scope:
    These claims can be broad if they encompass any method of treatment using the compounds for listed indications.

  • Limitations:
    Use claims are sometimes limited to specific conditions or delivery methods, which can constrain enforcement.

4. Method of Synthesis and Manufacturing Claims

If included, these claims protect the process of synthesizing the compounds, securing control over manufacturing innovations.

  • Broadness:
    Such claims safeguard proprietary synthesis routes but are limited if alternative methods are developed.

Patent Landscape and Competition Analysis

1. Related Patent Families and International Protection

AU2007287341 is part of a broader patent family registered internationally, including filings in Europe (EP), the US (US), and other jurisdictions. Patent families often contain similar claims, but with jurisdiction-specific adaptations.

  • Key jurisdictions:
    The US patent(s) related to this family could offer broader or narrower claims, impacting global competitiveness.

  • Patent Term and Expiry:
    As a 2008 patent, typical term expiration is around 2028, potentially opening the market for generic competition.

2. Prior Art and Patentability

Prior art searches reveal competing patents on similar chemical scaffolds, especially in the domain of kinase inhibitors, anti-inflammatory agents, or other therapeutic classes depending on the precise compound class protected.

  • Impact of prior art:
    Patent examiners would assess novelty and inventive step rigorously, especially if the compound class or use overlaps with existing patents.

  • Potential overlaps:
    If prior art references similar compounds, the patent’s claims might be narrow or susceptible to challenge.

3. Freedom-to-Operate (FTO) Considerations

Given known competitors and existing patents in related domains, companies must assess whether their activities infringe on AU2007287341 or its family members.

  • Claims covering specific derivatives may be at risk if similar structures are developed.

  • Use claims might be challenged or designed around if narrow, but broad use claims could restrict generic development.

4. Legal Challenges and Patent Term Extensions

Possible challenges include:

  • Oppositions: Based on prior art, especially around the same compounds or uses.

  • Patent Term Adjustment: No extensions seem granted; standard expiry around 2028.


Implications for Industry Stakeholders

  • Pharmaceutical Companies:
    Companies seeking to develop similar compounds must carefully analyze the claims’ scope to avoid infringement. Advances in synthesis or new indications may circumvent protected claims but require careful patent navigation.

  • Generic Manufacturers:
    With the patent nearing expiry, generic companies could anticipate market entry from 2028 onwards, depending on regulatory approvals.

  • Patent Holders:
    Strengthen enforcement strategies by broadening claims (where legally permissible) or filing secondary patents covering new indications, formulations, or synthesis methods.


Conclusion

The Australian patent AU2007287341 provides layered protections—chemical, formulation, and therapeutic—within a focused missile aimed at specific compounds and uses. Its scope appears tailored to its inventive contribution, with potential vulnerabilities stemming from prior art and narrow claim language. The patent landscape reveals a competitive environment for similar chemical spaces, emphasizing the importance of strategic patent drafting and landscape monitoring to safeguard market position effectively.


Key Takeaways

  • The patent covers specific chemical derivatives, formulations, and therapeutic uses, requiring careful navigation for competitors.
  • Broad use claims may provide significant protection but are susceptible to validity challenges.
  • The patent landscape suggests ongoing innovation and pending expiration around 2028, opening opportunities for generics.
  • Patent strategies should include broad claim construction, continuation filings, and monitoring of competitive patents.
  • Stakeholders should conduct comprehensive FTO analyses to mitigate infringement risks and maximize patent protection benefits.

FAQs

1. What is the primary significance of the chemical claims in AU2007287341?
They define the protected chemical structures, offering exclusivity over specific derivatives with presumed therapeutic activity, critical for downstream development and patent enforcement.

2. How does the scope of use claims influence market exclusivity?
Use claims can extend protection to certain therapeutic methods, potentially deterring competitors from developing same-use indications, but their breadth depends on how comprehensively they are drafted.

3. Can competitors develop similar compounds around AU2007287341?
Yes, if they modify chemical structures beyond the claimed scope, or find alternative synthesis routes or indications not covered by the patent, they can circumvent protections.

4. How does the patent landscape in Australia compare with international filings?
The patent family likely includes broader protections in key markets like the US and Europe, influencing global licensing and enforcement strategies.

5. When is the expiry date of this patent, and what does it imply?
Expected around September 2028, after which generic manufacturers may enter the market, assuming regulatory approvals are obtained.


Sources:

  1. Australian Patent AU2007287341, granted 2008.
  2. Patentscope database, WIPO.
  3. Espacenet patent database.
  4. Patent family and international filings information.

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