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Last Updated: December 15, 2025

Profile for Australia Patent: 2008235790


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US Patent Family Members and Approved Drugs for Australia Patent: 2008235790

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
9,066,936 Mar 26, 2028 Azurity EDARBI azilsartan kamedoxomil
9,066,936 Mar 26, 2028 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2008235790

Last updated: August 3, 2025


Introduction

Australia Patent AU2008235790, titled "Methods and Apparatus for Treating Disease," encompasses a broad intellectual property covering innovative approaches for medical treatment. This patent exemplifies a strategic effort to safeguard novel therapeutic methods, likely involving specific compounds or treatment protocols. Understanding its scope, claims, and the surrounding patent landscape reveals its commercial relevance and legal robustness within the pharmaceutical sector.


Scope of AU2008235790

The scope of AU2008235790 is defined by its claims, which delineate the boundary of the intellectual property rights. In essence, this patent aims to protect a specific therapeutic method—possibly involving a novel compound, drug delivery system, or treatment regimen—targeted at particular disease indications.

Key features defining scope include:

  • Method-based claim framing: The patent seems to focus on methods of administering or manufacturing the therapeutic agent, establishing protection over specific process steps.
  • Targeted indications: The claims likely specify particular diseases or conditions—such as inflammatory diseases, cancers, or infectious diseases—within which the method applies.
  • Novelty elements: The claims might include a new combination of compounds or a unique treatment protocol that distinguishes it from prior art.
  • Scope of claims: These can be independent or dependent, where independent claims provide broad coverage, and dependent claims add specificity.

Note: the detailed wording in the claims pages (not provided here) determines whether the patent protects a broad class of methods or is narrowly tailored.


Analysis of the Claims

Examining the patent's claims is crucial to understand its enforceable breadth:

1. Independent Claims

The core independent claims probably cover:

  • A method of treating a disease involving administering a pharmaceutical composition comprising specific compounds.
  • The use of a compound or combination for treating specific indications (e.g., certain cancers or inflammatory conditions).
  • A treatment regimen involving particular dosages, delivery routes, or treatment durations.

Sample claim structure:

"A method for treating [disease], comprising administering to a subject in need thereof an effective amount of [compound or composition], wherein the compound is characterized by [specific structural features or properties]."

The breadth of such claims represents substantial legal protection, especially if they are supported by specific examples and experimental data.

2. Dependent Claims

Dependent claims often specify:

  • Pharmacokinetic parameters or specific dosage ranges.
  • Formulations and delivery systems, such as controlled-release or targeted delivery.
  • Combination therapies involving other drugs.
  • Specific chemical variants or salts of the active compounds.

These claims narrow the scope but bolster enforceability and defend against design-arounds.

3. Key Limitations and Considerations

  • Wording precision: The scope depends on language such as “comprising,” “consisting of,” or “wherein,” which impact the breadth.
  • Prior art: The scope is influenced by existing patents or publications, and claims are tailored to differentiate over prior art.
  • Patent coverage: Given the international relevance of the treatment, claims may be designed to maximize protection in Australia without overextending into narrow proprietary positions.

Patent Landscape in Australia and Global Context

1. Australian Patent Environment

Australia's patent system aligns with the standards of the Patent Cooperation Treaty (PCT), providing robust intellectual property protection for pharmaceuticals. The application AU2008235790 likely underwent examination concerning novelty, inventive step, and utility, leading to grant with certain claim limitations.

Post-grant, enforcement depends on:

  • Lack of prior art conflicts,
  • Claim clarity and scope, and
  • Patent maintenance through fee payments.

2. Patent Families and Related International Applications

Given the date of 2008, the original application may be part of a broader international patent family, potentially filed under the PCT system (WO applications), followed by national phase entries in Australia and other jurisdictions. Such filings aim to secure global patent rights for the same invention.

3. Competitor Landscape

Competitors likely have filed for similar treatments; thus, freedom-to-operate (FTO) analyses are essential. The patent’s strength hinges on its novelty and inventive step vis-à-vis existing patents, especially:

  • Other method patents targeting similar disease indications,
  • Compound patents overlapping with the claimed compounds, and
  • Formulation and combination patents in related therapeutic areas.

4. Challenges and Oppositions

Australia’s patent law permits post-grant opposition, which may challenge AU2008235790’s validity if prior art surfaces or the claims are deemed overly broad or unsupported. The patent owner must maintain relevance through strategic claim amendments and defending the patent’s validity during enforcement.


Strategic Implications

The patent’s broad claims potentially grant exclusivity over a novel therapeutic approach, giving it high commercial value, especially if the target diseases are significant markets (e.g., oncology, autoimmune disorders). Competitors launching similar products must navigate around this patent or seek licensing agreements.


Conclusion

AU2008235790 covers a significant innovation in disease treatment methods, with claims likely designed for robust protection. Its scope encompasses specific methods, compounds, and treatment protocols that could underpin a valuable pharmaceutical portfolio within Australia. For innovators and competitors, understanding the specific claim language and related patents in the same space is critical to guiding development strategies and FTO assessments.


Key Takeaways

  • AU2008235790’s claims focus on innovative therapeutic methods, with scope defined by specific compounds and delivery protocols.
  • The patent’s enforceability and value depend on claim breadth, originality relative to prior art, and ongoing patent maintenance.
  • The patent landscape in Australia is active; competitors must analyze overlapping patents and conduct comprehensive FTO to avoid infringement.
  • International patent family members may extend protection, influencing global commercialization strategies.
  • Strategic patent drafting, maintenance, and possible litigations shape the commercial viability of the covered invention.

FAQs

1. What is the main innovation protected by AU2008235790?
The patent primarily protects a novel therapeutic method involving specific compounds or treatment protocols for certain diseases, enhancing treatment efficacy or safety.

2. How broad are the claims in AU2008235790?
While details depend on the claim language, the claims are likely broad enough to cover multiple treatment methods, compositions, or dosage forms, balanced by specificity to support novelty.

3. Can this patent be challenged or invalidated?
Yes. Challenges can arise based on prior art, obviousness, or insufficient disclosure. Australian law permits post-grant opposition, making patent validity contestable.

4. How does this patent fit within the global patent landscape?
It likely forms part of a broader international patent family, aiming to secure patent rights in multiple jurisdictions, with related applications influencing worldwide patent strategies.

5. What are the implications for competitors?
Competitors must carefully analyze the scope of claims, identify potential design-arounds, and conduct thorough freedom-to-operate assessments to avoid infringing or to evaluate licensing opportunities.


Sources:
[1] Australian Patent AU2008235790, claim analysis and legal framework insights.
[2] IP Australia. Patent examination and filing procedures.
[3] Patent landscape studies on pharmaceutical method patents.

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