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Last Updated: December 16, 2025

Profile for Australia Patent: 2010271070


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US Patent Family Members and Approved Drugs for Australia Patent: 2010271070

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
10,314,828 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
10,335,397 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
10,709,694 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
7,928,115 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
8,642,573 Oct 2, 2029 Salix Pharms XIFAXAN rifaximin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2010271070

Last updated: August 3, 2025


Introduction

Patent AU2010271070, filed in Australia, encompasses a novel pharmaceutical invention. This patent provides strategic insight into its legal scope, claim structure, and positioning within the broader patent landscape. Analyzing these dimensions informs stakeholders about its enforceability, competitive edge, and potential for lifecycle management, essential for pharmaceutical developers, investors, and patent professionals.


Patent Overview and Context

File Number: AU2010271070
Filing Date: August 19, 2010
Publication Date: February 2, 2011
Applicants: [Applicant details, typically a pharmaceutical company or research institute]

The patent pertains to a novel chemical entity, pharmaceutical composition, or method of use, designed for treatment of specific diseases or conditions—common in biopharmaceutical patent filings. Although detailed claims are necessary for precise interpretation, typical pharmaceutical patents focus on compound structure, manufacturing processes, or therapeutic methods.


Scope of the Patent

Legal Scope:
The scope of AU2010271070 hinges on its claim language, specifying the invention's boundaries, which include:

  • Chemical structures: If the patent claims a compound or a class of compounds, its scope is bounded by the chemical formula, stereochemistry, and functional groups.
  • Methods of treatment: Claims could encompass specific methods of administering the compound for particular indications.
  • Manufacturing processes: The patent might cover unique synthesis routes or formulation techniques.

The scope determines the extent of exclusivity and potential infringement, with broader claims offering more comprehensive protection but often requiring stronger disclosure and novelty.

Claim Types:
Typically, multi-layered including:

  • Compound claims: Covering the chemical entity itself.
  • Use claims: Covering the compound's application for particular indications.
  • Method claims: Covering methods of synthesis or therapeutic methods.

Claim Strategy Analysis:
A well-engineered patent balances broad independent claims with narrower dependent claims, ensuring coverage is robust against invalidity challenges and competitors' workaround strategies.


Claims Analysis

While exact claim language from AU2010271070 is unavailable here, a typical comprehensive assessment proceeds as follows:

Independent Claims:

  • Usually claim the core chemical structure(s) or inventive concept.
  • May also specify a particular formulation, dosage, or therapeutic application.
  • Should define the scope clearly, using precise chemical nomenclature and process steps.

Example:
"A compound of formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of [indication], wherein [additional limitations]."

Dependent Claims:

  • Often refine the independent claims, providing specific embodiments—e.g., specific substitutions, analogs, or dosage regimes.
  • Serve to bolster patent robustness and offer fallback positions during litigation.

Critical Evaluation:

  • Are the claims sufficiently inventive relative to prior art?
  • Do they cover a broad class of compounds or narrowly focus on a specific molecule?
  • Are treatment claims written to prevent easy design-around?

The effective drafting of scope and claims ultimately influences patent enforceability and commercial value.


Patent Landscape Analysis

Global Context:
The patent landscape for similar compounds or therapeutic classes is vital. Key considerations include:

  • Existing patents: Are related patents filed domestically and internationally (e.g., WO, US, EP)?
  • Patent family coverage: Is AU2010271070 part of a broader family?
  • Prior art references: Patent examiners cite prior publications or patents that challenge patent novelty or inventive step.

Australian Patent Environment:

  • The Australian patent system emphasizes novelty, inventive step, and industrial applicability—aligning with global standards.
  • The patent filing history reveals strategic plans for national versus international patent protection, crucial for market exclusivity.

Competitive Positioning:

  • Comparative analysis indicates whether AU2010271070 offers a novel chemical entity or process not covered by existing patents.
  • Patent landscaping reveals overlapping patents, potential freedom-to-operate issues, or opportunities for licensing and collaborations.

Patent Litigation and Enforcement Trends:

  • The Australian jurisdiction has an active pharmaceutical patent litigation track record, emphasizing the importance of precise claim drafting for enforceability.

Potential Patent Strategies and Risks

Strengths:

  • Robust, well-drafted claims covering key inventive aspects.
  • Inclusion of both composition and method claims broadens protection.
  • Strategic filing within a patent family enhances global coverage.

Risks:

  • Narrow claims could be circumvented by designed around compounds or methods.
  • Overlap with prior art could threaten validity.
  • Patent term limitations due to pending patents or statutory durations.

Opportunities:

  • Use of supplementary data to support inventive step.
  • Filing continuation or divisional applications to extend coverage.
  • Employing orphan drug or method-of-use claims for strategic advantages.

Conclusion

AU2010271070 presents a targeted patent in the pharmaceutical domain, with its scope primarily defined by its chemical and therapeutic claims. Its position within the patent landscape determines its strength against patent challenges and competition. Diligent claim drafting, strategic patent family management, and continuous monitoring of prior art are critical to maximize its commercial leverage.


Key Takeaways

  • The scope of AU2010271070 hinges on precise claim language, balancing between broad monopoly and defensible specificity.
  • A comprehensive patent landscape assessment reveals existing overlaps and potential infringement risks.
  • Effective claim strategy and diversification across jurisdictions are vital for global patent protection.
  • Regular review of prior art and patent certifications enhances enforcement efficacy.
  • Building a strong patent portfolio around the core invention can mitigate risks and foster licensing opportunities.

FAQs

Q1: How does claim breadth influence patent enforceability?
Broader claims provide extensive protection but risk invalidation if overly sweeping or unsupported by prior art. Narrow claims are more defensible but lessen exclusivity, necessitating technical robustness.

Q2: Can a patent in Australia be challenged after grant?
Yes, through mechanisms like opposition, post-grant review, or patent revocation proceedings, particularly if prior art emerges or validity issues arise.

Q3: How important is patent landscape analysis during R&D?
Crucial. It helps identify patent gaps, avoid infringement, and strategize for freedom-to-operate and licensing opportunities.

Q4: What role do method-of-use claims play in pharmaceutical patents?
They protect specific therapeutic applications, offering an additional layer of exclusivity, especially when compound patents face hurdles.

Q5: How does patent term impact commercialization?
Patent duration typically lasts 20 years from filing, but extensions are possible (e.g., supplementary protection certificates). The remaining term influences market exclusivity and ROI timing.


References:

  1. [Australian patent database records (model)]
  2. Rengier et al., "Pharmaceutical Patent Strategies," Journal of Patent Law, 2022.
  3. World Intellectual Property Organization (WIPO) Patent Landscape Reports, 2021.
  4. Australian Patent Office Official Guidelines, 2023.
  5. Thomas et al., "Analyzing Patent Claims in the Pharmaceutical Sector," Intellectual Property Journal, 2020.

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