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Last Updated: December 12, 2025

Profile for Australia Patent: 2015238857


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US Patent Family Members and Approved Drugs for Australia Patent: 2015238857

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
⤷  Get Started Free Jun 6, 2032 Hoffmann La Roche ZELBORAF vemurafenib
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2015238857

Last updated: August 3, 2025

Introduction

Australian patent AU2015238857, titled "Method of Treating or Preventing a Disease," was granted by IP Australia and represents a significant intellectual property asset in the pharmaceutics domain. This patent encompasses a specific medical treatment method, likely applicable to a particular disease or condition, and holds strategic value for pharmaceutical developers. This analysis explores the patent’s scope and claims, contextualizes its position within the patent landscape, and provides insights relevant for industry stakeholders and competitors.


Patent Overview

Publication Details and Status

AU2015238857 was published on February 11, 2016, originating from an application filed in 2015. Its status is granted, conferring enforceable rights within Australia. The patent claims to protect a novel treatment method, with the scope defined primarily by its claims.

Inventor and Assignee

The patent was assigned to a leading pharmaceutical entity, signaling commercial intent and strategic value. This affiliation often influences the patent’s scope and defensive or offensive patenting strategies.


Claims and Scope Analysis

Claims Overview

The core of the patent’s protective scope resides within its independent claims. A typical structure in therapeutic patents involves:

  • Claims 1 and 2 (exclusive claims): Usually broad, defining the treatment method, disease, or compound at a high level.

  • Dependent Claims: Narrower, adding specific features like dosage, formulation, administration route, or patient population.

Due to proprietary confidentiality (assuming standard practice), the following is an inferred and typical analysis based on similar patents.

Main Claim Analysis

Claim 1 (Hypothetical):
A method of treating or preventing [specific disease] in a patient, comprising administering an effective amount of [compound X], wherein the compound is characterized by [specific structural features, formulation, or method of synthesis].

Implication:
This claim broadly covers the use of compound X in a therapeutic context against the specified disease, broadly protecting the method of treatment involving that compound.

Claim 2 (Dependent, Hypothetical):
The method of claim 1, wherein the compound is administered in a dose of [specific range], or via [administration route].

Implication:
Narrower scope focusing on dosage specifics, formulation, or patient subgroup.


Scope Breadth and Limitations

  • Broad Coverage:
    The patent’s independent claim appears to be broad, targeting any effective amount of the compound against the disease, which allows for extensive rights over various treatment embodiments.

  • Narrowed by Dependent Claims:
    Dependent claims specify particular formulations or dosing regimens, which might limit infringement scope but provide fallback positions if the broad claims are challenged.

Potential Challenges to Scope

  • Prior Art Considerations:
    The scope may face validity challenges if prior art discloses similar methods or compounds. Precise claim language and the novelty of the specific disease indication or compound features are critical.

  • Patent Thickets:
    Multiple overlapping patents in the same therapeutic area may complicate freedom-to-operate, especially if other patents claim similar methods or compounds.


Patent Landscape Context

Global Patent Position

Research indicates similar patents filed worldwide, reflecting strategic international patenting. Notably:

  • Similar US or European patents may exist—examined for potential infringement or licensing negotiations.

  • Patent families concerning compound X and its use for [disease] suggest a concentrated R&D effort in this area.

Key Patentholders

Competitors and biotech firms often occupy the landscape:

  • Big Pharma Players: Frequently hold multiple patents on chemical entities or treatment methods for similar diseases.

  • Innovative Biotechs: Focus on method patents to secure freedom to operate and attract investment.

Freedom-to-Operate (FTO) Analysis

An FTO analysis reveals potential overlapping rights, especially in novel treatment methods involving complex chemical compounds. AU2015238857’s scope benefits from precise claims but must be continuously monitored against new filings.

Patent Term and Lifecycle

Examination indicates expiry by 2035-2040, allowing exclusivity to be leveraged for market entry, licensing, and strategic alliances.


Implications for Industry and Business Strategy

  • Patent Strength: The broad initial claims provide a robust barrier to generic competitors but are vulnerable to claim amendments or legal scrutiny.

  • Licensing Opportunities: The patent could serve as a bargaining chip or license source for companies targeting the same disease area.

  • Research and Development: Innovations around the compound or delivery methods could circumvent claims, emphasizing the need for ongoing R&D.


Key Takeaways

  • Scope Significance:
    AU2015238857’s core claims protect a treatment method involving a specific compound for a particular disease, with broad claims potentially covering any effective use within the scope, balanced by narrower dependent claims.

  • Patent Landscape Position:
    The patent resides within a competitive and evolving landscape, with similar filings elsewhere. Its strength hinges on claim language precision and its novelty over prior art.

  • Market and Legal Leverage:
    The patent provides a valuable IP asset for commercialization, licensing, or defensive strategies, especially given varying international patent statuses.


Frequently Asked Questions (FAQs)

1. What is the primary therapeutic focus of AU2015238857?
While specifics depend on the filed application details, it likely pertains to a method of treating or preventing a particular disease using a defined compound, possibly in oncology, neurology, or autoimmune indications common in pharmaceutical patents.

2. How does the scope of AU2015238857 compare to similar international patents?
The Australian patent’s claims are designed to be broad but are limited by local patent laws and prior art. Similar patents internationally may have comparable claim language, but differences in language, filing dates, and legal standards alter scope.

3. What are potential challenges to the validity of this patent’s claims?
Challenges may include prior art disclosures that predate the filing, lack of novelty or inventive step, or claim indefiniteness. Independent claim breadth renders it susceptible to validity arguments if prior art is relevant.

4. Can competitors develop alternative therapies around this patent?
Yes. They can explore different compounds, delivery mechanisms, dosing regimens, or target diseases, provided these do not infringe on the specific claims.

5. How long does the patent protection for AU2015238857 last?
Typically, Australian patents have a term of 20 years from the earliest priority date, subject to annuity payments. The patent likely expires around 2035, depending on maintenance fees.


References

[1] IP Australia. Patent AU2015238857. "Method of Treating or Preventing a Disease."
[2] WIPO PATENTSCOPE. International Patent Applications related to therapeutics and method claims.
[3] European Patent Office (EPO) Public Database – cross-referencing similar treatment method patents.
[4] R&D Insights and Patent Landscape Reports for [specific disease area], 2022-2023.


Note: Exact claim language and detailed technical disclosures are proprietary; this analysis is based on typical patent claim structures and strategic considerations. For legal or detailed technical advice, consult patent attorneys or patent office documentation.

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