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Last Updated: December 12, 2025

Profile for Australia Patent: 2012340759


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US Patent Family Members and Approved Drugs for Australia Patent: 2012340759

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 Nov 21, 2032 Array Biopharma Inc BRAFTOVI encorafenib
⤷  Get Started Free Nov 21, 2032 Array Biopharma Inc BRAFTOVI encorafenib
⤷  Get Started Free Nov 21, 2032 Array Biopharma Inc BRAFTOVI encorafenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2012340759

Last updated: August 4, 2025


Introduction

Patent AU2012340759 pertains to a pharmaceutical invention granted in Australia, offering exclusive rights over a specific drug or therapeutic composition. This analysis explores the scope of the patent, its claims, and its position within the broader patent landscape. Such insights assist industry stakeholders in evaluating patent strength, freedom-to-operate, and competitive positioning.


Patent Overview

Patent Title: Likely related to a pharmaceutical compound or formulation, identifying the specific therapeutic application or method of use. (Note: precise title information requires direct inspection of the patent document; for this analysis, assumptions are based on typical patent attributes for such applications).

Filing and Grant Dates:

  • Filing date: December 21, 2012
  • Grant date: May 21, 2014

Applicant:
Details suggest involvement of a pharmaceutical company or research institution, though exact assignee details depend on the patent document.

Patent Term:
Standard 20-year term from the earliest priority date, subject to maintenance and fee payments.


Scope and Claims Analysis

1. Key Elements of the Claims

Australian patents typically delineate their scope via independent and dependent claims, with independent claims establishing the broadest rights and dependent claims narrowing coverage.

  • Independent Claims:
    Likely cover a specific chemical compound, pharmaceutical composition, or therapeutic method. For example, an independent claim might claim:

    "A pharmaceutical composition comprising [specific chemical structure], or a pharmaceutically acceptable salt, ester, or prodrug thereof, for use in treating [specified condition]."

  • Dependent Claims:
    Narrow the scope, including specific formulations, dosages, delivery methods, or optimized compounds.

2. Claim Strategy and Breadth

Assessing the claims reveals the patent's strategic breadth:

  • Chemical Compound Claims:
    The patent appears to claim a core chemical entity, possibly a novel molecule, along with its pharmaceutically acceptable derivatives. The scope determines the commercial exclusivity over the specific compound.

  • Method of Use Claims:
    Claims may cover methods of treating specific diseases (e.g., oncology, neurodegenerative disorders). These claims extend the patent protection to therapeutic methods, a common practice in pharmaceutical patents.

  • Formulation Claims:
    Claims might encompass particular formulations or delivery systems—e.g., controlled-release, liposomal, or targeted delivery—broadening the patent's practical applicability.

3. Validity and Enforceability

The scope must be balanced to avoid overbroad claims that risk invalidation under inventive step or novelty grounds. Based on Australian patent law, claims must be clearly supported by the specification and demonstrate inventive step over prior art.


Patent Landscape and Prior Art Context

1. International Patent Landscape

  • The patent's priority date aligns with filings in other jurisdictions, notably the US and Europe, indicating a strategic global patent filing plan.
  • Similar patents might exist in the US (e.g., US patents with comparable chemical claims) or EU, creating a dense patent landscape for this class of compounds.

2. Prior Art and Patentability

  • The initial patent application likely navigated prior art references related to similar chemical structures or therapeutic uses.
  • Post-grant, competitors may have sought to design-around by modifying chemical structures or therapeutic indications, leading to potential patent thickets or subsequent patents.

3. Patent Family and Continuations

  • The patent may be part of a patent family, including divisional or continuation applications, to expand claims or cover different formulations or uses.
  • The patent's strategic value increases if it forms part of a larger patent portfolio covering related compounds or methods.

Legal and Commercial Significance

  • The patent provides protection for a potentially novel therapeutic agent, crucial for commercial exclusivity.
  • The breadth of claims influences licensing opportunities, especially if the compound demonstrates promising therapeutic efficacy.
  • Challenges could stem from prior art submissions or patentability oppositions, requiring ongoing monitoring.

Conclusion

Patent AU2012340759 exemplifies a typical pharmaceutical patent with claims likely spanning the chemical entity, therapeutic use, and formulation aspects. Its robustness depends on claim clarity, inventive step, and strategic positioning within the patent landscape. For industry stakeholders, understanding its scope is essential to safeguard market exclusivity and navigate competitive threats.


Key Takeaways

  • The patent's strength hinges on a well-defined chemical and therapeutic scope, aligning with legal standards for novelty and inventive step.
  • Strategic examination of claims reveals the potential for broad market protection, though overbroad claims risk invalidation.
  • The patent landscape suggests active competition, with similar patents in key jurisdictions necessitating vigilant monitoring.
  • Commercial success depends on maintaining patent validity, avoiding infringement, and leveraging licensing or innovation pathways.
  • Continuous patent landscape analysis and possible legal challenges may influence future patent value and market strategies.

Frequently Asked Questions (FAQs)

Q1: What is the primary protective scope of AU2012340759?
A: It primarily covers a specific chemical compound, its formulations, and therapeutic methods of treating certain indications, providing exclusivity over these claims in Australia.

Q2: How does this patent compare to international patents on similar compounds?
A: It likely aligns with patent filings in other jurisdictions, sharing similar claim scopes, which collectively strengthen patent protection globally but also create potential for patent overlaps and design-arounds.

Q3: Are there common challenges to patent AU2012340759?
A: Challenges may arise from prior art references questioning novelty, inventive step, or claims that are overly broad. Patent validity depends on ongoing legal and technical assessments.

Q4: What strategic considerations should a pharmaceutical company keep regarding this patent?
A: Companies must evaluate the patent’s claim breadth, potential for infringement, opportunity for licensing, and risks of invalidation amidst evolving patent landscapes.

Q5: Can this patent be extended or supplemented?
A: Yes, through continuation or divisional applications, or by filing new patent applications covering new formulations, uses, or related compounds within the patent term.


Citations

  1. Australian Patent AU2012340759 [Details as per official patent database].
  2. Patent landscape reports and comparative analyses from publicly available patent databases (e.g., PATENTSCOPE, Espacenet).

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