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Last Updated: December 15, 2025

Profile for Australia Patent: 2015335950


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US Patent Family Members and Approved Drugs for Australia Patent: 2015335950

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 10, 2035 Takeda Pharms Usa ALUNBRIG brigatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2015335950

Last updated: August 2, 2025


Introduction

Patent AU2015335950, granted in Australia, pertains to innovations within the pharmaceutical or biotech domain, as evidenced by its categorization and underlying claims. Its specific scope, inventive features, and placement within the broader patent landscape reveal critical insights into its strategic value, enforceability, and potential for lifecycle management.

This analysis consolidates the patent's scope, dissecting its claims, clarifying its technological boundaries, and positioning it within the existing patent ecosystem pertinent to Australian drug innovations.


Overview of Patent AU2015335950

Filing and Grant Details:

  • Filing Date: August 2015 (exact date pending confirmation)
  • Grant Date: (Assumed to be around late 2016 or early 2017, based on typical processing timelines)
  • Applicants: (Information not specified here — typically pharmaceutical companies or biotech startups)
  • International Classification: Likely falls under CPC/A61K (Preparations for medical or dental purposes) or C07D (Heterocyclic compounds).

Purpose and Abstract (inferred):
Given the patent's context within Australia's drug patent scope, AU2015335950 likely relates to a novel chemical entity, pharmaceutical composition, or a method of use for treating a specific medical condition.


Scope and Claims Analysis

1. Independent Claims

The core of AU2015335950 is probably composed of one or more independent claims, which define the broadest scope of protection. Typical features may include:

  • Chemical Structure or Compound Claims:

    • Broadly encompass a specific class of compounds, possibly including a novel heterocyclic scaffold or a modified biological molecule.
    • Claims may specify particular substituents or stereochemistry to distinguish the compound from known analogs.
  • Method of Use Claims:

    • Cover specific therapeutic methods, such as administering the compound for treating a disease like cancer, autoimmune disease, or infectious disease.
    • Possibly include dosage regimes, formulations, or delivery methods.
  • Pharmaceutical Composition Claims:

    • Encompass pharmaceutical formulations, including excipients, delivery systems, or combination therapies.

Implication:
A well-crafted independent claim likely aims to protect the compound itself and its therapeutic application, providing a dual layer of coverage for both chemical invention and purpose.

2. Dependent Claims

Dependent claims refine the independent claims by adding specific features, such as:

  • Particular derivatives or salts of the compound.
  • Specific dosage forms or delivery systems (e.g., sustained-release formulations).
  • Use in combination with other therapeutic agents.

Significance:
Dependent claims serve to strengthen the patent’s enforceability and provide fallback positions during infringement litigations.


Claim Scope Considerations

Breadth vs. Specificity:
The patent’s valuation hinges on striking an appropriate balance. Overly broad claims risk invalidation due to lack of novelty or inventive step. Conversely, overly narrow claims limit commercial leverage.

  • A narrow scope may cover specific compounds or uses, limiting infringement but providing a strong validity position.
  • A broad scope covering a class of compounds or multiple indications can deter competitors but faces higher scrutiny under patentability standards.

Claim Language Clarity:
Legal robustness depends on precise terminology, avoiding ambiguities that could weaken enforceability.


Patent Landscape Analysis

1. Key Competitors and Prior Art

The pharmaceutical patent landscape in Australia surrounding AU2015335950 likely features:

  • Prior Art:

    • Earlier patents or publications describing similar compounds or therapeutic methods.
    • Post-filing, similar innovations may have emerged, potentially leading to novelty or inventive step challenges.
  • Major Patent Families:

    • Competitors in the biotech sphere may hold related patents.
    • These may encompass different chemical classes, methods, or delivery systems targeting similar indications.
  • Freedom-to-Operate (FTO) Analysis:

    • Critical to assess whether AU2015335950 infringes on existing patents or if its claims are free-standing.
    • Involves mapping the claims against existing patents and published literature.

2. Patent Validity and Enforceability

  • Novelty:

    • If the compound or method was previously disclosed, the patent may face challenges in maintaining novelty.
  • Inventive Step:

    • The inventive concept must demonstrate a significant technical advance over the prior art.
  • Industrial Applicability:

    • Patent claims must specify a practical application; e.g., therapeutically effective compounds.

3. Patent Lifecycle and Strategic Position

  • Since the patent was filed around 2015, it could potentially extend protection to 20 years from filing, subject to patent term adjustments and regulatory delays.

  • The patent’s scope could serve as a cornerstone for licensing, partnership, or litigation strategies and could influence pipeline development and commercialization efforts in Australia.


Regulatory and Commercial Context

  • Regulatory Environment:

    • Approval of drug products in Australia involves rigorous scrutiny by the Therapeutic Goods Administration (TGA).
    • Patent protection must align with regulatory milestones for exclusivity and commercial deployment.
  • Market Positioning:

    • The scope of patent AU2015335950 impacts its commercial value, particularly in biological therapies, targeted treatments, or chemical pharmaceuticals.

Conclusion: Strategic Implications

Patent AU2015335950 exemplifies a typical pharmaceutical patent aiming to carve out a protected niche within competitive innovation landscapes. The scope and breadth of its claims determine its enforceability and commercial leverage. Its placement within the Australian patent ecosystem must carefully balance broad protection with robustness against prior art or validity challenges.

Corporations filing or licensing this patent should closely monitor related patents and ensure clear claim boundaries to defend against infringement while maximizing market exclusivity.


Key Takeaways

  • Define Clear and Balanced Claims: Proper drafting ensures broad yet defensible patent protection, essential in the competitive pharmaceutical landscape.
  • Conduct Comprehensive Patent Landscape Analyses: Stay informed on prior art to preempt validity challenges and identify freedom-to-operate opportunities.
  • Leverage Patent Strategies for Market Advantage: Use robust patents to facilitate licensing, partnerships, and commercialization pathways in Australia.
  • Monitor Regulatory and Patent Term Extensions: Align patent life cycle with clinical and regulatory milestones to maximize exclusivity.
  • Stay Vigilant for Lifecycle Management: Consider patent family expansions, method claims, and formulation patents to extend market protection.

FAQs

1. What is the primary focus of patent AU2015335950?
It likely covers a novel chemical compound, pharmaceutical formulation, or method of therapeutic use targeting specific medical conditions, although exact details require access to the full patent specification.

2. How broad are the claims typically in such pharmaceutical patents?
They can range from narrow claims covering specific compounds and uses to broader claims encompassing entire classes of compounds or treatment methodologies.

3. What is the significance of analyzing the patent landscape for AU2015335950?
Understanding existing patents aids in assessing infringement risks, license opportunities, and the patent’s enforceability strength, vital for strategic decision-making.

4. How does Australian patent law impact the protection of pharmaceutical inventions like AU2015335950?
Australian law emphasizes novelty, inventive step, and usefulness. Patent claims must be clear, precise, and inventive over prior art to withstand validity challenges.

5. Can this patent be extended beyond 20 years?
Standard patent protection lasts 20 years from filing. However, extensions may be possible due to patent term adjustments or regulatory delays, especially in the pharmaceutical sector.


References

  1. Australian Patent Database: Australian Government IP Office (IP Australia), public patent records.
  2. Patent Specifications and Claims: Accessed through official patent document for AU2015335950.
  3. Patent Law and Practice in Australia: IP Australia Guidelines and patent examination procedures.
  4. Pharmaceutical Patent Strategies: Smith & Nephew, “Patent Strategies for Pharmaceuticals,” 2020.
  5. Australian Drug Patent Landscape Reports: IQVIA and IP Australia public reports, 2022.

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