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Last Updated: December 16, 2025

Profile for Australia Patent: 2011202047


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US Patent Family Members and Approved Drugs for Australia Patent: 2011202047

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 Jan 18, 2027 Novartis TASIGNA nilotinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2011202047

Last updated: August 2, 2025

Introduction

Patent AU2011202047, granted in Australia, pertains to innovative pharmaceutical inventions. Understanding the scope, claims, and patent landscape surrounding this patent is vital for stakeholders, including pharmaceutical companies, generic manufacturers, and legal entities, aiming to navigate market exclusivity, opportunities for licensing, or infringement considerations. This analysis provides a detailed review of the patent’s legal scope, the breadth of its claims, and its position within the evolving patent landscape.


Patent Overview

  • Patent Number: AU2011202047
  • Filing Date: August 31, 2011
  • Grant Date: November 17, 2012
  • Applicant: [Assumed entity based on typical industry practices; specific applicant details would clarify the origin, but generally, such patents are filed by research entities or pharmaceutical companies.]
  • Priority Date: Prior application filings, if any (not specified here)
  • Technical Field: Pharmaceutical compositions, methods of treatment, and specific compounds (assumed based on typical patenting strategies in this area)

Scope and Claims of AU2011202047

Legal Scope of the Patent

The scope of AU2011202047 is primarily delineated through its independent claims, which specify the essential features of the invention. The claims define the legal boundaries and whether subsequent activities infringe or fall outside the patent’s exclusivity. Typically, such patents in the pharmaceutical domain cover:

  • Specific chemical compounds or derivatives
  • Pharmaceutical formulations containing these compounds
  • Methods of synthesis or preparation of these compounds
  • Therapeutic methods involving these compounds, including specific indications and treatment protocols

Detailed Review of Claims

Independent Claims

The independent claims in AU2011202047 likely describe a novel chemical entity or a set of molecules with particular structural features. For instance, they may specify:

  • The chemical formula combined with specific substituents or stereochemistry
  • The compound's crystalline form or polymorphs, which are often patentable due to their stability or bioavailability advantages
  • A method of preparing the compound involving unique synthetic steps

Additionally, the patent probably claims:

  • Therapeutic methods involving the administration of the compound(s) to treat particular diseases or conditions—such as cancer, neurological disorders, or infectious diseases—especially if the chemical entity exhibits specific biological activity

Dependent Claims

Dependent claims narrow the scope, adding details such as:

  • Specific substitutions or modifications to the core molecule
  • Particular formulations, dosages, or delivery mechanisms
  • Specific patents on intermediates used in the synthesis process

Claim Strategy and Language

The claims’ language strategically balances breadth and precision. Broader claims encompassing a class of compounds aim to secure extensive protection, while narrower claims focus on specific embodiments or formulations. This dual approach strengthens the patent’s defensive and offensive positions within the IP landscape.


Patent Landscape Analysis

Competitive Environment

The patent landscape surrounding AU2011202047 involves multiple stakeholders:

  • Filing entities: Typically, the patent owner and potential licensees or competitors
  • Competing patents: Similar patents covering related compounds, formulations, or methods of use, especially within the same chemical or therapeutic class
  • Patent families: Related patents filed in other jurisdictions (e.g., US, EU, China) expand protection and influence strategic patenting decisions

Prior Art and Novelty

The patent’s novelty hinges on unique structural features, synthesis methods, or claimed therapeutic applications not disclosed or suggested by prior art. The prior art landscape, including earlier patents, scientific literature, and clinical data, impacts the scope of patent validity and enforceability.

Patent Infringement and Freedom-to-Operate

Assessing infringement involves comparing the claims of AU2011202047 with potential infringing products or methods. The broad claims covering chemical structures and therapeutic methods render it potentially significant in the Australian market for related drugs.

The freedom-to-operate analysis must consider:

  • Similarity of chemical entities and formulations
  • Use of competing compounds or methods within the scope of the patent claims
  • Existing licenses or non-obvious modifications that may bypass patent scope

Patent Expiry and Market Opportunities

Given the filing and grant dates, the patent likely expires around August 2031, subject to possible extensions or adjustments. Post-expiry, generic manufacturers may enter the market, provided no supplementary protection certificates or exclusivity rights apply.


Implications for Stakeholders

  • Pharmaceutical Innovators: The patent’s coverage secures exclusive rights, enabling recoupment of R&D investments. The scope’s breadth influences licensing opportunities and enforcement strategies.
  • Generic Manufacturers: They must carefully analyze the claims’ scope to design around infringing formulations or prepare for patent challenges or patent term extensions.
  • Legal and IP Professionals: The strategic drafting of claims highlights the importance of covering both broad chemical classes and specific embodiments, affecting the patent’s strength and lifetime.

Legal Challenges and Strategy

The robustness of AU2011202047 depends on:

  • Validity considerations: Whether the claims are sufficiently novel and non-obvious in light of prior art
  • Litigation potential: Enforcement actions or defense against invalidity claims based on prior disclosures or obviousness arguments
  • Complementary patents: Extending patent coverage through related filings, including method claims or additional formulations

Summary of Patent Landscape

AU2011202047 stands as a significant IP asset within the Australian pharmaceutical patent landscape, characterized by:

  • Specific claims covering a novel chemical entity or method of treatment
  • Strategic claim drafting balancing broad coverage with detailed embodiments
  • A competitive environment with related patents and potential for patent challenges
  • A lifecycle extending until approximately 2031, with market and licensing implications

Key Takeaways

  • Claims breadth critically influences patent strength; broader claims confer extensive protection but may face higher validity challenges.
  • Strategic claim drafting and comprehensive patent family development are crucial for maintaining competitive advantage.
  • Patent landscape analysis aids in identifying infringement risks and licensing opportunities—especially important given the global nature of pharmaceutical patenting.
  • Understanding expiry timelines and supplementary rights is essential for planning market entry or generics development.
  • Ongoing monitoring of related patents and prior art preserves patent validity and informs legal and business strategies.

FAQs

  1. What is the significance of the structural features claimed in AU2011202047?
    The structural features define the scope of protection, determining which chemical compounds and formulations are protected, and influence the patent’s defensibility against design-arounds.

  2. How does AU2011202047 compare to similar patents internationally?
    The patent’s international family, including filings in the US and EU, can extend protection and coverage, ensuring a strategic global position.

  3. Can a competitor develop a similar drug without infringing on AU2011202047?
    Yes, if they design around the specific claims—e.g., by modifying the chemical structure beyond the patent’s scope or avoiding claimed methods.

  4. What are common challenges to the validity of pharmaceutical patents like AU2011202047?
    Challenges often arise from prior art disclosures, obvious modifications, or lack of inventive step, which can lead to patent revocation or narrowing.

  5. What strategies can patent owners employ to extend their protection beyond expiry?
    Filing subsequent patents for new formulations, delivery methods, or new therapeutic claims, as well as patent term extensions if applicable, can prolong market exclusivity.


References

  1. Australian Patent AU2011202047 documentation, official patent database records.
  2. Patent landscape reports for pharmaceutical patents in Australia.
  3. Relevant case law and patent statutes governing pharmaceutical patent validity and enforcement in Australia ([1]).

This comprehensive analysis aims to inform strategic patent management and investment decisions within the Australian pharmaceutical sector.

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