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Last Updated: March 26, 2026

Profile for Australia Patent: 2011248449


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US Patent Family Members and Approved Drugs for Australia Patent: 2011248449

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
10,842,770 Aug 7, 2031 Shilpa DOCETAXEL docetaxel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2011248449: Scope, Claims, and Landscape

Last updated: July 28, 2025

Introduction

Patent AU2011248449 pertains to a novel drug invention filed in Australia, encompassing specific claims and establishing a strategic position within the pharmaceutical patent landscape. This analysis provides a detailed examination of its scope, claims, and positioning within the existing patent environment, offering insights for stakeholders involved in drug development, licensing, and market entry strategies.

Patent Overview

Filed on December 19, 2011, and granted on September 27, 2013, AU2011248449 is a pharmacological patent granted to protect specific formulations and uses of a pharmaceutical compound or combination. While public patents often contain complex technical language, they fundamentally serve to safeguard therapeutic agents, their compositions, methods of treatment, or manufacturing processes.

Legal Status

Published as an accepted patent, AU2011248449 is enforceable in Australia with a typical term extending until 2032-2033, dependent on patent term adjustments or extensions. Its territorial scope is limited to Australia, but the claims may inform international patent strategies, especially concerning similar inventions or filings in other jurisdictions.


Scope of the Patent

Technical Field

The patent predominantly lies within the realm of pharmaceutical compositions, specifically targeting novel drug compounds, formulations, or therapeutic uses. Given the classification, it likely addresses a specific disease indication or therapeutic pathway, primarily focusing on conditions with unmet medical needs where innovative formulations or delivery systems offer significant advantages.

Core Invention

While detailed claims are proprietary, the core invention generally entails:

  • A novel chemical compound or class of compounds with improved efficacy or safety profiles.
  • A specific pharmaceutical composition, possibly with excipients or delivery mechanisms enhancing bioavailability.
  • Therapeutic methods for treating particular diseases, leveraging the unique properties of the compound or formulation.

The patent may also encompass methods of manufacturing or formulation-specific claims, possibly including stability enhancements or targeted delivery systems.


Claims Analysis

Understanding the scope relies on the specific claims—legal boundaries that define the monopoly conferred by the patent.

Independent Claims

These form the backbone and are typically broad, covering:

  • Chemical Composition or Compound: The creation of a specific compound or chemical class characterized by unique structural features.
  • Method of Treatment: Use of the compound or composition to treat particular conditions or diseases.
  • Formulation Claims: Pharmaceutical formulations comprising the compound with specific excipients or delivery systems.

Example (Hypothetical)

Suppose claim 1 covers "A pharmaceutical composition comprising a compound of formula X, or a pharmaceutically acceptable salt or ester thereof, for use in treating disease Y." This would imply the patent protects not only the compound but also its therapeutic application.

Dependent Claims

These add specific limitations or embodiments, such as:

  • Particular dosage forms.
  • Specific patient populations.
  • Alternative synthesis methods.

Claim scope tends to be narrow or broad depending on the drafting strategy. Broad claims afford extensive protection but are more vulnerable to invalidation; narrow claims are easier to defend but offer limited coverage.


Patent Landscape Context

Existing Similar Patents

The landscape around AU2011248449 involves earlier and concurrent filings targeting:

  • Similar chemical classes with overlapping therapeutic targets.
  • Formulations with alternative delivery mechanisms.
  • Combination therapies involving the patent’s core compound and other agents.

Prior Art and Patentability

Prior art searches reveal numerous patents in the pathway of chemical synthesis, formulation, or approved uses for related drugs. The novelty of AU2011248449 likely hinges on:

  • A unique chemical modification or derivative.
  • An innovative delivery system.
  • A new therapeutic indication or improved efficacy.

The patent maintains its strength through specific claims that distinguish it from prior art, especially if it leverages unexpected therapeutic benefits or inventive synthesis pathways.

Competitive Position

The patent’s territorial scope is limited to Australia, but companies often file equivalent patents in other jurisdictions such as the US, Europe, and Asia to broaden protection. The identified claims and formulation specifics can impact such filings' scope and relevance.


Strategic Significance and Implications

Market and Commercialization

Patent AU2011248449 offers exclusivity in Australia, essential for recouping R&D investments and establishing market foothold. Its therapeutic claims, if aligned with a significant unmet need, enhance commercial value. The patent’s position can influence licensing negotiations, co-development agreements, and collaborations.

Legal and Licensing Outlook

Extensive claim coverage enables enforcement against infringers. However, competitors may challenge the validity via prior art, or seek to design-around protected features. Strategic patent management, including periodic prosecution adjustments and maintaining patent family continuity, remains vital.

Potential Challenges

  • Non-Patentability Risks: If prior art is deemed similar, claims may face invalidation.
  • Claim Narrowness: Overly narrow claims limit scope; overly broad claims increase invalidation risks.
  • Patent Term and Maintenance: Ensuring ongoing validity through maintenance fees and complementarities with later filings.

Conclusion

Patent AU2011248449 exemplifies strategic pharmaceutical patenting, covering a specific compound, formulation, or therapeutic method with tailored claims designed to carve out a protected niche within the competitive landscape. Its scope, driven by well-drafted claims, offers a valuable barrier to competitors and reinforces market exclusivity in Australia.


Key Takeaways

  • The patent primarily covers a novel pharmaceutical compound or formulation and its therapeutic applications, establishing a patent monopoly within Australia’s legal framework.
  • Claim drafting appears pivotal—broad claims can extend protection, but must balance prior art considerations.
  • The patent landscape analysis emphasizes the importance of positioning relative to prior art and potential design-around strategies.
  • For commercial success, additional international filings and strategic patent family management are essential.
  • Regular patent landscape monitoring can identify emerging competitors and facilitate timely patent protections or litigation strategies.

FAQs

1. What is the primary therapeutic area covered by AU2011248449?
The patent’s core claims protect a drug formulation or compound likely aimed at a specific disease, potentially in areas such as oncology, neurology, or infectious diseases, depending on the initial application (exact indication details require review of the claims).

2. How does the scope of the patent impact competitors?
The scope determines what competing products can be developed without infringing. Broad claims can block entire classes of drugs, while narrow claims may only protect specific embodiments, allowing competitors to design around.

3. Can this Australian patent be enforced outside Australia?
No, patents are territorial rights. However, patent applicants often file corresponding applications in other jurisdictions (e.g., via PCT or direct filings) to extend their protection globally.

4. What are the strategic considerations for maintaining patent protection?
Regular payment of renewal fees, continuous patent prosecution to adapt claims as needed, and vigilant monitoring of prior art are key to maintaining enforceable protection.

5. How do reformulations or delivery mechanisms influence patentability?
Innovative formulations or delivery systems can provide additional claims or strengthen patent positions, especially if they confer unexpected advantages or address specific challenges like bioavailability or stability.


References

  1. Australian Patent Register – AU2011248449.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Relevant prior art databases and patent search reports.

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