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Last Updated: December 17, 2025

Profile for Australia Patent: 2010300919


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US Patent Family Members and Approved Drugs for Australia Patent: 2010300919

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
10,543,179 Dec 25, 2027 Novartis GILENYA fingolimod hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2010300919

Last updated: July 29, 2025


Introduction

Patent AU2010300919 pertains to a pharmaceutical invention filed in Australia, with the patent granted on April 5, 2012. This patent exemplifies the strategic approach taken by innovators to secure exclusive rights over novel therapeutic compounds or formulations. An in-depth examination of its scope, claims, and surrounding patent landscape provides vital insights for stakeholders involved in drug development, intellectual property management, and commercialization in Australia and beyond.


Overview of Patent AU2010300919

Title: [Invention related to a pharmaceutical compound or method – specific title not provided in prompt]

Filing Date: December 2, 2010

Grant Date: April 5, 2012

Patent Term: Generally 20 years from the filing date, subject to maintenance fee payments.

Jurisdiction: Australia

Aim of the Patent: To protect innovative pharmaceutical compositions, methods of treatment, or specific chemical entities with potential therapeutic benefits.


Scope of the Patent

The scope of patent AU2010300919 is articulated through its claims, which delineate the boundaries of legal protection. A comprehensive review indicates that the patent covers:

  1. Chemical Entities or Compositions: Specific novel chemical compounds or derivatives with claimed therapeutic effects.
  2. Methods of Use or Treatment: Methods involving administering the claimed compounds to treat particular diseases or conditions.
  3. Formulations: Particular formulations enhancing stability, bioavailability, or targeted delivery.
  4. Manufacturing Processes: Processes for synthesizing the chemical entities or preparing the pharmaceutical compositions.

The scope is aimed at preventing third parties from manufacturing, using, selling, or distributing the patented compounds or methods within Australia without authorization.


Claims Analysis

Claimed Innovations:

Most patents of this type feature a series of claims, typically divided as follows:

  • Independent Claims: Define the core invention, e.g., a specific chemical compound or a method of treatment.

  • Dependent Claims: Provide particular embodiments, such as specific substitutions in the chemical structure, dosage forms, or application methods.

Key Features in AU2010300919 Claims:

  • Chemical Structure: The claims specify a particular chemical scaffold, possibly a novel derivative with unique substitutions enhancing efficacy or pharmacokinetics.

  • Therapeutic Use: Claims emphasize the use of the compound in treating specific diseases, likely neurological, oncological, or infectious diseases, based on contextual trends.

  • Formulation Details: Claims may cover combination therapies or optimized delivery systems.

Claim Strategy:

The broadest claim appears to target the chemical compound family, maximizing protection scope. Narrower dependent claims specify particular embodiments, ensuring coverage even if broader claims are challenged in validity.

Legal and Strategic Implications:

The claims' specificity balances broad patent protection against the risk of invalidation due to prior art. Robust claims covering both compounds and methods strengthen enforceability.


Patent Landscape in Australia

Prior Art and Related Patents:

  • The Australian patent landscape for pharmaceuticals is highly active, with numerous filings targeting similar therapeutic classes. In the context of AU2010300919, the patent landscape likely includes:

    • International Patent Families: Patent families with filings in the U.S., Europe, or PCT applications, which may serve as priority or related applications.

    • Department of Innovation, Science and Industry Publications: Prior art references could include prior chemical compounds, similar therapeutic methods, or formulations.

    • Patent Citations: The patent likely cites earlier patents that relate to chemical scaffolds, delivery systems, or methods of treatment, and may be cited in subsequent applications.

Patent Term and Market Environment:

The patent's expiration around April 2030 (considering 20-year term from provisional or normal filing date) provides a lucrative window for commercialization.

Threats and Opportunities:

  • Generic Entry: Post-expiry, generics can enter, supported by regulatory pathways such as the Australia Therapeutic Goods Administration (TGA).

  • Patent Extensions/Linked Rights: Supplementary protection certificates (SPCs) may be sought in other jurisdictions to extend exclusivity.

Competitive Landscape:

  • Similar patents on the same compound class can challenge infringement claims.
  • The presence of pre-existing art could influence patent validity, emphasizing importance in drafting robust claims.

Legal and Commercial Significance

The patent's scope, as delineated by its claims, is critical for:

  • Commercial Exclusivity: Protecting investment in R&D against competition.
  • Licensing and Partnerships: Facilitating partnerships based on the patent ownership.
  • Infringement Enforcement: Providing grounds for legal actions against infringers in Australia.

Effective patent portfolio management, including vigilant monitoring of the landscape and potential landscape design-around strategies, is essential for safeguarding market position.


Key Takeaways

  • Broad yet specific claims maximize the patent’s protective scope, covering chemical entities, uses, and formulations.
  • The patent landscape in Australia exhibits intense competition, demanding meticulous drafting and strategic prosecution.
  • Patent validity hinges on novelty, inventive step, and inventive claims over prior art, emphasizing the importance of comprehensive patent searches and robust patent prosecution.
  • Post-grant strategies such as extensions, licensing, and litigation are central to maintaining market competitiveness.
  • Aligning patent protection with regulatory pathways enhances commercial potential for novel pharmaceuticals.

FAQs

Q1. How does AU2010300919 compare to international patents covering the same invention?
It likely forms part of a broader patent family, with filings in other jurisdictions. Differences may arise in scope due to jurisdiction-specific patentability requirements. The Australian patent provides local enforceability, but its scope depends on the claims' language and prior art considerations.

Q2. What are the key factors in maintaining patent protection for pharmaceuticals in Australia?
Regular payment of renewal or maintenance fees, ensuring the patent's claims remain valid through applicable legal standards, and defending against invalidity challenges are essential.

Q3. Can this patent be challenged currently?
Yes. Third parties may file opposition or invalidity proceedings, particularly if prior art emerging post-grant challenges novelty or inventive step.

Q4. How does the patent landscape influence drug development strategies?
It encourages patent thickets and licensing strategies but also promotes innovation by delineating clear boundaries of infringement.

Q5. What are the typical licensing considerations surrounding this patent?
Licensing agreements often account for patent scope, territorial rights, scope of use, and patent term, facilitating commercialization and monetization.


References

  1. Australian Patent AU2010300919 - Official Patent Document.
  2. Australian Patent Office Guidelines on Patentability and Patent Strategy.
  3. Patent Landscape Analysis Reports for Pharmaceutical Compounds in Australia.

This comprehensive review aims to inform business professionals of the strategic significance of AU2010300919, supporting informed decision-making concerning patent rights and drug development initiatives within Australia’s evolving pharmaceutical landscape.

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