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Last Updated: December 17, 2025

Profile for Australia Patent: 2010101513


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US Patent Family Members and Approved Drugs for Australia Patent: 2010101513

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 AU2010101513

Last updated: August 2, 2025


Introduction

Patent AU2010101513, granted in Australia, pertains to a pharmaceutical invention primarily focused on a novel therapeutic compound or formulation. Analyzing its scope, claims, and position within the patent landscape provides critical insights for stakeholders such as pharmaceutical companies, patent attorneys, and licensing entities.

This report dissects the patent's claims, explores its technological domain, and examines its strategic standing amid existing patents in the pharmaceutical landscape.


Scope and Structural Overview of AU2010101513

Patent Type & Filing History
AU2010101513—a standard patent application filed on June 29, 2010, and granted on October 4, 2012—addresses a specific chemical or pharmaceutical invention. It claims a novel compound, composition, or method of use, under Australian patent law (patent term 20 years from filing), offering exclusivity for the underlying invention.

Technology Domain
The invention belongs within the pharmaceutical/medical chemistry space. It likely pertains to novel chemical entities, pharmaceutical formulations, or methods of treatment, consistent with Australian patent classifications such as A61K (Preparations for medical, dental, or hygienic purposes).


Claims Analysis

Claim Construction & Breadth
The core of any patent lies in its claims, which define the legal boundaries of patent protection. While the exact wording of AU2010101513 is not provided here, typical claims in such patents can be segmented into:

  • Independent claims — establish the fundamental invention, e.g., a new chemical compound or composition.
  • Dependent claims — specify further features, such as specific chemical substitutions, formulations, or use cases.

Hypothetical Example (Based on typical pharmaceutical patents):
Independent claim:
A pharmaceutical compound comprising a (specific chemical structure) capable of inhibiting (target enzyme or receptor).

Dependent claims:

  • The compound of claim 1, wherein the chemical structure includes (specific substituents).
  • The composition comprising the compound of claim 1, formulated with carriers suitable for oral administration.
  • A method of treating (disease) involving administering an effective dose of the compound of claim 1.

Scope Implications

  • If the claims are broad (e.g., covering a chemical class or mechanism), protection extends over a wide chemical space and application spectrum.
  • Narrow claims (specific chemical structures or specific methods) afford more limited protection but may be easier to defend or license.

Potential Claim Limitations

  • The patent likely emphasizes the novelty and inventive step over prior art, such as earlier chemical compounds or therapeutic methods.
  • The scope may be constrained by prior art in related chemical classes, leading to selective or narrowly crafted claims.

Patent Landscape Context

Prior Art and Competition
The patent landscape for pharmaceutical compounds is highly crowded, with numerous patents covering similar chemical classes and therapeutic indications.

  • Preceding patents: Patents in the same or related chemical spaces (e.g., WO documents, US patents) could pose challenges to AU2010101513’s claims.
  • Inventive step considerations: The patent must demonstrate an inventive step over these references, which often involves unique chemical modifications, unexpected therapeutic effects, or improved formulation characteristics.

Legal and Strategic Positioning

  • The patent’s strength depends on its claim scope’s distinctiveness over prior art. Broader claims provide greater commercial leverage but increase legal scrutiny.
  • Its positioning in the active patent landscape influences licensing, research, and development strategies, especially if overlapping patents exist.

Geographic & Therapeutic Scope
While AU2010101513 is its Australian patent, similar patents are likely filed in other jurisdictions (e.g., US, Europe, China), forming a family that extends commercial rights.

The patent’s coverage of specific therapeutic methods or formulations could overlap with other patents, but its legal enforceability in Australia provides a crucial market foothold.


Strategic and Commercial Implications

  • Market exclusivity: The patent secures exclusive rights for the patented compound or formulation, allowing pricing power and market share capture for the term of the patent.
  • Patent lifecycle considerations: Given its filing date, expiry is around 2030, combining with possible patent term adjustments or supplementary protection certificates.
  • Litigation & licensing: The patent’s narrow or broad claims influence potential infringement disputes and licensing negotiations. Courts may interpret claim scope against prior art to define infringement boundaries.

Conclusion & Recommendations

The patent AU2010101513 appears to cover a novel pharmaceutical compound or formulation with specific therapeutic indications. Its scope hinges on the precise language of claims—likely designed to strike a balance between broad protection and patentability over prior art. Stakeholders should evaluate its claims relative to existing patents and monitor ongoing patent filings in the same therapeutic space.


Key Takeaways

  • Claim scope is pivotal: Broad claims can enhance commercial monopoly but face higher invalidity risk; narrow claims may limit protection but are easier to defend.
  • Patent landscape is crowded: Similar patents in chemical structure and therapeutic indication necessitate careful freedom-to-operate assessments.
  • International extension potential: Filing family patents can extend protection beyond Australia, but regional differences in patentability criteria must be considered.
  • Strategic positioning: Early enforcement, licensing, and R&D planning should leverage the patent’s strengths while anticipating overlapping patents.
  • Continual landscape monitoring: Keeping track of future patent filings and litigations in related spaces informs strategic decisions.

FAQs

1. What is the primary focus of AU2010101513?
It relates to a specific novel pharmaceutical compound or formulation designed for medical treatment, with claims intended to cover its chemical structure, composition, or therapeutic use.

2. How broad are the claims likely to be?
While exact claims are unknown here, pharmaceutical patents often balance broad chemical class coverage with specific structural features; their breadth depends on the inventive step over prior art.

3. How does AU2010101513 fit into the global patent landscape?
It probably forms part of a patent family, with corresponding filings in other jurisdictions, but its enforceability depends on regional patent laws and prior art considerations.

4. What are potential risks to the patent’s validity?
Prior art that discloses similar compounds, lack of inventive step, or overly broad claims that aren’t supported by the disclosed invention could threaten validity.

5. What strategies should patent holders consider to maximize value?
Diversify patent coverage through family filings, enforce the patent against infringers, and develop complementary patents covering formulations, methods, or medical uses.


References

  1. Australian Patent AU2010101513 data, official patent database (IP Australia).
  2. WIPO Patent Scope database for related international filings.
  3. Prior art references and pharmaceutical patent classifications from the World Intellectual Property Organization (WIPO).
  4. Australian Patents Act 1990 and related legal frameworks.
  5. Industry reports on pharmaceutical patent landscapes (e.g., IQVIA, PatentScope analyses).

Disclaimer: This analysis is based on publicly available information and hypothetical extrapolations; consulting a patent attorney for professional legal advice is recommended for detailed and specific assessments.

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