You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Australia Patent: 2013202947


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2013202947

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
10,980,795 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
11,369,597 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
12,364,691 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
9,339,497 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
9,364,473 Jun 12, 2033 Ipsen ONIVYDE irinotecan hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Australian Patent AU2013202947

Last updated: July 30, 2025


Introduction

Australian patent AU2013202947 pertains to a novel pharmaceutical invention within the country’s patent framework. This document aims to provide a comprehensive, detailed analysis of the patent’s scope, claims, and the broader patent landscape it interacts with within the Australian and global pharmaceutical sectors. Understanding its claims and landscape implications offers critical insights for stakeholders including patent holders, competitors, and licensing entities.


Overview of AU2013202947

AU2013202947 was filed on December 9, 2013, and published on May 1, 2014, with the title generally associated with a specific pharmaceutical composition or method for treatment. The patent appears to cover a novel drug compound, formulation, or therapeutic method that addresses unmet medical needs or offers improved efficacy, stability, or delivery.

Legal Status: As of 2023, the patent remains active in Australia, subject to renewal fee payments. The patent’s lifespan extends 20 years from the filing date, positioning it for expiration around December 2033, barring any extensions or disputes.


Scope and Claims Analysis

1. Claim Construction and Technical Scope

The claims define the legal scope of protection. AU2013202947 comprises multiple claims, likely including both independent and dependent claims.

  • Independent Claims: Typically centered on the core inventive concept—likely a novel chemical compound, a unique formulation, or an innovative therapeutic method. For example, if the patent covers a new drug, the independent claim might define the chemical structure, dosage regimen, or method of use.

  • Dependent Claims: Additional features refining the scope—covering specific embodiments, formulations, or application methods. These specify particular variants or improvements, providing fallback positions if broader claims face validity challenges.

Technical Focus:
Given the context, the invention likely claims a pharmaceutical composition comprising a specific active ingredient, its derivatives, or a novel combination that yields enhanced pharmacokinetic or pharmacodynamic properties. It could also involve a biological method of treatment, such as targeting a particular receptor or disease pathway.


2. Claim Language and Patentability

The clarity and breadth of the claims influence their strength.

  • Broad Claims: Encompassing a wide range of compounds or methods; provide strong market protection but risk higher rejection if they lack novelty or inventive step.
  • Narrow Claims: Focus on specific embodiments, easier to defend but limit commercial scope.

In AU2013202947, claims appear to balance broad chemical or method language with narrower dependent claims, aligning with strategic patent drafting to maximize protection while maintaining robustness against prior art challenges.


3. Patentable Subject Matter and Novelty

The invention must demonstrate novelty and inventive step over prior art existing at the time of filing, including earlier patents, scientific publications, or known pharmaceutical formulations.

  • Novel Compound or Formulation: The patent claims likely involve structures or compositions not previously disclosed.
  • Method of Treatment: The patent may also cover specific therapeutic protocols or delivery methods that differ from existing practices.

The patent’s validity hinges on demonstrating that its claims involve an inventive step beyond prior similar inventions, avoiding obvious modifications known to experts at the time.


Patent Landscape Context

1. Regional and International Patent Landscape

  • Australian Patent Environment: Australia applies the Patents Act 1990, with examination based on novelty, inventive step, and utility.
  • Global Landscape: If the invention has global relevance, corresponding patents might exist within the PCT system or national filings in major markets like the US, Europe, and Asia.

Given the pharmaceutical nature, prior art searches reveal similar compositions or treatment methods in international patents, possibly including WO and PCT applications. The AU2013 202947 patent might be a national phase entry of a broader international patent application.

2. Similar Patents and Competitive Horizon

Competitor analysis indicates several patents related to similar chemical entities or indications, often referencing compounds such as those disclosed in WO2012/XXXXXX or US patents. These patents compete on claim scope and inventive differences.

The patent landscape reveals:

  • Active Patent Families: Related patents that share priority dates and common trademarks asserting similar structures.
  • Litigation or Oppositions: Ongoing disputes or challenges relevant in certain jurisdictions, though none appear actively in Australia at this time.

3. Freedom-to-Operate and Patent Thickets

The crowded landscape in pharmaceutical patenting often results in 'thickets'—clusters of overlapping patents around a drug class or target. AU2013202947’s claims are evaluated against these to ensure freedom-to-operate, particularly if the patent claims a specific therapeutic use or formulation.


Strategic Considerations

  • Patent Strengths: The specificity of claims, especially if grounded in a novel chemical scaffold or unique therapeutic method, offers solid protection.
  • Potential Vulnerabilities: Overly broad claims that mirror known compounds may face validity challenges, especially if prior art demonstrates obvious modifications.
  • Patentability of Follow-on Innovations: Future improvements or formulations based on the patent could generate a pipeline of subsequent patents, extending market exclusivity.

Regulatory and Commercial Implications

The patent provides a critical barrier to market entry for potential biosimilar or generic competitors, effectively controlling commercial rights. Combined with regulatory approvals and clinical data, the patent’s scope informs licensing opportunities and R&D direction within the Australian pharmaceutical landscape.


Conclusions

AU2013202947 represents a strategically drafted pharmaceutical patent aimed at protecting a novel therapy. Its claims likely balance broad chemical or method claims with specific embodiments, providing a robust legal position while navigating prior art constraints.

Its position within the patent landscape underscores its importance: as a potential cornerstone for a new drug product in Australia, influencing licensing negotiations, competition strategies, and R&D innovation pathways.


Key Takeaways

  • The patent’s claims are designed to cover a specific pharmaceutical invention, potentially including novel compounds or therapeutic methods, with a strategic balance of breadth and specificity.
  • Its validity depends on demonstrating clear novelty and inventive step relative to existing patents and scientific literature.
  • The Australian patent landscape for pharmaceuticals is crowded; this patent’s strength depends on claim clarity and inventive differentiation.
  • For patent holders, maintaining the patent’s integrity through proactive monitoring and defending against challenges is critical.
  • The patent’s expiration, assuming no extensions, truncates around late 2033, after which generic entry might be permitted barring regulatory or legal barriers.

FAQs

1. What is the primary legal scope of AU2013202947?
The patent primarily covers a specific pharmaceutical composition or method, including particular chemical compounds or therapeutic protocols, as defined in its independent claims.

2. How does AU2013202947 compare with international patents?
It may be a national phase entry of an earlier international or PCT application, sharing core claims but tailored for the Australian market, with potential counterparts filed in other jurisdictions.

3. What are challenges that could threaten the validity of this patent?
Prior art demonstrating similar compounds or methods, obvious modifications, or lack of inventive step could pose challenges. Proper claim drafting and strategic prosecution mitigate these risks.

4. How long is this patent effective?
Assuming standard patent term calculations, it will expire around December 2033, 20 years from the filing date, unless extension or patent term adjustments apply.

5. What impact does this patent have on the Australian pharmaceutical market?
It grants exclusive rights to the patent holder, controlling manufacturing, licensing, and sales of the protected drug, with significant implications for market competition and innovation.


References

[1] Australian Patent AU2013202947.
[2] Patents Act 1990 (Australia).
[3] World Intellectual Property Organization (WIPO). Patent landscape reports.
[4] Australian Patent Office (IP Australia). Patent examination guidelines.
[5] Recent patent filings in the pharmaceutical sector Australia and internationally.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.