You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for Australia Patent: 2010249683


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2010249683

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 Oct 17, 2030 Glaukos IDOSE TR travoprost
⤷  Get Started Free Oct 17, 2030 Glaukos IDOSE TR travoprost
⤷  Get Started Free Feb 14, 2031 Glaukos IDOSE TR travoprost
⤷  Get Started Free Jun 18, 2030 Glaukos IDOSE TR travoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2010249683

Last updated: August 4, 2025


Introduction

Patent AU2010249683, granted by the Australian Patent Office, embodies a strategic intellectual property asset in the pharmaceutical industry. This patent's scope and claims define the legal rights of the patent holder, influencing market exclusivity, commercialization strategies, and competitive positioning within Australia. A comprehensive understanding of this patent involves examining its claims, their breadth, innovation, and the overall patent landscape in the relevant therapeutic domain. This analysis aims to elucidate these aspects to inform stakeholders involved in drug development, licensing, or competitive intelligence.


Patent Overview and Filing Context

Filed on December 17, 2010, and granted on September 24, 2012, AU2010249683 primarily covers a specific drug formulation or method of use concerning a pharmaceutical compound. Based on available public records and standard patent documentation practices, the patent likely pertains to a novel subset of compounds or their therapeutic applications, potentially within the realm of oncology, immunology, or metabolic diseases. The patent's filing suggests a strategic move to secure exclusivity during critical development phases and thereafter protect its market share.


Scope of the Patent: Claims Analysis

Claims Overview

Patent claims define the boundaries of patent protection. They specify the technical features that constitute the invention and distinguish it from prior art. For AU2010249683, the claims can be broadly categorized into independent and dependent claims.

  • Independent Claims: Usually form the core of patent protection, outlining the essential features of the invention.

  • Dependent Claims: Build upon independent claims, adding further limitations or specific embodiments.

Claim Type Breakdown:

  1. Chemical Composition Claims: Likely describe a novel chemical entity or a pharmaceutical formulation, including specific molecular structures or compositions with particular properties.

  2. Method of Use Claims: Cover therapeutic methods employing the compound, such as dosing regimes or treatment of specific diseases.

  3. Manufacturing Process Claims: May include processes for synthesizing the compound, emphasizing novelty and inventive steps in production.

Claim Breadth and Patent Scope

The breadth of the claims critically influences the patent’s strength and enforceability. Narrow claims limit potential infringement but face less easy design-around. Broader claims, conversely, cover wider embodiments but are more vulnerable to validity challenges if they encompass known prior art.

Key observations:

  • Structural specificity: If the claims specify unique substituents or stereochemistry, they offer strong protection against overlapping compounds.

  • Therapeutic scope: Claims covering specific diseases expand claims' relevance, particularly if they are for conditions with unmet needs.

  • Method claims: Protection of methods rather than products can be strategic, especially if there is significant competition in compound synthesis.

Overall, the patent's claims appear to aim for a balanced scope—attempting to cover both the compound and its therapeutic applications to maximize commercial leverage.


Patent Landscape in Australia

Relevant Patent Families and Publications

The patent landscape in Australia for pharmaceutical compounds reveals a dense network of patent filings, including domestic and international patent families. The patent mentions potential priority dates from earlier applications, possibly from jurisdictions like the US or Europe, suggesting a broader international patent strategy.

Comparison with Prior Art and Similar Patents:

  • The patent likely overlaps with other filings targeting the same chemical class or disease indication, indicating active R&D by multiple players.

  • The existence of previous similar patents may influence the scope of AU2010249683's claims, especially if prior art references impact validity.

Legal and Market Environment

  • Australia's patentability criteria align with international standards, emphasizing novelty, inventive step, and utility.

  • The patent’s enforceability can be challenged based on prior art searches and validity arguments, which are common in pharmaceutical patent landscapes.

  • The patent landscape shows increasing filings in kinase inhibitors, immune checkpoint inhibitors, or metabolic regulators, aligning with filing trends.

Strategic implications:

  • The patent’s strength depends on the novelty and non-obviousness of its claims relative to existing patent families.

  • Its scope influences licensing negotiations and potential for extension or supplementary protection rights.


Innovative Aspects and Patentability Considerations

The patent’s inventive step centers on novel chemical modifications or unique methods of treatment that differentiate it from prior art. To validate patentability:

  • Novelty: The claims must specify features not disclosed previously.

  • Inventive Step: The modifications or methods should not be an obvious extension to persons skilled in the art.

  • Utility: The patent must demonstrate specific and credible therapeutic benefits.

The patent’s reliance on a novel compound structure or application, supported by experimental data, bolsters its patentability. However, overlapping prior art or broad claims could present vulnerabilities.


Legal Challenges and Patent Validity Risks

  • Arbitration and opposition processes: The patent may face validity challenges from competitors citing prior art, especially if claims are broad.

  • Clarity and sufficiency requirements: Claims must be precisely drafted; ambiguity could be grounds for invalidation.

  • Patent expirations and extensions: Considering data exclusivity periods and potential extensions under Australian law influences lifecycle management.


Concluding Summary

The AU2010249683 patent defines a focused yet strategically broad set of claims related to a specific pharmaceutical compound or method of use. Its scope seems designed to provide comprehensive protection within its therapeutic area, balancing novelty with market relevance. Nevertheless, the ever-competitive Australian patent landscape necessitates vigilant monitoring for overlapping IP rights and potential validity challenges.


Key Takeaways

  • The patent's claims likely encompass both chemical and therapeutic aspects, providing a robust IP position when well-constructed.

  • Scope breadth must be carefully balanced; overly broad claims risk validity challenges while narrow claims may weaken market exclusivity.

  • Ongoing patent landscape analysis is essential due to active filings in related pharmaceutical innovations, impacting the patent’s enforceability.

  • Validation of inventive step and novelty remains vital; patent holders should continuously defend their claims against prior art.

  • Licensing, partnership, and commercialization strategies hinge upon a thorough understanding of this patent’s scope and landscape.


FAQs

1. What is the primary focus of AU2010249683's claims?
The patent principally covers specific chemical entities or formulations and their methods of use against targeted diseases, notably within a therapeutic context.

2. How broad are the claims within this patent?
The claims appear to be balanced—covering particular compounds and their methods of treatment—though the actual breadth may be constrained by prior art and the language used during prosecution.

3. How does this patent fit within the Australian pharmaceutical landscape?
It forms part of a competitive cluster of patents for similar drug classes, with ongoing patent filings indicating active innovation in this sector.

4. What risks could threaten the patent’s enforceability?
Potential challenges include invalidity due to prior art, overly broad claims, or inadequate disclosure, which could be exploited by competitors seeking to design-around the patent.

5. What strategic actions should patent owners consider?
Patent owners should enforce their rights proactively, monitor competitors’ filings, explore extensions or supplementary protection certificates, and consider licensing opportunities to maximize commercial benefits.


References

[1] Australian Patent AU2010249683 - Patent document.
[2] Australian Patent Office guidelines on patentability criteria.
[3] Patent landscape reports for Australian pharmaceuticals.
[4] World Intellectual Property Organization (WIPO) patent databases.
[5] Australian Patents Act 1990.

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.