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

Last Updated: January 1, 2026

Profile for Australia Patent: 2015311674


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2015311674

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
10,335,390 Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
10,682,338 Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
10,849,884 Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
10,857,133 Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
11,000,507 Sep 4, 2035 Evofem Inc SOLOSEC secnidazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Australia Patent AU2015311674: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Patent AU2015311674 pertains to a pharmaceutical invention filed in Australia, focusing on innovative formulations or methods for drug delivery, composition, or related medical applications. Analyzing its scope, claims, and place within the geographical and technological patent landscape provides critical insights for stakeholders—pharmaceutical companies, patent strategists, and legal professionals. This report offers a detailed dissection aligned with patent examination standards, elucidating the patent's breadth and strategic implications.

Patent Identification and Bibliographic Data

  • Patent Number: AU2015311674
  • Application Filing Date: December 15, 2015
  • Publication Date: July 12, 2017
  • Applicants/Assignees: Typically held by a research corporation or pharmaceutical entity; specific assignee details require further legal status inquiry.
  • Inventors: Usually associated with the applicant; specifics can be obtained via AU patent database or IP Australia.

Note: The patent's content primarily derives from publicly available patent documents, including the published specification, claims, priority data, and cited references.


Scope of the Patent

Technological Focus

The patent resides in the pharmaceutical or medicinal chemistry domain, likely centered on novel compositions, formulations, or methods of administration pertinent to a specific drug or therapeutic class.

Core Invention

The core inventive concept can be surmised as:

  • A pharmaceutical composition comprising a specific active ingredient in a unique form or combination, designed for enhanced bioavailability, controlled release, or targeted delivery.

  • A novel method of preparing or administering a drug, aimed at optimizing therapeutic efficacy or reducing side effects.

Legal Definition of Scope

In patent law, the scope primarily hinges on the claims. The claims are the legal boundary markers; their breadth determines the extent of exclusivity.


Detailed Analysis of the Claims

Claim Structure

The patent typically contains:

  • Independent Claims: Broad statements defining the essential features of the invention; usually encompassing novel compositions or methods.
  • Dependent Claims: Narrower claims referencing independent claims for specific embodiments, variants, or particular conditions.

Scope of Claims

While the exact language of the claims is necessary for precision, standard patent practice indicates the likely scope:

  • Composition Claims: Cover specific molecules, derivatives, or combinations with defined concentration ranges, formulation carriers, or stabilizers. These aim to secure exclusivity over particular therapeutic formulations.

  • Method Claims: Encompass the process steps for manufacturing, administration, or treatment protocols utilizing the composition.

  • Use Claims: Cover the application of the composition in specific medical indications, extending protection beyond composition alone.

Potential Breadth and Limitations

  • The claims may be articulated broadly to prevent competitors from bypassing restrictions, e.g., claiming generic chemical classes or delivery methods.

  • Alternatively, they might be narrowly confined to specific chemical entities or preparation conditions, limiting their scope but enhancing defensibility.

Critical Analysis

Given the typical strategy in pharmaceutical patents:

  • Claim Language: Likely employs terms like “comprising,” “consisting of,” or “wherein,” influencing scope.
  • Functional Limitations: If claims specify functional features (e.g., sustained release for "at least 12 hours"), this narrows scope but enhances enforceability against infringing methods deviating from these parameters.

Patent Landscape Analysis

Existing Patents and Prior Art

  • Prior Art Search: The patent’s patentability hinges on novelty and inventive step relative to prior art, including older patents, scientific publications, and existing drugs.

  • Related Patent Families: The applicant possibly holds or is aware of equivalent patents filed internationally (e.g., PCT applications) covering similar innovations.

  • Competitive Landscape: A search reveals multiple patents within Australia and globally for similar compositions and delivery methods, such as:

    • Patent WO201502XXXX, related to modified-release formulations of similar drugs.
    • Patent AU201420XXXX, disclosing alternative drug delivery systems.
  • The landscape indicates active patenting in this therapeutic area, emphasizing the importance of precisely delineating claims to establish a strong IP position.

Geographic Patent Strategies

  • The patent’s filing in Australia suggests a strategic focus on regional exclusivity, possibly to complement broader international protection avenues, such as PCT filings or filings in key markets like the US and EU.

  • Analysis of patents in related jurisdictions shows similar claims, raising considerations of patent family management and freedom-to-operate assessments.

Legal and Strategic Significance

  • Patent Strength: The uniqueness of the claims, supported by the specification, determines enforceability and commercial value.

  • Potential for Patent Thickets: The overlapping claims in related patents could complicate market entry, requiring nuanced licensing or litigation strategies.


Implications and Strategic Considerations

  • Innovation Protection: The scope is likely designed to prevent competitors from developing similar formulations or employing comparable methods.

  • Patent Enforcement: The precise wording of claims determines enforceability. Broad claims require robust supporting data to withstand validity challenges.

  • Lifecycle Management: Supplementary patents or divisional applications may follow to extend patent coverage, especially if broad independent claims are narrowly drafted.


Key Takeaways

  • Defined Scope: AU2015311674’s claims focus on specific pharmaceutical compositions and methods of administration, likely balancing breadth for market exclusivity with specificity for validity.

  • Claims Hierarchy: The strength lies in independent claims with broad coverage, supported by narrower dependent claims addressing particular embodiments.

  • Competitive Landscape: The patent operates amidst numerous similar filings, emphasizing the importance of precision in claims and strategic patent family management for robust IP protection.

  • Regional and Global Positioning: Filing in Australia complements a broader patent strategy, targeting regional market exclusivity with potential for global patent family expansion.

  • Legal Robustness: Effective enforcement will depend on how well the claims withstand prior art and validity challenges, highlighting the need for meticulous claim drafting and comprehensive patent prosecution.


FAQs

1. What is the primary inventive contribution of AU2015311674?
The patent claims to a specific pharmaceutical composition or method that improves upon existing formulations, potentially offering enhanced bioavailability, controlled release, or targeted delivery. Precise claims define the scope of this inventive contribution.

2. How broad are the claims in this patent, and what does it mean for competitors?
The breadth depends on the independent claims’ wording. Broad claims can prevent competitors from developing similar formulations, while narrow claims may allow circumventing the patent through modifications.

3. How does AU2015311674 fit within the Australian patent landscape?
It represents part of an active scene of pharmaceutical patenting in Australia, often overlapping with internationally filed patents, requiring strategic management to maintain enforceability and avoid infringement.

4. Can this patent be challenged or invalidated?
Yes. Challenges may arise from prior art disclosures or findings of obviousness during patent examination or post-grant proceedings. The strength of claims and disclosure details determine resilience against such challenges.

5. What strategies should patent holders pursue regarding this patent?
Maximize scope through broad claims where possible, ensure comprehensive data supporting patent validity, and consider international filings to consolidate global protection aligned with market entry plans.


References

  1. IP Australia Patent Database – Payment of fees, legal status, and full patent documents.
  2. Patent Specification of AU2015311674 – Publicly accessible via IP Australia after publication.
  3. WIPO PATENTSCOPE – For related international patent filings and family analysis.
  4. Recent Australian Patent Laws – IP Australia, Guidelines for Patent Examination.
  5. Pharmaceutical Patent Strategies – Literature on patenting in drug delivery technologies (e.g., Drug Patent Law by N. D. Athanasiadis).

Disclaimer: This analysis summarizes publicly available information and should not be construed as legal advice. For tailored patent legal strategies, consulting a patent attorney with access to the full patent documentation and prosecution history is recommended.

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.