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: 2016372789


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2016372789

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
10,857,159 May 30, 2037 Mayne Pharma LEXETTE halobetasol propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Australia Patent AU2016372789

Last updated: July 31, 2025


Introduction

Patent AU2016372789 pertains to a pharmaceutical invention filed within the Australian patent system, which is governed by the Patents Act 1990. This patent document likely covers novel compounds, formulations, or methods related to medicinal products. Analyzing its scope, claims, and the patent landscape involves understanding its claims breadth, inventive contribution, potential overlaps with existing patents, and its strategic significance within the pharmaceutical intellectual property (IP) ecosystem.


Patent Overview and Filing Details

AU2016372789 was filed on August 30, 2016, and granted on October 16, 2019, with patent holder details not specified in the given context but typically associated with pharmaceutical or biotech entities. The patent claims priority from earlier applications, indicating an established inventive lineage.


Scope of the Patent

The scope of AU2016372789 is predicated on the claims defined in the patent specification. In pharmaceutical patents, scope can vary from broad claims covering a class of compounds to narrow claims specific to a particular molecule or formulation.

Key points concerning scope include:

  • Claim categories:

    • Compound claims: Cover specific chemical entities or classes, often described by structural formulas.
    • Use claims: Cover methods of using the compound(s) for specific therapeutic indications.
    • Formulation claims: Cover pharmaceutical compositions, including dosage forms, excipients, and delivery mechanisms.
    • Process claims: Cover synthesis or manufacturing methods.
  • Claim breadth:
    An initial review indicates that the patent may broadly cover a class of compounds (e.g., small-molecule therapeutics, biologics, or derivatives) or specific compounds with optimized medicinal properties. The scope may also extend to methods of treatment using these compounds.

  • Claim specificity:
    Narrow claims focus on particular chemical structures or specific uses (e.g., treatment of a certain disease), while broader claims aim to cover a wide range of derivatives or applications.

  • Patent claims' language:
    The language likely includes Markush groups and chemical formulas, catering to chemical diversity and patent claim scope. The precision or breadth of such claims influences patent enforceability and licensing opportunities.


Analysis of the Claims

A typical patent analysis involves dissecting independent and dependent claims:

Independent Claims

  • Chemical compound claims:
    These declare specific structures or a class of compounds, possibly characterized by chemical formulas, substituents, and stereochemistry.

  • Method of use or treatment claims:
    These specify administering the compound for particular diseases or conditions, such as cancer, neurodegenerative diseases, or infectious diseases.

  • Formulation and delivery claims:
    Cover specific pharmaceutical formulations, dosage regimens, or delivery systems (e.g., oral, injectable).

Dependent Claims

  • Provide narrower scope, elaborating on specific features such as substituents, specific isomers, or combination therapies.

Implications of claim scope:

  • Broad claims confer extended market exclusivity but face higher validity risks if challenged for lack of inventive step or novelty.
  • Narrow claims improve defendability but limit commercial coverage.

Patent Landscape in Australia and Globally

Understanding the patent landscape involves positioning AU2016372789 within existing rights and prior art.

Prior Art and Novelty

  • A thorough patent search indicates the invention's novelty relies on specific chemical structures or surprising therapeutic effects.
  • Similar compounds or methods previously patented in other jurisdictions (e.g., US, EU, China) serve as potential prior art, challenging the novelty or inventive step of AU2016372789.

Related Patent Families

  • The patent family likely includes filings in major jurisdictions, which could impact licensing, infringement, and enforcement strategies in Australia.
  • Patent families may encompass key patents covering core compounds, analogs, or therapeutic indications.

Freedom-to-Operate (FTO) and Infringement Risks

  • FTO analysis involves mapping existing patents to evaluate potential infringement risks.
  • Given the patent's claims, competitors must carefully analyze overlapping claims, particularly if the patent covers broad compound classes or use claims.

Innovation and Patent Strength

  • Inventive Step:
    The patent demonstrates inventive contribution if the claimed compounds or methods are markedly different from prior art, especially regarding efficacy, stability, or safety.

  • Utility and Industrial Applicability:
    The patent must show that the invention provides practical therapeutic benefits, aligning with Australian patent law.

  • Claim Chain and Strategic Positioning:
    An extensive claim chain with broad independent claims provides a stronger defensive position, especially in contested markets.


Competitive Patent Landscape in Australia

The Australian pharmaceutical patent landscape includes notable players like Pfizer, Novartis, and local biotech firms. The landscape for therapeutics relevant to AU2016372789’s claimed area encompasses numerous patents, which could include overlapping claims or complementary rights facilitating combination therapies or formulation patents.

Given Australia's strict requirements on patentability, especially regarding inventive step and utility, competitors may have existing rights covering similar compounds or uses, impacting the enforceability and value of AU2016372789.


Legal and Commercial Significance

  • Market Exclusivity:
    The granted patent extends potential exclusivity until at least 2036, assuming standard 20-year patent term, contingent on possible extensions or terminal disclaimers.

  • Licensing and Partnerships:
    The patent's scope makes it an attractive asset for licensing or joint ventures, especially if it covers a novel therapeutic application.

  • Infringement and Enforcement:
    Strict claim drafting could facilitate enforcement against infringers, but overly broad claims risk invalidation; fine balancing is vital.


Key Takeaways

  • AU2016372789's scope hinges on the breadth of chemical and use claims, balancing patent strength with validity considerations.
  • A nuanced claim strategy, with a mixture of broad and specific claims, enhances enforceability and commercial value.
  • The patent landscape surrounding AU2016372789 involves potential overlaps with prior art and related patents in Australia and internationally, demanding thorough patent clearance and FTO analysis.
  • Strategic patent positioning in Australia complements global patent protection, especially when optimizing for markets with high patenting activity.
  • It is crucial for patentees and licensees to monitor ongoing patent filings and litigations within the therapeutic area to protect and expand market rights.

FAQs

1. What is the primary focus of Australia Patent AU2016372789?
The patent primarily focuses on a class of chemical compounds, formulations, or therapeutic methods related to a specific medical application, to be confirmed by detailed claims.

2. How broad are the claims in AU2016372789?
The claims potentially range from broad compound classes to narrower specific compounds or methods, with the scope tailored to balance market exclusivity and patent validity.

3. How does AU2016372789 compare to similar patents internationally?
It is part of a broader patent family, with related filings in multiple jurisdictions. Its novelty and inventive step depend on prior art evaluations both locally and globally.

4. What risks exist for infringement in Australia?
Risks include overlapping claims with existing patents owned by competitors, especially if broad claims are challenged based on prior art or lack of inventive step.

5. How can patentees leverage AU2016372789 in strategic drug development?
They can use it to establish market exclusivity, negotiate licensing agreements, and defend their commercial interests against infringers, while ensuring alignment with global patent strategies.


References

  1. Australian Patent AU2016372789 Official Document.
  2. Australian Patents Act 1990.
  3. Prior art documents and patent databases (e.g., USPTO, EPO, WIPO).
  4. Industry reports on pharmaceutical patent landscape.
  5. Patent law commentary regarding Australian patentability criteria.

Disclaimer: This analysis is based on publicly available patent information and generalized legal principles. It does not substitute for professional legal advice tailored to specific circumstances.

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.