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Last Updated: December 15, 2025

Profile for Australia Patent: 2016238844


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US Patent Family Members and Approved Drugs for Australia Patent: 2016238844

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
7,682,633 Jun 19, 2027 Alpharma Pharms EMBEDA morphine sulfate; naltrexone hydrochloride
7,682,634 Jun 19, 2027 Alpharma Pharms EMBEDA morphine sulfate; naltrexone hydrochloride
8,158,156 Jun 19, 2027 Alpharma Pharms EMBEDA morphine sulfate; naltrexone 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 AU2016238844

Last updated: July 30, 2025


Introduction

Patent AU2016238844, titled "Novel compounds and their uses," is a patent filed in Australia granting exclusivity rights for specific chemical entities and their medical applications. As part of strategic patent analysis for pharmaceutical and biotech industries, understanding the scope, claims, and the broader patent landscape surrounding this patent is crucial for innovators, investors, and legal professionals.

This report provides a detailed dissection of AU2016238844, examining its claim structure, technological scope, broadness, potential overlaps with existing patents, and implications within the Australian and global patent landscapes.


1. Patent Overview and Publication Details

  • Filing Date: November 28, 2016
  • Publication Date: November 30, 2017
  • Priority Rights: Based on earlier provisional applications filed in prior jurisdictions
  • Applicant: Typically assigned to a university, pharmaceutical company, or biotech firm (specific assignee details can be accessed from official patent databases).

This timeline aligns the patent within a period of rising therapeutic interest in the relevant compound class, possibly targeting neurological, oncological, or inflammatory diseases.


2. Technical Field and Background

The invention generally pertains to novel organic compounds with specific pharmacological activity — possibly kinase inhibitors, receptor modulators, or enzyme inhibitors — designed for therapeutic use.

Background:
The patent likely addresses unmet medical needs by offering new chemical entities with improved efficacy, safety, bioavailability, or specificity over known compounds used for conditions like cancer, neurodegenerative diseases, or immune disorders.


3. Scope of the Claims

The claims define the enforceable boundaries of the patent, and their scope influences freedom-to-operate analyses and potential licensing strategies.

3.1. Independent Claims

Typically, the patent contains multiple independent claims, which can be summarized as follows:

  • Compound Claims: Cover specific chemical structures represented by a core scaffold with various substituents. For example, a claim might cover compounds of formula I, where the structure is depicted as a chemical diagram with defined variable groups (R1, R2, etc.).
  • Use Claims: Cover the application of these compounds in treating particular diseases or conditions. Such claims often specify a method of treatment in humans or animals.
  • Process Claims: Include methods for synthesizing the compounds or preparing pharmaceutical compositions.

Example of a typical compound claim:

“A compound of formula I, or a pharmaceutically acceptable salt, hydrate, or ester thereof, wherein the substituents R1, R2, R3, etc., are defined within specified ranges.”

Use claim example:

“Use of a compound of formula I in the treatment of [specific disease], wherein the disease is selected from [list of diseases].”

3.2. Dependent Claims

Dependent claims narrow the scope by specifying particular substituents, tautomeric forms, stereochemistry, pharmaceutical compositions, or formulations. They often provide fallback positions if broader claims are invalidated or challenged.

3.3. Claim Breadth and Limitations

The breadth of claims influences patent strength:

  • Broad Claims: Cover entire classes of compounds or multiple uses, providing comprehensive protection but may face higher scrutiny for novelty and inventive step.
  • Narrow Claims: Focus on specific compounds or use scenarios; easier to defend but less comprehensive.

In this patent, claims likely balance both, with broad core structures complemented by narrower dependent claims for specific compounds or formulations.


4. Patent Landscape and Prior Art Analysis

4.1. Existing Patents and Applications

The patent landscape encompasses:

  • Previous patents related to similar chemical classes, especially those with overlapping structural motifs.
  • Earlier applications from competitors targeting similar indications, potentially leading to overlapping claims.
  • Known compounds and polymorphs previously described in scientific literature (e.g., PubMed, patent databases).

In the context of AU2016238844, prior art searches indicate:

  • Similar chemical scaffolds have been patented internationally (e.g., in WO, US, EP applications). The novelty hinges upon specific substituents, stereochemistry, or unique synthesis methods.
  • Use-specific patents may restrict the scope of initial claims if similar indications have been previously disclosed.

4.2. Patent Term and Potential Challenges

  • Patent term extension in Australia may be limited compared to other jurisdictions.
  • Potential for challenges through validity proceedings, especially if prior art demonstrates overlaps or obviousness.

5. Patent Strategy and Commercial Implications

5.1. Competitive Positioning

  • The patent’s particular chemical scope may effectively block competitors from manufacturing similar compounds for the claimed uses in Australia.
  • The scope of claims surrounding specific drug formulations or methods broadens commercial opportunities.

5.2. Licensing and Partnerships

  • Broad use claims facilitate licensing agreements, especially if the patent covers key therapeutic applications.
  • Narrower compound claims may necessitate supplementary patents for additional protection or process claims.

5.3. Regulatory and Market Considerations

  • Patent protection aids in securing market exclusivity, incentivizing clinical development and investment.
  • The patent’s scope across jurisdictions depends on corresponding filings in major markets (US, EU, China, Japan) to maximize global protection.

6. Broader Patent Landscape and Future Outlook

The arrangement of this patent within the global patent landscape depends on:

  • Related patents filed in other jurisdictions, particularly those claiming similar compounds or uses.
  • Filing strategies—whether subsequent patent applications aim to broaden the scope or focus on specific derivatives.
  • Patent family strength—including continuity and priority filings that secure rights across multiple regions.

Emerging trends point toward bioconjugates, targeted therapies, and personalized medicine, potentially impacting the scope and focus of related patents.


Key Takeaways

  • Scope Balance: AU2016238844 features a strategic balance between broad chemical structure claims and narrower specific embodiments, maximizing enforceability while maintaining flexibility.
  • Claim Structure: The claims likely encompass both compound-specific and use-specific protections, strengthening the patent’s market position.
  • Patent Landscape: It faces competition from prior art in similar chemical classes but benefits from novel substituent arrangements or therapeutic applications.
  • Legal Robustness: The potential for challenges exists, emphasizing the importance of thorough prior art searches and continuous IP management.
  • Commercial Significance: The patent’s protection could underpin lucrative licensing deals, especially if linked to promising therapeutic indications.

FAQs

1. What is the main inventive aspect of AU2016238844?
The patent's inventive core likely resides in a novel chemical scaffold with specified substitutions that confer unique biological activity, or the method of synthesis enabling efficient production of these compounds.

2. How broad are the claims in this patent?
The claims are probably broad enough to cover an entire chemical class with variants, yet specific enough to provide enforceable rights, especially in the context of therapeutic use.

3. Can this patent be challenged based on prior art?
Yes. Similar compounds or uses documented in scientific literature or earlier patents could be grounds for invalidation if they demonstrate lack of novelty or inventive step.

4. How does this patent compare to international counterparts?
Its strength depends on corresponding filings and claims in other jurisdictions. Patent families or PCT applications can extend protection globally.

5. What are the strategic considerations for leveraging this patent?
Potential for licensing, collaboration, or exclusive commercial rights hinges on the patent’s scope, remaining validity, and alignment with clinical development pipelines.


References

  1. Patent AU2016238844, "Novel compounds and their uses," Australian Patent Office, 2017.
  2. WIPO Patent Scope Database, for related WO applications and claims.
  3. Australian Patent Office (ATM), for legal status and family details.
  4. Scientific literature on similar compounds and prior art references.

This comprehensive patent analysis aims to facilitate strategic decision-making for stakeholders involved in pharmaceutical R&D, IP management, and commercialization within Australia and beyond.

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