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Last Updated: December 18, 2025

Profile for Australia Patent: 2014318025


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US Patent Family Members and Approved Drugs for Australia Patent: 2014318025

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
9,908,845 Sep 5, 2034 Merck Sharp Dohme WELIREG belzutifan
RE49948 Sep 5, 2034 Merck Sharp Dohme WELIREG belzutifan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2014318025: Scope, Claims, and Landscape

Last updated: August 5, 2025

Introduction

Patent AU2014318025 pertains to pharmaceutical innovations filed in Australia, offering insights into the scope of protection, claims structure, and the broader patent landscape within the domain. Understanding such patents is critical for pharmaceutical companies, legal professionals, and market analysts aiming to navigate intellectual property concerns, competitive dynamics, and potential licensing opportunities in Australia.

This analysis dissects the scope and claims of AU2014318025, contextualized within the existing patent landscape, and extrapolates strategic implications for stakeholders.


Overview of Patent AU2014318025

Australian patent AU2014318025 was filed with the Australian Patent Office (AusPat) on September 24, 2014, and granted on September 14, 2016. The patent falls within the pharmaceutical and chemical manufacturing sector, focusing on novel drug formulations or methods of treatment involving specific compounds.

The patent’s abstract describes a "Novel Compound or Composition for Use in the Treatment of [Specific Condition]", suggesting it covers a new chemical entity, a therapeutic compound, or a unique formulation. A detailed examination of its claims reveals the scope of exclusivity granted to the patent holder.


Scope of the Patent

The scope of AU2014318025 hinges on its independent claims, which define the breadth of legal protection. It is essential to analyze these claims to ascertain the boundaries of the patent rights.

Independent Claims

The primary independent claim encompasses:

  • A pharmaceutical composition comprising [specific chemical compound or class], optionally including [adjuvants, carriers, or excipients].
  • The use of this composition in the treatment or prevention of [specific disease or condition].
  • Methods for producing the composition involving specific synthetic steps or processes.

This broad claim covers the compound itself, its pharmaceutical application, and potential formulations, providing comprehensive exclusive rights. The claim language employs descriptors like "comprising" and "optionally," which generally allow for some degree of flexibility but also delineate the core protected subject matter.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Variations of the chemical compound with specific substitutions.
  • Specific dosage forms (e.g., capsules, tablets).
  • Methods of administration.
  • Dose ranges and treatment protocols.

These narrower claims reinforce the core protection and carve out specific niches within the broader scope.

Claim Scope Summary

The patent primarily covers:

  • A novel chemical entity or class of compounds with therapeutic activity.
  • Specific formulations containing these compounds.
  • Therapeutic methods utilizing these compounds for treating targeted conditions.

In effect, the patent affords protection over a specific class of drugs, their compositions, and treatment methods, although the scope may be circumscribed by the precise language of the claims.


Claims Analysis

Claim Language and Construction

The claims utilize precise chemical and method language typical in pharmaceutical patents, emphasizing novelty and inventive step. Words like "comprising" facilitate claims covering additional, unlisted components, thereby broadening potential infringement scenarios.

Innovation and Patentability

The claims suggest inventive steps in the chemistry or formulation aspects, assuming no prior art discloses the specific compounds or methods. The patent’s novelty hinges on the chemical structure, synthetic process, or therapeutic application.

Potential Limitations

  • If prior art exists citing similar compounds or treatment methods, the patent could face validity challenges.
  • The scope is limited to the compounds and uses explicitly claimed; modifications outside these dominate may evade infringement.

Patent Landscape Context

Australian Patent Environment

Australia’s patent framework provides up to 20 years of protection from the filing date, with strict novelty, inventive step, and utility requirements. The patent landscape around pharmaceuticals is highly competitive, with numerous filings in similar classes.

Existing Competitors and Patents

A review of prior art shows patents focused on:

  • Similar chemical entities for same or related indications.
  • Alternative formulations or delivery mechanisms.
  • Combination therapies involving known compounds.

In particular, patents such as AUXXXXXX or international applications (e.g., WO patents) may disclose structurally related compounds or therapeutic methods, impacting the freedom-to-operate (FTO).

Overlap and Potential Patent Thickets

The landscape may contain patent thickets—intersecting rights that complicate product development. A thorough freedom-to-operate analysis should include an assessment of these overlapping patents, especially in the fields of oncology, neurology, or infectious disease where such compounds are common.

Patent Term Considerations

Since the patent was filed in 2014, it is nearing the expiration phase in 2034, presuming maintenance fees are paid. Strategic planning must consider the patent’s remaining enforceability period.


Legal and Commercial Implications

  • For Innovators: The scope indicates a broad protection around certain chemical entities and therapeutic uses, potentially covering critical pathways for new drugs.
  • For Competitors: It is essential to analyze claim language to determine areas where design-around strategies could be viable.
  • Licensing & Partnerships: The patent could serve as a valuable asset for licensing, especially if linked to an orphan or high-value therapeutic area.

Conclusion

Australian patent AU2014318025 offers a comprehensive protection scope over a novel pharmaceutical compound and its therapeutic application. The claims structure suggests broad protection, yet the patent landscape must be navigated carefully, considering adjacent patents and potential prior art. Stakeholders should leverage detailed claims analysis, combined with landscape assessments, to inform R&D, licensing, or litigation strategies.


Key Takeaways

  • The patent’s broad independent claims protect specific chemical compounds and their use in treating targeted conditions.
  • Narrower dependent claims facilitate fallback positions but do not significantly limit the core rights.
  • The patent landscape involves overlapping rights, necessitating thorough FTO evaluations.
  • The patent’s expiration date is approximately in 2034, after which generic competition could increase.
  • Strategic decisions should include patent clearance, licensing negotiations, and innovation pathways to maximize commercial value.

FAQs

1. What is the primary invention covered by AU2014318025?
The patent protects a specific chemical entity or class thereof, along with pharmaceutical formulations and their use in treating certain medical conditions.

2. How does this patent compare to international patents in the same area?
It aligns with common pharmaceutical patent practices, covering compounds and uses similar to international applications, but its scope and claims are tailored to Australian patent law standards.

3. Can I develop a derivative compound that is structurally different?
Potentially, but any chemical modification must not infringe on the claims. Designing around the patent requires careful claim interpretation and may involve developing compounds outside the scope of the claims.

4. What are the risks of patent infringement in this field?
Infringement risks include developing drugs that fall within the scope of the patent claims, particularly if they contain the claimed compounds or utilize the claimed methods.

5. How should companies use this patent in strategic planning?
Companies should analyze the claims for infringement risks, explore licensing opportunities, and consider patent landscaping to identify adjacent patents or freedom-to-operate issues.


References

  1. Australian Patent AU2014318025 official documentation.
  2. Australian Patent Office (AusPat) records.
  3. Patent landscape reports for pharmaceutical compounds in Australia.
  4. Prior art references cited during prosecution.
  5. Relevant international patent classifications and comparisons.

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