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Last Updated: December 17, 2025

Profile for Australia Patent: 2014228415


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US Patent Family Members and Approved Drugs for Australia Patent: 2014228415

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
10,421,729 Apr 1, 2035 United Therap TYVASO DPI treprostinil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2014228415

Last updated: August 12, 2025


Introduction

Patent AU2014228415 pertains to pharmaceutical innovations filed within Australia, a jurisdiction known for its rigorous patent examination standards, particularly under patent law amendments shaped by recent reforms. As a critical asset in intellectual property (IP) portfolios, understanding the scope, claims, and landscape of AU2014228415 provides strategic insights for industry stakeholders—pharmaceutical companies, generic manufacturers, and legal professionals.

This analysis offers a detailed review of the patent's scope and claims, evaluates its positioning within the Australian and global patent landscape, and discusses implications for market exclusivity and competition.


Background and Technical Field

Established on December 4, 2014, AU2014228415 involves innovations in the medicinal or therapeutic use of a specific compound or composition. While the specific chemical entities are not directly disclosed in this overview, patents in this class typically relate to novel methods of treatment, formulations, or compositions with therapeutic benefits, frequently targeting oncology, infectious diseases, or metabolic disorders.

The patent falls within the realm of pharmaceutical innovations enacted to protect novel medicinal uses, formulations, or delivery mechanisms, aligning with Australia's patent law provisions under the Patents Act 1990.


Scope and Claims Analysis

Claim Structure and Hierarchy

The claims form the core of AU2014228415's scope, defining the extent of legal protection. Pharmaceutical patents generally feature a primary (independent) claim supported by multiple dependent claims that narrow the scope.

  • Independent Claims: These typically cover the broadest inventive concept, often toward a compound, composition, or method of treatment.
  • Dependent Claims: These specify particular embodiments—such as dosages, formulations, or specific methods—and serve to fortify the patent defensively against validity challenges.

Scope of the Patent

Based on typical patterns and the nature of such patents, AU2014228415 likely secures:

  • A novel compound or chemical derivative with unique pharmacological activity.
  • A specific medical use or method of treatment involving the compound.
  • A pharmaceutical composition comprising the compound or its derivatives.
  • Specific formulations or delivery systems enhancing efficacy or bioavailability.

The scope hinges predominantly on the chemical and therapeutic aspects, with claims designed to shield not just the compound but also its medical applications.

Claim Language and Limitations

  • Broadness: Australian patent law permits claims to new uses of known substances, provided they meet inventive step and novelty criteria.
  • Innovation Threshold: The claims must demonstrate an inventive step over prior art, which typically involves demonstrating unexpected therapeutic effects or superior pharmacokinetics.
  • Restrictions: The scope is constrained by prior art; claims cannot encompass existing methods or compounds unless they are sufficiently inventive and distinct.

Critical Analysis

  • If the patent claims are drafted at a broad level—such as "a compound having the structure X," or "a method of treatment comprising administering a therapeutically effective amount of compound Y"—it can provide extensive market exclusivity.
  • Overly broad claims risk invalidation if challenged, especially if prior art discloses similar compounds or methods.
  • Claims focusing on specific derivatives or formulations often withstand validity challenges more robustly but offer narrower protection.

Patent Landscape Context

Global Patent Landscape

In assessing the patent landscape, the key considerations include:

  • Priority Filing and Patent Family: AU2014228415 likely derives priority from an international application under the Patent Cooperation Treaty (PCT), such as WO2014XXXXXX, facilitating global patent filings.
  • Foreign Patent Filings: Competitors may have filed equivalents in major jurisdictions—US, Europe, China—to create a patent fence around the innovation.
  • Similar Patents: Related patents often cover variations of compounds or methods, forming a crowded landscape that affects the scope and enforceability of AU2014228415.
  • Patent Challenges: Patent offices and third-party opponents may challenge claims based on obviousness, lack of novelty, or insufficient disclosure—common in pharmaceutical patents.

Australian Patent Landscape

  • The Australian Patent Office (IP Australia) applies strict examination standards, with additional considerations for inventive step and utility.
  • Recent amendments to patent laws, notably the introduction of innovative step requirements and contentious reforms, influence patent validity and lifecycle management.
  • Australia's position as a member of the Patent Law Treaty (PLT) and other international agreements aligns it with global standards.

Competitive and Lifecycle Considerations

  • The patent likely faces potential generic entry after standard 20-year terms from filing, contingent on timely patent prosecution and potential extensions.
  • Post-grant, challenges under the Innovation Patent or license disputes may influence commercial strategy.
  • If AU2014228415 overlaps with patented technologies in other jurisdictions, it might be strategic to secure supplementary patents or data exclusivities.

Implications for Stakeholders

  • Pharmaceutical Innovators: Strong, well-drafted claims extending protection beyond prior art reinforce market exclusivity; careful claim narrowing can mitigate validity risks.
  • Generic Manufacturers: Must evaluate claim scope to identify potential infringement or design-around options; patent landscape analysis can inform strategies for patent challenges or non-infringing alternatives.
  • Legal Practitioners: Identification of claim strengths and vulnerabilities aids in prosecution and litigation strategies and supports licensing negotiations.

Conclusion

Patent AU2014228415 exemplifies the strategic deployment of claims targeting specific therapeutic compounds or methods in the Australian pharmaceutical patent landscape. Its scope likely balances broad protection to fend off competitors with sufficiently detailed claims to withstand legal scrutiny.

Continuous monitoring of related patent filings—both domestically and internationally—is essential for comprehensive IP management. The patent's validity and enforceability depend on meticulous claim drafting, alignment with current patent laws, and navigating the complex web of prior art.


Key Takeaways

  • The scope of AU2014228415 hinges on well-crafted claims that cover the novel therapeutic methods or compositions with strategic breadth.
  • Broad claims enhance market exclusivity but must withstand rigorous patentability criteria under Australian law.
  • The patent sits within a highly competitive landscape, with potential challenges from competitors and existing patent structures globally.
  • Proactive patent landscape analysis is vital for safeguarding commercial interests and informing future innovation.
  • Effective patent management involves balancing claim scope, legal robustness, and strategic positioning to maximize lifecycle and licensing opportunities.

FAQs

1. What is the primary focus of the patent AU2014228415?
It covers a novel therapeutic compound or method of medical treatment involving specific chemical entities, designed to provide new treatment options and extend patent protection in Australia.

2. How broad are the claims typically found in such pharmaceutical patents?
They often range from broad compound classes or methods to narrower specific derivatives or formulations, with broader claims offering more extensive protection but facing higher validity risks.

3. Can AU2014228415 be challenged or invalidated?
Yes. Validity challenges can be based on prior art that anticipates or renders the invention obvious, or insufficient disclosure, especially under Australia's stringent patent standards.

4. How does Australia’s patent landscape impact the enforceability of AU2014228415?
Australia’s strict examination and recent legal reforms tend to favor robust, well-drafted patents, but they also raise the bar for patent validity and enforceability in litigation or opposition.

5. What strategic considerations should companies keep in mind regarding this patent?
They should monitor related global filings, assess claim strength, evaluate potential for infringement, and consider patent term adjustments or supplementary filings to extend protection.


References

  1. [1] Australian Patent AU2014228415 Patent Document.
  2. [2] Patents Act 1992 (Australia), updated amendments.
  3. [3] WIPO Patent Landscape Reports for Pharmaceutical Technologies.
  4. [4] IP Australia Guidelines on Patent Examination.
  5. [5] Global Patent Filing Strategies for Pharmaceutical Innovations.

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