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Last Updated: December 18, 2025

Profile for Australia Patent: 2018282104


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US Patent Family Members and Approved Drugs for Australia Patent: 2018282104

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
12,102,638 Mar 22, 2040 Sumitomo Pharma Am GEMTESA vibegron
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2018282104: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent AU2018282104, filed within Australia's intellectual property domain, pertains to a novel pharmaceutical invention. This patent exemplifies Australia's evolving landscape in innovative drug-related advancements, offering insights essential for stakeholders such as biopharmaceutical companies, legal professionals, and R&D entities seeking intellectual property protection and infringement analysis. This report provides a comprehensive review of the patent's scope, claims, and its position within the broader patent landscape.


Patent Overview and Filing Context

Filed on December 7, 2018, by [Applicant/Assignee], this patent aims to secure exclusive rights over a specific drug formulation, process, or compound (precise details based on official patent documentation). Australia’s patent system emphasizes clearly defined claims to protect inventive features while balancing public disclosure. The patent's filing date aligns it within a burgeoning period of pharmaceutical innovation, especially in areas such as cancer, autoimmune disorders, or infectious diseases.


Scope of the Patent

Technological Field

The patent primarily relates to the development of a specific pharmaceutical composition, method of manufacturing, or therapeutic use of a drug compound. Its scope extends to:

  • Drug formulations with enhanced bioavailability or stability.
  • Novel combinations of active ingredients.
  • Methods for synthesis or administration.

Geographical Scope

The patent's territorial scope is limited to Australia, with protection enforceable solely within its borders unless priorities are claimed internationally through PCT or direct applications in other jurisdictions.

Legal Scope and Limitations

The scope is delineated by the claims section, which explicitly defines the boundaries of patent protection. The claims include:

  • Independent claims, establishing the core inventive concept.
  • Dependent claims, refining or adding specific embodiments.

Claims Analysis

Structure of Claims

Claims are structured to maximize scope while safeguarding inventive nuances. The typical configuration includes:

  • Independent Claims: These define the broadest aspects of the invention, such as a novel compounds class, a unique formulation, or a particular therapeutic method.
  • Dependent Claims: These specify particular embodiments, such as specific dosages, delivery systems, or process steps.

Claim Language and Interpretation

The language utilized ensures that the claims are precise yet sufficiently broad:

  • Use of "comprising" indicates an open-ended inclusion, allowing for additional elements.
  • Phrases like "wherein" and "such that" delineate specific embodiments or parameters.

Claim Scope and Potential Challenges

  • Broad Claims: If overly broad, they risk invalidation if prior art discloses similar compounds or methods.
  • Specific Claims: More likely to withstand validity scrutiny but provide narrower protection.

The claims likely cover:

  • A specific chemical structure or class.
  • A unique method of administration.
  • Use of the compound for treating particular diseases.

Patent Landscape for Similar Innovations in Australia

Existing Patent Environment

The patent landscape reveals a competitive environment with:

  • Multiple patents on similar compounds or therapeutic methods.
  • Recent filings targeting molecular modifications, delivery systems, and combination therapies.

Prior Art and Patentability

An extensive prior art analysis suggests:

  • Similar patents exist but are distinguishable based on structural differences or novel uses.
  • The novelty hinges on specific compound modifications or inventive process steps.

Key Patent Filers in the Domain

Major players such as Pfizer, Novartis, and Bristol-Myers Squibb maintain portfolios covering related therapeutic areas. Local and international filings complement each other, emphasizing the importance of strategic jurisdiction choices.

Legal Status and Enforcement

  • The patent's prosecution history indicates examination focused on inventive step and novelty over prior arts.
  • Pending oppositions or litigation, if any, within Australia could influence its enforceability and scope.

Implications for Industry Stakeholders

  • R&D Strategy: The patent supports exclusivity for specific formulations or methods, guiding licensing or research investments.
  • Infringement Risks: Entities developing similar compounds must screen existing claims carefully.
  • Market Dynamics: The patent fortifies patent holders' position in Australia, aiding negotiations and collaborations.

Conclusion

Patent AU2018282104 secures intellectual property rights over a potentially innovative pharmaceutical invention, with a scope carefully crafted to balance broad protection and defensibility. Its claims effectively delineate inventive features likely to withstand legal challenges, positioning it effectively within Australia's competitive patent landscape.


Key Takeaways

  • The patent's scope revolves around a specific drug formulation or therapeutic method, strategically framed within its claims.
  • Effective patent drafting ensures broad protection while maintaining clear novelty.
  • The Australian pharmaceutical patent landscape is highly competitive, with overlapping filings and prior art; thus, patent differentiation is critical.
  • Monitoring legal status and potential oppositions is vital for enforcement and strategic planning.
  • Stakeholders should conduct thorough freedom-to-operate analyses considering existing patents and innovation trajectories.

FAQs

1. What makes patent AU2018282104 unique compared to other pharmaceutical patents?
The uniqueness stems from specific structural modifications, formulation techniques, or therapeutic uses claimed in the patent's independent claims, which distinguish it from prior art.

2. How broad are the claims in AU2018282104, and can they be challenged?
While claims aim to be broad enough to encompass various embodiments, they are constructed within legal limits and can be challenged if found to lack novelty or inventive step outside Australian patent law standards.

3. Can this patent be enforced against generic competitors?
Yes, once granted, patent holders can license or litigate against infringing products that fall within the scope of the claims, provided the patent remains in force and valid.

4. How does this patent impact the development of similar drugs in Australia?
It acts as a barrier to competitors attempting to market similar formulations or methods without licensing, influencing R&D pathways and collaboration opportunities.

5. Is this patent likely to be part of a broader international patent family?
Given the strategic importance of pharmaceuticals, the patent likely forms part of a patent family extended via PCT or regional filings in key markets such as the US and Europe, ensuring global IP coverage.


References

  1. Australian Patent Office. Patent AU2018282104: Full Patent Specification. [Official Document]
  2. WIPO Patent Scope Database. International Patent Families and Related Filings.
  3. PATFT (Patent Full-Text and Image Database). Prior art search reports.
  4. Patent Analytics Reports. (2022). Australian Pharmaceutical Patent Trends.
  5. Relevant legal statutes, including Patents Act 1990 (Australia).

Disclaimer: This analysis is based on publicly available information and should not substitute legal advice or comprehensive patent searching.

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