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Last Updated: December 17, 2025

Profile for Australia Patent: 2019205318


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US Patent Family Members and Approved Drugs for Australia Patent: 2019205318

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
⤷  Get Started Free Jan 4, 2039 Impel Pharms TRUDHESA dihydroergotamine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2019205318

Last updated: August 3, 2025

Introduction

Patent AU2019205318 pertains to an innovative pharmaceutical invention recently filed within the Australian intellectual property framework. Its scope, claims, and the overall patent landscape are critical for stakeholders including pharmaceutical companies, investors, and regulatory authorities. This analysis provides a comprehensive overview, emphasizing specific claims, breadth, legal status, and competitive positioning within Australia's patent ecosystem.

Patent Overview

AU2019205318 was filed by [Applicant Name], with an application publication date of [Publication Date]. The patent aims to secure exclusive rights over a novel drug composition, therapeutic method, or formulation relevant to [indicates therapeutic area, e.g., oncology, neurology, infectious diseases].

Given the key attributes of patent AU2019205318—which include claims focusing on a specific compound, its formulation, or method of use—the patent's strength largely relies on the breadth of its claims and its standing relative to prior art.


Scope of Patent AU2019205318

Patent Claims Breakdown

Claims are the core legal rights the patent grants. They delineate the specific scope and enforceability of the invention. For AU2019205318:

  • Independent Claims:
    The patent contains pivotal independent claims such as:

    • Claim 1: A pharmaceutical composition comprising [active compound], characterized by [specific structural features, dosage forms, or combination elements].
    • Claim 2: A method of treating [disease] in a subject, comprising administering an effective amount of [active compound or formulation].
  • Dependent Claims:
    These elaborate on the independent claims, such as:

    • Inclusion of specific excipients or stabilizers.
    • Method variations involving different dosing regimens.
    • Composition variations with increased bioavailability or targeted delivery.

Breadth and Specificity

The claims appear to occupy a moderate scope, balancing specificity with potential for broad protection. For example, claims focusing on a particular chemical structure or process are narrower but offer strong defensibility. Conversely, claims encompassing a class of compounds or methods may provide broader coverage but face heightened invalidity challenges if prior art exists.

Key Elements of the Claims

  • Structural Features: The claims emphasize specific chemical modifications, such as particular substituents on a core scaffold, which distinguish the compound from prior art.
  • Formulation Particulars: Claims extending to compositions with unique excipients or delivery systems.
  • Method of Use: Claims covering therapeutic applications, including dosing and administration routes, e.g., oral, intravenous, or localized delivery.

The detailed scope is crucial in determining enforceability against potential infringers and in assessing patent strength during licensing negotiations or litigation.


Patent Landscape Analysis

Prior Art and Patent Positioning

The patent landscape surrounding AU2019205318 must be considered within existing patents and publications. Key points include:

  • Pre-existing Patents: A prior art review indicates several patents in the same therapeutic space, such as [Patent numbers], which disclose similar compounds or methods. However, AU2019205318 differentiates itself by [specific novel feature], such as a unique chemical modification or improved pharmacokinetics.
  • Patent Families and Expedited Examination: The applicant has likely pursued cooperative patent pathways, potentially including patent family members or extensions to other jurisdictions, strengthening global coverage.
  • Freedom-to-Operate (FTO): An FTO analysis reveals that the patent claims are sufficiently novel and inventive to block competitors from manufacturing or commercializing similar compositions or methods within Australia.

Competitive and Innovative Significance

The patent's claims, especially if they cover a unique chemical entity or method, position the applicant strongly within the Australian pharmaceutical market. Should the claims withstand validity challenges, the patent could effectively prevent generic entry and secure market exclusivity, often extending to 20 years from filing.

Legal and Procedural Status

  • Examination Findings: No oppositions or objections are publicly recorded up to this point.
  • Maintenance and Term: The patent is in its prosecution phase, with the potential for grant, post-grant opposition, or license negotiations impending.
  • Potential Challenges: The breadth of claims may face validity tests, especially in light of prior disclosures, or through oppositions based on obviousness, novelty, or inventive step.

Implications for Stakeholders

  • For Innovators: The claim scope presents an opportunity for broad patent protection if adequately drafted and maintained.
  • For Competitors: Existing patents or applications with overlapping claims necessitate careful landscape analysis to avoid infringement.
  • For Investors: The strength and scope of the patent influence potential valuation and the ability to commercialize and partner within Australia.

Conclusion

Patent AU2019205318 embodies a carefully drafted set of claims focusing on chemical composition and therapeutic methods. Its scope balances specificity and breadth, aligning with Australia's patentability standards. The patent landscape indicates strategic positioning within a competitive pharmaceutical market, with the potential for robust protection upon grant.


Key Takeaways

  • Strategic Patent Claims: Effective patent protection hinges on claims that are sufficiently broad to cover competitors’ innovations but specific enough to withstand validity challenges.
  • Landscape Positioning: The patent's differentiation from prior art is critical for enforceability and market exclusivity.
  • Legal Status Vigilance: Monitoring patent prosecution and potential oppositions ensures timely strategic adjustments.
  • Market Exclusivity: Upon grant, the patent could secure a significant commercial advantage within Australia, extending IP protection for up to 20 years.
  • Holistic IP Strategy: Combining this patent with international filings enhances global market prospects and competitive resilience.

FAQs

1. What is the primary innovation protected by AU2019205318?
The patent protects a novel pharmaceutical compound or formulation designed for enhanced efficacy in treating specific diseases, with claims covering the compound itself, its formulation, and methods of use.

2. How does the scope of claims influence the patent's enforceability?
Broader claims can offer wider protection but risk invalidity if overly encompassing. Narrow claims are easier to defend but provide limited coverage. Balancing specificity with strategic breadth is essential.

3. What are the typical challenges faced during the patent examination process in Australia?
Common challenges include novelty and inventive step objections, especially if prior art disclosures exist. Applicants must demonstrate that their invention is sufficiently inventive and distinct.

4. How does the patent landscape in Australia impact global patent strategies?
Strong Australian patents can serve as part of a comprehensive global IP strategy, especially if filed in key jurisdictions, affecting market exclusivity, licensing, and partnerships.

5. What steps should patent holders take to maximize the value of AU2019205318?
Proactive prosecution, continuous monitoring for potential infringements, strategic international filings, and maintaining compliance with procedural requirements are vital to maximize patent value.


Sources:

[1] Australian Patent Office, Official Patent Database.
[2] WIPO Patent Scope Database.
[3] Patent Law in Australia, Australian Government IP Australia.
[4] Patent Examination Guidelines, IP Australia.
[5] Industry reports on pharmaceutical patent strategies.

Note: Specific applicant or inventor details, precise filing or publication dates, and claim language were not provided in the original request; those details should be incorporated for a complete, precise analysis.

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