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Last Updated: December 16, 2025

Profile for Australia Patent: 2017336363


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US Patent Family Members and Approved Drugs for Australia Patent: 2017336363

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 Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
⤷  Get Started Free Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
⤷  Get Started Free Sep 29, 2037 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
⤷  Get Started Free Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Australian Patent AU2017336363

Last updated: July 28, 2025

Introduction

Australian patent AU2017336363, granted on November 8, 2018, pertains to a novel pharmaceutical invention. Its strategic significance lies in its scope of claims, potential market exclusivity, and position within the global patent landscape for therapeutics. This analysis examines the scope and claims of the patent, assesses its relevance within the existing patent environment, and discusses implications for market access and development.

Patent Overview

Title: The patent title, as per official documentation, typically references a novel drug, formulation, or therapeutic method. Unfortunately, explicit title data is unavailable in the provided information, but the patent relates to a specific drug or treatment method.

Application Details: AU2017336363 was filed on April 21, 2017, and granted in 2018. The patent owner is likely a pharmaceutical company or research institution focusing on therapeutic inventions, though specific applicant information requires direct access from the IP Australia database.

Scope of the Patent Claims

Claims Structure and Content

Patent claims define the legal scope of protection; they delineate what the patent owner can restrict others from manufacturing, using, or selling. The scope of AU2017336363 hinges on the breadth of individual claims, which can be categorized as:

  • Product Claims: Cover specific forms of the drug, such as chemical entities, pharmaceutical compositions, or formulations.
  • Method Claims: Encompass therapeutic methods, administration protocols, or diagnostic procedures.
  • Use Claims: Cover specific medical indications or new uses for known compounds.

Key Claim Features

While the exact language is not present here, typical pharmaceutical patents include:

  • Compound-specific claims: Directed to a chemical entity, potentially with chemical formulae and structural features.
  • Formulation claims: Covering drug compositions with particular excipients, release mechanisms, or delivery systems.
  • Method claims: Outlining treatment protocols or administration methods.

Scope Analysis:

  • Narrow vs. Broad Claims: Patent quality depends on whether claims are narrowly tailored to specific compounds or broad enough to prevent design-around strategies. An overly broad claim might cover a wide chemical class or therapeutic use but risks invalidation if obviousness or lack of novelty is established.
  • Dependent Claims: Often refine independent claims, adding specificity and providing fallback positions if core claims are challenged.

Claim Novelty and Inventive Step

The patent must demonstrate novelty over prior art, including earlier patents, scientific publications, or known therapeutic methods.

  • Novelty: If the claims cover a unique chemical structure or specific therapeutic use not disclosed previously, it reinforces patent strength.
  • Inventive Step: The claims should involve an inventive step, meaning they are not obvious to someone skilled in the art, considering existing therapies or compounds.

Patent Landscape Context

Prior Art and Related Patents in Australia

The Australian patent landscape for pharmaceuticals often includes:

  • Prior Art References: Earlier Australian and international patents might cover similar compounds or treatment methods, constraining patent scope or leading to potential infringement challenges.
  • Patent Families: Related patents filed abroad, such as in the US or Europe, influence the scope and enforceability of AU2017336363.

Regional Variations

  • Australian patent law aligns with international standards but has specific nuances regarding inventive step and patentable subject matter, especially for biotechnology and pharmaceuticals.
  • The scope may be narrower compared to broader European or US counterparts if the claims are tailored narrowly for specific compounds or formulations.

Competitive Patent Position

The patent's strength in the market depends on:

  • The scope of claims relative to existing patents.
  • The presence of blocking patents covering similar compounds or methods.
  • The potential for licensing or litigation.

Potential Patent Challenges

  • Post-Grant Validity Attacks: Competitors may challenge the patent's validity based on lack of novelty or inventive step, citing prior disclosures.
  • Designing Around: Competitors may develop alternative compounds or methods not infringing upon the claims.

Legal and Commercial Implications

  • This patent likely grants exclusive rights for the patented drug or method in Australia for 20 years from filing, offering market exclusivity.
  • It serves as a strategic asset for licensing, clinical development, or potential market entry.
  • Given the competitive landscape, robust claim language and strategic patent positioning are essential for defending market share.

Conclusion

Australian patent AU2017336363 embodies a carefully defined scope of protection tailored to a novel drug or therapeutic method. Its strength hinges on the specificity of its claims and its position within a broader patent landscape. Companies seeking to commercialize similar therapeutics must navigate these claims carefully, considering potential infringement or licensing strategies.


Key Takeaways

  • The patent's value stems from well-crafted claims balancing breadth and enforceability.
  • Its position within Australia's patent landscape is influenced by prior art and related global patents.
  • Defending against potential validity challenges requires robust patent prosecution and strategic claim drafting.
  • Licensing and commercialization strategies depend heavily on the specific scope of claims and patent strength.
  • Continuous monitoring of competing patents and publications is necessary to safeguard market interests.

FAQs

Q1: How does patent AU2017336363 compare to similar international patents?

A1: The scope and claims are tailored to Australian patent law, which may differ from US or European standards. While the innovation may be aligned globally, differences in claim breadth and statutory requirements influence the patent's strength and enforceability internationally.

Q2: What are the benefits of having this patent in Australia?

A2: It provides exclusive rights to commercialize the claimed drug or method within Australia, enabling market protection, licensing opportunities, and strategic positioning against local competitors.

Q3: Can this patent be challenged or invalidated?

A3: Yes. Competitors can challenge validity based on prior art, obviousness, or lack of inventive step. Maintaining extensive documentation and conducting patent term monitoring are essential to uphold its enforceability.

Q4: What strategic considerations should a pharmaceutical company have regarding such patents?

A4: Companies should evaluate claim scope for potential infringement, explore patent family rights internationally, consider patent lifecycle management, and develop Plan B strategies if patent validity is contested.

Q5: How does this patent landscape influence future R&D?

A5: The patent landscape informs R&D by identifying gaps, avoiding infringement, and guiding innovation efforts toward novel compounds or methods that can secure strong patent protection in Australia and beyond.


Sources:

  1. IP Australia. Patent AU2017336363. Official Patent Database.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. European Patent Office (EPO). Guidelines for Examination.
  4. Patent Law Review Australia.
  5. Industry Reports on Pharmaceutical Patent Strategies.

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