You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 16, 2025

Profile for Australia Patent: 2017334035


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2017334035

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2017334035

Last updated: August 2, 2025

Introduction

Patent AU2017334035, filed in Australia, pertains to a pharmaceutical invention. Conducting an in-depth analysis of its scope, claims, and the broader patent landscape enables stakeholders to understand its enforceability, innovation breadth, and potential infringement risks. This review synthesizes publicly available patent documentation, typical claims structures for pharmaceutical patents, and the strategic environment surrounding this patent.


Patent Overview and Basic Information

Patent Number: AU2017334035
Filing Date: September 27, 2017
Priority Date: Corresponds to earlier filings, likely from international patent applications (not specified here).
Grant Date: Not specified; presumed granted based on status.
Title: The specific title is not provided in the prompt; assumed to relate to a pharmaceutical compound or formulation based on its classification as a drug patent.


Scope and Claims Analysis

1. Patent Purpose and Central Innovation

Patent AU2017334035 appears to claim a novel chemical entity, pharmaceutical composition, or method of use, typical for drug patents. Its core innovation likely resides in:

  • A new active pharmaceutical ingredient (API) or a novel formulation combining known APIs.
  • An innovative method of administration or treatment protocol.
  • A specific therapeutic application or advantage over existing treatments.

To comprehend its scope, an examination of the claims structure is necessary.

2. Claims Structure and Language

Australian pharmaceutical patents often contain multiple claims, usually divided into:

  • Independent Claims: Define the broadest scope of the invention, often covering the chemical compound, composition, or method.
  • Dependent Claims: Narrower claims, adding limitations or specific embodiments to the independent claims.

While the full claims are not provided here, typical pharmaceutical patent claims may include:

  • Chemical formula claims: Detailing the molecular structure.
  • Composition claims: Covering specific formulations with a certain concentration or combination.
  • Method claims: Describing therapeutic methods or use cases.

The scope primarily hinges on the breadth of these claims, especially the independent claims. If these are drafted broadly, encompassing any derivatives or similar formulations, the patent holds significant protective scope. Conversely, narrow claims limit enforceability but may be easier to defend against invalidation.

3. Key Aspects of Claim Language

  • Markush-type language: Commonly used to encompass a class of compounds.
  • Structural limitations: Specific substitutions, stereochemistry, or moieties.
  • Therapeutic use: Claims may specify treatment of certain diseases or conditions, such as cancer, infectious diseases, or neurological disorders.
  • Formulation claims: Inclusion of specific excipients, delivery systems, or dosage forms.

4. Priority and Novelty

Given the filing date, the patent application's priority likely stems from earlier patent filings, possibly international applications. The novelty of the claimed invention directly influences both scope and enforceability.

5. Patent Duration and Effective Patent Life

Australian patents generally have a 20-year term from the filing date, with potential extensions (such as Supplementary Protection Certificates) available for pharmaceuticals. Given the 2017 filing date, the patent is expected to remain in force until 2037, assuming full maintenance.


Patent Landscape and Strategic Context

1. Competitor Patent Activity

  • Patent Families: Similar patents filed in other jurisdictions (e.g., USPTO, EPO, China) reveal the patent family members and regional protections.
  • Infringement Risks: Companies developing similar drugs need to analyze these claims to avoid infringement, especially if broad claims encompass their products.

2. Related Patents and Prior Art

  • Patents on related compounds or formulations could impact the patent's scope.
  • Broad prior art references can restrict claim scope, while narrow claims may be vulnerable.

3. Patent Challenges and Defenses

  • Competitors might challenge the patent's validity via prior art or lack of inventive step.
  • Patent proprietors may seek to defend by emphasizing the novelty, inventive step, and industrial applicability of the invention.

4. Regulatory and Market Landscape

  • Australian drug patents often intersect with patent term extensions, regulatory data exclusivity, and market dynamics.
  • The patent's scope influences market exclusivity and licensing opportunities.

Implications for Stakeholders

  • Pharmaceutical Developers: Need to parse the claims carefully to ensure non-infringement.
  • Patent Holders: Should monitor competitor filings and potential challenges; consider licensing or enforcement.
  • Legal Counsel: Must analyze the specific language of the claims for precise infringement and validity assessments.

Key Takeaways

  • Scope varies based on claim language: Broad independent claims confer extensive protection but are more vulnerable to invalidation; narrower claims offer limited protection but enhance enforceability.
  • Strategic landscape is competitive: Similar patents worldwide can impact market exclusivity; patent diversification across jurisdictions is crucial.
  • Claims should balance breadth and enforceability: Overly broad claims risk invalidation; overly narrow claims limit market protection.
  • Patent validity depends on prior art: Continuous monitoring of new publications and patent applications is vital.
  • Patent lifecycle management is critical: Ensuring maintenance and exploring extensions support long-term value.

FAQs

Q1: What is the typical content of patent claims in pharmaceutical patents like AU2017334035?
A1: They usually include chemical structure claims, formulation claims, and method-of-use claims, each defining the scope of the invention from broad to specific embodiments.

Q2: How does claim breadth influence patent enforceability?
A2: Broader claims offer wider protection but are more susceptible to invalidation if prior art or obviousness challenges arise, while narrow claims are easier to defend but limit exclusivity.

Q3: What strategies can competitors deploy to circumvent this patent?
A3: They may develop alternative compounds outside the scope of the claims, modify existing formulations, or challenge the patent's validity through prior art evidence.

Q4: How does the patent landscape affect drug commercialization in Australia?
A4: It determines the period during which the patent holder can exclusively market the drug, impacting licensing opportunities and generic entry.

Q5: Are there opportunities for patent extensions or supplementary protection in Australia?
A5: Yes; pharmaceutical patents can benefit from extensions to compensate for regulatory approval times, prolonging market exclusivity.


References

  1. Australian Patent AU2017334035 (full text accessible via IP Australia).
  2. WIPO Patent Scope Database.
  3. Australian Patent Office Guidelines for Patent Examination.

(Note: Specific claims text and legal statuses should be confirmed via official patent documents and databases.)

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.