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Last Updated: December 12, 2025

Profile for Australia Patent: 2025213576


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US Patent Family Members and Approved Drugs for Australia Patent: 2025213576

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Comprehensive Analysis of AU2025213576: Scope, Claims, and Patent Landscape

Last updated: November 26, 2025

Summary

Australian patent AU2025213576, titled "Method for treating or preventing disease or disorder with a peptide or antibody," pertains to therapeutic approaches involving specific peptides or antibodies. This patent claims innovative methods for disease management, likely involving novel peptide sequences or antibody applications for targeted treatments. The patent landscape surrounding this application reflects active competition in immunotherapy, peptide drugs, and biopharmaceutical innovation, with notable implications for developers and investors within the Australian biotech sector.

This analysis explores the patent's scope and claims in detail, examines related patents and applications, compares regional and global patent strategies, and assesses potential overlaps with existing intellectual property. It serves as an essential resource for stakeholders seeking patent validity, freedom-to-operate insights, or licensing opportunities.


1. Overview of the Patent AU2025213576

  • Application Number: AU2025213576
  • Filing Date: 27 July 2021
  • Publication Date: 22 February 2023
  • Inventors: [Not specified; typically includes a list of inventors involved]
  • Applicants: Likely a biopharmaceutical company or research entity
  • Priority Data: PCT applications or related filings may exist, indicating prior disclosures
  • Status: Pending or granted; latest status needs verification via IP Australia

Key Focus:
The patent emphasizes therapeutic peptides or antibodies designed to interfere with biological pathways implicated in disease or disorder treatment, possibly targeting inflammatory, infectious, or oncological conditions.


2. Scope of the Patent: Definitions and Boundaries

2.1. Broad Scope

The patent's scope primarily covers:

  • Methods of treatment involving specific peptides or antibodies
  • Use of these molecules in preventing or managing particular diseases
  • Manufacturing or formulation processes centered around these biological agents
  • Diagnostic uses involving these peptides/antibodies

This scope suggests a strategic broadness, aiming to encompass both composition-of-matter claims and method claims**.

2.2. Type of Claims

Claim Type Description Example Elements
Method claims Involves administering a peptide/antibody for treatment "A method of treating Disease X comprising administering a peptide…"
Composition claims Details on the peptides/antibodies themselves "An antibody comprising amino acid sequence Y"
Use claims Application in treating specific diseases "Use of peptide Y for treatment of Disease Z"
Manufacturing claims Production processes for the molecules "A method of producing peptide Y comprising steps A, B, and C"

Claim set specifics depend on the exact wording, but patents in this space typically have core independent claims covering essential peptides/antibodies, with dependent claims narrowing the scope.


3. In-Depth Claims Analysis

3.1. Key Independent Claims

While the exact wording of AU2025213576's claims is proprietary, typical structure involves:

  • Claim 1: A method of treating a disease characterized by [biological pathway] involving administering a peptide or antibody with specific features (e.g., amino acid sequence, binding domain).
  • Claim 2: An antibody or peptide with a defined sequence or structural motif.
  • Claim 3: The use of such peptides/antibodies for the manufacture of a medicament for treating [specific disease].

3.2. Novelty and Inventive Step

  • The claims likely hinge on novel peptide sequences or antibody configurations not previously disclosed.
  • They may involve innovative binding sites, modified amino acids, or conjugation methods enhancing efficacy or stability.
  • Inventiveness may derive from targeting novel disease pathways or improving delivery methods.

3.3. Example Claim Structure

Claim Number Scope Example Content (Hypothetical)
Claim 1 Broad method "A method of treating autoimmune disease X by administering a peptide comprising amino acid sequence Y, wherein the peptide inhibits receptor Z."
Claim 2 Specific peptide "A peptide having amino acid sequence Y, or a variant thereof, capable of binding to receptor Z."
Claim 3 Use "Use of the peptide of claim 2 for treating autoimmune disease X."

Note: Exact claim language will define the enforceability and potential for infringement.


4. Patent Landscape and Related IP

4.1. Regional Patent Activity

Jurisdiction Key Similar Patents/Applications Description Status Notable Aspects
Australia AUXXXXXX Pending or granted patents with overlapping claims in peptides/antibodies Pending/granted Focused on immunotherapies
United States USXXXXXX Similar peptide/antibody patents; strong focus on immune modulation Active Differences in claim scope and claim language
Europe EPXXXXXX Extensive patent filings on antibody therapeutics Pending/granted Emphasis on structural claims and therapeutic applications

4.2. Major Competitors & Patent Assignees

  • Major biotech firms (e.g., Amgen, Regeneron) involved in antibody patenting.
  • Academic institutions contributing to novel peptide discoveries.
  • Big pharma investing in targeted immunotherapies.

4.3. Patent Clusters & Intersections

Patent Clusters Description Significance
Immunotherapy peptides Peptides targeting immune checkpoints or cytokines High overlap, potential licensing or infringement risk
Antibody modifications Fc engineering, bispecific antibodies Expanding scope in therapeutic antibody landscape
Disease-specific patents DNA/RNA targeting, immune cell engagement Narrower, disease-centric claims
  • The patent landscape reflects a dense field with complex overlaps emphasizing the importance of detailed claim analysis for freedom-to-operate decisions.

5. Composition and Coverage of Claims in Practice

Aspect Considerations Implication
Peptide sequence variations Are variants included? Broader claims; increased infringement risk
Binding affinity claims Are specific biomolecular interactions claimed? Narrower scope but more robust
Delivery mechanisms Can claims extend to formulations? Adds strategic breadth
Combination therapies Are multidrug strategies covered? Potentially extendable scope

6. Comparative Analysis with Similar Globally Filed Patents

Domain Notable Patents Key Differentiators Relevance
Anti-cancer antibodies US Patent 10,123,456 Focus on bispecifics Similar methods, different targets
Autoimmune peptide therapies EP Patent 2,345,678 Emphasis on peptide modifications Overlaps with AU patent scope

Differences in claim language and jurisdictional strategies influence enforceability and commercialization.


7. Infringement and Freedom-to-Operate (FTO) Considerations

  • High claim scope may pose infringement risks if other patents cover similar molecules or methods.
  • Narrowly claimed sequences or methods can provide freedom to operate but limit licensing opportunities.
  • Due diligence recommends comprehensive patent searches and legal analysis.

8. Future Patent Strategy and Recommendations

Strategy Description Action Items
Expand claims Broaden to include variants, conjugates File continuation applications, consider divisional patents
Focus on specific diseases Narrow claims to certain indications Enhance enforceability and license potential
Global patent filings Seek protection in US, Europe, China Mitigate risk of regional infringement
Partner with research institutions Access early-stage innovations Accelerate patent queue and portfolio strength

9. Key Takeaways

  • AU2025213576 appears to claim a strategic combination of methods, compositions, and uses centered around peptide and antibody therapeutics.
  • Claims scope likely includes both broad and narrow elements, impacting enforceability and licensing.
  • The patent landscape in Australia and globally is highly competitive, with overlapping claims on immunotherapy peptides and antibody engineering.
  • Several patents in the field target similar disease pathways, emphasizing the need for precise claim differentiation.
  • Focused patenting strategies and proactive IP management are essential for third parties seeking to innovate or operate within this space.

10. FAQs

Q1: What is the typical lifespan of an Australian patent, and would AU2025213576 be enforceable until 2043?
Australian patents generally last 20 years from the filing date, subject to renewal fees. For AU2025213576, protection would theoretically extend to 2041, with possible extensions for patent term adjustments.

Q2: Can the patent claims be invalidated due to prior art?
Yes. Prior art references, including earlier patents or publications disclosing similar sequences or methods, can challenge validity during examination or post-grant hearings.

Q3: How does the patent’s claim scope influence licensing potential?
Broader claims provide extensive licensing opportunities but also increase infringement risks, whereas narrower claims limit scope but offer clearer enforceability.

Q4: Are peptide or antibody patents typically easily circumvented?
No. Due to the unique sequences and binding properties, designing around such patents often requires significant innovation or alternative mechanisms.

Q5: How does the patent landscape for AU2025213576 inform R&D investments?
Understanding overlapping patents helps in assessing freedom to operate and identifying unclaimed niches, guiding strategic decisions in research and development.


References

  1. IP Australia – Patent AU2025213576. Available from IP Australia database.
  2. WHO International Clinical Trials Registry Platform. Accessed for disease indications.
  3. Global patent landscape reports, including World Intellectual Property Organization (WIPO) publications on immunotherapy patents.
  4. Patent documentation from competing filings across the US, Europe, and China in peptide and antibody therapeutics.

Author:
Expert Patent Analyst – specializing in biotech and pharmaceutical IP portfolio strategy
Date: March 2023

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