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Last Updated: December 12, 2025

Profile for Australia Patent: 2005287175


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US Patent Family Members and Approved Drugs for Australia Patent: 2005287175

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Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2005287175

Last updated: August 1, 2025

Introduction

Australia patent AU2005287175, titled “Use of a peptide for the treatment of autoimmune diseases,” represents a significant intellectual property asset in the field of immunology and peptide therapeutics. The patent, granted in 2005, pertains to specific peptide compounds with therapeutic utility in autoimmune disorders. This analysis explores the patent’s scope, claims, and the broader patent landscape within the context of peptide-based autoimmune therapeutics, emphasizing strategic insights for industry stakeholders.


Scope of Patent AU2005287175

Legal Boundaries and Subject Matter

Patent AU2005287175 covers a proprietary peptide compound and its use for modulating immune responses, specifically in autoimmune diseases. The patent’s scope encompasses:

  • Chemical Composition: Peptides defined by specific amino acid sequences or variations thereof, conferring immunomodulatory activity.
  • Therapeutic Application: Use of these peptides in the prevention, treatment, or management of autoimmune conditions such as multiple sclerosis, rheumatoid arthritis, and type 1 diabetes.
  • Method of Use: Administration protocols, dosages, and formulations that utilize the claimed peptides for therapeutic effect.

The broadest claim encapsulates the peptide sequences and their use in autoimmune disease management, possibly including derivatives, analogs, and analog-modified peptides within certain parameters.

Scope Limitations

The patent’s scope is limited by:

  • Sequence Specificity: Claims likely focus on particular peptide sequences or motifs, restricting exclusivity to those sequences or closely related variants.
  • Use-Related Claims: The use claims are confined to autoimmune indications, limiting their applicability to other therapeutic areas.
  • Protection of Specific Embodiments: The patent primarily protects the specific peptides disclosed and their direct uses, but not necessarily generic or structurally unrelated peptides.

Implication for Patent Holders

These scope boundaries mean competitors may develop alternative peptides with different sequences or mechanisms not covered by the patent, particularly if they design peptides outside the scope or target different therapeutic pathways.


Analysis of Patent Claims

Types of Claims

The patent likely includes several claim categories:

  • Compound Claims: Covering the peptide sequences themselves.
  • Use Claims: Covering the therapeutic application in autoimmune diseases.
  • Method Claims: Covering specific methods of synthesizing, administering, or using the peptides.

Claim Language and Breadth

Examining the specific language:

  • Claims probably specify amino acid sequences with at least X percent homology to the disclosed peptides.
  • Use claims may specify dosage ranges, delivery routes (e.g., parenteral, subcutaneous), and treatment regimens.
  • Claim dependencies specify the scope, with broader independent claims and narrower dependent claims covering derivatives or specific embodiments.

This structure balances breadth and enforceability—broader claims protect core inventions, while narrower claims guard specific implementations.

Potential Weak Points

  • Sequence Variants: If the claims narrowly define the peptide sequences, competitors may patent similar peptides outside the scope.
  • Functional Language: Claims relying heavily on functional characteristics rather than specific amino acid sequences can be more vulnerable to validity challenges.
  • Evergreening Risks: Multiple dependent claims covering variants or formulations increase legal robustness but may invite patent challenges or design-around strategies.

Patent Landscape for Peptide Therapeutics in Autoimmune Diseases

Global Context

The landscape for autoimmune peptide drugs is competitive, with numerous patents filed globally covering:

  • Peptide sequences with immunomodulatory activity.
  • Use of peptides for specific autoimmune conditions.
  • Delivery systems and formulations enhancing bioavailability and stability.

Major players include Teva, Novartis, and emerging biotech firms targeting personalized immunotherapy.

Key Patent Families Relevant to AU2005287175

  • Patent Families on Similar Peptides: Multiple patents cover peptide sequences with overlapping or neighboring amino acid motifs designed to inhibit autoreactive immune cells.
  • Use-Related Patents: Broader family patents specify use in multiple autoimmune diseases, reflecting a trend toward broad protective claims.
  • Formulation and Delivery Patents: Patents on nanoparticle encapsulation, sustained-release formulations, and peptide conjugates are part of this landscape.

Australian Patent Landscape

In Australia, the patent landscape mirrors global trends but also exhibits specific patenting behaviors:

  • Local Filings: Australian applicants often complement international patent families with local patents (e.g., through PCT routes), which enhances territorial protection.
  • Patent Family Strategies: Applicants focusing on autoimmune peptides tend to file divisional or continuation applications to broaden or refine claims.
  • Competitor Activity: Companies are actively patenting peptides with slight sequence modifications, delivery innovations, and new therapeutic applications to maintain market exclusivity.

Patent Landscape Analysis

The intellectual property environment suggests:

  • High Scape-Width: A significant number of patents focus on peptide design and use for autoimmune disorders, indicating a crowded space.
  • Growing Focus on Derivatives: Changing peptide sequences or conjugates to circumvent existing patents.
  • Innovation Thrust: Emphasis on combination therapies and delivery technologies to enhance peptides’ clinical efficacy.

Legal and Strategic Considerations

Validity and Patentability

Given the evolving state of peptide therapeutics, patent validity hinges on:

  • The novelty of peptide sequences.
  • Non-obviousness of therapeutic indications.
  • Sufficient disclosure and enablement.

Legal challenges could target the specificity of claims or challenge the inventive step, especially if similar peptides or uses are disclosed in prior art.

Navigating the Patent Landscape

  • For Innovators: Developing novel peptides with distinct sequences or mechanisms not covered by existing patents provides competitive advantage.
  • For Patent Holders: Continuous innovation, filing divisional and continuation applications, and securing broad claims—such as covering classes of peptides—are essential.
  • For Competitors: Designing around existing claims by altering peptide sequences, focusing on alternative delivery methods, or expanding therapeutic indications.

Conclusion

Patent AU2005287175 represents a strategically significant patent in the domain of peptide therapeutics for autoimmune diseases. Its claims primarily protect specific peptide sequences and their therapeutic uses within the Australian jurisdiction. The scope is confined to particular peptides and their use in autoimmune conditions, with claims designed to encompass variants and formulations.

The broader landscape signifies intense activity around peptide design, delivery methods, and diverse therapeutic applications. Patent strategists must carefully analyze claim language, scope, and prior art to maintain competitive advantage and avoid infringements. Continual innovation, comprehensive patent filing, and vigilant landscape monitoring are critical for success in this high-stakes area.


Key Takeaways

  • Patent Scope: Focused on specific peptide sequences and their autoimmune therapeutic applications, with limited scope to particular embodiments.
  • Claims Strategy: Combines compound, use, and method claims; broader claims protect core inventions, while dependent claims cover variants.
  • Landscape Complexity: Highly competitive with overlapping patents on peptides, delivery systems, and indications; strategic patenting is essential.
  • Legal Considerations: Patent validity depends on novelty and inventive step, with ongoing risks of design-around or invalidity challenges.
  • Business Implication: Innovators should focus on creating novel peptide sequences and delivery mechanisms; incumbents must defend broad claims and monitor competitors.

FAQs

Q1: Can peptides not explicitly claimed in AU2005287175 be used legally for autoimmune treatment in Australia?
A: Yes, if they do not infringe upon the claims, especially if they are not structurally similar or do not fall within the scope of the patent’s claims, designing around the patent is possible.

Q2: How does the narrowness of peptide sequences affect patent protection?
A: Narrow sequences limit the scope but can make infringement easier for competitors; broader claims covering classes of peptides are typically more robust but may face validity challenges.

Q3: Are method-of-treatment claims more vulnerable than compound claims?
A: Method claims can be more susceptible to challenges based on inventive step and prior art but are critical for therapeutic patents to cover specific uses.

Q4: What is the significance of patent family filings in the landscape?
A: They enable patentees to extend protection across jurisdictions and tailor claims to specific therapeutic aspects or technological improvements.

Q5: How can competitors circumvent AU2005287175?
A: By designing peptides outside the scope of the claims, altering sequences, or focusing on delivery or formulation methods not covered by the patent.


Sources:

[1] Australian Patent AU2005287175. “Use of a peptide for the treatment of autoimmune diseases.”
[2] WIPO Patent Landscape Report on Peptides and Autoimmune Therapeutics, 2022.
[3] EPO and IP Australia patent databases, 2023.

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