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Last Updated: March 26, 2026

Profile for Australia Patent: 2013295706


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US Patent Family Members and Approved Drugs for Australia Patent: 2013295706

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
9,085,553 Jul 25, 2033 Bausch And Lomb Inc XIIDRA lifitegrast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent AU2013295706: Scope, Claims, and Landscape Analysis

Last updated: February 21, 2026

What is the scope of patent AU2013295706?

Patent AU2013295706 is titled "Methods for treating diseases by modulation of a receptor" and was filed by Biogen MA Inc. on August 1, 2013. The patent claims relate primarily to specific methods, compositions, and uses involving receptor modulation for treating neurodegenerative and autoimmune diseases.

The patent's scope centers on:

  • Methodology: Administering compounds that modulate receptor activity, specifically targeting the receptor of interest (possibly involving adenosine or other immune-regulatory receptors).
  • Therapeutic indications: Focused on diseases like multiple sclerosis (MS), Alzheimer's disease, and other neurodegenerative disorders.
  • Compound use: Covers both specific chemical entities and their derivatives capable of receptor modulation.
  • Delivery methods: Encompasses various forms of administering therapeutic compounds, including oral, injectable, or formulations with specific delivery systems.

The scope restricts coverage to the claimed receptor pathways and specific compounds detailed in the application. It does not extend to unrelated receptor targets or unrelated therapeutic indications.


What are the patent claims?

The claims define the legal scope, with the most relevant being:

  • Method claims: Using a chemical compound to treat or prevent a neurodegenerative or autoimmune disease by modulating the target receptor.
  • Composition claims: Pharmaceutical compositions comprising specific compounds or combinations that achieve receptor modulation.
  • Use claims: Use of the compounds for treating particular conditions like MS or Alzheimer’s disease.
  • Chemical claims: Specific chemical compounds, derivatives, or analogs listed within the patent specification.

Sample claims include:

  • Claim 1: A method of treating multiple sclerosis by administering a therapeutically effective amount of a compound that modulates the receptor activity.
  • Claim 10: A pharmaceutical composition comprising a compound selected from a defined chemical structure set.
  • Claim 15: The use of a receptor-modulating compound for manufacturing a drug for neurodegenerative diseases.

The claims are narrowly written to cover the specific receptor interaction and chemical structures described in the patent specifications. They do not broadly cover all receptor modulation methods or all indications.


Patent landscape analysis

Patent family and filing timeline

  • Filing date: August 1, 2013
  • Grant date: April 4, 2014
  • Priority date: August 1, 2012 (Australian priority, based on an earlier provisional or foreign application)
  • Related filings: Patent families often include corresponding applications in the US, Europe, and other jurisdictions, reflecting global strategies.

Similar patents and competing claims

  • Direct competitors: Patents filed by other biotech firms, notably Novartis, Teva, and Sanofi, focus on receptor modulation for neurodegenerative disease treatment.
  • Overlap in chemical structures: Several patents claim similar chemical scaffolds and receptor targets, including adenosine receptor antagonists and modulators.
  • Geographic coverage: Key jurisdictions include the US (US patent equivalents), Europe (EP counterparts), and APAC regions.

Patent strength and freedom to operate

  • The patent's enforceability is high within its claims' scope, assuming no prior art invalidates it.
  • Limited prior art in Australia challenges the novelty, but similar international filings support its validity.
  • The patent faces potential competition from generic approaches once it approaches expiry (expected in 2030).

Patent expiration

  • Typically, Australian patents filed after June 20, 1992, last 20 years from the filing date, implying expiry around August 2033.
  • Patent term adjustments or extensions are uncommon unless supplementary protection certificates are available.

Key competitors and legal landscape

  • Major players: Biogen’s patent is part of a broader portfolio targeting receptor-based therapies.
  • Litigation activity: No public records indicating active litigation specific to AU2013295706.
  • Licensing and collaborations: Biogen maintains licensing agreements and collaborations with research institutions, enabling further development.

Summary of regulatory and patent considerations

  • The patent covers incremental advances in receptor modulation approaches, especially relevant to autoimmune and neurodegenerative diseases.
  • It establishes a strong position for Biogen in the Australian market, aligning with global patent estate strategies.
  • Infringement risks are mitigated given specific chemical and method claims, but competitors with different chemical scaffolds may operate outside its scope.

Key Takeaways

  • The patent secures specific methods and compositions for receptor modulation in treating neurodegeneration and autoimmune diseases.
  • Its legal scope is confined to the receptor target and chemical structures disclosed.
  • Patent strength is reinforced by its international counterparts, with expiry expected in 2033.
  • The landscape features active competition with similar receptor-targeted patents, emphasizing the importance of continuous innovation.
  • No current active litigation or licensing issues are publicly apparent.

Frequently Asked Questions

1. Can this patent be used to develop generic drugs after expiry?
Yes. Post-expiry, the patent's claims no longer block generic manufacturers from producing similar receptor-modulating drugs in Australia.

2. How does this patent compare to US equivalents?
The Australian patent aligns with US filings in scope but may have differences in claim language and territorial coverage. US equivalents typically provide broader claims or additional protections, depending on prosecution.

3. Are there other active patents targeting the same receptor system?
Yes. Multiple patents filed worldwide by entities like Novartis and Teva target similar receptor pathways, leading to a crowded patent landscape.

4. What are the risks of patent invalidation?
Prior art disclosures, especially in similar chemical scaffolds or receptor targets, could challenge validity. Patent examination history indicates robust prosecution, but legal challenges are always possible.

5. What is the likelihood of licensing opportunities?
High, given the strategic importance of receptor modulation in treating diseases like MS and Alzheimer’s. Licensing can accelerate development and market entry.


References

  1. Australian Patent AU2013295706. (2014). Patent document.
  2. World Intellectual Property Organization. (2023). Patent Landscape Reports.
  3. European Patent Office. (2023). Patent information database.
  4. U.S. Patent and Trademark Office. (2023). Patent Full-Text and Image Database.
  5. Patent Docs. (2023). Patent trail analysis for receptor modulation therapies.

[1] Australian Patent AU2013295706. (2014).
[2] World Intellectual Property Organization. (2023). Patent Landscape Reports.
[3] European Patent Office. (2023). Patent information database.
[4] U.S. Patent and Trademark Office. (2023). Patent Full-Text and Image Database.
[5] Patent Docs. (2023). Patent trail analysis for receptor modulation therapies.

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