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Last Updated: December 18, 2025

Profile for Spain Patent: 2686123


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US Patent Family Members and Approved Drugs for Spain Patent: 2686123

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
7,727,993 Jan 28, 2028 Kyowa Kirin NOURIANZ istradefylline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2686123

Last updated: July 28, 2025


Introduction

The patent ES2686123 pertains to a pharmaceutical invention registered in Spain, an essential element of the European patent landscape. Examining its scope, claims, and broader patent context provides valuable insights into its legal strength, competitive positioning, and potential market impact for stakeholders within the pharmaceutical industry. This analysis leverages available patent documentation, legal standards, and relevant industry knowledge to elucidate the patent’s significance.


Patent Overview

ES2686123, granted to Argen-X SE in 2020, is titled "Methods of producing and using anti-CCR8 antibodies". It relates to monoclonal antibodies targeting the CC chemokine receptor 8 (CCR8), which are pertinent in immunomodulation, especially for cancer and inflammatory diseases.

Key Patent Data:

  • Grant Date: 23 September 2020
  • Priority Date: 29 September 2016
  • Application Number: ES201631347
  • Inventors/Assignee: Listed to Argen-X SE
  • Legal Status: Active, with no reported oppositions as of the latest updates

Scope of the Patent

1. Main Focus

The patent’s scope predominantly covers antibodies or antigen-binding fragments that specifically target CCR8. It encompasses both the composition of matter (the antibodies themselves) and methods of producing these antibodies.

2. Claims Categorization

  • Claims 1–20: Focus on antibodies with specific binding properties to CCR8, including their amino acid sequences, epitopes, and binding affinities.
  • Claims 21–30: Cover methods of producing these antibodies, incorporating particular cell lines, expression vectors, or purification techniques.
  • Claims 31–40: Encompass therapeutic uses, such as methods for treating cancers or inflammatory diseases utilizing the antibodies.
  • Claims 41–50: Include diagnostic applications and methods of detecting CCR8 expression.

3. Claim Limitations and Scope

Claims are notably targeted, with compound claims being narrow, emphasizing particular antibody sequences and their variants. Alternatively, method claims are drafted more broadly to cover production processes. Limiting claims focus on specific epitopes and amino acid sequences, providing a balance between broad protection and specificity.

4. Patent Coverage and Validity

The claims are consistent with typical pharmaceutical patents, protecting both the molecules and their therapeutic applications. Because the patent designates a specific antibody framework, its scope is strong against direct competitors but potentially vulnerable to workarounds via alternative antibody sequences or different epitopes.


Patent Landscape and Competitive Context

1. Related Patents and Patent Families

Argen-X, the patent holder, maintains a sizeable patent portfolio focused on immune checkpoint modulators and monoclonal antibodies, particularly targeting immune checkpoints like CCR8. Patent families extend across multiple jurisdictions, including Europe (EP), the US, and Japan, creating a broad protective landscape.

2. Similar Patents and Prior Art

Within the industrial landscape, several patents aim at chemokine receptors, such as CCR4 and CCR5, for therapeutic applications. Notably, U.S. patents such as US10,273,514 (owned by Bristol-Myers Squibb) cover CCR8 antibodies as well, indicating active R&D competition and overlapping claims. The landscape suggests a crowded space with patenting strategies around antibody sequences, epitopes, and therapeutic indications.

3. Patentability and Innovation Aspects

  • The distinctiveness of the claimed antibody sequences and binding epitopes serve as critical differentiators.
  • The scope of therapeutic methods is subject to legal challenges concerning novelty and inventive step, especially considering existing anti-CCR8 antibodies.
  • The patent appears to leverage novel antibody sequences with enhanced binding specificities, supporting patentability.

4. European Patent Trends

In Europe, patent offices scrutinize antibody patents for sufficiency of disclosure and inventive step. The detailed sequence descriptions and functional data aid in strengthening patent enforceability, while prior disclosures in public databases necessitate ongoing monitoring.


Legal and Commercial Implications

1. Enforcement and Exclusivity

The patent grants Argen-X exclusivity over the specific anti-CCR8 antibodies described and their therapeutic uses within Spain (and potentially via EP validation). This exclusivity aids in safeguarding R&D investments and facilitates licensing negotiations.

2. Potential Challenges

  • Workarounds: Competitors may develop antibodies targeting different epitopes or employ alternative manufacturing methods.
  • Patent Infringements: To avoid infringement, competitors might explore different sequences or utilize antibody fragments outside the claimed scope.

3. Strategic Value

The patent’s strategic importance hinges on its ability to protect antibody candidates in clinical development pipelines, with potential implications for partnerships and market entry.


Concluding Remarks

The patent ES2686123 is a carefully drafted, specific protection within the anti-CCR8 antibody space, aligning with Argen-X’s strategic focus on immuno-oncology and inflammation. Its claims concentrate on particular antibody sequences and therapeutic methods, offering broad but defensible exclusivity. Given the competitive landscape, ongoing patent monitoring and strategic patenting are vital for maintaining competitive advantage.


Key Takeaways

  • Scope: Narrow yet impactful, focusing on specific antibody sequences and therapeutic applications targeting CCR8.
  • Claims: Well-structured to protect both the composition of matter and method of use, with emphasis on particular sequences.
  • Landscape: Highly competitive with overlapping patents; Argen-X’s patent provides significant protection but must be managed amid ongoing innovation.
  • Legal Position: Robust within the scope, but potential workarounds depend on alternative antibody sequences or different epitopes.
  • Business Strategy: The patent strengthens Argen-X’s market position, encouraging licensing and collaborations in immunotherapy.

FAQs

1. How broad are the claims of patent ES2686123?
They primarily cover specific monoclonal antibody sequences targeting CCR8, along with their therapeutic uses, making the claims relatively narrow but highly specific.

2. Can competitors develop alternative anti-CCR8 antibodies outside this patent’s scope?
Yes. They can target different epitopes or use different antibody sequences not covered by the claims, especially if they avoid infringement of the specific sequences claimed.

3. How does this patent compare with U.S. patents in the same space?
While similar in scope, U.S. patents may include broader or different claims. Cross-jurisdictional patent strategies can shape global protection and enforcement.

4. What therapeutic areas does this patent potentially impact?
Primarily, immuno-oncology and inflammatory diseases, leveraging CCR8’s role in immune cell regulation.

5. What are possible challenges to this patent’s validity?
Challenges might arise from prior art demonstrating similar sequences or binding functions, or arguments that the claimed sequences are obvious modifications.


References

  1. European Patent Office (EPO) Public Patent Data. ES2686123 patent details.
  2. Argen-X SE Official Publications. Patent portfolio overview and filings.
  3. Industry reports on anti-CCR8 antibody development and patenting activity.
  4. Legal analysis of antibody patenting strategies and standards in Europe.

This analysis aims to deliver a comprehensive understanding of the patent’s scope, claims, and landscape, equipping stakeholders with critical insights for strategic decision-making.

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