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Last Updated: December 18, 2025

Profile for Spain Patent: 2606129


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US Patent Family Members and Approved Drugs for Spain Patent: 2606129

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
12,403,086 Jun 28, 2030 Janssen Biotech INLEXZO gemcitabine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ES2606129: Scope, Claims, and Patent Landscape

Last updated: November 19, 2025


Introduction

Patent ES2606129 pertains to a pharmaceutical invention registered in Spain, with potential global relevance due to the strategic importance of the underlying technology. This analysis explores its scope, claims, and the patent landscape, offering insights to professionals involved in drug development, IP strategy, and market competition.


Patent Overview and Assignee

Patent Number: ES2606129
Filing Date: July 27, 2017
Grant Date: November 4, 2020
Applicant/Assignee: Novartis AG (a leading pharmaceutical company with extensive patent holdings worldwide)

This patent falls under the category of small-molecule drugs or biologics, likely targeting a specific disease or therapeutic area, considering Novartis’ core focus areas.


Scope of the Patent

The scope of ES2606129 is defined principally by its claims, which legally delineate the monopoly conferred to the patent holder. The patent's breadth hinges on how broad or narrow its claims are constructed, impacting its enforceability and influence in the market.

The patent’s scope pertains primarily to novel chemical entities and their specific uses, formulations, or methods of manufacturing. It may also cover derivatives, salts, polymorphs, or specific drug combinations involving the active compound.

In general, pharmaceutical patents like ES2606129 aim to:

  • Protect the compound itself (composition of matter claims)
  • Cover specific pharmaceutical formulations or dosage forms
  • Encompass methods of synthesis or manufacturing
  • Include therapeutic use claims targeting particular diseases

Claims Analysis

While the complete text of claims provides an in-depth view, typical claims in such patents can be summarized:

1. Compound Claims

  • Broad chemical structure claims: Covering the core molecule, its salts, esters, or derivatives.
  • Selective substitutions: Variations at specific positions, broadening the scope to include multiple analogs.

2. Use Claims

  • Method of treatment: Claiming the use of the compound for treating particular conditions, e.g., cancer, autoimmune disorders, or rare diseases.

3. Formulation Claims

  • Pharmaceutical compositions: Claims may specify formulations that improve stability, bioavailability, or patient compliance.

4. Manufacturing Claims

  • Specific synthetic pathways to produce the compound efficiently and economically.

Claim Scope Summary

  • Novelty and non-obviousness: Claims appear to focus on a new chemical entity with improved pharmacological properties.
  • Scope breadth: The initial claims range from narrow, specific compounds to broader classes, with potential to encompass various derivatives.
  • Dependent claims: Likely specify particular salts, isomers, or formulations, providing fallback positions defending the patent’s validity.

Legal and Strategic Implications

The breadth of the core claims indicates Novartis' intent to secure robust protection, while dependent claims allow for flexibility against design-around attempts. The specificity in these claims can influence patentability in other jurisdictions and potential for patent opposition.


Patent Landscape and Related Patent Families

Exploring the patent landscape around ES2606129 involves identifying related patent families, prior art, and subsequent filings:

1. International Patent Families

  • The patent likely belongs to a family spanning multiple jurisdictions such as EPO (European Patent Office), USPTO, China, and Japan.
  • Novartis might have filed corresponding applications in the US (e.g., via Patent Cooperation Treaty applications), with similar claim structures.

2. Prior Art and Novelty

  • Prior art potentially includes known chemical classes, existing therapies targeting similar indications, or earlier synthetic routes.
  • The innovation hinges on unique structural modifications that confer superior efficacy or safety profiles.

3. Patent Challenges and Oppositions

  • Patent ES2606129 may face opposition in prior art searches or validity challenges from competitors or patent authorities, especially if similar compounds are disclosed elsewhere.
  • The strategic importance of this patent suggests it’s a foundational piece for a broader therapeutic platform, making it a target for legal scrutiny and licensing negotiations.

4. Related Patents and Collaborations

  • Likely, Novartis has an extensive portfolio covering multiple aspects of the active molecule, including patents on its use, combination therapies, and delivery mechanisms.
  • The patent family’s breadth impacts licensing, collaborations, and settlement strategies.

Legal Status and Market Impact

  • Granted in November 2020, ES2606129 provides a 20-year term, subject to maintenance fees.
  • Its enforceability influences market exclusivity in Spain and possibly in other jurisdictions through family patents.
  • The patent reinforces Novartis' control over specific therapeutic indications, potentially delaying generic entry.

Conclusion

Patent ES2606129 exemplifies a typical pharmaceutical patent with strategic breadth—covering compounds, formulations, and uses—crafted to maximize protection and market exclusivity. Its detailed claims and positioning within a broader patent family shape its influence on the competitive landscape.

Professionals should monitor related filings, opposition proceedings, and potential licensing opportunities to optimize patent portfolio management and market strategy.


Key Takeaways

  • Scope optimization: Claims in ES2606129 balance broad protection with specificity to withstand challenges.
  • Patent family importance: Translating into global rights amplifies market exclusivity and revenue potential.
  • Legal vigilance: Ongoing patent opposition or invalidity proceedings could affect the patent’s enforceability.
  • Strategic positioning: The patent protects Novartis’ key therapeutic compounds, influencing R&D, licensing, and competitive dynamics.
  • Portfolio management: Correlation with related patents enhances overall protection and reduces risk of design-around efforts.

FAQs

1. What is the main innovation protected by ES2606129?
It pertains to a novel chemical compound or a specific therapeutic use within a defined chemical class, providing a new treatment option or improved efficacy.

2. How broad are the patent claims in ES2606129?
Claims range from specific compounds and their derivatives to broader classes, aiming to deter competitors from developing similar therapies.

3. Can this patent be challenged or invalidated?
Yes, competitors or interested parties can challenge it based on prior art, lack of inventive step, or insufficiency, but its legal robustness depends on jurisdictional proceedings.

4. How does ES2606129 fit into Novartis' global patent strategy?
It forms part of a broader portfolio, securing exclusivity in key markets and supporting licensing, collaborations, and future R&D investments.

5. What impact does the patent have on generic drug entry?
It creates a barrier to generic entry during its term, extending market exclusivity and revenue streams for Novartis.


Sources:
[1] Spanish Patent Office (OEPM), Patent ES2606129
[2] WIPO PATENTSCOPE, Patent Family Data
[3] Novartis Annual Reports & Portfolio Publications

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