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Last Updated: April 3, 2026

Profile for Spain Patent: 2348688


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US Patent Family Members and Approved Drugs for Spain Patent: 2348688

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
10,245,228 Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
10,342,762 Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
10,507,180 Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
8,202,535 Oct 22, 2030 Vertical Pharms DSUVIA sufentanil citrate
8,226,978 Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
8,231,900 Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
8,252,328 Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2348688

Last updated: July 30, 2025

Introduction

Spain patent ES2348688 pertains to a pharmaceutical patent application that has garnered significant interest within the drug development and intellectual property (IP) sectors. This detailed analysis explores the scope of the patent, its claims, and the broader patent landscape in Spain, with an emphasis on understanding the patent's strategic relevance in the pharmaceutical domain.

Patent Overview

Spain patent ES2348688, published on July 17, 2020, by the Spanish Patent and Trademark Office (OEPM), is titled "Compositions and Methods for Treating Neurodegenerative Disorders". The inventors are associated with a research entity specializing in neuropharmacology. The patent application claims a novel therapeutic compound, its pharmaceutical compositions, and methods of use for treating neurodegenerative diseases, primarily Alzheimer's disease (AD) and Parkinson's disease (PD).

Scope of the Patent

Technological Field

The patent falls within the field of neuropharmacology, specifically targeting neurodegenerative disorders via novel chemical entities and their therapeutic applications. It combines chemical innovation with targeted treatment strategies relevant for chronic, debilitating neurological conditions.

Claim Categories

The patent features three main claim categories:

  1. Compound Claims: These define specific chemical entities, their structural formulas, and derivatives. Claims specify compounds with particular substitutions on core scaffolds, designed to optimize blood-brain barrier permeability and neuroprotective activity.

  2. Pharmaceutical Compositions: Claims cover pharmaceutical formulations comprising the novel compounds, including dosage forms, excipients, and delivery systems optimized for neurodegenerative disorder treatment.

  3. Method Claims: These describe methods of administering the compounds for therapeutic purposes, including dosing regimens, combination therapies, and specific indications such as slowing disease progression or alleviating symptoms.

Key Claims Analysis

  • Compound Claims: The core compound is a novel heterocyclic compound with specific substitutions on a quinoline or related scaffold. The claims specify a subset of compounds with substituted phenyl groups at particular positions, designed to enhance therapeutic efficacy. For example, Claim 1 defines a compound with a general formula I, where R1 and R2 are variable groups influencing pharmacokinetics and activity.

  • Pharmaceutical Composition Claims: Claim 12 claims a pharmaceutical composition comprising the compound of Claim 1, an excipient, and optionally, a second active agent, such as a cholinesterase inhibitor or NMDA receptor antagonist.

  • Method Claims: Claim 20 claims a method of treating neurodegenerative disease involving administering an effective amount of the compound to a patient in need, with particular emphasis on doses that cross the blood-brain barrier effectively.

Limitations and Scope

The patent claims are narrowly scoped around specific chemical structures, primarily derivatives with particular substitutions. They do not extend to broad classes of heterocyclic compounds but focus on specific structural motifs. This narrow scope incentivizes safeguarding distinct novel compounds rather than broad chemical classes, reducing the risk of generic challenge but requiring continuous innovation to extend claims.

Patent Landscape in Spain and Globally

Regional Context: Spain

Spain's patent system adheres to European Patent Convention (EPC) standards, providing a robust environment for pharmaceutical patents. Patent ES2348688 leverages Spain's patent laws that provide 20-year patent rights from the filing date, with strict novelty and inventive step criteria. The patent's visibility within Spain's research ecosystem underscores its strategic importance, especially given Spain's growing biotech sector.

European and International Patent Environment

Since the patent application aligns with the EPC, applicants may seek validation in multiple European countries, enabling broad market coverage in Europe. The patent landscape in neurodegenerative therapeutics is highly competitive, with multiple patents filed by multinational pharmaceutical firms and biotech startups. Similar patents often focus on:

  • Alpha-synuclein aggregation inhibitors
  • Tau protein modulators
  • Cholinesterase inhibitors with enhanced CNS penetration
  • Novel neurotrophic factors

The novelty and non-obviousness of ES2348688 hinge on the specific chemical modifications claimed. Competitors may challenge the patent via prior art searches focusing on similar heterocyclic compounds.

Globally, the patent landscape is complicated by competing filings in the U.S., China, and Japan, where large pharma entities actively patent therapeutics targeting neurodegenerative disorders. The patent's narrow claims might be tailored to avoid infringement issues while asserting a unique chemical space.

Patent Life Cycle and Litigation Trends

With a 20-year lifespan from the priority date, the patent managed to secure early national protection. While no ongoing litigation has been publicly recorded, the high-value nature of neurodegenerative drugs suggests potential for patent oppositions or licensing disputes, especially in Europe.

Key Patent Strategies

  • Claim Narrowing: The patent employs narrow claims focused on specific derivatives, likely intended to withstand validity challenges.

  • Combination Claims: Inclusion of claims for combination therapies enhances scope, potentially offering broader competitive advantages.

  • Method of Use: Method claims add versatile protection, potentially covering specific treatment regimens, which are critical in neurodegenerative therapy patenting.

  • Patent Family and Continuations: The applicant may seek continuations and divisionals to extend patent life and claim additional derivatives.

Legal Status and Commercial Implications

As of 2023, the patent's legal status indicates it remains in force, with no oppositions registered. Its broad commercial implications depend on subsequent clinical trial success and regulatory approvals. Pending patent expirations could affect lifecycle management strategies, emphasizing the importance of strategic patent filings.

Conclusion

Spain patent ES2348688 reflects a targeted innovation in neurodegenerative therapeutics, with scope primarily around specific heterocyclic compounds and their use. Its narrow claims provide a strategic barrier against challenges while incentivizing further innovation towards related chemical entities. In the broader European and global patent landscape, the patent aligns with ongoing efforts to secure IP rights in a competitive therapeutic domain.


Key Takeaways

  • The patent protects specific heterocyclic compounds designed for neurodegenerative disease treatment, with narrow chemical scope for strong validity.

  • Strategic formulation and method claims expand the patent's protective reach, covering compositions and therapeutic methods.

  • The Spanish patent landscape offers robust protection, with opportunities for filing in Europe and beyond, considering international patent strategies.

  • Ongoing clinical development and patent maintenance are critical for maximizing therapeutic and commercial value.

  • Future patent filings may focus on broader derivatives and combination therapies to extend IP protection in this competitive field.


FAQs

Q1. What is the primary innovation claimed in Spain patent ES2348688?
It claims specific heterocyclic compounds with particular substitutions designed to treat neurodegenerative diseases, primarily Alzheimer's and Parkinson's.

Q2. How broad is the patent's scope?
The scope is narrow, focusing on specific chemical structures and derivatives, which helps in defending against invalidation but limits coverage to particular compounds.

Q3. Can this patent be validated in other countries?
Yes, through the European Patent Convention, applicants can pursue validation in multiple European countries, and potentially through PCT applications for broader international protection.

Q4. What strategic advantages does this patent provide?
It protects a novel class of compounds and methods, enabling potential licensing, partnerships, or exclusive rights during clinical development.

Q5. How does this patent impact competitors in the neurodegenerative field?
It constrains competitors from using similar compounds within the scope of claims, encouraging the development of alternative chemical structures or different therapeutic approaches.


Sources:

  1. Spanish Patent and Trademark Office (OEPM). Patent ES2348688 publication details.
  2. European Patent Office (EPO). Patent landscape reports on neurodegenerative therapeutics.
  3. WHO International Patent Classification (IPC) codes related to neuropharmacology.
  4. Recent market reports on biotech patent filings in Spain and Europe.

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