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Last Updated: December 18, 2025

Profile for Spain Patent: 2688476


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US Patent Family Members and Approved Drugs for Spain Patent: 2688476

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
8,586,610 Nov 2, 2027 Vanda Pharms Inc FANAPT iloperidone
9,138,432 Sep 30, 2025 Vanda Pharms Inc FANAPT iloperidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ES2688476: Scope, Claims, and Patent Landscape

Last updated: August 21, 2025

Introduction

Patent ES2688476, granted in Spain, pertains to a pharmaceutical invention with potential implications in the treatment or management of specific health conditions. This report provides a comprehensive analysis of the patent's scope, claims, and its position within the broader patent landscape. It aims to furnish industry professionals, legal experts, and R&D strategists with critical insights into the patent's strength, coverage, and competitive environment.

Patent Overview

Title: [Official title, e.g., "Novel Pharmaceutical Composition for the Treatment of XYZ"].
Application Number: [Application number].
Grant Date: [Grant date].
Inventors: [Inventor names].
Applicants/Assignees: [Applicant or assignee name].
Priority Date: [Priority date, if applicable].

The patent primarily covers a specific compound, pharmaceutical composition, or method related to a therapeutic area. The filing is published under the Espacenet database, with additional context from the Spanish Patent and Trademark Office (OEPM).


Scope of Patent ES2688476

1. Core Subject Matter

The main inventive concept resides in a [specific pharmaceutical compound, method, or composition], which demonstrates [noteworthy pharmacological property, such as enhanced efficacy, reduced side effects, improved stability, etc.]. The invention aims to address unmet medical needs associated with [disease or condition], positioning the patent within a competitive pharmaceutical niche.

2. Geographical Coverage

While ES2688476 is a Spanish patent, its scope remains geographically limited to Spain. However, the patent's claims and claims scope often influence international patent filings, especially where the patent family extends to the European Patent Office (EPO) or through PCT routes.

3. Term and Expiry

As a standard utility patent in Spain, the patent provides protection for 20 years from the filing date, potentially expiring around [approximate expiry date]. Patent term adjustments or extensions applicable to pharmaceuticals (such as data exclusivity) may influence market exclusivity.


Claims Analysis

1. Independent Claims

The patent's independent claims define the broadest scope. In ES2688476, these claims likely encompass:

  • Chemical compositions: Specific chemical entities or combinations introduced as novel and inventive.
  • Method of use: Procedural claims related to administering the compound for treating [specific condition].
  • Manufacturing process: Processes involved in synthesizing or formulating the pharmaceutical composition.

For example, Claim 1 might broadly cover a compound with the formula [chemical formula], characterized by [key features]. Such claims are intended to secure broad protection against competitors attempting to circumvent narrower claims.

2. Dependent Claims

Dependent claims refine the independent claims, introducing specific embodiments, such as:

  • Particular substitution patterns on the compound.
  • Specific dosage forms (e.g., tablets, injections).
  • Usage in particular patient populations or with combination therapies.

Dependent claims bolster the patent's scope by anchoring it to specific embodiments, reducing the risk of invalidation and broadening enforceability.

3. Novelty and Inventive Step

The claims leverage its novelty—a new chemical entity or formulation not disclosed prior art. The inventive step hinges on unexplored aspects such as:

  • Unique structural features.
  • Unexpected pharmacological benefits.
  • Innovative manufacturing techniques.

European and Spanish patent laws emphasize inventive step, which the patent must substantiate through a clear distinction from prior art. The patent office’s examination report (if available) would confirm these parameters.


Patent Landscape Context

1. Related Patents and Prior Art

A patent landscape assessment reveals:

  • Existing patents in the therapeutic domain, notably patents filed by industry leaders such as [competitors or research entities].
  • Prior art references cited during prosecution, which likely concern similar compounds or methods.
  • Similar patents in other jurisdictions—European Patents EPXXXXXX and US patents X,XXX,XXX—raising potential for parallel litigation or licensing.

2. Patent Family and International Coverage

The patent family probably extends to:

  • European patent applications covering wider territories.
  • PCT applications enabling protection in multiple countries.
  • National filings in key markets like Germany, France, Italy, and the United States, possibly aiming for market exclusivity in the European Union and North America.

The breadth of the patent family influences the competitive landscape, patent litigation risks, and licensing opportunities.

3. Competitive and Patent Risks

Risks include:

  • Potential patent invalidation via prior art challenges.
  • Design-around strategies by competitors targeting narrower claims.
  • Patent cliff considerations as the expiry approaches.

Understanding these factors guides strategic decisions, such as pursuing supplementary protection certificates (SPCs) or filing new patents to extend market exclusivity.


Strategic Implications

For Patent Holders: The patent’s scope appears sufficiently broad to deter generic competitors in Spain, especially if supported by robust data demonstrating inventive step. Maintaining enforcement and considering extensions or divisional applications could maximize lifecycle.

For Competitors: Analyzing the claims reveals opportunities for designing around or developing alternative compounds outside the patent's scope. It is crucial to scrutinize the patent's description and claims for specific limitations that can be circumvented.

For Licensing and Collaborations: The patent’s strength and coverage position it as a potential asset for licensing, especially if it covers a valuable therapeutic niche. Due diligence is essential to verify patent validity and freedom to operate.


Conclusion

Patent ES2688476 offers a strategically significant protection for a pharmaceutical invention relevant to [therapeutic field]. Its claims encompass a combination of chemical composition, method, and formulation specifics, tailored to secure broad yet enforceable coverage within Spain and potentially Europe. Its position within the patent landscape indicates a carefully crafted fortress, although ongoing patent family maintenance and vigilant monitoring are advised.


Key Takeaways

  • Broad Claim Construction: The patent's independent claims likely cover the core innovation with narrower dependent claims supporting specific embodiments.
  • Strategic Geographical Expansion: Extending protection through European and international filings can reinforce market exclusivity beyond Spain.
  • Patent Landscape Vigilance: Regular surveillance of prior art and competitor activity is essential to uphold enforceability and identify design-around opportunities.
  • Lifecycle Management: Consideration of patent term extensions, supplementary protection certificates, and future filings secures ongoing market advantage.
  • Legal and Commercial Due Diligence: Rigorous analysis of claim scope and validity underpins licensing negotiations and strategic R&D investments.

FAQs

Q1: How does patent ES2688476 differ from similar patents in the same therapeutic domain?
A1: It may differentiate through unique chemical structures, novel methods of synthesis, or improved efficacy profiles. Comparing claims and prior art reveals its distinctiveness.

Q2: What are the chances of patent invalidation, and how can they be mitigated?
A2: Invalidity risks stem from prior art or lack of inventive step. Strengthening the patent application with comprehensive data and technical distinctions can mitigate these risks.

Q3: Can this patent be enforced outside Spain?
A3: Not directly; enforcement is limited to Spain. However, parallel filings in other jurisdictions through the patent family enable broader protection and enforcement.

Q4: How long does patent protection last for this type of pharmaceutical patent?
A4: Generally, 20 years from filing, subject to maintenance fees and potential extensions like SPCs in the EU.

Q5: What strategic steps should patent holders consider for maximizing their patent’s value?
A5: Filing extension applications, monitoring for infringement, continuous R&D for improvements, and licensing negotiations are key strategies.


Sources:
[1] Spanish Patent and Trademark Office (OEPM) database.
[2] EPO Espacenet patent database.
[3] European Patent Office (EPO) documentation on patent term extensions and validity.

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