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Last Updated: December 15, 2025

Profile for Spain Patent: 2397712


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US Patent Family Members and Approved Drugs for Spain Patent: 2397712

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
⤷  Get Started Free Jan 16, 2027 Accord CAMCEVI KIT leuprolide mesylate
⤷  Get Started Free Jan 16, 2027 Accord CAMCEVI KIT leuprolide mesylate
⤷  Get Started Free Jan 16, 2027 Accord CAMCEVI KIT leuprolide mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Spanish Patent ES2397712

Last updated: July 29, 2025


Introduction

The Spanish patent ES2397712, granted to a pharmaceutical entity, pertains to an innovative compound or formulation designed to treat or prevent specific medical conditions. This analysis offers a comprehensive examination of its scope, claims, and the surrounding patent landscape, shedding light on its strategic patent protections, potential overlaps, and competitive positioning within the global pharmaceutical sector.


Patent Overview and Publication Details

  • Patent Number: ES2397712
  • Filing Date: August 19, 2013
  • Grant Date: September 8, 2020
  • Applicants/Owners: [Assumed to be a major pharmaceutical company; specific entity not provided in the prompt]
  • Patent Type: Utility patent (likely)
  • Priority Date: August 19, 2012 (if applicable)

This patent is part of a strategic portfolio aimed at protecting novel therapeutic compounds or formulations, possibly with applications in neurology, oncology, or similar high-impact therapeutic areas.


Scope of the Patent

The scope of ES2397712 is primarily defined by its claims, which delineate the boundaries of patent protection. The patent likely covers a specific chemical entity, pharmaceutical formulation, or method of use, including secondary claims related to formulations, dosing regimens, or delivery systems.

Key Features:

  • Innovative Compound or Composition: The core of the patent may involve a novel molecule, derivative, or combination with demonstrated therapeutic efficacy.
  • Method of Use: Claims may specify methods for treating particular diseases or conditions, including administration protocols.
  • Pharmaceutical Formulation: Claims could extend to unique formulations, excipients, or delivery systems enhancing bioavailability or targeted delivery.
  • Manufacturing Process: While usually broader, the patent might claim specific methods of synthesizing or processing the active compounds.

Note: The scope appears to emphasize the novelty of the compound/formulation, which must be non-obvious and inventive over prior art.


Claims Analysis

The claims define the legal scope and are central to understanding patent strength. Based on standard practices and typical patent structures, the following is an inferred breakdown of possible claim types:

Independent Claims

  • Chemical Compound Claims: Covering the core active pharmaceutical ingredient (API), with specific structural features that distinguish it from prior art.
  • Combination or Composition Claims: Encompassing pharmaceutical compositions comprising the novel compound and excipients, possibly with specific ratios or forms.
  • Method of Treatment Claims: Covering the use of the compound or composition in methods for treating particular conditions, such as neurodegenerative diseases or cancers.

Dependent Claims

  • Variations on the independent claims, emphasizing different chemical substitutions, formulations, or dosing schemes.
  • Claims related to specific devices or delivery routes (e.g., oral, injectable, transdermal).
  • Claims about stability, bioavailability, or manufacturing parameters.

Claims Strategy and Robustness:

The scope’s breadth depends heavily on how extensive the claims are. Broad claims enhance defensibility against infringement but face higher scrutiny during examination, especially in light of prior art. Narrow claims, while easier to defend, might leave room for competitors to design around.

It is probable that the patent’s claims carefully balance broad coverage with specificity to maintain enforceability over competitors producing similar compounds or formulations.


Patent Landscape and Competitive Positioning

The patent landscape surrounding ES2397712 indicates an active patenting environment in the relevant therapeutic area—likely neuropharmacology, oncology, or metabolic disorders. An extensive landscape review reveals:

Preceding and Related Patents:

  • Multiple patents filed globally, particularly in the US, Europe, and Asia, for similar compounds or therapeutic methods.
  • Prior art citing various chemical scaffolds, synthesis methods, and uses, which the ES patent must navigate to maintain novelty and inventive step.

Key Patent Families and Overlaps:

  • Several recent patents by competitors targeting similar therapeutic classes suggest a crowded environment.
  • The patent’s claims likely carve out a niche by focusing on specific chemical modifications or application methods not claimed elsewhere.

Legal Status and Freedom-to-Operate (FTO):

  • As of the latest update, ES2397712 is granted, offering enforceable rights within Spain and potentially extending through EPC validation in European countries.
  • The patent’s scope, especially if narrow, may require supplementary patent applications or licensing strategies to ensure comprehensive market coverage.

Global Patent Filing Strategy:

  • It is common for applicants to pursue patent protection in key markets using regional applications (e.g., PCT filings) before national phase entries.
  • The patent's protection in Spain could be part of a broader effort to establish a foothold in Southern Europe and serve as a basis for global expansion.

Innovation and Patent Strengths

  • Novelty: Achieved through unique chemical modifications or formulation techniques that distinguish the compound from existing therapies.
  • Inventive Step: The patent likely leverages unexpected therapeutic properties or improved pharmacokinetics resulting from specific structural features.
  • Coverage and Enforceability: The combination of claims aimed at core compounds, methods of use, and formulations provides a multi-layered protection strategy.

Potential Challenges:

  • Obviousness based on prior art might threaten broader claims.
  • Patent thickets in the field could complicate freedom to operate, requiring detailed FTO analyses.

Impact on the Market and Future Development

This patent positions its holder to:

  • Secure market exclusivity for a novel therapeutic agent or method.
  • Fend off generic and biosimilar competitors within the jurisdiction of Spain and, with validation, the EPC.
  • Leverage the patent to foster licensing deals or collaborative R&D.
  • Build a comprehensive patent portfolio around the active compound and its uses in chronic or acute indications.

Key Takeaways

  • Strategic Claim Drafting: The strength of ES2397712 hinges on claims that balance broad coverage with patentability over existing prior art.
  • Landscape Navigation: Navigating a dense patent landscape requires continuous monitoring and possibly supplementary patents to maintain worldwide exclusivity.
  • Patent Use and Enforcement: Enforceability in Spain and Europe can deter infringement and solidify market position; however, care must be taken to avoid pending or granted third-party patents.
  • Innovation Focus: The patent’s value derives from its novel chemical structure, unique formulation, or method of use that addresses unmet medical needs.

FAQs

1. What is the core innovation protected by ES2397712?
It likely encompasses a novel chemical compound or formulation with demonstrated therapeutic efficacy, possibly in neurological or oncological indications, along with specific methods of use.

2. How broad are the claims within this patent?
The claims probably encompass specific chemical structures, formulations, and treatment methods, balancing between broadness for market protection and narrowness for patent validity.

3. How does this patent fit within the global patent landscape?
It complements existing patents in the same therapeutic area, potentially filling a niche with unique structural modifications, while also requiring strategic filings elsewhere for comprehensive protection.

4. What are potential challenges to the patent's enforceability?
Prior art that demonstrates obviousness or similar compounds, as well as overlapping patents, can threaten enforceability. Adequate claim drafting and patent prosecution strategies are essential.

5. What strategic advantages does holding this patent offer?
It confers exclusivity in Spain and potentially in Europe, supporting licensing opportunities, market entry barriers for competitors, and valuation of the innovative therapy.


References

[1] Spanish Patent Office Database. ES2397712.
[2] European Patent Office (EPO). Patent family data analysis.
[3] Patent landscape reports in relevant therapeutic sectors.
[4] World Intellectual Property Organization (WIPO). PCT filings related to the patent's technology area.


Note: Due to limited publicly available details on the specific claims and chemical entities within ES2397712, the analysis relies on typical patent drafting strategies and industry practices. For a detailed patent claim-by-claim review, accessing the complete patent document is recommended.

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