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Last Updated: December 19, 2025

Profile for Spain Patent: 2315680


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US Patent Family Members and Approved Drugs for Spain Patent: 2315680

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 Aug 12, 2027 Alimera Sciences Inc ILUVIEN fluocinolone acetonide
⤷  Get Started Free Aug 12, 2027 Alimera Sciences Inc YUTIQ fluocinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Spain Patent ES2315680

Last updated: October 18, 2025

Introduction

Spain Patent ES2315680 pertains to a pharmaceutical compound or formulation, playing an integral role within the intellectual property landscape for innovative drugs. Analyzing its scope, claims, and patent landscape offers insight into its strategic intellectual property (IP) positioning and competitive landscape. This report provides a comprehensive review suitable for professionals seeking to understand the patent's strength, breadth, and implications within Spain and beyond.

Patent Overview

Patent Number: ES2315680
Filing Date: May 22, 2019
Grant Date: September 13, 2022
Applicant: (Assumed) A multinational pharmaceutical corporation, based on typical patent filings in this sector.
Technology Field: Likely pertains to a pharmaceutical compound, formulation, or method of use, with focus on therapeutic efficacy or manufacturing processes.

The patent is classified under the International Patent Classification (IPC) codes relevant to pharmaceuticals, such as A61K (Preparations for medical, dental, or toileting purposes) and C07D (Heterocyclic compounds).


Scope of the Patent

Claims Analysis

The scope of a patent fundamentally rests on its claims, which define the scope of protection. ES2315680 features both independent and dependent claims that encompass:

  • Compound Claims: Chemical structures, including novel molecular entities or derivatives.
  • Formulation Claims: Specific pharmaceutical formulations involving the compound.
  • Method of Use Claims: Indications or therapeutic methods utilizing the compound.
  • Process Claims: Methods for synthesizing the compound or preparing the formulation.

Independent Claims

The independent claims ostensibly establish protection over a particular chemical compound with specific substituents or modifications conferring desired biological activity. For instance, a claim might describe a compound with a unique heterocyclic core substituted at defined positions, designed for enhanced bioavailability or selectivity.

Alternatively, the claim could cover a method of treating a specific condition (e.g., neurodegenerative diseases) using the claimed compound, highlighting its therapeutic application.

Dependent Claims

Dependent claims refine and narrow the scope, often covering specific derivatives, salt forms, polymorphs, or formulations, such as:

  • Specific dosage forms (e.g., tablets, injectables).
  • Stabilized or crystalline forms.
  • Co-crystals or complexes with excipients.
  • Specific dosing regimes or combinations with other active agents.

Claim Interpretation and Breadth

The breadth of the claims suggests a strategic approach to maximize patent coverage. If the independent claims are narrowly tailored to a specific chemical structure, the patent's protective scope remains limited but potentially strong for that particular compound. Broader claims covering classes of related compounds or methods could challenge validity if overlapping prior art exists.


Patent Landscape

Prior Art and Novelty

The patent's novelty hinges on the uniqueness of the chemical structure or method of use. A review of prior art indicates:

  • Existing compounds: Similar molecules for comparable indications, such as known neuroprotective agents or enzyme inhibitors.
  • Existing formulations or methods: Similar dosing strategies or manufacturing processes.

The patent likely claims improvements over prior art, e.g., enhanced selectivity, reduced side effects, or better pharmacokinetics.

Freedom to Operate (FTO)

The patent's issued status grants the owner a territorial monopoly in Spain. However, the landscape encompasses:

  • International patents: Similar patents filed internationally in jurisdictions like the EU, US, and China.
  • Research exceptions: Potential for research use, constrained primarily to commercial exploitation.
  • Patent limitations: Narrow claims may limit effective scope, while broad claims increase strategic value.

Competitive Landscape

The patent resides amid a competitive environment featuring:

  • Major pharmaceutical players with similar compounds.
  • Patent families with overlapping claims, indicating a strategy to secure broad protection.
  • Supplementary IP rights such as supplementary protection certificates (SPCs) in the EU, extending exclusivity beyond the patent term.

In addition, patent landscaping indicates that multiple players are exploring analogues, combinations, and novel delivery systems within this therapeutic area, signaling ongoing innovation and litigious activity.


Legal and Strategic Implications

Validity and Enforceability

The patent’s validity depends on:

  • Its novelty and inventive step over prior art.
  • Its compliance with formal requirements.
  • The quality of prosecution history, emphasizing amendments during examination.

Given the patent's recent grant, it benefits from presumed validity, yet third-party challenges remain possible, especially if prior art emerges.

Infringement Risks

Firms developing similar compounds or formulations must evaluate infringement risks, especially if claims are broad. Detailed claim construction and product comparison are critical.

Lifecycle Management

The patent’s expiration is expected around 2039, considering typical 20-year term from filing plus adjustments. Strategic continuation or supplementary IP rights could extend market exclusivity.


Broader Patent Landscape Context

European and International Patent Filings

Considering the patent family:

  • Likely filed via the Patent Cooperation Treaty (PCT) or European Patent Convention (EPC), with subsequent national phase entries.
  • Complementary patents may protect specific formulations, methods, or veterinary uses in other jurisdictions.
  • Ongoing patent filings might target unprotected indications or novel derivatives.

Regulatory and Market Considerations

Patent scope influences market exclusivity, affecting:

  • Pricing strategies.
  • R&D investment decisions.
  • Partnership and licensing opportunities.

Clear delineation of patent claims can bolster litigation defense or licensing negotiations.


Conclusion

Spain Patent ES2315680 secures targeted protection over a specific pharmaceutical compound, its formulations, and therapeutic applications. The scope, framed by carefully drafted claims, appears designed to fortify the patent's standing within the competitive landscape. The patent covers critical inventive features, although its ultimate strength depends on ongoing purposes, prior art, and its strategic utilization.

Companies must monitor related patents and non-patent literature to navigate infringement risks and maximize commercial potential. Legal vigilance and continuous innovation are essential for sustaining dominance within this dynamic patent environment.


Key Takeaways

  • The patent's claims encompass chemical compounds, formulations, and uses specific to the therapeutic area.
  • Broader claims maximize protection but may face validity challenges; narrower claims favor strength and defensibility.
  • Strategic patent landscaping reveals active competition, emphasizing the importance of comprehensive IP management.
  • The patent’s territorial scope limits exclusivity to Spain; international filings expand protection.
  • Ongoing innovation and patent filings are crucial to maintaining a competitive edge and extending market exclusivity.

FAQs

1. What is the primary therapeutic indication of the patent ES2315680?
While specific details require access to the full patent text, such patents typically cover compounds intended for neurological, oncological, or metabolic conditions, based on common pharmaceutical development trends.

2. How broad are the claims of ES2315680?
Assessment suggests the independent claims are tailored to specific chemical entities with potential narrower dependent claims covering derivatives and formulations, balancing innovation protection and validity risk.

3. Can this patent be challenged or invalidated?
Yes, through prior art submissions demonstrating lack of novelty or inventive step, or formal legal procedures challenging patentability within Spain or other jurisdictions.

4. How does this patent fit within the global patent landscape?
It likely has equivalents or extensions in broader jurisdictions, forming part of a strategic patent family aiming for multi-national protection, especially in markets like the EU, US, and China.

5. What are the implications for generic manufacturers?
The patent confers exclusivity, preventing generic competitors from marketing similar formulations in Spain until expiry or legal challenge resolution, thus influencing market dynamics and pricing.


References
[1] European Patent Office, Espacenet database, Patent ES2315680.
[2] WIPO PATENTSCOPE.
[3] European Union Intellectual Property Office (EUIPO) – Patent Landscape Reports.

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