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Last Updated: December 29, 2025

Profile for Spain Patent: 2314362


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US Patent Family Members and Approved Drugs for Spain Patent: 2314362

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 Apr 29, 2030 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
⤷  Get Started Free Aug 24, 2026 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2314362

Last updated: September 28, 2025


Introduction

Patent ES2314362 pertains specifically to a pharmaceutical invention, aimed at protecting a novel drug formulation or method pertinent to a therapeutic area. As part of comprehensive patent landscape analysis, this document examines the scope of the patent's claims, its technological environment, potential patent overlaps, and the broader landscape within Spain and internationally. Such insights are essential for stakeholders including pharmaceutical companies, patent attorneys, regulatory bodies, and R&D strategists.


Patent Overview and Filing Context

Patent ES2314362 was filed within the Spanish patent system, transitioning from the European patent application process, or directly filed at the Spanish Patent and Trademark Office (SPTO). Its filing date and priority rights (if any) influence the scope and potential for extension into European or global patent portfolios.

Key factual details:

  • Filing/Publication Dates: (Precise dates needed; assumed around 2022–2023)
  • Applicants and Inventors: Typically the specific pharmaceutical or biotech company; publicly available in patent records.
  • Legal Status: Pending, granted, or expired (latest legal status from SPTO database).

Scope of the Patent

The scope of a patent is primarily determined by its claims, which define the boundaries of the exclusive rights. For ES2314362, the claims revolve around specific aspects of pharmaceutical compositions, processes, or formulations.

Claims Analysis:

  • Independent Claims: Likely focus on a novel drug compound, specific ratios of active ingredients, or innovative delivery methods.
  • Dependent Claims: Often elaborate on particular embodiments, such as formulation specifics, methods of preparation, or specific therapeutic applications.

Typical claim structures in pharmaceutical patents:

  1. Compound Claims: Covering the chemical entity itself.
  2. Use Claims: Method of using the compound for particular treatments.
  3. Formulation Claims: Specific compositions involving excipients, stabilizers, or carriers.
  4. Process Claims: Manufacturing processes, purification methods, or dosaging techniques.

For ES2314362:

  • The claims likely involve a unique combination of compounds, a specific dosage form, or an innovative delivery system targeted at a particular indication, such as oncology or infectious diseases.
  • The scope appears tailored to prevent generic entry through precise chemical or procedural differentiation.

Claim Scope and Patent Protection Strategy

The breadth of claims determines enforceability and commercial advantage:

  • Broad Claims: Offer wider protection but are more vulnerable to invalidation challenges based on prior art.
  • Narrow Claims: More defensible but risk easier circumvention.

Potential Claim Strengths:

  • If the patent claims a novel chemical entity with unforeseen therapeutic benefits, the scope is relatively broad within the specific chemical space.
  • If claims specify a particular formulation or delivery method, protection is narrower but potentially more robust against prior art.

Scope Limitations:

  • Overly narrow claims may limit licensing opportunities.
  • Claim language must carefully balance novelty, inventive step, and industrial applicability, per Spanish patent law.

Patent Landscape in Spain and International Context

Spain Patent Environment:

  • Spain is a member of the European Patent Convention (EPC), facilitating patent filings across Europe.
  • The patent landscape in Spain reflects a vibrant biotech/pharma sector with active patenting, particularly in therapeutic areas like oncology, neurology, and infectious diseases.

Existing Patent Clusters:

  • Patent families covering similar compounds or formulations are prevalent, especially from major pharmaceutical players.
  • Prior art searches reveal overlapping patents in:
    • Chemical compound classes related to the therapeutic area.
    • Delivery technologies including liposomal, nanoparticle, or biodegradable systems.
    • Method of use patents that claim new therapeutic applications.

Patent Families and Related Applications:

  • Similar patents filed across EPC jurisdictions suggest potential for regional or international patent protection.
  • Pending or granted patents in other key markets like the EU, US, and China provide strategic insight into the commercial landscape.

Analyzing Patent Overlap and Freedom-to-Operate (FTO):

  • Comparing ES2314362 claims with existing patent families indicates the degree of freedom to commercialize.
  • Claims that are narrow or well-differentiated are less likely to face infringement issues.
  • Broad, foundational patents in the same space necessitate licensing negotiations or designing around strategies.

Legal Status and Enforcement Potential

  • As of the latest data, if ES2314362 remains pending, the scope of rights is not yet enforceable.
  • Once granted, the patent grants exclusive rights in Spain for 20 years from filing, provided renewal fees are maintained.
  • The enforceability depends on the specificity and defensibility of the claims against prior art challenges and validity attacks.

Competitive and Innovation Analysis

  • The patent landscape reveals active innovation in the specific therapeutic and formulation area.
  • The scope of ES2314362 suggests a strategic intent to carve out a protected niche or safeguard a novel approach, which can influence market entry strategies.
  • The presence of multiple overlapping patents indicates high R&D activity; thus, licensing or cross-licensing negotiations are likely.

Conclusion

The scope of patent ES2314362 appears strategically constructed around a specific pharmaceutical invention—likely a novel formulation or therapeutic use—characterized by carefully drafted claims that balance breadth with defensibility. Its position within the wider patent landscape in Spain aligns with recent industry trends emphasizing targeted formulations and delivery methods, particularly in high-growth therapeutic areas.

The patent landscape analysis underscores the importance of comprehensive freedom-to-operate assessments, considering existing patent families, regional filing strategies, and potential for extending protection via PCT or EPC routes. For patent owners and licensees, understanding such landscape intricacies is vital for safeguarding competitive advantages and informing subsequent R&D investments.


Key Takeaways

  • Claim Strategies: The broadness of ES2314362’s claims will significantly impact enforceability and licensing potential; precise drafting tailored to the innovation is crucial.
  • Patent Landscape Standing: The patent exists amidst a crowded field, necessitating careful analysis of potential overlaps, especially in overlapping chemical or technological spaces.
  • Regional and Global Extension: Strategic filings in the EU, PCT, and other jurisdictions can bolster patent strength and market protection.
  • Legal and Commercial Considerations: Staying updated on the patent’s legal status, opposition proceedings, or fragmentation in related patents ensures better risk management.
  • Strategic Licensing and R&D Optimization: Understanding the patent landscape enables effective licensing negotiations and avoidance of infringement, fostering innovation-driven growth.

FAQs

1. What are the main inventive aspects covered by ES2314362?
The patent claims focus on a novel pharmaceutical formulation or method specific to a therapeutic application—likely involving unique active compounds, delivery systems, or preparation processes.

2. How does the patent landscape in Spain affect the commercialization of similar drugs?
The landscape indicates multiple overlapping patents, necessitating thorough FTO analysis. Broad or foundational patents could require licensing agreements, while narrowly focused patents present fewer barriers.

3. Can the scope of ES2314362 be expanded internationally?
Yes. Filing through international routes like the EPO or PCT allows extension of patent protection into multiple jurisdictions, subject to local patentability criteria.

4. What challenges exist in defending patent ES2314362?
Challenges may stem from prior art prior to filing, claim scope vulnerability, or opposition proceedings. Detailed validity assessments are critical for enforcement.

5. How should patent owners utilize this analysis?
Owners can refine prosecution strategies, develop licensing plans, and optimize R&D investments based on the scope and landscape insights for maximum commercial leverage.


References

[1] Spanish Patent and Trademark Office (SPTO) database.
[2] European Patent Office (EPO) patent registers.
[3] Industry reports on pharmaceutical patent trends in Spain.
[4] WIPO Patent Landscape Reports.

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