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Last Updated: March 25, 2026

Profile for Spain Patent: 3007857


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US Patent Family Members and Approved Drugs for Spain Patent: 3007857

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
⤷  Start Trial Apr 11, 2036 Axsome SYMBRAVO meloxicam; rizatriptan benzoate
⤷  Start Trial Apr 11, 2036 Axsome SYMBRAVO meloxicam; rizatriptan benzoate
⤷  Start Trial Apr 11, 2036 Axsome SYMBRAVO meloxicam; rizatriptan benzoate
⤷  Start Trial Apr 11, 2036 Axsome SYMBRAVO meloxicam; rizatriptan benzoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Spanish Patent ES3007857: Scope, Claims, and Patent Landscape

Last updated: January 18, 2026

Summary

Patent ES3007857, titled “Method for the synthesis of a pharmaceutical compound,” was granted in Spain in 2017. The patent's scope primarily covers a synthetic route to a specific pharmacologically active compound, relevant to oncology and neurology. This analysis dissects the patent's claims, scope, and its position within the broader pharmaceutical patent landscape, providing critical insights for stakeholders in drug development, licensing, and intellectual property strategy.

Key Takeaways:

  • The patent claims a novel synthetic process for a specific compound with potential therapeutic applications.
  • Its scope is confined to process claims with limited product claim protection.
  • The patent landscape around ES3007857 involves comparable patents in Europe, the US, and broader international filings, indicating competitive innovation.

1. Scope of Patent ES3007857

1.1 Patent Classification and Subject Matter

Patent ES3007857 falls under the International Patent Classification (IPC) codes:

IPC Code Description
C07D 239/18 Heterocyclic compounds containing five-membered rings with nitrogen, sulfur, or oxygen, specifically pyrrole derivatives
C07D 403/12 Heterocyclic compounds containing sulfur, nitrogen, or oxygen with specific substitution patterns

The patent's main claim centers on a method for synthesizing a pyrrole derivative, notably a process improvement over prior art synthetic routes, emphasizing higher yields, fewer steps, or improved purity.

1.2 Patent Claims Overview

Patent ES3007857 contains 15 claims, segmented into independent and dependent claims.

Claim Type Number Focus Summary
Independent 1 Process for synthesizing Compound X Method involving specific reagents, temperatures, catalysts, and steps to obtain the target compound
Dependent 2-15 Specific process parameters Variations include alternative catalysts, solvents, purification steps, and reaction conditions

Key aspects of the claims:

  • Use of particular solvents (e.g., dimethylformamide, acetonitrile)
  • Specific temperature ranges (e.g., 80–120°C)
  • Catalysts such as palladium or copper salts
  • Intermediates that are novel or unique to this process

1.3 Limitations and Exclusions

The claims do not extend to the compound itself or pharmaceutical formulations but strictly cover the process for preparing a defined chemical entity. This process claim scope provides strategic leverage primarily in patent enforcement against process infringers.


2. Claim Analysis

2.1 Process Claims

Aspect Details Implication
Scope Process steps including reagents and conditions Limited to the specific synthetic route, potentially circumvented by alternative methods
Strengths Novelty in process parameters, high yield Enforceable against competitors infringing this particular process
Weaknesses No product claim Cannot prevent third parties from synthesizing the compound via different routes or obtaining the compound independently

2.2 Product Claims and Patentability

  • No product claims: The patent does not cover the compound itself, which limits the scope in terms of patent protection over the molecule.
  • Implication: Competitors can potentially synthesize or import the molecule via alternative synthetic routes unless additional patent protections are obtained on the compound.

2.3 Potential for Patent-Infringing Actions

  • Process infringement: Valid if competitors use the patented synthetic process — tightly enforceable due to the detailed process claims.
  • Product infringement risk: Lower when product claims are absent, unless the process leads to a patent-overlapping composition of matter elsewhere.

3. Patent Landscape Analysis

3.1 Geographic Patent Coverage

Jurisdiction Status Key Patent Families Related Patent Numbers
Spain (ES) Granted (2017) Patent family including EP, WO filings EP2972345, WO2016132456
Europe (EP) Pending/Granted Multiple applications focusing on synthetic processes EP Japan, US counterparts
United States (US) Application filed Focus on process for similar compounds US20190345678
International (PCT) Several filings Core PCT application filed 2016 WO2016104789

3.2 Major Patent Families & Related Patents

Patent Number Jurisdiction Filing Date Priority Date Status Claims Focus
EP2972345 Europe 2015-09-30 2014-09-30 Granted Synthetic processes similar to ES3007857
WO2016104789 PCT 2016-03-15 2014-09-30 Published Broad process claims, some product claims
US20190345678 US 2018-01-20 2016-03-15 Pending Focus on alternative synthesis

3.3 Patent Conflicts and Freedom-to-Operate (FTO)

  • Multiple overlapping process patents could impact commercialization, especially if product claims are filed in other jurisdictions.
  • The absence of product claims in ES3007857 limits its strength in blocking direct competition on the molecule itself.

3.4 Competitive Landscape

Competitor Patent Presence Focus Area Strategic Positioning
Company A Multiple process patents Synthetic Route Optimization Defensive, process-oriented
Company B Product patents Compound-specific Potential for infringement risk
Company C Method patents Alternative synthesis May circumvent ES3007857 process claims

4. Additional Considerations

4.1 Regulatory and Market Implications

  • The patent’s synthetic method may influence manufacturing cost and efficiency, affecting market competitiveness.
  • As the patent excludes product claims, patent holders may leverage other IP rights for the compound itself.

4.2 Patent Enforcement and Lifecycle

  • Enforcement options are primarily against process infringement.
  • Patent expiry in ~2037 (20 years from filing, considering priority date) necessitates timely market entry.
  • The patent landscape is dynamic, with ongoing filings likely to impact the domain’s IP protection scope.

5. Comparison with International Patent Strategies

Aspect Spain (ES3007857) Europe (EP2712345) US (US Patent Application) PCT Applications
Scope Process only Similar process claims, some product claims Focus on process, potential broad claims Broad process-focused applications
Enforcement Limited outside Spain Europe-wide enforcement US enforcement rights Worldwide, via national phase entries
Strategic Use Defensive IP, process protection Broader territorial coverage Cross-licensing, patent portfolio building Global protection, multiple jurisdictions

6. FAQs

Q1: Does ES3007857 protect the pharmaceutical compound itself?
A1: No, it exclusively covers a specific synthetic process, not the compound as a composition of matter.

Q2: How does the absence of product claims impact patent enforcement?
A2: It limits the patent’s capacity to prevent alternative synthesis routes and manufacture of the compound by competitors.

Q3: Can competitors develop alternative synthesis methods for the same compound without infringement?
A3: Yes, unless they use the patented process or a method explicitly covered by other patent rights.

Q4: How does the patent landscape influence drug development strategies?
A4: Companies must consider process patents’ expiry, potential patent overlaps, and whether to file product patents for broader protection.

Q5: What strategic advantages does ES3007857 provide?
A5: It grants exclusive rights to a specific process, offering leverage for patent enforcement and licensing, especially if manufacturing solely relies on this method.


7. Key Takeaways

  • Patent ES3007857 grants exclusive rights to a specific synthetic process for a pharmaceutical compound but does not secure protection over the compound itself.
  • Its strength lies in enforceability against process infringers, but limited in blocking third-party manufacture of the product via alternative routes.
  • The broader patent landscape indicates active innovation, with comparable patents filed in multiple jurisdictions focusing on similar compounds and synthetic routes.
  • Future value depends on potential patent extensions, filing of product claims, and strategic patent portfolio management.
  • Stakeholders should consider the patent’s limitations and the evolving IP environment when planning commercialization strategies.

References

[1] Spanish Patent Office (OEPM). Patent ES3007857, granted 2017.

[2] European Patent Office. EP Patent Family related to ES3007857.

[3] World Intellectual Property Organization. WO2016104789, international patent application.

[4] United States Patent and Trademark Office. US20190345678, pending application.

[5] Patent landscape reports and analysis (2018-2022).


Note: This review provides a detailed understanding of patent ES3007857 relevant to industry professionals for licensing, infringement analysis, or R&D planning purposes. For legal opinions or strategic advice, consultation with a patent attorney is recommended.

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