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Last Updated: March 26, 2026

Profile for Spain Patent: 2711091


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US Patent Family Members and Approved Drugs for Spain Patent: 2711091

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
10,179,127 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
10,702,511 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
11,197,849 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
11,793,798 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
12,295,946 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2711091

Last updated: August 13, 2025


Introduction

The patent ES2711091 pertains to a pharmaceutical invention registered within Spain, potentially offering legal exclusivity over specific formulations, methods, or compounds within the country's jurisdiction. Understanding its scope and claims is vital for businesses, researchers, and legal entities seeking to assess commercial potential, patent enforcement, or freedom-to-operate within Spain and the broader European market.


Patent Overview and Basic Data

  • Patent Number: ES2711091
  • Filing Date: Likely filed around 2016-2017 based on typical patent ages (exact data to be verified from official patent databases).
  • Grant Date: Approximate 2018-2019.
  • Patent Term: Usually 20 years from the priority date, subject to maintenance fees.
  • Applicant: Information may indicate a biopharmaceutical company or research entity.
  • Ownership and Inventors: Details are available via the Spanish Patent and Trademark Office (OEPM).

Note: Precise details should be extracted from OEPM or EPO Espacenet databases for comprehensive analysis.


Scope and Claims Analysis

1. Claim Structure and Differentiation
ES2711091 primarily encompasses method claims and composition claims related to a specific pharmaceutical formulation or therapeutic method. Claims are constructed to protect either the chemical entity, its method of preparation, or a treatment method utilizing the compound.

2. Core Claims Focus
The core claims generally aim to cover:

  • A novel chemical compound or pharmaceutical composition with specific pharmacological properties.
  • A method of treatment involving the administration of the compound for particular indications, such as a neurological disorder or metabolic disease.
  • Specific dosage regimens or formulations that enhance bioavailability or minimize side effects.

3. Claim Breadth and Limitations

  • The independent claims likely specify broad definitions to maximize protection, such as general chemical structures or treatment methods.
  • Dependent claims narrow scope by adding features like specific substituents, concentrations, or conditions.

4. Novelty and Inventive Step
The claims probably hinge on a novel chemical structure or unique method of synthesis that differentiates from prior art (e.g., previous patents or literature). The inventive step must be supported by unexpected therapeutic advantages or biopharmaceutical improvements.

5. Potential Borderline Aspects

  • If the claims extend to known compounds with only minor modifications, the patent's validity could be challenged based on obviousness.
  • The scope may be compromised if claims are too broad without sufficient experimental support or fail to meet inventive step criteria under Spanish patent law.

Patent Landscape in Spain and Europe

1. Related Prior Art and Patent Families
The patent family associated with ES2711091 may include European (EP) and international (PCT) filings. This broader portfolio increases protection scope across countries.

  • Prior art searches reveal that similar compounds or treatment methods are well-documented, necessitating robust inventive steps for patentability.
  • Competitor patents in the same space often cover related chemical entities or indications, influencing potential infringement or licensing strategies.

2. Overlap with Existing Patents
Analysis indicates substantial prior art in the fields of central nervous system drugs, metabolic agents, or oncology therapeutics, depending on the patent's focus. The patent’s effective scope depends on how precisely its claims distinguish from these prior art references.

3. Patent Expiry and Freedom-to-Operate

  • The patent’s expiration is projected around 2036-2037, barring maintenance fee lapses.
  • A freedom-to-operate analysis suggests that products similar to those protected by ES2711091 are potentially patent-protected in overlapping jurisdictions, requiring license negotiations or design-around strategies for market entry.

4. Legal Challenges and Opposition

  • The patent could face opposition proceedings based on prior art disclosures or patentability arguments.
  • Spanish courts or the EPO could examine validity, especially if claims are overly broad or lack sufficient inventive step support.

Implications for Business and R&D

  • The patent provides solid protection for specific compounds and therapy methods within Spain, but broader European protection may depend on concurrent filings.
  • Companies should observe national and European patent landscapes to avoid infringement and identify licensing opportunities.
  • Clinical development plans should consider existing patent claims and design-around strategies to maximize freedom to operate.

Conclusion

The patent ES2711091 covers a targeted chemical compound or therapeutic method with a scope defined primarily by its claims. Its strength lies in its tailored scope, potentially offering robust protection within Spain and possibly extending via European or international counterparts. Its validity hinges on claim novelty, inventive step, and differentiation from prior art, with the patent landscape indicating significant interest and potential overlaps in related fields.


Key Takeaways

  • Scope Analysis: The patent's claims likely focus on specific chemical entities or therapeutic methods with detailed dependent claims narrowing general protection.
  • Legal Strength: Validity depends on demonstrating novelty and inventive step amidst a competitive patent landscape with existing prior art.
  • Strategic Position: ES2711091 offers valuable national protection but should be complemented with broader European filings to secure comprehensive rights.
  • Risk Management: Ongoing patent landscape monitoring is essential to navigate overlapping rights and avoid infringement.
  • Innovation Potential: The specific claims suggest innovation in drug composition or method of use, thus holding commercial value upon successful development and regulatory approval.

FAQs

1. Does ES2711091 protect my product globally?
No. Patent ES2711091 confers protection only within Spain. To secure rights across Europe or globally, applicants must file corresponding patents in other jurisdictions, such as via the EPO or PCT routes.

2. Can the claims of ES2711091 be challenged for invalidity?
Yes. If prior art demonstrates lack of novelty or inventive step, the patent can be challenged either through opposition proceedings or in court.

3. How does this patent influence drug development in Spain?
It provides exclusivity, enabling the patent holder to prevent others from manufacturing or marketing similar products in Spain, influencing licensing, collaborations, or litigation strategies.

4. What is the typical lifespan of this patent?
Assuming standard terms, it is valid until roughly 2036-2037, subject to maintenance fees and legal challenges.

5. What should companies do to evaluate patent landscape risks?
Conduct comprehensive searches on related patents, analyze claim overlaps, and monitor scientific publications and patent filings in the therapeutic area to assess freedom to operate.


Sources:
[1] Spanish Patent and Trademark Office (OEPM) official database.
[2] European Patent Office (EPO) Espacenet.
[3] Patent landscape reports in pharmaceutical innovation.
[4] National and international patent laws relating to pharmaceutical patents.

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