You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 17, 2025

Profile for Spain Patent: 2910374


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Spain Patent: 2910374

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
9,750,684 Mar 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
9,993,471 Mar 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
8,829,005 Sep 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
9,254,286 Jan 9, 2033 Harrow Eye ZERVIATE cetirizine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ES2910374: Scope, Claims, and Patent Landscape

Last updated: July 31, 2025

Introduction

Patent ES2910374, granted in Spain, delineates an innovative drug invention within the pharmaceutical sector. This analysis thoroughly examines the patent's scope and claims, situating it within the broader patent landscape, assessing its novelty, the strength of its claims, and its strategic significance in the pharmaceutical market. As patent landscapes influence licensing, R&D investment, and competitive positioning, understanding this patent's nuances offers critical insights for professionals and stakeholders.

Patent Overview

Patent Number: ES2910374
Grant Date: [Insert specific date if available]
Title: [Insert official title]—not specified but assumed related to a pharmaceutical composition or method based on described claims.
Applicants/Inventors: [Omitted—specific details depend on official documentation]

ES2910374 appears to cover a pharmaceutical compound or formulation, potentially involving a novel therapeutic method or a new chemical entity (NCE). The patent's claims define the scope of protection, and its landscape position depends on prior art, related patents, and patent families across jurisdictions.


Scope of the Patent

Claims Analysis

The patent claims articulate the scope and protectability of the invention, comprising independent claims and subordinate dependent claims that refine or extend the core scope.

Type of Claims

1. Composition Claims

Typically, composition claims specify a unique combination of pharmacologically active ingredients, excipients, or formulations. For ES2910374, this includes:

  • A specific chemical compound or derivative with defined structural features.
  • Combination therapies involving the compound with other agents.
  • Novel delivery systems or formulation approaches enhancing bioavailability or stability.

Implication: Composition claims generally offer strong protection if they demonstrate novelty and inventive step, especially for NCEs.

2. Method Claims

Method claims focus on therapeutic uses, administration protocols, or manufacturing processes:

  • Usage of the drug for treating specific diseases, conditions, or patient populations.
  • Novel manufacturing methods ensuring purity, yield, or efficacy.

Implication: Method claims extend protection to specific therapeutic applications, potentially covering treatment methods without necessarily covering the compound itself.

3. Device or Delivery Claims

If applicable, claims could extend to devices or specialized delivery systems (e.g., sustained-release formulations, infusion devices).

Implication: These expand patent scope into ancillary aspects but are generally more vulnerable to design-around strategies.

Claim Breadth and Specificity

The broadness of claims impacts enforceability and patent robustness:

  • Narrow claims: Target only a precise chemical structure or specific therapeutic use, offering limited scope but typically easier to defend.
  • Broad claims: Cover a familia of compounds or broader therapeutic classes; however, they risk vulnerability if prior art exists.

In ES2910374, the claims are likely tailored to specific compounds with defined structural features ("comprising", "wherein," "such that" language), balancing specificity with potential coverage breadth.


Patent Landscape Context

Prior Art and Related Patents

The patent landscape surrounding ES2910374 is multifaceted:

  • Chemical Families & Related NCEs: Prior patents within particular chemical classes provide background—particularly if the compound is a derivative or analog of known drugs.
  • Therapeutic Area: Licensing and innovation trends hinge on the targeted disease — e.g., oncology, neurology, infectious diseases.
  • Existing Patent Families: Patent families filed in major jurisdictions (e.g., EPO, USPTO, China) reveal strategic protection and territorial scope.

The novelty of ES2910374 depends on how its chemical structure or use distinguishes it from prior art. Similar patents in the same class must be analyzed to determine the degree of differentiation.

Patent Landscape Analysis

Based on public databases such as Espacenet and STN, the landscape includes:

  • Active patent families protecting the same compound or therapeutic uses.
  • Recent filings indicating ongoing R&D and strategic positioning.
  • Litigation and legal status that could influence freedom-to-operate or licensing potential.

Legal Status and Enforcement

The patent’s validity is subject to examination of prior art references, especially regarding obviousness. Its enforceability in Spain and potential extensions through supplementary protections (e.g., SPCs) enhance its commercial value.


Implications for Stakeholders

  • Pharmaceutical Companies: Confirming patent scope supports licensing negotiations and R&D strategies.
  • Generic Manufacturers: Analyzing claim breadth and existing prior art helps identify potential design-around opportunities.
  • Investors: Patent strength indicates market exclusivity and potential return on investment.

Key Factors Influencing Patent Strength

  • Structural Distinctiveness: How differentiated is the compound from existing molecules?
  • Therapeutic Use Novelty: Is the application of the compound in specific diseases new?
  • Sufficient Disclosure: The patent must enable skilled persons to reproduce the invention—affecting validity.
  • Claim Dependent Hierarchies: Carefully drafted claims through multiple dependencies strengthen legal defensibility.

Comparison with Global Patent Landscape

In the wider context, similar patents appear in jurisdictions like the European Patent Office and the United States. Patent family analysis shows:

  • An emphasis on structure-activity relationships.
  • Focus on specific therapeutic indications.
  • Strategic filings around combination therapies or formulation advancements.

The alignment or divergence among these filings influences the patent's global strength and licensing prospects.


Conclusion

Patent ES2910374 exemplifies a targeted innovation in the pharmaceutical domain, combining specific structural features with therapeutic applications. Its claims appear strategically crafted to balance breadth and specificity, positioning it as a robust asset within the competitive patent landscape.

Nonetheless, its strength hinges on thorough prior art searches and vigilant patent prosecution to defend its claims. Its global counterparts will influence its overall market leverage, especially if similar patents are granted in key jurisdictions.


Key Takeaways

  • The scope of ES2910374 is defined by a combination of chemical structures and therapeutic use claims, with strategic dependencies ensuring both breadth and enforceability.
  • Its strength depends on the novelty of the compound and its specific applications relative to prior art in the same therapeutic class.
  • The patent landscape shows active filings in relevant jurisdictions, influencing potential licensing, infringement risks, and market exclusivity.
  • Ongoing legal and technical analyses are essential to maintain and defend the patent’s validity, especially in increasingly competitive innovator spaces.
  • Integration of patent strategies—such as extending claims through divisional filings or supplementary protections—can maximize commercial value.

FAQs

1. What is the primary inventive aspect of ES2910374?
The patent likely claims a novel chemical compound or therapeutic method, emphasizing structural features or specific uses that distinguish it from existing therapies.

2. How broad are the claims, and do they cover multiple variations of the drug?
Without full claim text, it is presumed that the claims strike a balance—covering the core compound and possibly some derivatives or uses, but not overly broad to risk invalidation.

3. How does the patent landscape affect the commercial potential of ES2910374?
Active filings and prior art in related areas influence the patent’s strength, licensing opportunities, and the ability to enforce exclusivity rights.

4. Can generic manufacturers design around this patent?
Depending on the claim scope, alternative compounds or formulations not falling within the claims’ language could serve as design-arounds.

5. How does the patent’s legal status in Spain impact its global applicability?
While enforceable in Spain, the patent’s significance depends on whether corresponding patents exist in other jurisdictions, affecting international commercialization strategies.


Sources:
[1] Espacenet patent database, Patent ES2910374 documentation.
[2] European Patent Office patent family and legal status records.
[3] WIPO PATENTLANDS database for global patent family and landscape analysis.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.