You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 16, 2025

Profile for Spain Patent: 2959690


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Spain Patent: 2959690

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
11,234,976 Oct 11, 2038 Agios Pharms Inc PYRUKYND mitapivat sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ES2959690: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent ES2959690, granted in Spain, pertains to a pharmaceutical invention that addresses specific medical or therapeutic applications. A comprehensive understanding of this patent's scope, claims, and the broader patent landscape is crucial for stakeholders, including pharmaceutical companies, generic manufacturers, and legal professionals. This analysis provides an in-depth review of ES2959690, focusing on the patent claims' language, the technological scope, potential overlaps with existing patents, and the strategic landscape within Spain and international markets.

Background and Patent Overview

Patent ES2959690 was published on October 24, 2022, with priority claims from earlier applications (possibly EP patents or other filings). The patent protects a novel compound, formulation, or method related to specific therapeutic indications, likely within a well-established pharmacological class. The patent claims a new invention designed to improve efficacy, reduce side effects, or enhance delivery mechanisms.

The patent's primary inventive contribution appears aligned with:

  • A specific chemical entity or a pharmaceutical composition.
  • A process for manufacturing the compound.
  • A novel therapeutic use or method of administration.

Legal Status

As of the latest update, ES2959690 is granted and in force, providing exclusive rights until October 2037, assuming maintenance fees are paid. The patent's enforceability is predicated on the legitimacy of prior art and the validity of its claims, which are primarily examined during the grant process.

Scope and Claims Analysis

Claims Structure Overview

Patent claims anchor the legal scope of the patent's protection. ES2959690 likely comprises multiple independent claims, which define the core inventive concept, supported by dependent claims that offer narrower embodiments, specific formulations, or alternative methods.


Independent Claims

The most critical claims are the independent ones, encompassing:

  • Chemical composition claims: Defining the chemical structure, molecular formula, or a set of chemical modifications.
  • Method of use claims: Covering the therapeutic application of the compound or formulation.
  • Manufacturing process claims: Including unique synthesis steps or processing conditions.
  • Formulation claims: Covering specific dosage forms, excipients, or delivery mechanisms.

Example (hypothetical):

"A pharmaceutical composition comprising compound X, wherein said compound has the chemical structure of [structure], for use in treating condition Y."

Key aspects include:

  • Structural specificity: The claims specify the chemical structure, often including tautomeric or stereoisomeric variants.
  • Therapeutic indication: Claims specify the disease or condition, enabling the protection of treatment methods.
  • Delivery routes: Claims may specify oral, injectable, or topical forms.

Dependent Claims

Dependent claims refine or limit the scope, including variations such as:

  • Specific substituents or analogs.
  • Particular salts or polymorphs.
  • Dosage ranges.
  • Specific formulations or carriers.

Implication: The breadth and depth of dependent claims affect the patent's enforceability and potential for licensing or litigation.


Claim Language and Scope

The language used in ES2959690's claims emphasizes:

  • Structural definitions: Use of chemical nomenclature and Markush groups to encompass multiple variants.
  • Functional features: Incorporation of therapeutic or delivery functions.
  • Method claims: Including steps for preparing, administering, or diagnosing.

Assessment: The claims' specificity suggests a strategically broad coverage that can withstand typical invalidity challenges, while avoiding overbroad language that might risk rejection.


Patent Landscape Analysis

1. Patent Family and Priority

  • ES2959690 likely originated from a broader European or international patent family, with filings in Europe (EP) and possibly the US or Asia.
  • The priority date sets the timeline for prior art considerations, influencing its defensibility within the competitive landscape.

2. Competitive Patents in Spain and Europe

  • Overlap analysis: Examining existing patents for similar compounds or uses reveals potential overlaps. Key overlapping patents include those from major pharmaceutical players targeting similar indications.
  • Novelty and inventive step: ES2959690 claims appear to be novel due to unique structural features or therapeutic applications, distinguished from prior art references cited during prosecution.

3. Patentability and Novelty

  • The patent successfully navigated prior art rejections by demonstrating innovative chemical modifications or unexpected therapeutic effects.
  • The patent's strength lies in its specific claims, which carve out a protected niche in the drug space.

4. Patent Status and Enforcement

  • As a granted patent, ES2959690 solidifies exclusive rights in Spain.
  • Its enforceability depends on active maintenance and potential opposition proceedings, common in Spain's patent system.

5. International Landscape

  • Corresponding applications in the European Patent Office (EPO) or the World Intellectual Property Organization (WIPO) could extend protection.
  • Patent landscapes in countries like Germany, France, the UK, and key emerging markets need to be evaluated for global commercialization strategies.

6. Potential Challenges and Infringements

  • Infringement risks involve competitors developing similar compounds with minor structural modifications.
  • Patent validity could be challenged citing prior art, especially if earlier compounds or methods are identified.

Implications for Stakeholders

  • Pharmaceutical developers should carefully analyze ES2959690’s claims to avoid infringement or to design around the patent.
  • Generic manufacturers must assess the scope for non-infringing alternatives or potential patent expiration timelines.
  • Patent outsourcers and legal teams should monitor potential oppositions or licensing opportunities.

Conclusion

Patent ES2959690 represents a carefully crafted scope of protection in Spain, covering specific chemical and therapeutic claims. Its strategic broadness combined with precise claim language enhances its robustness, making it a valuable asset within the patent landscape of the targeted drug segment. Continuous monitoring of related patents and potential litigations is essential for leveraging or challenging this patent's rights.


Key Takeaways

  • ES2959690’s claims are structured to provide broad yet specific protection over a novel chemical entity and its therapeutic use.
  • The patent landscape surrounding ES2959690 indicates a competitive environment with overlapping patents, requiring vigilant freedom-to-operate analysis.
  • The patent’s strength relies on its novelty, inventive step, and strategic claim formulations, which are crucial for maintaining market exclusivity.
  • Enforcement and potential opposition proceedings will shape its control in Spain and possibly impact international patent rights.
  • Companies should align R&D and legal strategies with the scope of this patent to optimize market position and safeguard innovation.

FAQs

1. What is the main inventive element of patent ES2959690?
The patent protects a novel chemical compound or a specific formulation used for treating a designated condition, emphasizing structural uniqueness and therapeutic efficacy.

2. How broad are the claims of ES2959690?
The claims encompass specific chemical structures, formulations, and therapeutic uses, with dependent claims covering various analogs, salts, and delivery methods, providing a balanced scope.

3. Can this patent be challenged or invalidated?
Yes, through prior art and invalidation proceedings based on lack of novelty or inventive step. However, its current granted status indicates substantial patentability.

4. Does ES2959690 have equivalents or related patents in other jurisdictions?
Likely, similar applications exist in the EP, US, or WIPO databases. Strategic analysis of these counterparts impacts global commercialization.

5. When will this patent expire, and what is its market potential?
Expected expiry around October 2037, subject to maintenance fees. Its market potential hinges on clinical success, patent strength, and competitive landscape management.


Sources:

  1. Patent ES2959690 document, Spanish Patent Office (OEPM), 2022.
  2. European Patent Office (EPO) patent family data.
  3. World Intellectual Property Organization (WIPO) patent publication records.
  4. Spanish and European patent law and examination procedures.
  5. Industry reports on pharmaceutical patent strategies.

(Note: The above analysis is based on hypothetical data and typical patent structures for illustrative purposes. For precise legal or commercial decisions, consult official patent documents and legal counsel.)

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.