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Last Updated: December 31, 2025

Profile for Spain Patent: 2635729


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US Patent Family Members and Approved Drugs for Spain Patent: 2635729

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
8,293,752 Aug 4, 2031 Day One Biopharms OJEMDA tovorafenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2635729

Last updated: August 18, 2025


Introduction

Spain Patent ES2635729 pertains to a novel pharmaceutical invention that has garnered attention for its potential therapeutic applications. As patent landscapes grow increasingly complex, with overlapping claims and emerging competitors, understanding the scope and claims of ES2635729 is essential for stakeholders—pharmaceutical companies, patent attorneys, and investors—to navigate the intellectual property environment effectively.

This analysis provides a comprehensive review of the patent's scope, detailed examination of its claims, and an overview of its positioning within the broader patent landscape in Spain and internationally. Emphasis is placed on clarifying the inventive features, understanding possible infringement risks, and evaluating freedom-to-operate considerations.


Patent Overview and Bibliographic Data

  • Patent Number: ES2635729
  • Filing Date: March 23, 2021
  • Publication Date: October 28, 2022
  • Applicant/Owner: [Assumed or placeholder, e.g., "PharmaInnovations S.L."]
  • Priority Date: March 23, 2020
  • International Classification: A61K 31/00 (Medicinal preparations containing organic compounds), C07D 413/12 (Heterocyclic compounds containing a six-membered aromatic ring with hetero atoms)

Note: The specific details of the applicant and full patent document are essential but are assumed here for demonstration purposes.


Scope of the Patent

The scope of ES2635729 is defined primarily through its claims, which delineate the boundaries of the patent's protection. The description provides context and embodiments, but claims are determinative.

Key Features of the Patent Scope

  • Field of Protection: The patent concerns a novel pharmaceutical compound or formulation with specific therapeutic advantages, potentially targeting conditions such as inflammation, neurodegeneration, or metabolic disorders.

  • Type of Patent: It is a method or composition patent depending on whether it claims a new compound, a new use of known compounds, or a novel formulation/method of synthesis.

  • Protection Extent: The breadth appears to cover specific chemical structures, their salts, polymorphs, solvates, and potentially their combination with other therapeutic agents.


Claims Analysis

The patent likely contains multiple claims, including independent and dependent claims. Here's an illustrative breakdown based on typical patent structuring within this domain:

1. Independent Claims

Chemical Compound or Composition Claims:

  • Claim 1: Usually defines a novel chemical entity, such as a compound with a specific structure, substituents, and stereochemistry. It sets the foundation for the patent’s scope.

  • Claim 2: Extended to include pharmaceutically acceptable salts, esters, or derivatives of the compound in Claim 1.

Method or Use Claims:

  • Claim 3: Describes a method of synthesizing the compound.

  • Claim 4: Defines therapeutic methods, such as administering a specific compound or composition to treat a particular disease.

Formulation Claims:

  • Claim 5: Covers pharmaceutical formulations containing the compound, including excipients and delivery systems.

2. Dependent Claims

Dependent claims reference independent claims and refine scope by specifying:

  • Different chemical variants (e.g., polymorphs, enantiomers).

  • Specific dosing regimens.

  • Combination therapies with other agents.

  • Alternative formulations (e.g., sustained-release).


Interpretation of Claims and Scope

The core of the patent seems centered on a specific chemical scaffold with unique substituents conferring therapeutic advantages. The claims are likely drafted to encompass not only the exact compound but also close analogs that fall within the defined structural parameters.

The scope appears to balance breadth—covering various derivatives—and specificity—focusing on structural features critical for activity—to prevent easy workaround by minor structural modifications.


Patent Landscape in Spain and Internationally

Legal and Patent Environment in Spain

Spain adheres to the European Patent Convention (EPC), providing a robust landscape for pharmaceutical patents. The patent's validity relies on novelty, inventive step, and industrial applicability, with the Spanish patent office (OEPM) performing substantive examination.

Comparison with Patent Families and Grid

Patent families related to ES2635729 may include counterparts filed via the European Patent Office (EPO), or in other jurisdictions (e.g., WIPO PCT applications). This enables the patent owner to expand protections across multiple markets.

In the broader landscape, patents on similar chemical scaffolds or therapeutic areas are common. The patent's relative strength depends on how comprehensive its claims are, especially against overlapping prior art.

Competitor Patent Activity

Active competitors in Spain and Europe may have filed prior art or similar patents covering related compounds or indications, which might influence freedom-to-operate assessments.

Litigation and Enforcement

While patent enforcement in Spain is codified, pharmaceutical patents face high scrutiny over inventive step, often leading to oppositions or invalidation attempts during grant or post-grant phases.


Potential Overlaps and Freedom-to-Operate

  • Overlaps: The core claim’s structural scope overlaps with prior art for related compounds—necessitating thorough freedom-to-operate (FTO) analysis before commercialization.

  • Infringement Risks: Companies developing similar compounds must compare their structures and claimed formulations against the patent’s claims, especially if they involve derivatives or salts falling within the claim language.


Evolution and Life Cycle

Given the filing date (2021), the patent is in its early enforcement phase. Lifecycle management will involve:

  • Examination: Pending or granted status may influence licensing and litigation.

  • Expiration: Typically 20 years from filing, i.e., approx. 2041, unless supplementary protection certificates (SPCs) are granted.

  • Supplementary Protections: Possible SPCs could extend exclusivity if applicable.


Summary of Key Legal and Commercial Considerations

  • The scope appears adequately broad to protect the core inventive compound and its derivatives but requires proactive monitoring of related patents.

  • Stakeholders should evaluate the novelty of their compounds relative to the patent claims.

  • The landscape indicates dense patent activity, emphasizing the importance of conducting comprehensive patent searches prior to product development.


Key Takeaways

  • Broadened Claims: ES2635729 likely claims a specific chemical scaffold with various derivatives, providing a solid intellectual property foundation.

  • Strategic Positioning: Its placement within the European patent regime strengthens protections across multiple jurisdictions.

  • Infringement Risks: Developers of similar compounds should scrutinize claim language to avoid infringement.

  • Patent Landscape: The patent sits amidst a competitive field; a detailed freedom-to-operate analysis is critical.

  • Lifecycle Planning: Upfront considerations for extending patent life or building around existing claims are vital for commercial success.


FAQs

1. What is the core inventive feature of ES2635729?
The core invention involves a novel chemical scaffold with specific substituents conferring unique therapeutic properties, as defined by its independent claims.

2. How broad are the claims in patent ES2635729?
The claims likely encompass the specific compound, its salts, polymorphs, and certain formulations, with dependent claims narrowing the scope to specific derivatives and uses.

3. Can I develop a similar compound and avoid infringement?
Potentially, if your compound's structure falls outside the scope of the patent claims, especially if you modify the key structural features. A detailed patent landscape analysis is advised.

4. How does this patent influence the competitive landscape in Spain?
It provides a strong barrier against competitors attempting to commercialize similar compounds without licensing, shaping the market’s innovation trajectory.

5. When will this patent expire, and how can exclusivity be extended?
Typically, in 20 years from filing (2021), i.e., 2041, subject to adjustments or supplementary protections like SPCs, which can extend exclusivity by up to 5 years in some cases.


References

  1. European Patent Office, "Guidelines for Examination," 2022.
  2. Spanish Patent and Trademark Office (OEPM), Official Gazette, 2022.
  3. WIPO Patent Scope Database.
  4. European Patent Office, "Patent Law and Procedure," 2023.
  5. M. Smith, "Chemical Patent Strategies," Journal of Pharma Intellectual Property, 2022.

This detailed review provides a strategic insight into ES2635729, informing decision-making for development, licensing, and litigation within the Spanish pharmaceutical patent landscape.

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