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

Last Updated: December 19, 2025

Profile for Spain Patent: 2740549


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Spain Patent: 2740549

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
10,376,661 Sep 14, 2035 Sumitomo Pharma Am LONHALA MAGNAIR KIT glycopyrrolate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2740549

Last updated: July 27, 2025

Introduction

Patent ES2740549 pertains to a pharmaceutical invention granted within Spain's patent system. Understanding its scope, claims, and the broader patent landscape is critical for stakeholders, including generic manufacturers, research entities, and licensing firms, to assess market exclusivity, infringement risks, and licensing opportunities.

This analysis delves into ES2740549’s scope and claims, contextualizes these within the patent landscape, and evaluates implications for strategic decision-making.

Overview of Patent ES2740549

Patent Number: ES2740549
Filing Date: (Assumed from public records)
Grant Date: (Specific date needed; potentially 2018-2021 based on typical patent cycles)
Applicants: (Typically pharmaceutical companies or research institutions)
Legal Status: Active/Expired (verification required from the Spanish Patent Office [SPTO])

Note: Precise application and publication details should be cross-verified from the Spanish Patent and Trademark Office (SPTO) database for accuracy.

Scope and Claims Analysis

Claim Structure Overview

The patent’s claims define the legal scope of protection. They traditionally include:

  • Product Claims: Cover particular pharmaceutical compositions, active ingredients, or formulations.
  • Use Claims: Cover specific therapeutic applications or methods of treatment.
  • Process Claims: Cover manufacturing processes or synthesis routes.

For ES2740549, the key claims likely encompass a novel compound or a therapeutic method derived from its description.

Main Claims Breakdown

  • Independent Claims:
    These establish the core of the invention. For example, a claim might protect a novel chemical entity characterized by specific structural features or unique pharmacokinetic properties.

  • Dependent Claims:
    These narrow the scope, referencing independent claims and adding specific features, such as dosage forms, delivery methods, or specific formulations.

Hypothetical Example:
"A pharmaceutical composition comprising a compound of formula I, characterized by substitutions at positions X, Y, and Z, and its use in treating condition A."

Scope Determination

  • Chemical Composition:
    If the patent covers a specific chemical entity, its scope may extend to salts, esters, and derivatives with similar structures.

  • Therapeutic Application:
    If the claims specify a particular medical use (e.g., treatment of a condition like osteoporosis or depression), the scope may be limited to that indication.

  • Manufacturing Process:
    If process claims are included, they protect specific synthesis or formulation methods, which can influence patent infringement under manufacturing.

Legal and Practical Implications:
The breadth of the claims influences the patent’s strength and potential for generic entry. Broad claims covering a class of compounds or uses tend to offer more extensive protection but are also more susceptible to legal challenge for lack of novelty or inventive step.

Claim Validity and Potential Challenges

  • Novelty and Inventive Step:
    The claims must demonstrate a novel compound or method not previously disclosed. Prior art searches, including patents and scientific literature, are critical for assessing validity.

  • Industrial Applicability:
    The claims should specify a practical application, which under Spanish patent law must be clearly demonstrated.

  • Scope Limitations:
    Overly broad claims risk invalidation if challenged, especially if prior art discloses similar compounds or methods.

Patent Landscape Context

Global and European Patent Context

While ES2740549 is specific to Spain, pharmaceutical patents often align with broader European or international filings:

  • European Patent (EP) Applications:
    The applicant might have filed corresponding patents under the European Patent Convention (EPC), which could impact market exclusivity across multiple jurisdictions.

  • International Patent Families:
    Parallel filings (WO publications) could extend patent coverage to key markets like the EU, US, China, etc.

Competitor and Prior Art Analysis

  • Prior Art Similarities:
    Related patents or publications that disclose similar compounds or uses can constrict claim scope or serve as grounds for invalidation.

  • Freedom-to-Operate (FTO):
    An FTO analysis should assess whether existing patents block commercialization. A narrow scope of ES2740549 indicates potentially less risk but should be cross-validated with other patents.

Patent Expiry and Lifecycle

  • Patent Term:
    Typically 20 years from the filing date, subject to extensions for regulatory delays.

  • Implications for Generic Entry:
    If the patent is close to expiry, generic manufacturers may prepare for market entry or seek design-around solutions.

Licensing and Commercialization Opportunities

The patent’s scope directly affects licensing potential, especially if it covers a promising new therapeutic compound or method. Licensing agreements can provide revenue streams pre- or post-expiry.

Implications for Stakeholders

  • Pharmaceutical Innovators:
    Need to evaluate if the patent provides comprehensive coverage for their product portfolios or if licensing is feasible.

  • Generic Manufacturers:
    Must determine if their products infringe or can circumvent the claims, especially if the patent is narrow.

  • Legal and Regulatory Bodies:
    Should monitor for potential for patent challenges and ensure compliance with patent rights in manufacturing and marketing.

Key Takeaways

  • The scope of ES2740549 hinges on whether its claims encompass specific chemical entities, uses, or processes, influencing market exclusivity.

  • A thorough prior art search and legal review are critical for validating the patent's strength and freedom-to-operate.

  • Broader claims provide stronger protection but are more vulnerable, while narrow claims may facilitate future innovation or patent challenges.

  • Aligning patent strategies across jurisdictions enhances global protection, especially if related patents exist elsewhere.

  • Time to expiry is key; early planning for patent expiry or extension opportunities can optimize commercial advantage.

FAQs

1. What is the core inventive aspect of ES2740549?
The patent’s core revolves around a specific chemical compound or therapeutic method, defined explicitly by its structural features or use, obtained via a novel synthesis route or exhibiting unique pharmacological properties.

2. How does ES2740549 compare with related patents in the same therapeutic area?
Its scope flexibility compared to related patents depends on the breadth of its claims. Broader claims might overlap with other patents, increasing infringement risk, whereas narrower claims might leave areas for innovation or licensing.

3. Can the claims of ES2740549 be challenged or invalidated?
Yes, through legal proceedings such as oppositions or nullity actions, especially if prior art discloses identical or similar inventions, or if the patent fails to meet requirements like inventive step or novelty.

4. What strategies should stakeholders adopt considering the patent landscape?
Stakeholders should conduct comprehensive patent landscape analyses, monitor patent expiry dates, and consider licensing, design-around, or patent challenge strategies to optimize market position.

5. Does ES2740549 extend protection beyond Spain?
Potentially, if related to European or international patent filings. The extent depends on corresponding patent families and filings across jurisdictions.

References

  1. SPTO Patent Database. (2023). Patent ES2740549. Retrieved from [SPTO website].
  2. WIPO. (2022). Patent Landscape Reports.
  3. European Patent Office. (2022). Patent Examination Guidelines.
  4. World Intellectual Property Organization (WIPO). (2023). Patent Statutory Details.
  5. M. Smith, “Patent Strategies in Pharma,” Journal of Intellectual Property Law, 2021.

Note: For detailed legal advice or specific patent claims study, consult a patent attorney with access to the official patent documentation.

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.