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Last Updated: December 12, 2025

Profile for Spain Patent: 2621915


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US Patent Family Members and Approved Drugs for Spain Patent: 2621915

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
⤷  Get Started Free Oct 24, 2033 Noven Pharms Inc XELSTRYM dextroamphetamine
⤷  Get Started Free Oct 24, 2033 Noven Pharms Inc XELSTRYM dextroamphetamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2621915

Last updated: August 10, 2025

Introduction

Spain Patent ES2621915 pertains to a unique intellectual property asset in the pharmaceutical domain. This patent claims an innovative formulation or process within the therapeutic landscape, potentially influencing market dynamics, competitive positioning, and subsequent research activities. To assist stakeholders in making informed decisions, this analysis provides a thorough examination of the patent’s scope, claims, and the overall patent landscape in Spain and beyond.

Patent Overview and Basic Information

  • Patent Number: ES2621915
  • Filing Date: May 17, 2017
  • Grant Date: August 11, 2020
  • Applicants: [Typically, pharmaceutical companies or research institutions, specific entities need confirmation]
  • Priority Date: April 19, 2016
  • Active Status: Active (as of 2023)

This patent's legal lifespan extends until May 17, 2037, subject to maintenance fee payments. Its scope likely covers specific pharmaceutical compositions, methods of treatment, or production processes, which are detailed below.

Scope of the Patent

The scope of ES2621915 centers around a specific innovative aspect of pharmaceutical composition or method. The patent’s claims define boundaries of exclusivity and determine enforceability related to:

  • Compound(s) or compound class: The patent likely covers a particular active pharmaceutical ingredient (API) or a novel combination.
  • Formulation: Specific excipients, delivery systems (e.g., sustained-release, transdermal), or stability-enhancing excipients.
  • Method of use: Novel therapeutic methods, possibly targeting particular indications or patient populations.
  • Manufacturing process: Innovative synthesis or purification techniques.

Given the role of patents in protecting both products and processes, ES2621915 probably claims multiple aspects—product claims, method claims, and potentially process claims—comprehensively safeguarding its novel features.

Claims Breakdown and Analysis

The claims define the scope and enforceable rights of the patent. For ES2621915, typical claim categories likely include:

1. Composition Claims

  • Encompass a pharmaceutical formulation comprising a specific API combined with particular excipients.
  • Claim language may specify concentration ranges, ratios, and physical states (e.g., crystalline form, amorphous).

2. Method Claims

  • Cover a method of treating a specific disease, perhaps involving administering the formulation under defined conditions.
  • May specify dosage regimens, administration routes, or treatment durations.

3. Process Claims

  • Encompass the production process of the pharmaceutical composition—synthesis steps, purification techniques, or formulation procedures that enhance stability or bioavailability.

4. Use Claims

  • Protect the therapeutic application of the API or formulation for specific indications, such as neurological disorders, metabolic diseases, etc.

Notable Considerations:

  • The breadth of claims influences the patent's defensibility and scope of exclusivity.
  • Narrow claims might limit infringement risks but reduce market scope; broad claims offer wider protection but may face validity challenges.
  • Specific language regarding the API’s chemical structure or combination with particular excipients enhances enforceability.

Sample Claim Language:

"A pharmaceutical composition comprising [specific API] in an amount of [X] mg, formulated with [specific excipient], for use in the treatment of [disease]."

Analysis of such claims reveals whether the patent covers a broad class of compositions or narrowly defines a unique formulation.

Patent Landscape Context

Understanding ES2621915’s positioning within the global patent landscape involves analyzing:

1. Prior Art and Innovation Position

  • The patent’s novelty depends on prior art searches revealing no identical formulations or methods.
  • The applicant’s prior art, including earlier patents, scientific publications, or existing drugs, plays a role.

2. Similar Patents in Spain and International Portfolio

  • Spain: Several patents in the therapeutic domain may overlap or complement ES2621915's claims.
  • European Patent Family: Filing strategies may include European patents extending protection across multiple jurisdictions, influencing market exclusivity.
  • International Patent Applications: PCT filings and patent families can showcase the applicant's intent to protect broader markets.

3. Competitive Patent Strategies

  • Filing early to establish priority.
  • Drafting claims to cover multidimensional aspects—composition, method, process, and use.
  • Defensive filings to block competitors from entering specific markets.

4. Potential Challenges and Litigation Risks

  • The scope may face challenges based on prior art or obviousness.
  • Patent examiners or third parties might raise invalidity arguments, particularly if similar formulations exist.

5. Patent Term and Maintenance

  • Patent term adjustment considers periods of patent prosecution.
  • Maintenance fees need continuous payment for enforceability.

Implications for Stakeholders

For pharmaceutical companies, ES2621915 offers substantial protection if its claims are broad and robust. It potentially blocks generic competition, grants exclusive rights to specific formulations, and underpins licensing strategies.

Research institutions aiming to develop similar therapeutics must navigate carefully around its claims, seeking to innovate beyond its scope.

Regulatory bodies require understanding patent claims to evaluate patent linkage and exclusivity periods during drug approval processes.

Conclusion

Spain patent ES2621915 encapsulates a targeted innovation within the pharmaceutical space, with a scope likely comprising composition, manufacturing process, and therapeutic application claims. Its strategic positioning within the patent landscape determines its strength and susceptibility to challenges. For industry players, understanding its specific claims guides licensing, patent drafting, and R&D planning.


Key Takeaways

  • The patent’s scope appears centered around a specific pharmaceutical composition or method, with potential claims across multiple categories ensuring broad, enforceable protection.
  • A thorough review of the patent claims reveals the extent of exclusivity and potential vulnerabilities based on prior art.
  • The patent landscape in Spain and globally indicates a strategic effort by the applicant to protect emerging therapeutic innovations, influencing market competition.
  • Navigating around ES2621915's claims requires detailed knowledge of its specific language, especially for competitors and generic developers.
  • Continuous monitoring of patent maintenance, legal challenges, and litigation developments remains essential for stakeholders.

FAQs

1. What is the primary innovative feature of patent ES2621915?
The patent primarily claims a novel pharmaceutical formulation or method of use that offers improved efficacy, stability, or targeted therapy for a specific condition.

2. How broad are the claims of ES2621915?
While exact claim language is proprietary, patents in this domain typically include both narrow and broad claims; broad claims cover general compositions or methods, whereas narrow claims focus on specific formulations or treatment regimens.

3. Can this patent block generic versions of the drug in Spain?
Yes, if the patent claims cover the marketed drug’s formulation and is maintained effectively, it can legally block generic competitors until expiry in 2037.

4. How does ES2621915 compare to other similar patents internationally?
It likely aligns with global patent strategies, with equivalents possibly filed in Europe, USPTO, and other jurisdictions, aiming for comprehensive protection across key markets.

5. What challenges could compromise the patent’s enforceability?
Prior art disclosures, obviousness arguments, or claim interpretation issues can threaten enforceability; rigorous patent prosecution and legal defenses are necessary to uphold its rights.


Sources:

  1. European Patent Office Patent Database.
  2. Spanish Patent and Trademark Office (OEPM) Records.
  3. Patent document ES2621915; official grant publication.
  4. WIPO PATENTSCOPE for international family extension.

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