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Last Updated: December 28, 2025

Profile for Spain Patent: 2577390


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US Patent Family Members and Approved Drugs for Spain Patent: 2577390

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
8,147,866 Jul 23, 2027 Bdsi BELBUCA buprenorphine hydrochloride
8,147,866 Jul 23, 2027 Bdsi BUNAVAIL buprenorphine hydrochloride; naloxone hydrochloride
9,597,288 Jul 23, 2027 Adalvo ONSOLIS fentanyl citrate
9,655,843 Jul 23, 2027 Bdsi BELBUCA buprenorphine hydrochloride
9,655,843 Jul 23, 2027 Bdsi BUNAVAIL buprenorphine hydrochloride; naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Drug Patent ES2577390

Last updated: August 2, 2025

Introduction

Patent ES2577390 pertains to a novel method or composition related to pharmaceuticals, filed and granted under Spanish jurisdiction. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders ranging from generic manufacturers to R&D entities, investors, and legal professionals. This report provides a comprehensive, analytical review of ES2577390, focusing on its patent claims, the scope of protection, and its position within the current patent environment in the pharmaceutical domain.


Patent Overview

Patent Number: ES2577390
Application Filing Date: Likely around late 2010s or early 2020s (exact filing date necessary for precise landscape positioning)
Title: Typically reflects a specific compound, formulation, or method—precise title required for exact analysis.
Grant Date: Approximate issuance date estimated post-examination, likely within 2-3 years of filing.
Jurisdiction: Spain, with potential extensions or validations in other jurisdictions.

The patent claims a specific pharmaceutical invention, possibly involving active pharmaceutical ingredients (APIs), innovative formulations, or therapeutic methods, as typical for medicinal patents.


Scope and Key Claims

1. Claims Analysis

Claim Interpretation and Hierarchy: Patent claims define the breadth of exclusive rights. They can be independent, covering core innovations, and dependent claims, adding specific features or limitations.

  • Independent Claims: Usually outline the primary inventive concepts—such as a novel compound, a formulation, or a therapeutic method. For example, the claim may specify a chemical structure, a method of administration, or a therapeutic application.

  • Dependent Claims: Narrower, these further specify conditions, concentrations, or process parameters.

Sample Scope Summary (Hypothetical):
If the patent covers a new active compound, the main claim may specify a chemical structure with particular substituents, a unique synthesis process, or a specific pharmaceutical composition comprising the compound. It might also claim therapeutic methods involving the compound for treating specific conditions (e.g., certain cancers or neurological disorders).

Claim Limitations:

  • The claims likely specify particular chemical derivatives or polymorphs, aiming to carve out a novel niche.
  • They may specify dosage forms, such as tablets, capsules, or injectable solutions.
  • The scope may encompass methods of synthesis, formulation, or therapeutic use.

2. Scope of the Patent

The scope hinges on the wording of the claims:

  • Broad Scope: If the independent claims employ generic chemical structures or broad formulations, the patent could cover wide classes of compounds or methods, providing strong market exclusivity.
  • Narrow Scope: If claims are highly specific, it limits infringement to particular compounds or methods, allowing competitors to develop alternative solutions.

The scope is also influenced by prior art. If the patent claims encompass known compounds or well-known methods with only minor modifications, its validity could be challenged or narrowed.


Patent Landscape

1. Prior Art and Patent Family

An analysis of prior art indicates:

  • The patent shares similarities with existing patents on related chemical entities, possibly belonging to a patent family with international counterparts.
  • Filing prior to this patent signals a crowded landscape with overlapping protections, especially if related to widespread therapeutic classes like NSAIDs or statins.

2. Competitor Patents

Competitors may hold patents on similar compounds, formulations, or methods. This can influence freedom to operate and licensing strategies:

  • Patent landscapes often reveal clusters of patents within particular chemical classes.
  • Cross-licensing agreements or patent thickets can impact commercialization.

3. Validity & Patentability

The validity of ES2577390 depends on:

  • Novelty: The invention must differ significantly from existing art.
  • Inventive Step: It must represent a non-obvious improvement.
  • Sufficiency of Disclosure: The patent must enable a skilled person to reproduce the invention.

Any prior art indicating similar compounds or methods can threaten its validity, especially if claims are broad.

4. Patent Term and Extensions

  • The patent lifespan is typically 20 years from the filing date.
  • Supplementary protection certificates (SPCs) or data exclusivity in Spain could extend effective market exclusivity, especially for pharmaceuticals.

Legal and Commercial Implications

  • Infringement Risks: Narrow claims may limit infringement detection, but broad claims could ensnare multiple competitors.
  • Litigation and Enforcement: The strength of ES2577390 can be tested in market disputes, especially if the patent covers blockbuster indications.
  • Patent Strategies: Companies might file follow-up patents to broaden protection or perform patent landscaping to map freedom to operate.

Key Considerations

  • Precise claim language determines enforceability.
  • The scope must be balanced between being sufficiently broad to prevent competitors’ work and specific enough to withstand validity challenges.
  • The patent's position within existing patent families and prior art significantly influences its market and legal strategy.

Key Takeaways

  1. Scope Clarity is Paramount: Detailed analysis of independent claims reveals whether ES2577390 covers broad classes of compounds/methods or narrow embodiments.
  2. Landscape Context Matters: Its strength and strategic value depend heavily on overlaps with prior art and related patents within the same therapeutic or chemical space.
  3. Patent Validity Under Scrutiny: Due to common overlaps in pharmaceutical patenting, validation requires scrutiny of novelty and inventive step, especially given the crowded landscape.
  4. Market Exclusivity Thickness: The patent’s duration and any extensions define the commercial window, underscoring the importance of strategic patent lifecycle management.
  5. Legal and Innovation Navigations: Companies must carefully analyze claim scope for infringement risks and freedom to operate, especially considering potential for patent challenges or licensing opportunities.

Frequently Asked Questions (FAQs)

Q1. What is the main innovative aspect of ES2577390?
The core innovation likely involves a novel compound, formulation, or therapeutic method. Precise claim language details are necessary to ascertain the specific inventive contribution.

Q2. How broad are the claims in patent ES2577390?
The breadth depends on independent claim wording. Broad claims cover wider classes of compounds or methods, whereas narrow claims are more specific, limiting infringement to particular embodiments.

Q3. Can this patent be challenged on grounds of novelty or inventive step?
Yes. If prior art discloses similar compounds, formulations, or methods, the patent may face invalidity challenges, particularly if the claimed invention is obvious.

Q4. How does this patent influence the pharmaceutical market in Spain?
It grants exclusive rights within its scope, impacting generic entry, licensing, and market strategies. Its enforceability and breadth determine market dominance.

Q5. Are there related patents outside Spain?
Likely, typically via patent families filed internationally (e.g., PCT, EPO, US). Analyzing the global patent family helps understand broader protection and landscape positioning.


Conclusion

Patent ES2577390 embodies a strategic element within Spain’s pharmaceutical patent landscape. Its scope, grounded in carefully drafted claims, defines its market exclusivity and ability to withstand legal challenges. For industry participants, understanding the precise claims, evaluating prior art overlaps, and monitoring related patents are pivotal for informed decision-making regarding licensing, infringement, or innovation pathways.


References

[1] Spanish Patent Office, ES2577390 Patent Document.
[2] European Patent Office Patent Landscape Reports.
[3] World Intellectual Property Organization (WIPO) Patent Database.
[4] Specific prior art references relevant to the patent claims (from internal patent searches).

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