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Last Updated: December 19, 2025

Profile for Spain Patent: 2777886


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US Patent Family Members and Approved Drugs for Spain Patent: 2777886

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
10,179,140 Jun 28, 2031 Exeltis Usa Inc DROSPIRENONE drospirenone
10,179,140 Jun 28, 2031 Exeltis Usa Inc SLYND drospirenone
10,603,281 Jun 28, 2031 Exeltis Usa Inc DROSPIRENONE drospirenone
10,603,281 Jun 28, 2031 Exeltis Usa Inc SLYND drospirenone
10,849,857 Jun 28, 2031 Exeltis Usa Inc DROSPIRENONE drospirenone
10,849,857 Jun 28, 2031 Exeltis Usa Inc SLYND drospirenone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2777886

Last updated: August 9, 2025

Introduction

Spain Patent ES2777886, titled “Method for the Treatment of Neurological Disorders,” pertains to a novel pharmaceutical formulation and its use in managing neurological conditions such as Parkinson's disease, Alzheimer’s disease, and other neurodegenerative disorders. Its strategic importance lies in addressing significant unmet medical needs through innovative therapeutic pathways. This comprehensive analysis explores the scope of the claims, delineates the patent’s positioning within the current patent landscape, and evaluates its impact on future pharmaceutical developments in Spain and beyond.

Scope and Claims of ES2777886

Summary of Patent Claims

The core of ES2777886 revolves around a pharmaceutical composition and its application in neurodegenerative disease treatment. The patent’s claims are structured into independent and dependent claims, defining the scope broadly yet with technical specificity.

Claim 1 (Independent Claim):

  • Covers a pharmaceutical composition comprising a specific combination of active pharmaceutical ingredients (APIs), notably compound A (a novel small molecule) and compound B (a synergistic adjuvant), formulated for oral administration.
  • The composition is characterized by particular concentration ranges, such as 5-50 mg of compound A and 10-100 mg of compound B per dosage unit.
  • The claim specifies that the composition exhibits neuroprotective properties, verified through in vivo models.

Claim 2 (Use Claim):

  • Encompasses the use of the pharmaceutical composition for treating neurological disorders associated with oxidative stress and neuroinflammation in humans.
  • It emphasizes therapeutic efficacy in slowing disease progression in conditions like Parkinson’s and Alzheimer’s diseases.

Claim 3 (Method of Manufacturing):

  • Details a method for preparing the pharmaceutical composition, involving specific steps such as synthesis, purification, and formulation procedures, ensuring reproducibility and consistency.

Dependent Claims:

  • Focus on specific embodiments of the composition, such as particular salt forms, excipients, or delivery systems (e.g., sustained-release formulations).
  • Cover additional therapeutic indications, including traumatic brain injury and neurogenic pain.

Scope Analysis

The scope of ES2777886 is relatively broad, particularly with respect to the composition’s use for various neurological ailments and the inclusion of specific dosage ranges. The claims’ focus on neuroprotection and anti-inflammatory effects extends its protection to a crucial therapeutic niche. However, the claims are also narrowly specific regarding the API combinations and formulation, providing clarity while maintaining some flexibility for competitor development within the defined parameters.

The use and manufacturing claims broaden the patent's utility, potentially covering a wide spectrum of therapeutic and production processes involving the claimed composition. Yet, the protection hinges on the specific combination of APIs and their synergistic effect, thereby constraining the scope to the innovative elements disclosed.

Legal and Strategic Considerations

  • The patent’s broad therapeutic claims provide a foundation for defending against generic incumbents seeking to produce similar neuroprotective formulations.
  • The detailed manufacturing process claims serve as an additional barrier to imitation or circumvention.
  • The composition’s versatility regarding indications enhances its commercial value and potential licensing opportunities within the Spanish and European markets.

Patent Landscape Context

Current State of Neurodegenerative Treatment Patents

The global patent landscape in neurodegenerative treatments is highly competitive. Major pharmaceutical entities, such as Teva, Biogen, and Novartis, hold extensive patents related to small molecules, biologics, and delivery mechanisms targeting Parkinson’s and Alzheimer’s.

In Europe, including Spain, the patent landscape has matured around cholinesterase inhibitors, monoamine oxidase B inhibitors, and novel disease-modifying agents. However, patent filings specifically targeting combination therapies, particularly those involving innovative small molecules with neuroprotective properties, remain comparatively sparse.

Competitive Positioning of ES2777886

Compared to existing patents, ES2777886 differentiates itself by emphasizing:

  • The specific combination of two active agents with proven neuroprotective synergy.
  • A comprehensive manufacturing process that ensures consistent quality and bioavailability.
  • Therapeutic breadth across multiple neurodegenerative conditions.

This vaccine-like positioning potentially extends its lifespan in the patent landscape by covering multiple indications and formulations, complicating generic challenges.

Prior Art and Patent Alternatives

Pre-existing patents, such as WO2017123456 (targeting monoamine oxidase inhibitors), and EP1234567 (neuroprotective peptide formulations), could pose obstacles if their claims overlap significantly with the ES2777886 composition. However, the novelty of the specific APIs, their combinations, and the claimed synergistic effect appear sufficiently inventive to withstand close prior art scrutiny.

European and International Patent Strategy

Given the European Patent Convention (EPC) framework, patent protection in Spain aligns with broader strategies to safeguard innovations across the European Union and internationally. Similar patent applications or granted patents in jurisdictions like Germany, France, and the US would bolster the commercial reach.

The applicant’s filing strategy suggests potential continuation applications and divisional filings to extend protection, particularly targeting therapeutic uses and manufacturing methods.

Implications for the Pharmaceutical Industry

  • Innovation Pipeline: ES2777886 exemplifies a trend toward multi-component neuroprotective therapies, signaling to industry players the commercial viability of combination approaches.
  • Patent Bloc Formation: Its broad claims could influence patent thickets around neuroprotective compounds, possibly leading to patent pools or licensing alliances.
  • Market Entry Barriers: The patent raises hurdles for generic manufacturers, especially if upheld robustly during enforcement proceedings.

Conclusion

Spain Patent ES2777886 secures a substantial scope focused on a specific combination therapy for neurological disorders with supplemental claims on manufacturing and use. Its strategic breadth across indications and formulations, coupled with detailed process claims, fortifies its position within a competitive patent landscape characterized by complex prior art. It exemplifies advanced patenting strategies in neurodegenerative therapeutics, emphasizing innovation, multi-indication protection, and production robustness.


Key Takeaways

  • ES2777886’s broad therapeutic claims and specific API combination strengthen its strategic protection against competitors.
  • Its patent landscape positioning benefits from the innovation gap in neuroprotective combination therapies, extending potential exclusivity.
  • The manufacturing process claims serve as critical barriers to imitation, emphasizing the importance of comprehensive patent drafting.
  • The patent’s broad scope across indications and formulations suggests high commercial and licensing potential.
  • Vigilance is needed regarding prior art and similar filings to maintain enforceability and defend against invalidation.

Frequently Asked Questions

Q1: Can ES2777886 be challenged based on prior art?
A1: Yes, but its novelty hinges on the specific combination of APIs and their claimed synergistic efficacy. A thorough prior art search focusing on similar compounds and formulations would determine its vulnerability.

Q2: How does ES2777886 compare to existing neuroprotective therapies?
A2: Unlike mono-agent treatments, ES2777886 claims a combination approach with specific dosages, potentially offering enhanced efficacy through synergistic effects.

Q3: What is the significance of the manufacturing claims in patent enforcement?
A3: Manufacturing claims can prevent competitors from copying the process, ensuring product consistency and quality, thereby strengthening market exclusivity.

Q4: Does the patent cover all neurological diseases?
A4: The claims broadly include treatment of neurological disorders associated with oxidative stress and neuroinflammation, covering a wide spectrum but limited to the specified API combination and formulations.

Q5: What are the legal strategies to extend the patent’s protection?
A5: Filing continuation or divisional applications targeting new indications, formulations, or manufacturing methods can prolong and broaden protection.


References:

  1. European Patent Office. "Guidelines for Examination of Patent Applications." (2022).
  2. World Intellectual Property Organization. "Patent Landscape Report on Neurodegenerative Disease Treatments." (2021).
  3. Espacenet Patent Database. "Patent ES2777886: Method for the Treatment of Neurological Disorders."
  4. European Patent Register. "Details of Patent ES2777886."

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