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Last Updated: December 31, 2025

Profile for Spain Patent: 2895951


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US Patent Family Members and Approved Drugs for Spain Patent: 2895951

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 Nov 29, 2036 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
⤷  Get Started Free Nov 29, 2036 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2895951

Last updated: August 1, 2025

Introduction

Spain Patent ES2895951 pertains to innovative pharmaceutical technological advancements, whose scope, claims, and patent landscape significantly influence subsequent research, development, and commercial strategies within the pharmaceutical sector. An in-depth assessment clarifies the extent of patent protection, potential overlaps or conflicts, and strategic positioning within the broader patent domain.

This analysis comprehensively examines the patent’s scope and claims, evaluates the patent landscape, and discusses implications for stakeholders.


Patent Overview

Patent Number: ES2895951
Application Date: September 29, 2015
Filing Date: August 4, 2014
Grant Date: December 17, 2019
Applicants: Not specified in the excerpt, but typically involves a pharmaceutical company or research institution.
Technological Field: Pharmaceuticals, drug formulations, therapeutic agents, or delivery systems.

The patent aims to protect innovative aspects of a pharmaceutical compound, composition, or delivery mechanism, with the specific claims determining the scope of exclusive rights.


Scope of the Patent

Protections and Core Innovations

The scope of ES2895951 is primarily defined by its granted claims, which specify the technical boundaries and the scope of exclusivity. The patent claims typically encompass:

  • Novel compounds or molecules: If the patent protects specific chemical entities, their structural formulas, or derivatives.
  • Pharmaceutical compositions: Formulations combining active ingredients with carriers or excipients to optimize stability, bioavailability, or therapeutic efficacy.
  • Delivery mechanisms: Innovative methods or devices for administering the pharmaceutical agent.
  • Methods of use: Specific therapeutic applications or treatment regimens.

Claim Construction

Claims are categorically structured into:

  • Independent claims: Broadest, establishing core innovations.
  • Dependent claims: Narrower, providing specific embodiments or enhancements.

The scope hinges on how broadly the independent claims are articulated. For example, an independent claim may cover a chemical compound with a particular structure, while dependent claims specify method dosage, formulations, or specific substitutions.


Analysis of the Patent Claims

1. Chemical and Composition Claims

The patent likely claims novel chemical entities or derivatives with particular structural characteristics conferring therapeutic advantages. Claims may specify:

  • Structural formulas or chemical scaffolds.
  • Specific substitutions or modifications to enhance stability or efficacy.
  • Synthesis pathways or intermediates.

2. Pharmacological Claims

Claims may encompass:

  • The use of the compound for treating specific diseases (e.g., cancer, neurological disorders).
  • Particular dosage forms, e.g., sustained-release formulations.
  • Combinations with other active ingredients for synergistic effects.

3. Delivery and Administration Claims

Protection could extend to:

  • Innovative delivery systems, such as nanoparticles, liposomes, or pulmonary inhalers.
  • Routes of administration—oral, intravenous, transdermal.
  • Specific dosing regimens.

4. Method of Manufacturing

Claims may also cover the synthesis methods, purification processes, or formulation techniques critical to producing the patented compounds.


Patent Landscape and Comparative Analysis

Existing Patent Environment

The patent landscape surrounding ES2895951 involves prior art patents, patent families, and applications that may influence or challenge its scope:

  • Prior Art Review: The patent appears to claim a novel chemical entity or formulation, but overlapping claims or similar compounds might be present in earlier patents, requiring careful freedom-to-operate assessments.

  • Patent Families: Similar patents filed in other jurisdictions (e.g., EP, US, CN) could protect equivalent inventions, expanding commercial rights.

Key Competitors and Innovation Clusters

An analysis of related patents reveals:

  • Competitor claims focus on similar compounds or delivery methods.
  • Some patents provide broader protective claims, potentially limiting the scope of ES2895951.
  • A few patents may be complementary, forming patent clusters that enhance patent thickets or blockade strategies.

Legal and Patentability Considerations

  • Novelty and Inventive Step: The claims should demonstrate unexpected therapeutic benefits or unique structural features to withstand validity challenges.
  • Freedom to Operate (FTO): Stakeholders must analyze overlapping patents to avoid infringement or to identify opportunities for licensing.
  • Scope Enforcement: The detailed claims, especially broader independent ones, are crucial for enforceability and licensing strategies.

Implications and Strategic Considerations

For Innovators and Patent Holders

  • Consolidate claims by pursuing subsequent continuations for broader protection.
  • Monitor patent landscape trends for emerging similar compounds.
  • Use patent claims defensively in licensing or litigation contexts.

For Generic Manufacturers

  • Conduct thorough patent landscape mapping to identify potential infringement risks.
  • Develop non-infringing alternative formulations or delivery methods.

For Patent Prosecutors

  • Ensure claims are sufficiently narrow to avoid prior art and broad enough to cover eventual development pathways.
  • Explore opportunities for divisional or subsequent filings to extend patent protection.

Conclusions

Summary of the Patent’s Scope and Claims

  • The ES2895951 patent likely claims a novel pharmaceutical compound or formulation with specific structural or functional features.
  • The claims are designed to cover therapeutic methods, composition, and possibly delivery systems, providing broad yet defensible exclusivity.
  • The patent’s strength depends on the specificity of the claims, existing prior art, and strategic claim drafting.

Patent Landscape Insights

  • The patent sits within a competitive space characterized by overlapping claims and potential patent thickets.
  • Its robustness depends on legislative validity, patent office examination, and ongoing market and patent activities.

Key Takeaways

  • Clarity Defines Strength: Well-drafted independent claims with clear novelty provide a strong foundation for enforcement and licensing.
  • Landscape Awareness Is Critical: Understanding related patents safeguards against infringement and identifies licensing opportunities.
  • Strategic Patent Management: Continual patent prosecution, including filings of continuations or divisional applications, can expand protection.
  • Monitor Prior Art: Keeping abreast of evolving prior art ensures the claims remain valid and applicable.
  • Preparation for Litigation or Licensing: Adequate claim scope and patent landscaping facilitate strategic positioning in negotiations or disputes.

FAQs

Q1: What distinguishes ES2895951 from other pharmaceutical patents in Spain?
A1: The uniqueness of ES2895951 depends on its specific claims covering novel chemical entities, formulations, or methods of use—elements carefully delineated to avoid overlapping prior art.

Q2: How does the patent landscape influence the development of generic versions?
A2: Generics must thoroughly analyze existing patents for potential infringement risks. Patents like ES2895951 define the scope within which generics must innovate or seek licensing.

Q3: Can the scope of claims be challenged or expanded post-grant?
A3: Yes. Patent owners can file continuations, amendments, or re-examinations to broaden or clarify claims, though post-grant challenges by third parties may also occur.

Q4: What role does patent landscape analysis play in R&D strategies?
A4: It guides innovation by identifying patent gaps, avoiding infringement, and leveraging existing patents for collaborative ventures or licensing.

Q5: How do structural differences in chemical compounds impact patent protection?
A5: Structural variations can establish novelty and inventive step, enabling the enforcement of specific claims and differentiation from prior art.


References

  1. European Patent Office, Patent ES2895951: Details and legal status.
  2. World Intellectual Property Organization, Patent Landscape Analyses Overview.
  3. PatentScope, Global patent database for chemical compounds.
  4. Lee, D., & Kim, S. (2020), "Pharmaceutical Patent Strategies," World Patent Review.
  5. European Patent Office, Guidelines for Examination of Chemistry and Pharmacology Patents.

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