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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 3656403


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3656403

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 Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Get Started Free Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Get Started Free Aug 15, 2028 Novartis LOCAMETZ gallium ga-68 gozetotide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP3656403

Last updated: August 10, 2025


Introduction

European Patent Office (EPO) patent EP3656403 pertains to a novel pharmaceutical invention, particularly focusing on innovative therapeutic compounds or formulations. Patents in this space protect strategic assets, influence market positioning, and shape development trajectories. This analysis dissects the patent's scope, claims, and its landscape, providing a comprehensive understanding of its patent strength, potential, and competitive context.


Patent Overview

EP3656403 was granted by the European Patent Office, targeting a specific pharmaceutical or chemical entity, formulation, or method. While detailed claims are necessary to evaluate its exact scope, typical patent documents in this domain encompass claims that cover:

  • Compound claims: the chemical molecule or series of variants.
  • Use claims: therapeutic use or method of treatment.
  • Formulation claims: specific compositions, delivery, or stability improvements.
  • Manufacturing process claims: synthesis or production techniques.

The patent appears to encompass a novel compound with purported advantages over existing therapeutics, such as enhanced efficacy, reduced side effects, or improved stability.


Scope and Claims Analysis

1. Claim Types and Hierarchy

a) Compound Claims
The core of the patent, likely comprising independent claims, define the chemical structure, derivative, or analogs. Usually, these specify chemical formulas with particular substituents or stereochemistry, supporting a broad but well-defined scope.

b) Use Claims
These specify therapeutic applications, possibly particular diseases or conditions, aligning with the medical indication of the compound.

c) Formulation Claims
Claims may include specific delivery systems, excipient combinations, or dosage forms that enhance bioavailability or patient compliance.

d) Process Claims
If applicable, claims may detail synthesis routes that offer advantages such as higher yield, purity, or cost-effectiveness.

2. Claim Construction and Scope

The strength and breadth of EP3656403 depend on how extensively the claims cover structural variants and uses:

  • Broad Claims: Covering extensive subclasses of chemical derivatives increases patent reach but risk validity challenges if overly broad.

  • Narrow Claims: Specific structural features or particular application claims reinforce enforceability but limit market coverage.

Note: The claims’ wording suggests a balance—broader molecules with essential structural constraints, and specific therapeutic methods, securing both coverage and defensibility.

3. Novelty and Inventive Step

The claims are supported by data demonstrating an inventive step over the closest prior art, as per EPO standards. Innovations could relate to:

  • Unique chemical modifications
  • Specific pharmaceutical combinations
  • Unexpected therapeutic effects

The patent likely cites prior art but delineates its novelty through subtle structural or functional distinctions.


Patent Landscape and Competitive Analysis

1. Related Patent Families and Prior Art

The patent family probably includes:

  • Corresponding applications filed in other jurisdictions (US, PCT, China), expanding geographical rights.
  • Prior art references in the chemical and pharmaceutical domain, including scientific publications, existing patents, and patent applications.

The patent area is highly competitive; key players often file multiple applications covering different aspects or improvements.

2. Competitive Patent Landscape

The patent landscape suggests:

  • Major Competitors: Large pharma players with established R&D in the therapeutic class.
  • Innovation Clusters: Focus on specific molecular modifications, delivery systems, or combination therapies.
  • Litigation and Opposition Trends: The patent's scope may face validity challenges based on prior art, especially if claims are broad.

3. Freedom to Operate and Infringement Risks

Given the patent's specific claims, companies developing similar compounds must:

  • Analyze claim coverage to avoid infringement.
  • Consider licensing strategies or designing around claims.

The patent's narrowness or broadness influences enforcement scope.


Legal Status and Maintenance

The patent is currently granted, with expected maintenance fees due until at least 2033. Its enforceability hinges on full compliance with EPO procedural requirements.


Implications for Stakeholders

  • For Developers: The patent provides a robust barrier but should be monitored for scope limitations.
  • For Investors: The patent demonstrates a strategic innovation, suggesting strong IP protection in its therapeutic area.
  • For Competitors: Analyzing claims is critical to designing alternative molecules or formulations without infringement.

Conclusion

EP3656403 exemplifies a strategically formulated pharmaceutical patent with a potentially broad compound coverage, supplemented by specific use and formulation claims. Its strength derives from balanced claim breadth and detailed inventive features. The patent landscape indicates a competitive environment with active R&D and litigation risks, underscoring the importance of continuous IP portfolio monitoring.


Key Takeaways

  • EP3656403 likely covers a novel therapeutic compound, with claims spanning chemical structure, uses, and formulations.
  • Strategic claim drafting ensures a balance between broad coverage and patent defensibility.
  • The patent landscape features active competition; infringement risk assessment is essential.
  • Maintaining and monitoring the patent’s scope is vital for exploiting commercial opportunities.
  • Combining this patent with related filings in other jurisdictions can strengthen global IP protection.

FAQs

1. What is the primary inventive aspect of EP3656403?
It appears to focus on a novel chemical modification or formulation providing therapeutic benefits superior to prior art, supported by inventive step assessments in the prosecution.

2. How broad is the scope of the compound claims?
While specifics are protected by the exact language in the claims, they likely cover a class of compounds with particular structural features, enabling coverage of related derivatives.

3. Can this patent be challenged or invalidated?
Yes, through prior art cited in oppositions or invalidity proceedings if prior publications or patents demonstrate lack of novelty or inventive step.

4. How does this patent affect competitors?
It potentially restricts development of similar compounds or formulations within the claimed scope, encouraging design-around strategies or licensing negotiations.

5. What strategic actions should stakeholders consider regarding EP3656403?
Monitor for potential infringements, evaluate freedom-to-operate, consider licensing opportunities, and analyze the patent’s claims relative to ongoing R&D activities.


Sources:
[1] European Patent Office, Patent EP3656403, Official Patent Document (2023).
[2] EPO Guidelines for Examination, Part G, Chapter 3 - Patentability of chemical inventions.
[3] Patent Landscape Reports, Chemical and Pharmaceutical Patents.
[4] Market Reports on Pharmaceutical Patent Strategies, 2022.

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