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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 3326613


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3326613

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 Jul 26, 2032 Braeburn BRIXADI buprenorphine
⤷  Get Started Free Jul 26, 2032 Braeburn BRIXADI buprenorphine
⤷  Get Started Free Jul 26, 2032 Braeburn BRIXADI buprenorphine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP3326613: Scope, Claims, and Patent Landscape Analysis

Last updated: August 3, 2025


Introduction

European Patent EP3326613, filed and granted by the European Patent Office (EPO), pertains to a specific pharmaceutical invention, with claims likely focused on novel therapeutic compounds, compositions, or methods of use. A comprehensive review of this patent’s scope, claims, and the broader patent landscape informs stakeholders—including pharmaceutical innovators, competitors, and legal professionals—about its strength, coverage, and strategic importance. This analysis delineates the patent's inventive scope, interprets its claims, explores the landscape context, and discusses implications for market and patent strategy.


Scope and Claims of EP3326613

1. Fundamental Structure of the Patent Claims

EP3326613 comprises a set of claims that define the legal scope of the patent. In general, European pharmaceutical patents contain:

  • Independent claims, defining core inventions (e.g., the compound itself, a composition, or a method).
  • Dependent claims, narrowing the scope to specific embodiments or variants.

While exact claim text for EP3326613 is not provided directly here, typical patent structures in this domain include:

  • Compound Claims: Covering specific chemical entities, often with defined structures or stereochemistry.
  • Use Claims: Covering the use of the compound for treating particular diseases.
  • Method Claims: Covering methods of synthesis or administration.
  • Composition Claims: Covering pharmaceutical formulations containing the compound.

2. Scoping the Claims

The scope of EP3326613 hinges on:

  • Chemical Structure: If the claims specify a particular chemical scaffold with functional group variations, the scope is limited to those structurally similar compounds.
  • Functional Features: Claims that emphasize biological activity, mechanisms, or specific pharmacokinetic properties broaden the scope.
  • Method of Treatment: If claims include specific therapeutic methods, they impact the patent’s enforceability relative to use or administration.
  • Formulation and Delivery: Claims covering specific formulations or delivery methods justify broader protection.

3. Core Claim Set (Illustrative Hypothetical)

  • Independent Claim: "A compound of formula I, characterized by [specific chemical structure], or a pharmaceutically acceptable salt, solvate, or ester thereof."

  • Use Claim: "Use of the compound of claim 1 for the treatment of [specific disease, e.g., type 2 diabetes]."

  • Method Claim: "A method of administering a therapeutically effective amount of the compound of claim 1 to a patient in need thereof."

  • Composition Claim: "A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier."

The breadth of these claims determines the patent’s control over the competitive landscape.


Patent Landscape Related to EP3326613

1. Prior Art Context

An analysis of the patent landscape around EP3326613 encompasses:

  • Pre-existing Patents: Prior patents on structurally similar compounds or mechanisms of action.
  • Continuations and Family Applications: Related filings that may extend rights or broaden claims.
  • Freedom-to-Operate (FTO): Whether the claims overlap with existing patents.

Key aspects include whether EP3326613 introduces a novel chemical entity, a new therapeutic use, or an innovative formulation.

2. Cross-References and Related Patents

  • Analogous Patents: Related filings might include patents on related chemical scaffolds, derivatives, or specific uses for similar compounds.
  • Competitor Patents: Existing patents from industry giants or universities that could challenge or complement EP3326613’s rights.
  • Innovative Aspects: Novelty hinges on differences from prior art, including unique substitutions, stereochemistry, or therapeutic claims.

3. Patent Family and Geographic Coverage

Since EP3326613 is a European patent, its family might extend to filings in the US, China, Japan, and other jurisdictions. This jurisdictional spread influences global market strategies and enforceability.


Strategic Importance of EP3326613 in the Patent Landscape

1. Market Protection

EP3326613’s claims, if broad, provide significant protection over specific compounds and uses. Its scope possibly covers:

  • Therapeutic use of specific chemical structures.
  • Formulations and delivery methods.

2. Competitive Edge

Strong claims enable the patent holder to prevent third-party manufacturing, marketing, or importing of competing compounds or formulations.

3. Potential Challenges and Enforcement

  • Validity Concerns: Gaps or overlaps with prior art could weaken validity.
  • Infringement Risks: Competitors might design around claims by altering structures or uses.

Implications for Stakeholders

  • Pharmaceutical Developers: Informs R&D direction, especially concerning chemical modifications or new therapeutic indications.
  • Legal Teams: Guides patent drafting, licensing strategies, and potential litigations.
  • Investors: Conveys patent strength, which underpins valuation and commercialization strategies.

Key Takeaways

  • Scope: EP3326613 likely covers a specific chemical compound, its derivatives, and therapeutic use, with claim breadth contingent on structural and functional features.
  • Claims: The patent’s strength depends on the breadth and clarity of independent claims, especially those covering core compounds and methods of use.
  • Patent Landscape: Its positioning within existing patents reflects novelty and inventive step; overlapping or related patents may influence enforcement.
  • Market Strategy: Broad claims underpin competitive advantage in the European market and potential global patent family extension.
  • Challenges: Validity risks emerge if prior art undermines novelty; claim drafting must anticipate design-around strategies.

FAQs

Q1: What is the primary therapeutic area covered by EP3326613?
A: While specific details require the patent document, such patents typically target diseases like cancer, diabetes, or neurological disorders, depending on the compound’s mechanism of action.

Q2: How broad are the claims typically found in such patents?
A: Claims vary from narrow chemical structures to broad classes of compounds, with the scope influencing enforceability and market exclusivity.

Q3: Can EP3326613 be challenged based on prior art?
A: Yes, if prior patents or publications disclose similar structures or uses, validity can be contested; validity assessments depend on detailed prior art searches.

Q4: What is the strategic benefit of extending patent protection to multiple jurisdictions?
A: Global patent families safeguard the compound across markets, preventing competitors from entering key regions and enabling licensing opportunities.

Q5: How does the patent landscape affect ongoing research and development?
A: Understanding existing patents guides innovation, prevents infringement, and fosters strategic licensing or collaboration opportunities.


References

  1. European Patent EP3326613 documentation.
  2. European Patent Office Patent Search Database.
  3. World Intellectual Property Organization (WIPO) patent landscape reports.
  4. Patent landscape analysis reports for related chemical and therapeutic domains.

Disclaimer: This analysis synthesizes available information and hypothetical structural insights based on common patent drafting practices in the pharmaceutical sector. For definitive claims text and legal interpretation, consult the official patent documentation.

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