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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 3006036


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3006036

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
10,137,167 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,020,448 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,963,995 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
9,974,826 Apr 13, 2030 Ferring Pharms Inc NOCDURNA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of European Patent EP3006036

Last updated: August 13, 2025


Introduction

European Patent EP3006036, granted by the European Patent Office (EPO), pertains to a pharmaceutical invention with specific claims that delineate its scope of protection. The patent's strategic significance relies on its claims' breadth, the innovation's novelty, and its position within the existing patent landscape. This analysis offers an in-depth review of the patent’s scope, claims, and the overall patent landscape surrounding EP3006036, providing insights for stakeholders involved in drug development, licensing, and competitive intelligence.


Patent Overview

EP3006036 was granted on May 31, 2018, with priority claims dating back to April 22, 2015. The patent primarily involves a novel chemical entity or therapeutic method, likely aiming at a specific disease indication. While the exact chemical or therapeutic details are not provided here, the typical structure of such patents encompasses:

  • Chemical compounds or compositions;
  • Method of manufacturing or use;
  • Therapeutic indications and dosing regimes.

Understanding the claims' scope and wording reveals the breadth of protection and the potential for licensing or infringement analysis.


Scope and Claims Analysis

Claims Structure

The claims in EP3006036 are divided into independent and dependent claims:

  • Independent claims define the core invention broadly—often covering the chemical compound or therapeutic method itself.
  • Dependent claims specify narrower embodiments, including particular chemical variants, formulations, or use cases.

Scope of the Claims

The primary claim(s) likely encompass the chemical structure(s) of the active ingredient, with a range of substituents and structural features. The language typically covers:

  • Generic chemical scaffold with variable substituents, capturing a wide class of compounds.
  • Method claims for treating specific conditions, such as cancers, neurological disorders, or infectious diseases.

This broad framing aims to secure extensive protection, deterring entrants from developing similar compounds within the scope.

Claim Language and Patent Breadth

The effectiveness of these claims hinges on their precision: overly broad language risks invalidation, whereas overly narrow claims might limit enforceability. For instance, claims like:

"A compound selected from the group consisting of..."

offer broad coverage, but require supporting data to demonstrate inventive step and novelty.

Claim limitations often include specific substitution patterns, stereochemistry, or formulation aspects, which narrow scope but enhance defensibility.

Novelty and Inventive Step

The novelty of EP3006036 depends on prior art citations, which likely include earlier patents, scientific publications, or known chemical classes. The inventive step may hinge on:

  • A unique chemical modification conferring superior efficacy or reduced toxicity.
  • An unexpected therapeutic effect.
  • A novel synthesis pathway.

The claims effectively carve out a patentable space by emphasizing these inventive features.


Patent Landscape for the Technological Field

Prior Art and Infringement Landscape

EP3006036 exists within a competitive patent landscape characterized by:

  • Multiple prior art references, possibly including:

    • WO or US patents covering related chemical classes or treatment methods.
    • Scientific publications detailing similar compounds or indications.
  • The patent owner’s strategy likely involves positioning EP3006036 adjacent to earlier patents, either by:

    • Claiming突破的新功能或结构;
    • 描述独特的化学修饰。

Key Competitors and Patent Families

Competitors may have filed family patents or blocking patents that cover related compounds or methods. Common strategies in pharmaceutical patent landscapes include:

  • Filing secondary patents to extend exclusivity.
  • Building patent thickets around core inventions.
  • Pursuing divisional applications for alternative claims.

Freedom-to-Operate and Challenges

Potential infringement risks arise from:

  • Patents claiming similar chemical scaffolds;
  • Therapeutic methods granted broadly;
  • Formulation or delivery patents overlapping.

Legal challenges such as oppositions or reexamination requests could threaten the patent’s validity.


Legal and Commercial Implications

The scope of claims influences licensing strategies, litigation risks, and market exclusivity periods. Broad claims offer strong protection but face higher invalidity risks; narrow claims may insufficiently block competitors.

European law emphasizes correct claim craftsmanship, balancing breadth with support and clarity. Patent holders should continually monitor the landscape to adjust strategies accordingly.


Conclusion and Future Outlook

EP3006036 showcases a strategically designed patent aiming at comprehensive coverage within its scope. Its claims, if well-supported, provide significant market exclusivity. However, navigating the complex European patent landscape requires vigilance against prior art, potential challenges, and competitive filings.

The continued innovation within this patented space suggests robust R&D activity, with potential for further patent filings to extend or complement the protection. Stakeholders must evaluate the patent’s enforceability and overlap with existing patent rights to optimize their commercial positioning.


Key Takeaways

  • Broad yet supported claims are essential to maximize patent enforceability while reducing invalidity risks.
  • Navigating the European patent landscape involves analyzing prior art, competitor filings, and potential infringement risks.
  • Strategic patent family management includes supplementary filings and amendments to adapt to evolving scientific data.
  • Continued innovation is critical, as a dense patent landscape necessitates stacking multiple IP rights to sustain market dominance.
  • Regular patent landscape reviews support proactive licensing, litigation, or development strategies.

FAQs

Q1: What is typically included in the claims of a pharmaceutical patent like EP3006036?
A: Claims generally cover the chemical compounds themselves, their formulations, pharmaceutical uses, production methods, and specific dosing or treatment methods.

Q2: How does claim breadth impact patent enforceability in Europe?
A: Broader claims can provide extensive protection but risk invalidation if they lack novelty or inventive step. Narrower claims are easier to defend but offer limited scope.

Q3: What are common challenges to patents like EP3006036?
A: Challenges often stem from prior art disclosures, lack of inventive step, insufficient disclosure, or ambiguity in claim language.

Q4: How does the patent landscape influence drug development strategies?
A: It guides R&D focus, licensing opportunities, and the timing of filing supplementary patents to maintain market exclusivity.

Q5: What is the significance of patent families surrounding EP3006036?
A: Patent families extend coverage internationally and across different jurisdictions, strengthening market protection and blocking competitors.


References

  1. European Patent Office. (2018). Patent EP3006036 Details.
  2. Espacenet. Patent family and legal status information.
  3. WIPO. Patent Landscape Reports on pharmaceutical innovations.
  4. European Patent Convention (EPC) legal framework on patent claims.
  5. Strategic patent management in pharma: insights from IP professionals.

More… ↓

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