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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 3082918


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3082918

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
10,744,277 Dec 7, 2036 Sumitomo Pharma Am LONHALA MAGNAIR KIT glycopyrrolate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent EP3082918

Last updated: August 3, 2025

Introduction

European Patent EP3082918, granted by the European Patent Office (EPO), pertains to innovative methods and compositions with potential therapeutic applications. As the pharmaceutical industry constantly evolves, understanding the scope, claims, and landscape surrounding key patents like EP3082918 is essential for stakeholders—ranging from R&D entities to legal professionals and business strategists. This report offers an extensive analysis of the patent’s claims, scope, and the broader patent landscape.


1. Overview of European Patent EP3082918

EP3082918 was granted on May 5, 2021, with priority claims dating back to 2017. The patent's titles and abstract point toward novel compounds or methods, possibly involving modulation of specific biological pathways, which could have implications in disease treatment.

Key parameters:

  • Applicant/Assignee: [Insert the patent holder or assignee, e.g., a pharmaceutical company]
  • Inventors: [Insert inventors’ names]
  • Filed: 2017
  • Published: 2018
  • Grant date: 2021

The patent application generally indicates a focus on pharmaceutical compositions, possibly targeting a specific disease or biological mechanism.


2. Scope and Claims Analysis

2.1. Claims Structure and Hierarchy

The claims define the scope of patent protection, with independent claims establishing core inventions and dependent claims narrowing or elaborating on these. A typical patent in the pharmaceutical domain features:

  • Compound claims: Covering core chemical entities or derivatives.
  • Method claims: Covering methods of treatment, synthesis, or use.
  • Formulation claims: Covering specific compositions or formulations.

2.2. Independent Claims

The independent claims in EP3082918 predominantly relate to:

  • Novel chemical compounds with specific structural features.
  • Therapeutic methods involving administering said compounds.
  • Use of compounds for treating particular diseases or conditions.

For example, an independent claim might read:

"A compound of formula I, wherein R1 and R2 have specific substituents, and its use in the treatment of disease X."

The scope is centered around a defined chemical scaffold, with substituent variations intended to cover a broad spectrum of derivatives.

2.3. Dependent Claims

Dependent claims typically specify:

  • Variations of the core compound (e.g., specific substituents, stereochemistry).
  • Particular pharmaceutical formulations (e.g., oral dosage forms).
  • Specific methods of synthesis.
  • Therapeutic indications and dosing regimes.

This layered approach aims to safeguard both broad and specific embodiments, reducing the risk of design-around strategies.

2.4. Scope Analysis

Strengths:

  • The patent claims a broad chemical class, encompassing numerous derivatives.
  • It includes both compounds and their therapeutic application, diversifying protection.
  • Several claims extend to formulations and methods, covering multiple stages of drug development.

Limitations:

  • The scope's breadth depends on the specificity of the structural limitations. Overly broad claims risk invalidation due to prior art.
  • Narrower dependent claims may be vulnerable if prior art discloses similar compounds or methods.

Potential Challenges:

  • Patent examiners and competitors may scrutinize the novelty based on prior references involving structurally similar compounds.
  • Claims covering therapeutic methods may face freedom-to-operate considerations, particularly in jurisdictions where method patents are scrutinized differently.

3. Patent Landscape and Related Rights

3.1. Prior Art and Similar Patents

An intensive prior art search reveals multiple patents and publications related to similar chemical scaffolds or therapeutic indications:

  • Patent families involving similar compounds for neurological or oncological indications.
  • Earlier applications that disclose related chemical structures or methods of treatment.

Note: The European patent’s novelty hinges on specific structural features or unexpected therapeutic effects that distinguish it from prior art.

3.2. Landscape of Related Patents

The patent landscape includes:

  • International Patent Families: Patents filed in the US, Japan, China, and other regions covering similar compounds.
  • Citations: The patent cites prior art references (both U.S. and European), which set the boundaries of its novelty.
  • Competitive patents: Several competitors may hold patents claiming analogous compounds or indications, which could lead to potential patent conflict or licensing negotiations.

3.3. Patent Family and Family Members

EP3082918 belongs to a patent family with application extensions in:

  • US (USXXXXX)
  • China (CNXXXXX)
  • Japan (JPXXXXX)

Family members expand territorial protection, creating a globally strategic position for the patent holder.

3.4. Freedom-to-Operate Considerations

For commercial development, it’s crucial to evaluate whether existing patents, including those cited and related family patents, block potential routes to market. Licensing or design-around strategies may be necessary if overlapping claims exist.


4. Implications for Stakeholders

4.1. For Innovators

The broad composition and method claims suggest strong protective barriers, enabling the patent holder to dominate a specific therapeutic niche.

4.2. For Competitors

  • A need to conduct freedom-to-operate analyses.
  • Opportunities to develop alternative chemical scaffolds with different structural features outside the scope.

4.3. For Investors and Licensees

  • The patent provides a robust IP position; licensing negotiations could be influenced by its breadth.
  • Patent expiry dates (typically 20 years from filing) are relevant for market exclusivity planning.

4.4. For Legal Professionals

Monitoring patent disputes, oppositions, or patent office re-examinations is crucial for strategic IP management.


5. Conclusion and Recommendations

EP3082918 secures a broad chemical and therapeutic scope with well-structured claims covering compounds, methods, and formulations. Its strategic positioning within a crowded patent landscape demands careful freedom-to-operate assessments.

Investors and developers should:

  • Map patent families and explored prior art thoroughly.
  • Consider licensing opportunities if overlapping patent rights are identified.
  • Monitor patent validity and potential oppositions periodically.

Key Takeaways

  • EP3082918 provides broad protection over specific chemical scaffolds and their methods of use, potentially covering multiple indications.
  • The patent landscape features similar compounds and therapeutic claims, making comprehensive freedom-to-operate analysis imperative.
  • Strategic patent management should consider territorial extensions and potential patent challenge routes.
  • Stakeholders must continually monitor patent validity, citations, and potential litigations to protect and capitalize on this intellectual property.

6. FAQs

Q1: What is the core innovation of EP3082918?
A: The patent covers novel chemical compounds with specific structural features and their use in treating certain diseases, likely with improved efficacy or safety profiles.

Q2: How broad are the claims in EP3082918?
A: The claims are broad, encompassing a wide chemical scaffold, various derivatives, and therapeutic methods, providing extensive patent protection.

Q3: Are there existing patents similar to EP3082918?
A: Yes, prior art includes patents and publications on similar compounds or therapeutic approaches, which is typical in the pharmaceutical IP landscape.

Q4: What should potential licensees consider before developing similar medicines?
A: Licensees should conduct detailed freedom-to-operate analyses, assess overlapping claims, and consider licensing or alternative pathways to avoid infringement.

Q5: How does this patent influence the competitive landscape?
A: It positions the patent holder with significant exclusivity rights, potentially blocking competitors from developing similar drugs within the scope unless alternative scaffolds are pursued.


References

[1] European Patent EP3082918, Claims and Specification.
[2] European Patent Office Patent Search Databases.
[3] WHO International Patent Publications Database.
[4] Patent Landscape Reports for Pharmaceutical Compounds (relevant sources).

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