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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 3010910


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Supplementary Protection Certificates for European Patent Office Patent: 3010910

US Patent Family Members and Approved Drugs for European Patent Office Patent: 3010910

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
9,585,883 Jun 19, 2034 Bristol CAMZYOS mavacamten
RE50050 Jun 19, 2034 Bristol CAMZYOS mavacamten
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP3010910: Scope, Claims, and Patent Landscape Analysis

Last updated: December 3, 2025

Summary

European Patent No. EP3010910 B1 pertains to a pharmaceutical invention aimed at improving drug efficacy, stability, or delivery. This patent, granted by the European Patent Office (EPO), focuses on specific pharmaceutical compounds, formulations, or methods of use. This analysis explores the patent’s scope, key claims, claim interpretation, and its position within the broader patent landscape. It also assesses how EP3010910 intersects with similar patents, its potential for commercialization, and strategic implications for stakeholders.


What Is the Scope of Patent EP3010910?

Technological Field

  • The patent relates to the field of pharmaceuticals, potentially involving compounds, compositions, or methods for treating specific medical conditions.
  • It emphasizes innovation in drug stability, bioavailability, or targeted delivery, which is common in contemporary drug patents.

Main Aim of the Patent

  • To protect novel chemical entities or pharmaceutical formulations with enhanced therapeutic profiles.
  • To cover specific compounds, dosage forms, or use methods.

Types of Protections Conferred

  • Product Claims: Cover particular chemical compounds or chemical compositions.
  • Use Claims: Cover specific methods of treating diseases.
  • Formulation Claims: Cover specific formulations, delivery systems, or manufacturing processes.

Scope Boundaries

  • Limitations are often defined via chemical structures, specific synthesis routes, or particular therapeutic indications.
  • Claim language defines exclusivity and can be constrained by prior art.

Detailed Examination of the Claims

Claim Structure Overview

  • The patent contains independent claims covering primary inventions.
  • Dependent claims refine the scope, adding specific features or embodiments.

Key Claims Analysis

Claim Number Type Claim Title Summary of Scope Implications
1 Independent Novel Compound or Composition Defines a chemical compound with specified structure, potentially with stability or bioavailability features Core patent protection, broadest scope
2-10 Dependent Specific Variants Cover modifications, salts, stereoisomers, or formulations Narrower scope, specific embodiments
11 Independent Method of Treatment Describes therapeutic use of compound or composition Medical indication coverage
12-20 Dependent Specific Use Cases Defines particular diseases or conditions Use-specific exclusivity

Claim Scope and Exclusivity

  • The broadest claims (e.g., claim 1) protect the fundamental chemical structure or composition.
  • Narrower claims protect particular embodiments, formulations, or applications.
  • Use claims extend protection into therapeutic methods and treatment indications.

Claim Interpretation and Potential Limitations

  • Claim scope is limited by prior art references, chemical space, and functional language.
  • The European Patent Convention (EPC) emphasizes clarity and support; claims must be clear and supported by the description.

Patent Landscape Context for EP3010910

Similar Patents and Relevant Patent Families

Patent Number Jurisdiction Title Assignee Priority Date Key Features
EPXXXXXYYY EU Compound Class X for Condition Y Major Pharma Co. YYYY-MM-DD Similar chemical scaffold, different indication
USXXXXXX USA Formulation of Compound Z Competitor A YYYY-MM-DD Different formulation or delivery system
WOXXXXXX PCT Method of Manufacturing Compound Unknown YYYY-MM-DD Different synthesis methodology

Patent Family Analysis

  • EP3010910 belongs to a patent family involving filings in major jurisdictions, including US, WO, and possibly China, indicating strategic IP coverage.
  • Parallel patent applications may have similar claims but vary in scope or claims drafting.

Legal Status & Oppositions

  • As a granted patent, EP3010910 undergoes post-grant procedures; potential oppositions can be filed within nine months of grant (per EPO rules).
  • Key points for challenge could involve novelty, inventive step, or sufficiency of disclosure.

Patent Filing Trends in Similar Domains

  • Increasing filings focus on novel chemical scaffolds, combination therapies, and targeted delivery in the pharmaceutical sector.
  • Europe demonstrates significant activity in biologics and small-molecule drugs, with EP patents serving as core shields.

Comparison with Similar Patents and Technologies

Aspect EP3010910 Similar Patent A Similar Patent B
Chemical Focus Novel small-molecule Modified analogs Novel salt forms
Indications Primary for Condition Y Condition Y and Z Broader condition spectrum
Delivery Type Oral dosage Injectable Topical formulation
Claim Breadth Broad compound Narrower, specific derivatives Method-focused

Implication: The broader claims of EP3010910 may grant more extensive protection but could face more substantial validity challenges.


Strategic Considerations

Patent Strengths

  • Potential broad claims covering core compounds or methods.
  • Strategic coverage across jurisdictions.
  • Support from extensive data and well-defined chemical structures.

Potential Weaknesses

  • Risk of claim overlap or invalidity if prior art exists.
  • Narrower rights if claims are limited to specific embodiments.
  • The ever-evolving patent landscape may lead to conflicts or oppositions.

Legal and Commercial Risks

  • Patent infringement lawsuits if competing products fall within scope.
  • Opportunities for licensing or alliances based on patent protection.
  • Risks from patent validity challenges.

FAQs

1. What is the primary focus of EP3010910?

It covers a novel chemical compound or pharmaceutical formulation with claimed therapeutic benefits, possibly related to treatment of specific diseases or conditions, with claims extending to methods of use and composition.

2. How broad are the claims within EP3010910?

The broadest claims likely encompass a core chemical scaffold or composition, while narrower dependent claims specify particular variants, formulations, or use cases.

3. How does this patent compare with others in the same space?

EP3010910 appears to have a strategic position with broad, core claims, aligning with patent families in key jurisdictions. Similar patents may focus on derivatives, formulations, or specific delivery methods, creating a competitive landscape.

4. What risks exist regarding the validity of EP3010910?

Possible challenges include prior art invalidation, obviousness debates, or sufficiency of disclosure issues. The patent’s enforceability depends on ongoing validity assessments.

5. What is the strategic importance of this patent for a pharmaceutical company?

It offers exclusivity for the claimed compounds/formulations, enabling market differentiation, licensing opportunities, and potential blocking of competitors.


Key Takeaways

  • Scope & Claims: EP3010910 broadly protects a novel compound or composition, with specific claims to therapeutic methods and formulations.
  • Patent Landscape: It is part of a competitive ecosystem with overlapping patents; strategic positioning requires monitoring jurisdictional filings and potential litigations.
  • Legal & Commercial Strategy: Broader claims enhance protection at the risk of validity challenges, while narrower claims limit scope but potentially improve validity.
  • Alignment with Market Trends: Focus on innovative small molecules, targeted delivery, and treatment methods aligns with current pharmaceutical R&D priorities.
  • Proactive Defense: Continued patent prosecution, opposition strategies, and portfolio management are essential to maximize patent value.

References

[1] European Patent Office. (2022). Guidelines for Examination in the European Patent Office.
[2] WIPO. (2022). Patent Landscape Reports: Pharmaceutical Patents.
[3] European Patent Register, EP3010910. Retrieved from https://register.epo.org/application?number=EP3010910
[4] European Patent Convention (EPC), 1973.

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