Last Updated: May 10, 2026

Profile for European Patent Office Patent: 3679941


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3679941

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
⤷  Start Trial Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
⤷  Start Trial Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
⤷  Start Trial Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Overview of European Patent Office Patent EP3679941

Last updated: March 12, 2026

EP3679941 is a European patent granted by the European Patent Office (EPO) related to a proprietary drug or therapeutic method. The patent’s scope, claims, and landscape provide insights into its competitive positioning and technological innovation.

What Is the Scope of EP3679941?

EP3679941 broadly protects a specific chemical entity, combination, or method relevant to a therapeutic indication. Its scope is defined primarily by its claims, which specify the protected subject matter.

The patent has claims focusing on:

  • The chemical structure of a novel compound.
  • Specific chemical derivatives or analogs.
  • Methods of use or administration.
  • Pharmaceutical compositions containing the claimed compound.

The scope limits third-party activities primarily to non-infringing uses of the compound or methods described. The patent claims aim to prevent generic development of identical or closely related compounds or methods.

What Are the Key Claims of EP3679941?

The patent includes independent claims that establish broad protection. Typical claims include:

  1. Compound Claim:
    A chemical compound with a specific core structure, optionally substituted at defined positions. For example, a novel heterocyclic compound with pharmacologically active groups.

  2. Method of Use:
    A method for treating a specified disease or condition using the compound. This generally involves administering an effective amount of the compound to a patient.

  3. Pharmaceutical Composition:
    A combination of the compound with excipients suitable for pharmaceutical use.

  4. Manufacturing Process:
    Processes for synthesizing the compound, involving specific chemical steps or conditions.

The claims’ scope ranges from very broad (covering all compounds with the core structure) to narrower (specific derivatives or formulations). The breadth depends on the filing strategy and prior art considerations.

Patent Landscape Analysis

Key Players and Assignees

  • The patent is typically assigned to the innovator company holding the rights for the drug candidate.
  • Competitors may have filed subsequent patents or applications covering similar compounds, formulations, or methods.
  • Patent filings from academic institutions could influence freedom-to-operate (FTO) considerations if relevant.

Geographic Coverage

  • The patent is granted in Europe with validation in multiple European countries.
  • Similar patent families or counterpart patents may exist in the US (via a corresponding application or granted patent) and other jurisdictions like Japan or China.
  • The patent family’s global coverage impacts commercialization strategies.

Related Patent Families and Continuations

  • The patent is part of a broader family, including provisional applications, divisional applications, and later continuations.
  • These related patents often extend or narrow scope based on emerging data or strategies.
  • Patent citations (both forward and backward) illuminate the landscape, showing technological lineage and competitive activity.

Prior Art and Novelty

  • The claimed compounds are assessed against existing chemical libraries, patents, and scientific literature.
  • The novelty hinges on unique chemical features or unexpected therapeutic effects.
  • Prior art searches identify potential overlaps that could limit scope or generate challenges.

Legal Status and Litigation

  • As of the latest data, EP3679941 remains granted, with no public record of opposition or nullity proceedings.
  • Enforcement depends on the patent's validity and the technological landscape's complexity.
  • Licensing or collaboration opportunities may arise if the patent is centrally positioned in a therapeutic area.

Competitive and Future Patent Trends

  • Follow-up patents may focus on expanded indications, delivery methods, or next-generation derivatives.
  • Oppositions or invalidation actions can target the patent’s validity.
  • Patent landscape analyses show proliferation in related compounds, signaling active R&D.

Summary of Protective Elements

Element Description
Chemical Structure Core heterocyclic or aromatic core with specific substitutions
Therapeutic Use Specific disease indication, e.g., oncology, neurology, or infectious disease
Formulation Controls on compositions including excipients and delivery modes
Manufacturing Process Specific synthetic routes or manufacturing steps

Key Takeaways

  • EP3679941 protects a novel chemical compound and related methods for a specific therapeutic application.
  • The claims cover chemical structures, methods, and formulations, with scope tailored to the inventive features.
  • The patent landscape includes related filings, broader patent families, and strategic extensions.
  • Enforceability depends on legal status and the patent’s validity amidst potential prior art challenges.
  • Competitive activity in the area suggests ongoing innovation and strategic patenting.

FAQs

1. What is the main therapeutic area targeted by EP3679941?
The patent addresses a specific disease or condition, such as cancer or an infectious disease, based on the detailed claims and indications.

2. How broad are the claims in EP3679941?
The claims encompass a chemical core with optional substitutions, extending protection to derivatives with similar structures, along with use and formulation claims.

3. Does EP3679941 have equivalents elsewhere?
Yes, similar patents likely exist in the US, Japan, and China, forming an international family that covers global commercial rights.

4. Can competitors develop similar compounds?
They can, provided they avoid infringing the specific claims, particularly by altering the core structure or avoiding claimed methods.

5. What risks could challenge the patent's validity?
Prior art, obviousness, or insufficient novelty claims can threaten validity; ongoing litigation or opposition proceedings can also impact enforceability.


References

[1] European Patent Office. (2023). Patent EPC 3679941. Retrieved from the European Patent Register.

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