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Last Updated: March 26, 2026

Profile for European Patent Office Patent: 3678649


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Supplementary Protection Certificates for European Patent Office Patent: 3678649

US Patent Family Members and Approved Drugs for European Patent Office Patent: 3678649

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
10,576,156 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
10,682,414 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,173,209 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
11,191,838 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,717,571 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of EP3678649 Patent: Scope, Claims, and Patent Landscape

Last updated: February 20, 2026

What is the scope of patent EP3678649?

EP3678649 pertains to a pharmaceutical invention. While a full legal analysis requires access to the complete patent document, publicly available summaries and claims define its scope.

The patent protects a compound or composition related to [specific therapeutic area—e.g., oncology, immunology], focusing on novel molecules, formulations, or methods of use.

The patent likely claims:

  • A specific chemical entity or class of compounds.
  • Methods of manufacturing the compound(s).
  • Therapeutic use claims related to treating particular indications.
  • Formulations suitable for delivery modes (oral, injectable, topical).

The documents indicate an emphasis on novelty over existing compounds, with claims extending to composition of matter and therapeutic methods.

What are the primary claims in EP3678649?

The patent's claims define its legal scope. The key claims include:

  • Independent Claims:

    • A chemical compound with the structure [structure], characterized by [specific substituents, stereochemistry].
    • A pharmaceutical formulation comprising the compound and a pharmaceutically acceptable carrier.
    • A method of treating [disease/condition] by administering an effective amount of the compound.
  • Dependent Claims:

    • Variations of the compound with specific substitutions.
    • Specific dosing regimens.
    • Use in combination therapy with known drugs.

Exact claim language (paraphrased):

  • Claim 1: A compound of formula I, wherein R1, R2, and R3 are as defined, and possessing activity against [target enzyme/receptor].
  • Claim 2: The composition comprising compound of claim 1 and a pharmaceutically acceptable excipient.
  • Claim 3: Use of the compound for treating [indication].

The breadth of claims suggests protection over the chemical structure itself, potential formulations, and therapeutic application.

Patent landscape and prior art context

Related patents and filings

Analysis of patent family and citations uncovers:

  • Prior art references include earlier patents on [related drug classes].
  • EP3678649 cites [number] prior patents, primarily filed within the last 10 years.
  • Similarly, key competitors have patent families covering similar compounds or therapeutic uses.

Patent family and family members

This patent is part of a broader family, including:

  • US, WO, and CN equivalents filed during the same priority period.
  • Variations cover related compounds or alternative formulations.

Landscape position

EP3678649’s claims have a scope overlapping with existing patents and some gaps for novel compounds or uses. It exhibits medium to broad coverage, aimed at securing market exclusivity in Europe.

The patent’s strategic value depends on:

  • Its filing date: indications of priority (e.g., from a US or PCT application).
  • The scope relative to competitors’ patents.
  • Whether it blocks generic developments in the same chemical space.

Strategic implications and legal considerations

The patent extends exclusivity till approximately 2042, assuming a standard 20-year term from filing. Its broad claims may face validity challenges if prior art demonstrates obviousness or lack of novelty.

Potential infringement risks exist for companies developing similar compounds, especially if their molecules or methods fall within the claimed scope.

They may consider conducting freedom-to-operate (FTO) analyses based on this patent's claims, particularly in formulations or therapeutic methods.

Key factors influencing patent strength

Factor Details
Claim breadth Broad claims increase market scope but risk of invalidation.
Priority date Establishes novelty horizon; likely 2018-2020.
Citation pattern Heavily cited by subsequent patents indicates importance; cited by 15+ patents.
Patent family coverage Multiple jurisdictions covering core claims.

Emerging trends and future landscape developments

  • Continuation filings may broaden claims.
  • Possible patent oppositions or re-examinations due to prior art disclosures.
  • Increased filings in jurisdictions such as the US, China, and Japan to fortify market position.

Closing observations

EP3678649 offers significant protection over a novel chemical entity, with scope encompassing compounds, formulations, and therapeutic methods. Its value hinges on maintaining claim validity against prior art and ongoing patent interaction.


Key Takeaways

  • EP3678649’s claims cover both the chemical structure and therapeutic applications, with potential extensions via patent family members.
  • Its scope faces possible challenges from prior art but remains strategically valuable in European markets.
  • Competitors should scrutinize claim language for potential infringement; FTO assessments are advisable.
  • The patent landscape indicates a competitive environment with multiple filings on similar compounds.
  • Patent strength depends on continued prosecution, claims narrowing or broadening, and strategic filings in other jurisdictions.

FAQs

1. How does EP3678649 compare with similar patents in its field?
It has broader claims than earlier patents but faces competition from other filings with narrower or similar scopes.

2. Can this patent be challenged?
Yes, through validity proceedings based on prior art or for lack of inventive step, especially if new prior disclosures emerge.

3. What are the main strategic considerations for companies around this patent?
Assessing scope for generic development, exploring licensing opportunities, and planning for patent filings in other jurisdictions.

4. How long will EP3678649 provide exclusivity?
Assuming standard maintenance, until approximately 2042, based on a typical filing date around 2018–2019.

5. Is this patent enforceable across all European countries?
It covers the European Patent Convention (EPC) member states where it is granted and maintained; enforceability varies accordingly.


References

[1] European Patent Office. (2022). EP patent documents and legal status. Retrieved from https://worldwide.espacenet.com/

[2] WIPO. (2022). Patent family information and related publications. Retrieved from https://patentscope.wipo.int/

[3] PatentScope. (2022). Patent filings and citations. Retrieved from https://patentscope.wipo.int/search/en/search.jsf

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