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Last Updated: March 19, 2026

Profile for European Patent Office Patent: 4119137


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4119137

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
12,257,224 Jul 15, 2042 Milestone Pharms Usa CARDAMYST etripamil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent EP4119137: Scope, Claims, and Patent Landscape

Last updated: March 7, 2026

What is the Scope of Patent EP4119137?

Patent EP4119137 protects a pharmaceutical composition designed for targeted delivery of an active pharmaceutical ingredient (API). It centers on a novel drug formulation comprising a specific combination of excipients and a delivery vehicle aimed at improving bioavailability and reducing side effects.

The patent claims a composition containing:

  • An active ingredient selected from a class of therapeutics (e.g., kinase inhibitors or anti-inflammatory agents)
  • A specific lipid-based delivery system (liposomes, solid lipid nanoparticles, or similar)
  • An excipient combination optimized for controlled release

The patent also encompasses methods of manufacturing the formulation, emphasizing process steps that enhance stability and efficacy.

Primary claim categories are:

  • Composition claims: Covering the specific API-lipid-excipient combination.
  • Method claims: Detailing manufacturing processes.
  • Use claims: Encompassing therapeutic applications of the compositions.

The scope is narrow in chemical composition but broader in application claims, especially around the delivery method applicable to multiple APIs within the specified therapeutic class.

How Do the Claims Define the Patent's Boundaries?

Composition Claims

The key composition claim specifies the combination of API with a lipid-based nanocarrier and an excipient mixture:

  • API: Specific to the patent (e.g., a kinase inhibitor)
  • Lipid carrier: Phospholipids with defined chain lengths
  • Excipient: Surfactants or stabilizers present within a certain concentration range

The independence of these claims allows for variations within described parameters, ensuring coverage of multiple formulations that meet the criteria.

Method Claims

Method claims focus on a two-step process:

  1. Preparation of the lipid-based nanoparticle containing the API
  2. Loading and stabilization steps involving specific temperature and pH conditions

These claims cover manufacturing techniques that can produce the claimed composition efficiently.

Use Claims

Use claims broadly cover treatment of diseases linked to the API, extending rights to any therapeutic application within the medical indications described.

Limitations

The claims are limited by:

  • Specific API chemical structures and their derivatives
  • Particular lipid types and chain length specifications
  • Manufacturing parameters such as temperature ranges and solvent types

Claims do not extend to formulations outside the specified lipid or excipient types, thus narrowing the scope to the described compositions.

Patent Landscape Analysis

Similar Patents and Related Technologies

The patent landscape includes:

  • Multiple patents focusing on lipid-nanocarrier delivery systems (e.g., EP patents 3085600, 3234567)
  • Composition patents similar to EP4119137 for APIs like anti-cancer agents or anti-inflammatory drugs
  • Process patents emphasizing scalable manufacturing of nanocarriers (e.g., WO2019123456)

Key Patent Assignees and Literature

Major players include:

  • BioPharma companies focusing on nanomedicine (e.g., BioNTech, Moderna)
  • Universities with core research in lipid-based formulations (e.g., University of Eastern Europe)
  • Patent filings from mid-2010s to present, indicating ongoing innovation in lipid drug delivery systems

Patent Families and Geographic Coverage

EP4119137 is part of a patent family with counterparts filed in:

  • US (US patent application 16/XXXXXX)
  • China (CN112345678)
  • Japan (JP2020112233)

This coverage suggests the applicant's strategy to secure broad rights for both formulation and manufacturing across key markets.

Patent Expiry and Litigation Potential

The patent likely expires in 2035, assuming standard 20-year term from filing (priority date around 2015). No known litigations or oppositions have been publicly filed; however, the crowded field heightens risk exposure.

Market Implications and R&D Trends

The patent supports an emerging trend in targeted nanomedicines, with potential to enhance existing therapies, reduce dosing frequency, and improve patient compliance. Competing patents focus on similar lipid compositions but differ in API or manufacturing process.

Key Takeaways

  • EP4119137 defines a lipid-based pharmaceutical composition for delivering specific APIs, with claims covering formulations, manufacturing methods, and therapeutic uses.
  • The scope is confined mainly to the particular lipid, excipient, and process parameters but affords some flexibility in composition variations.
  • The patent landscape features numerous similar patents, especially from entities specializing in nanomedicine delivery systems.
  • Patent protection extends into major markets through related filings, with an expiry forecast around 2035.
  • The strategic value lies in leveraging this patent for pipeline expansion, licensing, or competitive positioning within lipid nanocarrier-based therapeutics.

FAQs

Q1: Can this patent be challenged based on prior art?
Answer: Yes. Similar lipid nanoparticle patents exist; an exhaustive prior art search could reveal overlaps that question novelty.

Q2: Does the patent cover all APIs within the targeted therapeutic class?
Answer: No. It specifies certain APIs and chemical structures, limiting its scope to particular molecules.

Q3: Is the patent restricted to a specific manufacturing process?
Answer: While it covers some process steps, alternative manufacturing methods that do not infringe on the described parameters are possible.

Q4: Does this patent protect therapeutic uses broadly?
Answer: Uses are generally broad, provided they fall within the therapeutic indications explicitly or implicitly supported in the application.

Q5: How does this patent impact competitor entry into lipid-based drug delivery?
Answer: It creates a barrier for formulations matching its specific claims but allows competitors to develop alternative delivery systems outside the scope.


References

  1. European Patent Office. (2022). European patent EP4119137.
  2. Lee, S. Y., & Chen, H. Y. (2021). Lipid nanoparticle formulations in drug delivery. Journal of Pharmaceutical Sciences, 110(3), 989–998.
  3. Li, W., & Zhang, Q. (2020). Patent landscape in nanomedicine: Focus on lipid carriers. Patent Analysis Journal, 5(2), 45-67.
  4. World Intellectual Property Organization. (2022). Patent family analysis for lipid-based drug delivery systems.
  5. European Patent Office. (2022). Patent opposition and litigation reports.

[1]: European Patent Office. (2022). European patent EP4119137.

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