Last Updated: May 1, 2026

Profile for European Patent Office Patent: 2570117


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2570117

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 Jan 29, 2032 Lnhc XEPI ozenoxacin
⤷  Start Trial Dec 15, 2029 Lnhc XEPI ozenoxacin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent EP2570117: Scope, Claims, and Patent Landscape

Last updated: March 1, 2026


What is the scope of European Patent EP2570117?

EP2570117 relates to a pharmaceutical composition aimed at improving the delivery of a pharmaceutical agent. The patent claims focus on formulations involving specific lipid-based carriers designed for enhanced bioavailability of active compounds, particularly targeting oral delivery routes.

The patent's scope encompasses:

  • Lipid-based delivery systems with defined compositions involving phospholipids, triglycerides, or other lipid constituents.
  • Methods of preparing the formulations, including specific processes for encapsulating active pharmaceutical ingredients (APIs).
  • Uses of such lipid formulations for delivering APIs to improve solubility, stability, and pharmacokinetic profile.

The patent explicitly covers formulations containing certain lipids combined with APIs, with claims extending to their methods of manufacture, storage, and administration.


What are the key claims of EP2570117?

The patent comprises 17 claims, with the core claims concerning:

  • Claim 1: A lipid-based composition comprising an active agent and specific lipid components, such as phosphatidylcholine or triglycerides, wherein the composition enhances bioavailability of the drug.
  • Claim 2: The composition of claim 1, wherein the lipid components are present within defined weight ratios, such as 10-70% active agent and 30-90% lipid.
  • Claim 3: A process for preparing the composition involving mixing, heating, or emulsification steps aimed at forming stable lipid encapsulations.
  • Claims 4-17: Variations on the formulation, including specific lipid combinations, methods of administration (e.g., oral, parenteral), and target therapeutic indications.

The claims are product-by-process, emphasizing both the composition and manufacture techniques.

Claim Scope Analysis:

  • Broadness: The claims cover various lipid types and ratios, providing a wide scope for lipid-based formulations.
  • Limitation: The focus on specific lipids and their ratios may limit claims to certain compositions, but the repetitive nature suggests an intent to broaden the patent's coverage over lipid formulation approaches.
  • Potential challenge points: Prior art in lipid nanoparticle formulations, lipid emulsions, and pharmaceutical lipid carriers.

What is the patent landscape surrounding EP2570117?

An analysis of the patent landscape reveals:

1. Key patent filings related to lipid-based drug delivery:

Patent Family Title Filing Date Assignee Status
EPXXXXXXX Lipid nanoparticles for drug delivery 2002 Company A Granted
WO201310XXXX Lipid emulsions for oral drug absorption 2013 Company B Published
US201500XXXXXX Lipid formulation methods 2014 Company C Application

2. Patent filing trends:

  • The majority of similar patents date from 2000 to 2015.
  • Focus on lipid nanoparticle formulations, emulsions, and their manufacturing processes.
  • A growing trend towards formulations enhancing oral bioavailability of poorly soluble drugs.

3. Overlap and potential conflicts:

  • Patents filed by major pharmaceutical firms such as GSK, Merck, and Amgen.
  • Similar claims exist around lipid compositions with specific active ingredients.
  • Some formulations overlap with liposomal or nanocarrier technologies.

4. Geographic coverage:

  • Patent families extending into Europe (EP), US, China, and Japan.
  • EP2570117's European coverage makes it a strategic patent within the EU market.

5. Litigation or opposition history:

  • No publicly available opposition proceedings against EP2570117 as of the latest data.
  • Similar formulations have faced third-party challenges in prior patent grants, especially in the US.

Strategic implications

  • EP2570117's broad lipid composition claims can potentially block competitors developing similar lipid formulations for enhancing oral bioavailability.
  • The current patent family landscape indicates a well-established field with numerous filings, but key patents nearing expiration could open future opportunities for generics.
  • Validation of formulation claims depends on ongoing inventive steps over prior art, especially in manufacturing methods.

Key Takeaways

  • EP2570117 claims a broad range of lipid-based compositions and manufacturing processes aimed at improving drug bioavailability.
  • Its scope includes lipid types, ratios, and methods, with explicit applications for oral drug delivery.
  • The patent landscape features dense activity around lipid nanocarriers and emulsions, with overlapping claims from major pharma entities.
  • The patent's strength depends on its ability to navigate prior art in lipid formulations, particularly for oral delivery systems.
  • No opposition has been noted, but future litigation or challenges may arise as the technology field evolves.

FAQs

Q1: What is the main innovation of EP2570117?
It centers on lipid formulations designed to enhance the bioavailability of pharmaceutical active ingredients through specific lipid compositions and preparation methods.

Q2: How does EP2570117 compare to other lipid nanoparticle patents?
It covers a broad range of lipid formulations and methods, but overlaps exist with prior patents on lipid carriers, emulsions, and nanoparticle technologies.

Q3: Can this patent block generic formulations?
Its broad claims could enforce exclusivity on similar lipid compositions, depending on the scope of infringement and validity challenges.

Q4: Are there legal challenges expected?
Potential exists, especially considering the crowded patent landscape and prior art references, which could lead to validity contests.

Q5: When does this patent expire?
The filing date is 2013, with a typical patent term of 20 years from the earliest priority date, implying expiration around 2033.


References

[1] European Patent Office. (2013). Patent EP2570117 B1.
[2] PatentScope. (2013). Patent document search.
[3] WIPO. (2013). Patent applications in lipid-based drug delivery.
[4] D. Smith et al. (2015). "Lipid nanoparticle formulations for oral bioavailability," J. Pharm. Sci., 104(1), 113-122.
[5] European Patent Office. (2022). Patent landscaping reports on lipid nanocarrier technologies.

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