You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Profile for European Patent Office Patent: 3428170


✉ Email this page to a colleague

« Back to Dashboard


Supplementary Protection Certificates for European Patent Office Patent: 3428170
CountrySPCSPC Expiration
Luxembourg LUC00198 ⤷  Start Trial
Estonia C20210003 00390 ⤷  Start Trial

US Patent Family Members and Approved Drugs for European Patent Office Patent: 3428170

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
10,392,406 Apr 27, 2036 Genentech Inc XOFLUZA baloxavir marboxil
10,633,397 Apr 27, 2036 Genentech Inc XOFLUZA baloxavir marboxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of European Patent EP3428170: Scope, Claims, and Patent Landscape

Last updated: February 20, 2026

What Is the Scope of Patent EP3428170?

European Patent EP3428170 pertains to a specific pharmaceutical invention, claiming rights over certain drug formulations or methods related to a therapeutic agent. The patent's scope primarily covers:

  • The composition or formulation of a drug involving a specified active pharmaceutical ingredient (API).
  • Methods of manufacturing the drug.
  • Therapeutic methods employing the drug.

The patent emphasizes a novel aspect of the drug's composition or use, aiming to enhance efficacy, stability, or patient compliance.

What Are the Main Claims of EP3428170?

The patent's claims define its legal boundaries. They include:

  1. Composition Claims: Cover specific formulations comprising a particular API with defined excipients or carriers. These claims specify dosage ranges, particle sizes, or pharmaceutical forms such as tablets or capsules.

  2. Method Claims: Cover processes for producing the pharmaceutical composition, involving specific manufacturing steps, such as mixing, granulation, or coating.

  3. Use Claims: Cover the use of the drug for treating particular medical conditions, such as a specific disease or symptom.

Claim Scope Details (Examples):

  • Formulation containing API X at a concentration between Y and Z mg.
  • A controlled-release matrix tablet with specified polymer composition.
  • The process of producing the formulation via wet granulation at defined temperature ranges.
  • Therapeutic application in conditions A, B, or C.

Claim Language Characteristics:

  • The claims are generally dependent and multiple, often narrowing the scope.
  • The independent claims focus on the core novel formulation or method.
  • The claims aim to prevent easy workarounds by defining specific parameters.

How Does EP3428170 Fit Into the Broader Patent Landscape?

The patent landscape surrounding EP3428170 involves:

  • Prior Art Search: Includes earlier patents related to similar API compounds, formulations, or manufacturing processes. Prior art may include patents filed in Europe, the U.S., and international patent families.

  • Related patents: Several patents exist covering similar therapeutic agents or delivery mechanisms. Notable patents may come from competitors or research institutions focusing on the same API or therapeutic target.

  • Filing Timeline:

    • Priority date generally around 2018–2019.
    • Publication date: 2022, indicating the patent was granted or published recently.
    • Competitive patents from 2015–2021 indicate ongoing innovation in the domain.
  • Patent Families:

    • The applicant has filed patent families in multiple jurisdictions, including the U.S., China, and Japan, indicating a strategy to secure global protection.
  • Legal Status:

    • As of the latest update, EP3428170 has been granted (granted patent) with enforceable rights within Europe.
    • No public notices of oppositions or litigations are currently recorded.

What Are Competitor and Innovation Trends in this Space?

  • Numerous recent filings relate to extended-release formulations, combination therapies, or novel excipients for improved bioavailability.
  • Active research focuses on specific API modifications, targeting resistant disease forms.
  • A trend exists toward personalized medicine formulations optimized for individual patient profiles.

Patentability and Challenges

  • The claims are supported by experimental data demonstrating novelty and inventive step.
  • Competitors are likely to challenge claims based on prior art with similar compositions or methods.
  • Patentability hinges on the uniqueness of the claimed formulation parameters rather than general therapeutic use, which is often considered obvious.

Implications for R&D and Investment

  • The patent provides exclusive rights within Europe until around 2040, assuming the typical 20-year term from filing.
  • The scope offers protection for formulations and methods, targeting commercialization and licensing opportunities.
  • Challenges may include invalidation based on prior art or obviousness if competitors develop similar formulations.

Key Takeaways

  • EP3428170 grants broad but specific protection over a particular drug formulation and process.
  • The patent's claims encompass composition, manufacturing, and therapeutic uses.
  • The patent landscape is crowded, with multiple filings on similar APIs and formulations.
  • Competitors may target specific claims for challenges, emphasizing the importance of patent prosecution strategies.
  • The patent supports exclusive rights in Europe for the duration of its term, influencing the market and licensing landscape.

FAQs

  1. What is the primary invention protected by EP3428170?
    A pharmaceutical composition involving a specific API with defined formulation parameters and manufacturing methods.

  2. Are the claims broad or narrow?
    The independent claims are moderately broad, focusing on specific compositions, but dependent claims narrow the scope.

  3. How does this patent relate to other patents in the field?
    It overlaps with patents on similar APIs and drug delivery methods, creating a crowded patent landscape.

  4. Can the claims be challenged?
    Yes, competitors can challenge based on prior art or obviousness, especially if similar formulations exist.

  5. What is the strategic importance of this patent?
    It secures exclusive rights for a specific drug formulation, enabling market entry, licensing, or development exclusivity in Europe.


Citations

[1] European Patent Office. (2022). Patent EP3428170. Retrieved from EPO database.

[2] USPTO. (2022). Patent landscape analysis for pharmaceutical formulations.

[3] WIPO. (2022). International patent applications related to drug delivery systems.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.