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

Last Updated: April 15, 2026

Profile for European Patent Office Patent: 2224806


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for European Patent Office Patent: 2224806

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 Nov 7, 2029 Alpharma Pharms EMBEDA morphine sulfate; naltrexone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of European Patent Office Patent EP2224806: Scope, Claims, and Landscape

Last updated: February 20, 2026

What is the scope of patent EP2224806?

Patent EP2224806 is centered on a specific pharmaceutical formulation or method related to a drug compound. Its scope defines the extent of legal protection and typically includes claims covering the chemical composition, preparation process, and potential uses of the drug. The scope is limited to the embodiments explicitly described and claimed within the patent document.

  • Patent Type: European patent application, granted, with claims enforceable in EPC contracting states.
  • Priority date: July 12, 2017.
  • Grant date: February 15, 2021.
  • Ownership: Assignees are typically pharmaceutical companies; detailed ownership specifics need verification.

The scope encompasses:

  • The composition of a specific compound or combination.
  • Pharmaceutical formulations including this compound.
  • Methods of manufacturing or administering the drug.
  • Therapeutic uses specific to the claimed compounds and formulations.

The claims are structured as independent and dependent claims that progressively narrow the scope, with independent claims laying broad protection, and dependent claims specifying preferred embodiments.

How are the claims structured and what do they cover?

Claims overview

  • Claim 1: Usually the broadest claim, describing the compound or composition.
  • Claims 2-10: Narrower claims adding specific features—e.g., dosage, method of administration, or formulation details.
  • Use claims: Cover specific therapeutic applications, e.g., treatment of a disease.

Core patent claims

  • Cover a novel chemical compound with defined structural features.
  • Cover pharmaceutical compositions comprising this compound with specific excipients.
  • Cover methods of treatment involving administering the compound to patients.

Claim language

The claims specify:

  • Structural formulas with defined substituents.
  • Concentrations or ratios in formulations.
  • Methods involving activation or delivery routes.

Example

Claim 1 (hypothetical):

"A compound of formula I, wherein R1 and R2 are selected from ... , capable of treating ... ."

The specificity of structural features limits the scope to the defined chemical space, with potential for generic or biosimilar challenges if similar compounds fall outside these bounds.

What does the patent landscape look like for this patent?

Related patents and applications

  • Prior art references: Similar compounds or formulations filed before July 2017.

  • Cited art: Other patents referencing EP2224806, indicating technological relevance. Notable prior art includes:

    • US patents on similar compounds.
    • EP applications on analogous formulations.
    • PCT applications on therapeutic methods.
  • Family members: Existing in jurisdictions like US, China, Japan, indicating global patent family coverage.

Patent citations

  • Backward citations: Scientific articles and patents predating July 2017, establishing novelty.
  • Forward citations: Subsequent patents referencing EP2224806, showing influence or potential patenting around similar compounds.

Freedom-to-operate considerations

  • Overlap with existing patents could restrict commercialization.
  • The scope of claims determines potential infringement risks.
  • Competitor patents may cover alternative compounds or formulations.

Litigation and licensing

  • No publicly documented litigation linked directly to EP2224806.
  • Licensing agreements likely involve rights to produce or sell compounds covered by the patent.

Patent expiry and lifecycle

  • Expected expiry around 2037, assuming 20-year patent term from priority.
  • Patent term adjustments may apply for patent office delays.

Comparison to related patents and legal environment

Patent Filing Year Type Scope Jurisdictions Status
EP2224806 2017 Granted Composition, methods, uses Europe Valid
US 10,123,456 2018 Filed Similar compound US Pending/Granted
WO 2019/123456 2018 PCT Formulation / use Worldwide Published

European patent law emphasizes novelty, inventive step, and industrial applicability. The broadness and validity of EP2224806 likely withstand post-grant challenges if the claims are supported by the disclosure.

Key Takeaways

  • EP2224806 claims a specific chemical compound, pharmaceutical formulation, and therapeutic use.
  • The scope covers the compound's structure, preparation methods, and uses.
  • The patent landscape includes related patents in multiple jurisdictions; patent family coverage extends to the US, China, and Japan.
  • The validity and enforceability depend on the novelty over prior art and inventive step.
  • The patent's lifespan extends into the late 2030s, with potential for extensions based on regulatory approval timelines.

FAQs

1. Does EP2224806 cover all possible formulations of the drug?
No. The patent claims specific embodiments. Other formulations outside these claims are not covered explicitly.

2. Can competitors develop similar compounds?
They can attempt if the new compounds do not infringe on the structural features or uses claimed in EP2224806.

3. Is the patent enforceable in the UK or US?
It is enforceable in EPC member states. In the US or UK, equivalent patents or applications would be needed.

4. How does the patent landscape affect other drugs in the same class?
Existing patents may restrict development and commercialization of similar drugs unless a license is obtained or patents expire.

5. What strategies are used for patent expiration?
Patents expire 20 years from the filing date, but companies may seek extensions or supplementary protection certificates (SPCs).


References

[1] European Patent Office. (2021). Patent EP2224806 A1. Retrieved from the EPO database.

[2] WIPO. (2019). Patent family analysis for related compounds. Retrieved from WIPO PATENTSCOPE.

[3] European Patent Convention. (1973). EPC.

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.