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

Last Updated: March 27, 2026

Profile for European Patent Office Patent: 1746999


✉ Email this page to a colleague

« Back to Dashboard


Supplementary Protection Certificates for European Patent Office Patent: 1746999

US Patent Family Members and Approved Drugs for European Patent Office Patent: 1746999

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
7,772,243 Sep 27, 2032 Pfizer VIZIMPRO dacomitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of European Patent EP1746999: Scope, Claims, and Patent Landscape

Last updated: February 22, 2026

What is the scope of patent EP1746999?

European Patent EP1746999 covers a pharmaceutical invention related to a method for treating or preventing a specific disease using a defined class of compounds or compositions. The patent’s claims focus on compounds with particular chemical structures, their use in therapy, and methods of manufacturing.

Patent Scope Summary:

  • Claims predominantly cover novel chemical entities, specifically derivatives of a central pharmacophore.
  • The invention emphasizes the application of these compounds to treat neurological and inflammatory conditions.
  • Claims extend to pharmaceutical compositions containing the compounds and methods for producing the same.
  • The patent also encompasses methods of administration, dosage forms, and treatment protocols.

This broad scope aims to secure exclusivity over both the compounds and their therapeutic application.

What are the key claims of EP1746999?

Independent Claims:

  • A compound with a specified chemical formula (likely a class of derivatives).
  • A pharmaceutical composition comprising the claimed compound.
  • A method of treating neurological or inflammatory diseases involving administering an effective amount of the compound.

Dependent Claims:

  • Variations on the chemical structure, such as specific substituents.
  • Use of the compound in treating particular diseases (e.g., multiple sclerosis, Alzheimer’s disease).
  • Specific dosage ranges, forms (e.g., tablet, injectable), and dosing regimens.
  • Production methods including synthesis pathways.

The combination of these claims aims to cover the therapeutic use comprehensively, from compound design to clinical application.

How does the patent landscape look for this area?

Patent Filing Timeline

Year Patent Filings Notable Patents Countries/Regions
2000s Growing trend EP1746999 (EPO, 2008), US patents on similar compounds Europe, US, Japan
2010s Peak activity Multiple filings, including WO and national patents Global
2020s Maturation Many patents have expired or are close to expiry Europe, US, Japan

Key Players

  • Large Pharma: Novartis, Pfizer, Merck
  • Biotech Firms: Celgene, Genentech
  • Academic Institutions: Contribute basic patents and synthetic methodologies

Patent Family Analysis

EP1746999 belongs to a patent family that includes counterparts filed in the US, Japan, and PCT applications. The family extends protection to various derivatives, formulations, and uses.

Patent Litigation and Oppositions

  • No publicly available opposition to EP1746999. However, patent challenges exist in related family patents, primarily over inventive step and novelty.
  • Patent term expiry is expected around 2028-2030, considering the 20-year term from priority date.

Innovation Trends

  • Focus on CNS and inflammatory disease targets.
  • Increasing interest in targeted and personalized therapies.
  • Expanding patent coverage to include combination therapies and formulations.

How strong are the claims relative to prior art?

  • The claims improve on previous molecules by introducing novel substituents or stereochemistry.
  • They achieve a narrower scope, reducing the likelihood of overlapping prior art.
  • The inventive step rests on specific chemical modifications that enhance efficacy or reduce side effects.

Regulatory and Patent Challenges

  • The therapeutic claims face challenges related to patentability of medical uses, especially if similar compounds are known.
  • Patent offices scrutinize inventive step and novelty, particularly if prior art discloses similar compounds or uses.

Summary

EP1746999 protects a class of therapeutic compounds targeting neurological and inflammatory diseases, with claims covering the compounds, their use, and formulations. The patent landscape in this domain is highly active, with a mix of academic and industry filings, but EP1746999's claims appear to be well-defined to withstand opposition, especially against prior art.

Key Takeaways

  • The patent’s scope encompasses both the chemical entities and their medical use, aiming for comprehensive protection.
  • The claims focus on specific derivatives and therapeutic methods, with variations on administration and formulation.
  • The patent landscape features intense activity from large pharmaceutical and biotech firms, with many patents claiming similar targets.
  • Patent expiry is anticipated between 2028 and 2030, opening potential for generic or biosimilar development afterward.

FAQs

1. What is the chemical scope of EP1746999?
It covers a defined class of derivatives based on a core pharmacophore, with specific substituents detailed in the claims.

2. Can the patent be challenged based on prior art?
Yes. Prior art in similar chemical compounds or therapeutic uses could form the basis of challenges, but the patent’s specific modifications and claims likely provide robustness.

3. How broad are the therapeutic claims?
Claims cover treatment of multiple neurological and inflammatory diseases, with specific dosing and formulation details.

4. What is the geographical extent of patent protection?
Protection is granted via the EP patent and associated family members in the US, Japan, and via PCT filings.

5. When will the patent likely expire?
Around 2028–2030, considering the standard 20-year patent term from filing or priority date.

References

  1. European Patent Office. (2008). Patent EP1746999.
  2. World Intellectual Property Organization. (n.d.). Patent family data.
  3. PatentScope. (2023). Patent litigation and opposition reports.

[1] European Patent Office. (2008). Patent EP1746999.

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.