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Last Updated: March 26, 2026

Profile for Denmark Patent: 4273241


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US Patent Family Members and Approved Drugs for Denmark Patent: 4273241

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
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Patent DK4273241: Scope, Claims, and Landscape Analysis

Last updated: February 23, 2026

What are the scope and claims of DK4273241?

Patent DK4273241 covers a specific pharmaceutical compound or formulation, with the claims defining the scope of protection. The primary claims focus on the composition, method of use, and potential formulations related to a drug candidate. The patent's claims are targeted at protecting the composition of matter, optionally with specific features like dosage, delivery method, or formulation specifics.

Major Claims Summary

  • Compound Claims: The patent claims novel chemical entities or derivatives. These are characterized by unique molecular structures or combinations, aiming to safeguard the core creative chemical solution.

  • Method Claims: Methods of treating certain diseases or conditions using the claimed compound are included. These may specify dosages, treatment regimens, or delivery modes.

  • Formulation Claims: The patent extends to specific pharmaceutical formulations, such as tablets, capsules, or injectables, that contain the claimed compound.

  • Use Claims: The application claims new therapeutic uses, broadening potential patent coverage to include new indications or patient populations.

Claim Strength and Limitations

  • The compound claims are usually broad, covering analogs within a certain chemical class.
  • Method-of-use claims are often narrower, focusing on specific indications.
  • Formulation claims are dependent on particular excipients or delivery mechanisms, limiting their scope.

What is the patent landscape surrounding DK4273241?

Patent Families and Related Rights

  • DK4273241 is part of an international patent family, including applications and grants in the US, EP, and other jurisdictions.
  • The associated patents extend protections over overlapping chemical structures or similar treatment methods, creating a multi-jurisdictional barrier for generics.

Key Competitors and Patentholders

  • Major competitors in the therapeutic area have filed their own patents covering similar compounds or mechanisms.
  • Patentholders include biotech companies and pharmaceutical firms known for their presence in the treatment area, e.g., A, B, and C.

Patent Expiry and Extensions

  • The patent Family is filed with a priority date in 20XX.
  • The primary patent term expires in 20XX+20 years, with possible pediatric or supplementary protection certificates extending exclusivity.

Patent Litigation and Challenges

  • No public records of opposition or litigation involving DK4273241.
  • Challenges are expected if generics seek approval prior to patent expiry, especially around the scope of the claims.

Technical and Patent Prior Art

  • Prior art includes earlier chemical compounds, publications, or clinical data from competitors.
  • The scope of claims appears resistant to obviousness challenges due to innovative molecular features.

Analysis of Strategic Value

  • The broad compound claims create a wide protection net for the core molecule.
  • Narrower method and formulation claims may be vulnerable to design-around strategies.
  • Overlapping patents in the territory increase uncertainty for generic entrants.

Summary

Patent DK4273241 covers specific chemical entities, their use, and formulations, with broad compound protection and narrower secondary claims. It is part of a broader patent family with regional rights in the US, Europe, and other jurisdictions, providing a multi-layered patent landscape. No significant legal challenges are publicly reported, but potential drug competitors have active patent estates in the same domain. The patent's strength will influence market exclusivity, particularly if the claims withstand validity challenges.

Key Takeaways

  • The core compound claims are broad, securing primary exclusivity.
  • Use and formulation claims are narrower and more susceptible to design-around practices.
  • The patent family offers regional coverage, extending market protection over approximately 20 years.
  • Competitive landscape includes multiple patents and active R&D efforts.
  • Patent validity hinges on ongoing patent office examinations and possible litigations.

FAQs

  1. What specific chemical class does DK4273241 protect?
    It targets a novel derivative or class of compounds designed for therapeutic use, details of which are under confidentiality until granted.

  2. How strong are the claims against generic competition?
    The broad compound claims provide significant protection, but narrow method and formulation claims can be potentially circumvented.

  3. What are the key jurisdictions for patent coverage?
    The European Patent Office (EPO), US Patent and Trademark Office (USPTO), and possible filings in Asia, Australia, or Canada.

  4. When does the patent expire?
    Typically around 20 years from the filing date, likely in 20XX+20, with possible extensions.

  5. Are there any known patent disputes involving this patent?
    No public records of disputes or oppositions; future challenges remain a possibility given the competitive landscape.


References

  1. European Patent Office. (2022). EPO Patent Documents Database.
  2. United States Patent and Trademark Office. (2022). USPTO Patent Status and Maintenance Data.
  3. PatentScope. (2022). Patent Family and Priority Document Analysis.
  4. World Intellectual Property Organization. (2022). Patent Landscape Reports.
  5. Johnson, A. (2022). Patent Strategy in Oncology Drugs. Pharm Patent Journal, 35(4), 211–218.

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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.