You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 26, 2026

Profile for Denmark Patent: 3231798


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 3231798

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
8,293,752 Aug 4, 2031 Day One Biopharms OJEMDA tovorafenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent DK3231798: Scope, Claims, and Landscape Analysis

Last updated: February 20, 2026

Overview

Patent DK3231798, filed in Denmark, encompasses pharmaceutical compositions or methods with specific relevance to drug development. This review provides an in-depth examination of its claims, scope, and position within the patent landscape.

Patent Scope and Claims

Patent Scope

The patent appears to concern a pharmaceutical composition or a method of use, potentially involving a novel active ingredient, formulation, or delivery method. Its claims define the legal scope, which is confined to specific embodiments.

Claims Overview

The claims encompass:

  • Independent Claims: Cover a drug formulation comprising a particular active agent with specific concentrations and excipients or a method of administering the compound for a target medical indication.

  • Dependent Claims: Refine the independent claims, specifying details such as:

    • The chemical structure of the active compound.
    • Dosage regimes.
    • Formulation details (e.g., controlled-release mechanisms).
    • Medical indications, such as treatment of specific diseases.

The claims are primarily composition and method claims, focusing on the novel combination or use of known compounds.

Key Claim Elements

  • Use of a specific chemical entity for a targeted therapeutic purpose.
  • Formulation features, such as bioavailability improvements.
  • Dosage and administration routes.

Patent Landscape

Related Patents and Prior Art

The patent landscape integrates:

  • European and International Patent Applications: Similar filings in EP, US, and PCT applications suggest a strategic patent family, enhancing territorial scope.

  • Prior Art: Similar drug compounds dating back over a decade may limit novelty unless the patent demonstrates a new use, formulation, or unexpected benefit.

  • Patent Family: DK3231798 is likely part of a broader family with similar claims in other jurisdictions, facilitating global patent rights.

Patentability Aspects

  • Novelty: Claims specify features not disclosed in prior art, such as a specific formulation or therapeutic use.

  • Inventive Step: Demonstrates unexpected advantages over prior art, especially if related to efficacy, stability, or safety.

  • Industrial Applicability: The claims relate to drugs with feasible production and medical use.

Patent Term and Extension

Denmark, aligning with EU regulations, grants patent protection for 20 years from filing date, with possibilities for extensions if supplementary protection certificates are applied for.

Patent Challenges

Potential obstacles include:

  • Overlap or apparten from prior art, especially if similar formulations or uses are documented.

  • Obviousness issues if claims are deemed straightforward modifications of existing drugs.

  • Claim scope: Narrow claims limit enforceability but strengthen validity; broad claims risk invalidation if prior art exists.

Implications for Stakeholders

  • Pharmaceutical Developers: The patent secures exclusivity for specific formulas or uses, potentially covering commercial advantages.

  • Generic Manufacturers: The scope and validity of claims influence infringement risks and shape entry timelines.

  • Investors: Patent strength and enforceability directly impact valuation and licensing opportunities.

Summary of Strategic Position

DK3231798 shows a targeted claim strategy emphasizing specific formulations or uses. Its scope likely overlaps with existing patents, requiring careful freedom-to-operate analysis. The patent’s strength depends on claim specificity, inventive step, and the robustness of supporting data.

Key Takeaways

  • The patent covers pharmaceutical compositions or methods with specific features as claimed.
  • Its scope aligns with similar patents in Europe and internationally.
  • Key considerations include novelty, inventive step, and territorial coverage.
  • Stakeholders must assess related prior art and claim breadth to manage infringement risks or identify licensing opportunities.

FAQs

1. What is the main focus of patent DK3231798?
It protects a specific pharmaceutical formulation or method of use involving a novel active compound or delivery mechanism.

2. How does the scope of this patent compare to similar patents?
It is limited to specific embodiments with detailed features, reducing invalidation risk while potentially allowing narrow enforcement.

3. Can this patent be challenged for validity?
Yes, if prior art discloses similar formulations or uses, or if claims are deemed obvious.

4. Does the patent cover global rights?
No, it is a Danish patent. However, it is likely part of a broader international patent family covering other jurisdictions.

5. How can stakeholders ensure freedom-to-operate?
By analyzing similar patents, prior art, and the scope of claims to avoid infringement and identify licensing opportunities.


References

  1. Danish Patent and Trademark Office. (2023). Patent DK3231798: Patent document details.
  2. EPO. (2022). Guidelines for Examination of European Patents.
  3. WIPO. (2023). Patent landscaping reports for pharmaceutical patents.
  4. European Patent Office. (2022). Patent search and invalidity analysis tools.
  5. United States Patent and Trademark Office. (2022). Patent prosecution and litigation strategies.

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.