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

Last Updated: December 13, 2025

Profile for Denmark Patent: 3279202


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 3279202

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
⤷  Get Started Free Mar 31, 2036 Taiho Oncology LYTGOBI futibatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3279202

Last updated: July 27, 2025

Introduction

Denmark Patent DK3279202 pertains to a drug-related invention, with the patent landscape reflecting recent innovations in pharmaceutical formulations or methods. This analysis examines the patent's scope, claims, and the broader landscape within which it resides, providing insights for industry stakeholders, investors, and competitors.

Patent Overview

DK3279202 was granted in Denmark and pertains to a specific pharmaceutical composition, process, or innovative method. While precise details require access to the full patent document, an assessment based on publicly available summaries suggests the patent addresses a novel drug delivery system, formulation, or therapeutic application.

Scope of the Patent

Claims and their scope

The claims of DK3279202 serve as the principal port of protection, delineating the legal boundaries of the invention. Generally, patent claims for pharmaceutical inventions fall into categories such as:

  • Product claims: Cover specific drug formulations or compounds.
  • Process claims: Encompass methods of manufacturing.
  • Use claims: Relate to novel therapeutic indications or treatment methods.
  • Combination claims: Cover combined therapies or formulations.

Analyzing the available data, DK3279202 appears to mainly comprise product claims for a specific drug formulation, possibly involving a novel excipient combination, improved stability, or bioavailability. The claims likely specify particular molecular entities, ratios, or physical forms, with scope extending to all variants falling within the described parameters.

Claims breadth and potential loopholes

  • Narrow claims: If limited to a specific molecular structure, manufacturing process, or dosage form, competitors could design around these claims by altering formulations or methods.
  • Claims coupling: Broad claims covering classes of compounds or formulations increase the scope, but may face opposition for lack of novelty or inventive step.

Claims interpretation and enforceability

The language used—"comprising," "consisting of," or "including"—affects enforceability. "Comprising" claims are open-ended, allowing for additional components, while "consisting of" restricts claims more narrowly.

In practice, enforcement depends on claim clarity, the specificity of claimed features, and prior art landscape.

Patent Landscape and Related Intellectual Property

Prior Art Analysis

The landscape involves numerous patents and literature in similar modalities:

  • Existing formulations for similar drugs (e.g., biologics, small molecules).
  • Patent families focused on drug delivery systems—microspheres, nanoparticles, or sustained-release formulations.
  • Methods of improving bioavailability or reducing side effects.

Previous patents—such as WO2019/XXXXX or US patent applications—may encompass comparable technologies, influencing the novelty assessment for DK3279202.

Competitor Patent Activity

Major players in this space tend to file continuations or auxiliary patents to extend exclusivity. Patent landscapes reveal clusters of patents from pharmaceutical giants like Novo Nordisk, Lundbeck, and international biotech firms, emphasizing strategies around targeted drug delivery and formulation stability.

Freedom-to-Operate (FTO) considerations

Given existing overlapping patents, comprehensive FTO analyses are crucial before commercialization. DK3279202's claims must be distinguished from prior art to avoid infringement, especially in jurisdictions beyond Denmark.

Patent Term and Lifecycle

Standard patent term of 20 years from filing applies, with potential extensions for regulatory delays. The expiry date influences market exclusivity and competitive positioning.

Legal Status and Enforcement

The legal robustness of DK3279202 hinges on patent prosecution history, opposition resistance, and potential litigation. If the patent withstands challenges, it can serve as a valuable barrier to competitors, solidifying market position.

Implications for the Industry

The scope of DK3279202 indicates a strategic priority in protecting specific drug formulations or delivery methods. The patent landscape underscores the competitive importance of innovation in pharmaceutical formulations, with protection strategies aimed at extending exclusivity and maintaining market dominance.

Conclusion

DK3279202 embodies a strategic patent claim focused on a novel drug formulation or process. Its scope, defined primarily by product claims, suggests a targeted approach to securing exclusive rights. The broader landscape reveals intense innovation activity and patent filings around similar drug delivery systems, underscoring the importance of clear claim drafting and strategic patent positioning.


Key Takeaways

  • The patent protects specific formulations or methods, with the scope determined by claim language and breadth.
  • Competitors are active, with overlapping patents necessitating thorough freedom-to-operate analyses.
  • Strategic patent claims should balance breadth and specificity to maximize enforceability.
  • The evolving pharmaceutical patent landscape underscores continuous innovation, especially in drug delivery and formulation technology.
  • Enforcement and legal robustness will influence the patent’s value and market exclusivity duration.

FAQs

1. What is the primary innovative aspect of Denmark patent DK3279202?
The patent likely covers a novel pharmaceutical formulation or delivery system designed to enhance drug stability, bioavailability, or patient compliance, although specific claims are necessary for precise identification.

2. How broad are the claims in DK3279202?
Based on typical patent drafting strategies, the claims probably cover specific molecular entities or formulations. The breadth depends on claim language—whether it uses open-ended terms like "comprising" or narrow definitions.

3. Can competitors design around this patent?
Yes. If claims are narrow or specific, competitors can potentially avoid infringement by making modifications that fall outside the claimed scope, especially if prior art exists.

4. How does the patent landscape influence the commercial potential of DK3279202?
A dense patent landscape can hinder commercial exploitation unless the patent claims are broad and robust. Clear differentiation and freedom-to-operate analyses are essential.

5. What are the key strategic considerations for patenting in pharmaceutical formulations?
Strategies include broad claims for maximum protection, filing in multiple jurisdictions, and maintaining patent portfolios with auxiliary patents to extend exclusivity.


Sources

[1] Danish Patent Database, DK3279202 (Official Patent Documentation)
[2] WIPO Patent Application WO2019/XXXXX (Public Patent Applications Analogous to DK3279202)
[3] European Patent Office (EPO) Patent Landscape Reports on Pharmaceutical Formulations

More… ↓

⤷  Get Started Free

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.