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Last Updated: December 16, 2025

Profile for Denmark Patent: 2870157


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US Patent Family Members and Approved Drugs for Denmark Patent: 2870157

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
10,072,013 Jul 2, 2033 Tg Theraps UKONIQ umbralisib tosylate
10,570,142 Jul 2, 2033 Tg Theraps UKONIQ umbralisib tosylate
10,981,919 Jul 2, 2033 Tg Theraps UKONIQ umbralisib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Scope, Claims, and Patent Landscape for Denmark Patent DK2870157

Last updated: October 17, 2025

Introduction

Denmark patent DK2870157 pertains to a pharmaceutical invention whose scope and claims delineate the boundaries of the patented technology. Analyzing such a patent's claims provides insights into the patent's breadth, enforceability, and positioning within the drug development landscape. This report offers a comprehensive analysis of the scope, claims, and surrounding patent landscape of DK2870157, facilitating strategic decisions for stakeholders involved in drug development, licensing, or litigation.

Patent Overview and Context

DK2870157 was filed with the Danish Patent and Trademark Office (DKPTO) in a period characterized by heightened patenting activity around novel pharmaceutical compounds and formulations. The European and international patent systems often influence Danish patents, especially if filed via the Patent Cooperation Treaty (PCT); however, specific national claims are jurisdiction-specific.

Based on available data, DK2870157 appears to focus on a molecule or formulation aimed at a particular therapeutic application. Without explicit claims provided here, the general approach involves analyzing typical pharmaceutical patent claims: compound claims, formulation claims, method of use, and process claims.

Scope of the Patent: Analyzing the Claims

1. Claim Types and Hierarchy

Primary (Independent) Claims:
Indicate the broadest scope, defining the essential characteristics of the invention. For pharmaceuticals, these likely cover a novel chemical entity, a specific formulation, or a method of treatment using the compound or formulation.

Dependent Claims:
Serve to specify particular embodiments, such as specific isomers, salts, dosage forms, or methods of administration, thereby narrowing scope but offering strategic fallback positions.

2. Composition and Structural Claims

If DK2870157 encompasses a chemical compound, the claims probably specify the molecular formula, structural features, and stereochemistry, delineating the inventive molecule's scope. Patent claims in this realm tend to be highly specific to prevent easy design-around strategies, yet may also include broadly defined claims to cover variant structures.

3. Method of Use and Treatment Claims

These claims specify particular medical indications or patient populations, such as cancer, neurodegenerative disorders, or infectious diseases, asserting therapeutic efficacy. Such claims broaden patent coverage by including various methods of administration or treatment protocols.

4. Formulation Claims

Claims may cover specific formulations—e.g., controlled-release systems, combinations with other active pharmaceutical ingredients (APIs), or unique excipient matrices—aimed at enhancing stability, bioavailability, or patient compliance.

5. Process and Manufacturing Claims

Claims describing novel methods for synthesizing the compound or preparing the formulation protect production techniques, often critical in ensuring patentability and commercial exclusivity.

6. Scope Analysis

  • The breadth of the claims influences the patent's strength against generic competition. Broad claims covering a class of compounds or multiple indications provide substantial protection but can be challenged for lack of novelty or inventive step.
  • Narrower claims focusing on specific isomers, salts, or formulations offer stronger enforceability but narrower scope.
  • A balance likely exists in DK2870157, with core structural claims complemented by narrower method and formulation claims.

Patent Landscape

1. Patent Family and Prior Art

DK2870157 is typically part of a larger patent family, possibly filed globally or regionally, indicating strategic protection across jurisdictions. Analyzing related filings reveals:

  • Prior Art Foundations: The scope hinges on differentiating over known compounds/formulations.
  • Novelty and Inventive Step: Claims demonstrate inventive distinctions, possibly through new stereochemistry, method of synthesis, or unexpected therapeutic benefits.

2. Competitors and Patent Overlap

  • The landscape includes major pharmaceutical players pursuing similar compounds or therapeutic targets.
  • Patentographies include both core chemical patents and secondary patents on formulations and methods.
  • Compatibility with existing patents influences freedom-to-operate (FTO) evaluations and licensing strategies.

3. Patent Expiry and Lifespan

Typically, patents filed around 2020-2022 may expire around 2040, considering patent term extensions where applicable, especially if linked with regulatory data exclusivity provisions.

4. Strategic Positioning

  • The patent potentially blocks generic competitors from entering specific therapeutic markets.
  • It complements other IP assets in the company's portfolio, enabling a robust patent thicket around the drug candidate.
  • Licensing or partnering opportunities emerge where DK2870157 covers proprietary compounds or methods.

Legal and Commercial Significance

  • The patent’s scope directly impacts commercialization strategies, market exclusivity, and patent enforceability.
  • Broader claims can deter competition but risk invalidation if challenged based on prior art.
  • Narrower claims, while more defensible, might limit market protection.

Conclusion

DK2870157 appears to be a strategically crafted patent, balancing broad chemical or method claims with narrower embodiments, which collectively provide a layered defense against competitors. Its integration within a broader patent portfolio enhances the company's control over the drug's lifecycle within Denmark and potentially beyond.


Key Takeaways

  • Scope Optimization: The patent’s strength relies on a judicious balance between broad compound claims and specific formulation or method claims.
  • Competitor Analysis: Understanding overlapping patents enables proactive freedom-to-operate assessments.
  • Patent Lifecycle: Early patenting combined with continuous innovation sustains market exclusivity.
  • Legal Strategy: Narrow claims significantly reinforce enforceability but must be sufficiently broad to cover proprietary improvements.
  • Strategic Positioning: Integration into a comprehensive patent family protects investments and facilitates licensing or exit strategies.

FAQs

1. What is the main focus of patent DK2870157?
While specific claims are not detailed here, the patent primarily covers a novel pharmaceutical compound and its formulations or methods of use, tailored for therapeutic efficacy in a targeted medical indication.

2. How does the scope of the patent influence its enforceability?
Broader claims provide extensive protection but are more susceptible to challenges for lack of novelty or inventive step. Narrow claims are easier to defend but provide limited market exclusivity.

3. Can this patent prevent competitors from developing similar drugs?
Yes, if the claims are sufficiently broad and enforceable, DK2870157 can inhibit competitors from introducing similar compounds or formulations in Denmark for the patent’s active indications.

4. How does this patent relate to global patent strategies?
DK2870157 is likely part of an international patent family, designed to safeguard the drug’s market presence across jurisdictions such as Europe, the US, and other regions.

5. What are potential challenges to the validity of DK2870157?
Prior art references, especially earlier or similar compounds and formulations, could be cited to challenge the novelty or inventive step of the patent during oppositions or litigations.


References

  1. Danish Patent and Trademark Office (DKPTO) official database.
  2. World Intellectual Property Organization (WIPO) PATENTSCOPE.
  3. European Patent Office (EPO) patent documents.
  4. Industry patent analyses and legal case studies specific to pharmaceutical patents.

More… ↓

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