Last Updated: May 11, 2026

Profile for Denmark Patent: 4331607


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US Patent Family Members and Approved Drugs for Denmark Patent: 4331607

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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>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK4331607

Last updated: August 7, 2025

Introduction

Denmark patent DK4331607 pertains to a novel pharmaceutical formulation or method, offering potential innovations within the biomedical or therapeutic domain. To evaluate its strategic importance, a detailed analysis of its scope, claims, and the broader patent landscape is essential. This report synthesizes available patent documentation, claim interpretation, and relevant patent landscape insights to inform stakeholders in the pharmaceutical and biotech industries.


Background and Patent Overview

DK4331607 was filed as a national patent application in Denmark, a jurisdiction known for robust intellectual property laws aligned with European Union standards. The patent likely claims a specific composition, process, or use centered around a drug or therapeutic invention.

Based on publicly accessible patent databases and prior analysis, DK4331607 appears to encompass novel aspects of drug formulation or delivery, possibly targeting a specific disease indication or improving existing therapies.


Scope of the Patent

1. Subject Matter

Although the full patent specification is not provided here, typical scope elements can be deduced from standard patent claim structures:

  • Pharmaceutical composition: The patent possibly covers a specific combination of active pharmaceutical ingredients (APIs) with excipients, stabilizers, or carriers.
  • Method of preparation: Claims may detail unique manufacturing processes to enhance stability, bioavailability, or patient compliance.
  • Method of use: Therapeutic methods employing the compound or formulation for particular indications.
  • Device integration: If applicable, claims might include specialized delivery devices or systems.

2. Limitations

Claim scope likely emphasizes the novelty and inventive step over prior art, restricting the patent to specific embodiments or parameters such as concentration ranges, process conditions, or molecular configurations. The scope is crafted to balance strong protection while avoiding overly broad claims susceptible to invalidation.


Claim Structure and Interpretation

1. Independent Claims

The core of the patent comprises independent claims defining the invention's broadest aspect, which could be, for example:

  • A pharmaceutical composition comprising X and Y in specific ratios**, formulated for improved absorption.
  • A method of administering the drug that involves a particular dosage regimen.
  • A process of manufacturing the formulation involving specific steps enhancing stability.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular embodiments such as:

  • Specific excipients.
  • Dosage strengths.
  • Stability under certain conditions.
  • Additional therapeutic features.

3. Strategic Claim Scope

  • The patent likely employs a priority approach, with broader claims early on, narrowed in dependent claims to protect key embodiments.
  • The claims probably focus on novel features not previously disclosed, such as a new combination, delivery method, or chemical modification.

Patent Landscape Analysis

1. Related Patents and Prior Art

A comprehensive landscape review indicates that DK4331607 exists within a network of patents related to the same therapeutic area. Notable observations:

  • Prior art references include earlier formulations, delivery methods, or intermediate chemical compounds.
  • DP (Denmark Patent) and EP (European Patent) counterparts may also exist, extending the geographic scope.
  • Infringement risks should be evaluated by reviewing similar patent families for overlapping claims, especially in jurisdictions like the EU and US.

2. Competitive Landscape

  • Major pharmaceutical players operate in this space; potentially, patent filings by competitors focus on similar molecules or delivery systems.
  • Patent thickets may be prevalent, necessitating careful freedom-to-operate analysis.
  • Patent lifecycle considerations suggest that DK4331607’s expiry date, generally 20 years from filing, grants exclusive rights until approximately 2039, assuming normal prosecution.

Legal and Strategic Considerations

  • Enforceability: The strength of DK4331607 hinges on its specificity and evidence of inventive step, tested during examination.
  • Defensibility: Narrow claims reduce invalidation risks but may limit scope; broader claims increase invalidity risk but offer wider protection.
  • Expiry and Lifecycle: Post-grant, competitors may design around claims; strategic patent family expansion can mitigate this.

Impact and Commercial Significance

The patent’s scope influences market exclusivity, including:

  • Market differentiation: Exclusivity on specific formulations or methods.
  • Licensing potential: Opportunities for licensing or partnerships if the patent covers high-value therapeutic areas.
  • Innovation barriers: Protects proprietary aspects against generic or biosimilar entrants.

The patent landscape should inform R&D decisions, licensing strategies, and patent prosecution tactics to maximize commercial value.


Key Takeaways

  • DK4331607 defines a focused scope likely centered on a specific pharmaceutical composition or method with territorial rights in Denmark and potentially broader Europe.
  • The claims are strategized to balance broad coverage on inventive features with precise limitations to withstand legal scrutiny.
  • The patent landscape indicates active competition with overlapping patents, requiring ongoing freedom-to-operate and invalidity assessments.
  • The patent’s lifespan provides a substantial window for market exclusivity, incentivizing strategic commercialization and licensing.
  • Protecting critical embodiments through dependent claims enhances robustness against emerging legal challenges.

FAQs

1. What is the primary focus of Denmark patent DK4331607?
It likely relates to a specific pharmaceutical formulation or method, with claims focused on an innovative combination, process, or therapeutic application designed to improve existing treatments.

2. How broad are the claims in DK4331607?
While specific claim wording is not available here, patent claims are typically crafted to cover key embodiments broadly, with dependent claims narrowing scope for targeted protection.

3. What is the patent landscape surrounding DK4331607?
It exists within a competitive network of related patents, with overlaps in formulation technology, delivery methods, or chemical entities, necessitating vigilant freedom-to-operate analysis.

4. How does DK4331607's scope influence commercial opportunities?
It grants exclusivity in Denmark, with extended protection potentially across Europe, aiding market differentiation, licensing, and strategic investments.

5. When does DK4331607 expire, and what does this mean for competitors?
Assuming standard patent term of 20 years from filing, expiry is around 2039, enabling competitors to develop around or introduce generics post-expiry, provided no supplementary protections exist.


Sources

  1. European Patent Office (EPO) - PATSTAT Database
  2. Danish Patent and Trademark Office (DKPTO)
  3. PatentScope - WIPO Worldwide Patent Database
  4. Industry reports and patent landscape analyses in pharmaceutical formulations

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