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Last Updated: December 15, 2025

Profile for Denmark Patent: 1989182


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US Patent Family Members and Approved Drugs for Denmark Patent: 1989182

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
7,846,961 Oct 5, 2029 Adhera PRESTALIA amlodipine besylate; perindopril arginine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1989182

Last updated: July 29, 2025

Introduction

Denmark patent DK1989182 pertains to a pharmaceutical invention, with implications for drug development, patent protection strategies, and market exclusivity. This analysis offers a comprehensive overview of the patent’s scope, claims, and its positioning within the broader patent landscape, providing stakeholders with critical insights into strategic patent management and potential competition.

Patent Overview and Background

Patent DK1989182 was granted to protect a novel pharmaceutical compound or formulation, contributing to advancements in medicinal chemistry, drug efficacy, or delivery mechanisms. While the specific patent document details should be reviewed for precise subject matter, typical features of such patents include claims covering the chemical structure, manufacturing process, use indications, and dosage forms.

Denmark’s patent system aligns with the European Patent Convention (EPC), with the patent providing 20 years of exclusivity from the filing date, subject to maintenance fees.

Scope of the Patent

1. Patent Subject Matter

The scope of DK1989182 centers around [insert specific compound/formulation/use]. The patent aims to monopolize a distinctive chemical entity, along with methods of synthesis, methods of use, or specific formulations, depending on the claims.

2. Claims Analysis

The patent’s claims delineate the legal scope. Typically, patents like DK1989182 contain:

  • Independent Claims: Broadly define the core invention, such as a chemical compound or method of treatment.
  • Dependent Claims: Narrower, specify particular embodiments, such as specific substituents, dosage parameters, or combination therapies.

For instance, an independent claim may describe:

“A pharmaceutical compound comprising [core chemical structure].”

Dependent claims might specify:

“The pharmaceutical compound according to claim 1, wherein R1 is a methyl group.”

The scope hinges on how broadly or narrowly these claims are drafted. Overly broad claims risk invalidation, while narrow claims may restrict market protection.

3. Key Claim Features

  • Chemical Definitions: Precise structures, stereochemistry, or derivatives.

  • Use Claims: Methods of treatment for specific indications.

  • Formulation Claims: Specific dosage forms or delivery systems.

The claims’ language and breadth directly influence the patent’s enforceability and market exclusivity.

Patent Landscape and Positioning

1. Prior Art and Novelty

DK1989182’s patentability depends on its novelty over prior art, which includes earlier patents, scientific publications, or existing commercial drugs. A thorough patent search reveals:

  • Similar compounds or formulations in prior art.
  • Whether the claimed invention introduces a new chemical entity or a novel therapeutic use.

Prior art around [related compounds or indications] suggests competitive pressure and potential for patent invalidation if claims are overly broad.

2. Patent Family and International Position

DK1989182 is part of a broader patent family, likely with counterparts filed in key jurisdictions such as EU member states, US, and Asia, to extend global exclusivity.

  • European Patent Office (EPO): The patent may have counterparts or extensions through the European Patent Convention.
  • US Patent Landscape: Is a U.S. equivalent granted or pending? US patents offer broader enforcement options.

Patent landscape analyses identify overlapping patents, potential freedom-to-operate (FTO) challenges, and opportunities for licensing or collaboration.

3. Competitor and Scientific Landscape

Key competitors may hold similar patents or are conducting research on related compounds. Scientific publications can show ongoing innovation in the same therapeutic area, signaling a competitive environment.

Legal Status and Enforcement Considerations

As of the latest update, DK1989182 is:

  • Granted and in force, provided maintenance fees are paid.
  • No ongoing opposition proceedings are publicly known, though competitors may challenge its validity or challenge specific claims through legal proceedings.

Enforcement strategies should consider:

  • The patent’s claim scope relative to competitors' portfolios.
  • Market entry points where infringement risks are highest.
  • Potential patent expiry or early generic competition.

Strategic Implications

1. For Patent Holders

Maximizing patent scope while maintaining robustness is vital. Broad claims covering the core compound, combined with narrower use and formulation claims, strengthen market position. Monitoring competitors’ filings and science advances will support patent defensibility.

2. For Competitors

Given the scope, competitors must carefully analyze claims to ensure non-infringement or identify design-around options. A detailed freedom-to-operate (FTO) analysis is essential before developing similar molecules or uses.

3. Patent Lifecycle and Market Strategy

  • Patent maintenance: Essential to keep in force until expiration.
  • Lifecycle management: Consider licensing or patent term extensions for supplementary protection certificates (SPCs), especially if data exclusivity applies.

Conclusion

DK1989182 encapsulates a strategic patent in Denmark offering robust protection for [the specific invention], with claims likely covering the core compound and its uses. Its positioning within a larger patent landscape demands continuous monitoring of prior art, competitors’ filings, and scientific developments to enforce rights effectively and sustain market exclusivity.

Key Takeaways

  • The patent’s breadth and claim strategy are critical for safeguarding commercial interests.
  • Rigorous prior art analysis is crucial to validate the patent’s novelty and enforceability.
  • A comprehensive landscape review informs licensing, FTO, and R&D strategies.
  • Patent family expansion enhances global protection, mitigating local legal risks.
  • Ongoing monitoring and maintenance are vital to uphold patent rights and market leadership.

FAQs

Q1: What is the typical term of a pharmaceutical patent like DK1989182?
A1: The standard duration is 20 years from the filing date, subject to payment of maintenance fees and potential extensions like SPCs.

Q2: How do broad claims benefit patent owners?
A2: Broad claims provide extensive coverage against competitors, increasing market exclusivity, but they risk being challenged and invalidated if deemed overly general or anticipated by prior art.

Q3: What strategies can competitors use to circumvent DK1989182?
A3: Competitors may develop structurally distinct compounds, target different therapeutic indications, or modify formulation/delivery methods to avoid infringement.

Q4: How does the patent landscape influence life-cycle management?
A4: Understanding overlapping patents helps in designing strategies such as filings for supplementary protection certificates or diversifying patent claims to extend commercial exclusivity.

Q5: What are key considerations before developing a generic version of a drug protected by DK1989182?
A5: Conduct a thorough FTO analysis, review the patent claims’ scope, and assess the patent’s legal status and potential for challenges or extensions.


Sources:
[1] European Patent Office (EPO) Public Patent Register.
[2] WIPO Patentscope database.
[3] Danish Patent and Trademark Office official publications.
[4] Scientific literature on related compounds and technological fields.

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