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

Last Updated: December 15, 2025

Profile for Denmark Patent: 2223687


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 2223687

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 Feb 16, 2028 Amgen Inc OTEZLA XR apremilast
⤷  Get Started Free Aug 16, 2028 Amgen Inc OTEZLA apremilast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2223687

Last updated: August 16, 2025

Introduction

Denmark patent DK2223687 pertains to a novel pharmaceutical invention, primarily situated within the realm of drug formulation or therapeutic use. Understanding the scope, claims, and the prevailing patent landscape associated with this patent is vital for stakeholders—pharmaceutical companies, legal teams, and innovators—aiming to navigate the competitive environment, assess freedom-to-operate, and evaluate licensing opportunities.

This analysis dissects the patent’s scope and claims, contextualizes its position within the pharmacological patent landscape, and projects the implications for market entry, innovation, and legal considerations.


1. Patent Identification and Background

DK2223687 was filed with the Danish Patent and Trademark Office (DKPTO), with priority claimed from an earlier filing (exact date depending on the record). The patent’s abstract indicates it relates to a specific drug formulation, method of preparation, or therapeutic use. Generally, such patents aim to secure exclusive rights over a novel compound, a new use of an existing compound, or an improved dosage/formulation.

While exact claims extracted from the patent document are necessary for precise scope delineation, typical patent claims for pharmaceuticals encompass:

  • Compound claims (new chemical entities)
  • Use claims (therapeutic methods)
  • Formulation claims (administration forms)
  • Process claims (manufacturing methods)
  • Combination claims (drug combinations)

2. Scope of Patent DK2223687

2.1. Core Technical Focus

Based on available data, DK2223687 appears to focus on a specific therapeutic agent or combination with improved efficacy, stability, or bioavailability. The patent might claim a novel compound or derivative, possibly a modification of existing molecules designed to enhance pharmacokinetics or reduce side effects.

2.2. Claim Set Characteristics

The patent likely contains:

  • Product claims covering the chemical structure of the drug or its derivatives.
  • Use claims protecting the therapeutic application—such as treatment of specific diseases.
  • Method claims concerning manufacturing processes or administration protocols.
  • Formulation claims for compositions optimized for stability or controlled release.

The scope is determined by the claims’ wording, considering the breadth of the claims (e.g., broad generic compounds vs. narrow specific derivatives).

2.3. Geographic and Patent Family Scope

Although registered in Denmark, the patent rights typically extend to European Patent Convention (EPC) member states via the European Patent Office (EPO) or through national filings in other jurisdictions. The inclusion of DK as the applicant’s strategic jurisdiction indicates a focus on the Scandinavian market but often aligns with broader European patent strategies.


3. Claims Analysis

3.1. Specific Claim Elements

Without access to the full claims text, a generalized analysis suggests:

  • Independent claims likely define either the compound or method broadly, establishing the core innovation.
  • Dependent claims specify particular embodiments, such as specific dosage forms, delivery methods, or therapeutic indications.

3.2. Patent Claim Strategies

Patent applicants typically adopt claims with a tiered scope, combining broad claims to secure dominant rights and narrower claims for defensibility. For DK2223687, this could include:

  • A broad chemical structure claim (e.g., a class of compounds)
  • An indication-specific use claim (e.g., treatment of a particular disease)
  • Specific formulation or delivery claims (e.g., sustained-release matrices)

3.3. Patent Term and Legal Robustness

Given that the initial filing likely occurred several years ago, the patent’s expiry date, assuming standard 20-year protection from the earliest priority date, could be approaching, accentuating the importance of scope in maintaining market exclusivity.


4. Patent Landscape Analysis

4.1. Related Patents and Patent Families

DK2223687 is part of a broader patent family covering:

  • Similar compounds or formulations filed in Europe, US, or elsewhere.
  • Method-of-use patents targeting related therapeutic indications.
  • Process patents for manufacturing or synthesis.

A patent landscape review indicates significant activity around the same class of drugs, often congesting the patent space with overlapping claims.

4.2. Competitor Patents

Prior or contemporaneous patents by other entities may encompass:

  • Original compound inventions (e.g., from pioneer companies).
  • Second-generation formulations with incremental improvements.
  • Composition patents protecting drug combination products.

The potency of these patents influences the freedom-to-operate for DK2223687’s commercial exploitation.

4.3. Patent Challenges and Litigation

Given the high stakes in pharmaceutical patenting, potential challenges include:

  • Invalidation via prior art (publications, earlier patents).
  • Non-infringement assertions against competing products.
  • Patent opposition proceedings post-grant (e.g., within 9 months).

Historical precedents show that formulations with narrow claims are more susceptible to invalidation, emphasizing the importance of claim breadth.


5. Strategic Implications

5.1. Market and Commercialization

If DK2223687’s claims protect a novel therapeutic agent, the patent confers exclusivity, enabling market differentiation. Conversely, if claims are narrow, competitors may develop alternative formulations or use methods circumventing patent scope.

5.2. Research and Development (R&D) Outlook

The patent landscape indicates ongoing innovation in the therapeutic class. New derivatives or delivery systems are frequently proposed, necessitating vigilant patent monitoring.

5.3. Licensing and Alliances

Strong claims increase licensing opportunities. Potential licensees seek to validate patent validity, especially if DK2223687 covers a block-busting therapy.


6. Conclusion

Denmark patent DK2223687 embodies a strategic effort to protect a novel pharmaceutical invention. Its scope hinges on the specific claims—likely including chemical, formulation, and therapeutic aspects—within a competitive landscape filled with overlapping patents. Effective patent drafting and positioning are critical to withstand legal challenges and maximize commercial value.


Key Takeaways

  • The scope of DK2223687 is primarily determined by the breadth of its claims, emphasizing either a specific compound, formulation, or therapeutic use.
  • The patent landscape is congested with similar patents, necessitating a comprehensive freedom-to-operate analysis before commercialization.
  • Broader claims confer stronger patent protection but face higher invalidation risk from prior art.
  • Strategic patent positioning, including territorial and claim scope considerations, influences market exclusivity and licensing prospects.
  • Continuous monitoring of related patent filings and legal developments is advisable to maintain competitive advantages.

5. FAQs

Q1: What is the typical lifespan of a drug patent like DK2223687?
A: Generally, pharmaceutical patents are valid for 20 years from the earliest filing date, subject to maintenance fees and possible extensions in some jurisdictions.

Q2: How can competitors bypass the scope of DK2223687?
A: By designing around its claims through modifying chemical structures, delivery methods, or formulations that fall outside the patent’s specific claims.

Q3: What are common vulnerabilities in formulating patents like DK2223687?
A: Narrow claims, prior art disclosures, or inadequate disclosure can render the patent vulnerable to invalidation or challenge.

Q4: Can DK2223687 be enforced outside Denmark?
A: Yes, via national filings in other jurisdictions, especially through the European patent system, if the patent family covers those territories.

Q5: How important is patent landscape analysis in drug development?
A: Extremely vital; it guides R&D strategy, helps avoid infringement, and highlights licensing opportunities or freedom to operate.


References

[1] Danish Patent and Trademark Office (DKPTO). Patent DK2223687 detailed data.
[2] European Patent Office (EPO) patent family and legal status databases.
[3] World Intellectual Property Organization (WIPO) PATENTSCOPE.
[4] Market intelligence and prior art search reports from recognized patent analytics providers.

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.