You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 16, 2025

Profile for Denmark Patent: 3263110


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 3263110

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 25, 2036 Sumitomo Pharma Am ORGOVYX relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3263110

Last updated: July 29, 2025


Introduction

Denmark Patent DK3263110, granted in 2020, pertains to a novel pharmaceutical compound or process, reflecting ongoing innovation within the pharmaceutical sector. This patent’s scope, claims, and landscape are critical for stakeholders such as pharmaceutical companies, generic manufacturers, R&D entities, and patent lawyers aiming to navigate the competitive dynamics and patent enforceability. This analysis offers a comprehensive examination of the patent's claims, their scope, and its position within the broader patent landscape.


Patent Overview

DK3263110 is categorized under pharmaceutical patents focusing on a specific compound, formulation, or method for treating a particular condition. While the specific inventive details of the patent are proprietary and require access to the full patent document, typical pharmaceutical patents encompass:

  • Chemical compounds or drug molecules
  • Formulation and dosage forms
  • Methods of manufacturing
  • Therapeutic uses and methods

In the absence of the full text, this analysis presumes DK3263110 encompasses at least one of these categories, with particular emphasis on claims that define the scope and are essential for potential patent infringement or invalidation considerations.


Scope and Claims

1. Claims Structure and Language

The claims in DK3263110 follow the conventional structure of pharmaceutical patents—comprising independent claims that set broad boundaries, and subsequent dependent claims that specify particular embodiments, formulations, or use cases.

  • Independent Claims
    Likely define the core inventive concept—perhaps a novel chemical entity or novel use of an existing compound for treatment. The scope of the independent claims determines the breadth of patent protection.

  • Dependent Claims
    Narrower, providing specifics such as particular salts, dosage forms, methods of synthesis, or treatment regimens, thus creating a hierarchical protection scheme.

2. Key Elements and Notable Words

Important language in pharmaceutical claims often includes:

  • "Comprising": open-ended, allowing the inclusion of additional ingredients or steps.
  • "Consisting of": more restrictive, excluding other components.
  • "Effective amount": defining the dosage necessary for therapeutic effect.
  • "Pharmaceutically acceptable": referring to suitable excipients, salts, or formulations.

The scope hinges on these terms; broader usage of "comprising" can favor patent validity but may limit enforceability across variations, while restrictive language narrows scope but enhances defensibility.

3. Scope Analysis

Based on typical claim phrasing, the scope of DK3263110 likely covers:

  • Specific chemical compounds or drug combinations
  • Formulations including particular excipients
  • Methods of treatment involving these compounds
  • Manufacturing processes

The actual breadth depends on whether broad formulations or narrow specific compounds are claimed. For example, if the patent claims a "chemical compound comprising...", its scope extends to all derivatives or salts unless explicitly excluded.


Patent Claims Validity and Limitations

Potential Limitations:

  • Novelty: To maintain validity, claims must be novel relative to prior art, including patents, scientific literature, or known compounds.
  • Inventive Step: The claims should involve an inventive step beyond what is disclosed or obvious from prior art.
  • Industrial Applicability: The application must demonstrate utility in a pharmaceutical context.

Potential Challenges:

  • Prior Art Overlap: Existing patents or publications could threaten the novelty or inventive step.
  • Claim Breadth: Excessively broad claims risk invalidation if prior disclosures are similar.
  • Experimental Data: Limited data supporting therapeutic efficacy can impact the enforceability.

Patent Landscape Analysis

1. Regional and Global Patent Family

DK3263110 exists within a sizable and competitive patent landscape, with similar patents likely filed in major jurisdictions like the US, EP (Europe), China, and Japan. These parallel filings safeguard global market rights and prevent infringement.

  • Patent Families and Priority Claims:
    The patent probably belongs to a broader family claiming priority from earlier applications, such as PCT filings or related patent families.

  • Filing Strategies:
    Pharmaceutical companies often use national phases coupled with PCT applications to extend patent protection across key markets.

2. Competitive Landscape and Related Patents

Adjacent patents may involve:

  • Similar chemical scaffolds or derivatives
  • Alternative therapeutic methods
  • Formulation innovations

Standard patent landscapes reveal the following:

  • Infringement Risks: Competitors with similar compounds patentably distinguishable from DK3263110 may challenge its validity.
  • Freedom-to-Operate (FTO): Clearance for commercial activities depends on comprehensive landscape analysis, including prior art and live patent applications.

3. Patent Lifecycle and Maintenance

  • Expiry and Extensions:
    While the patent was granted in 2020, its expiry date will be 20 years from filing, subject to maintenance fees. Supplementary protection certificates (SPCs) can extend exclusivity for pharmaceuticals.

  • Lifeline of Innovation:
    Continuous R&D and filings in overlapping areas could threaten or reinforce the patent's strategic value.


Implications for Industry Stakeholders

Pharmaceutical Developers:
Understanding the scope of DK3263110 aids in designing novel compounds or formulations avoiding infringement, verifying patent infringement, or preparing for licensing negotiations.

Generic Manufacturers:
Analyzing claims for potential design-around strategies while assessing patent expiry timelines.

Legal and Patent Counsel:
Ensuring robustness of the patent’s claims and validity against prior art, especially considering the potential for future litigation or opposition.


Conclusion

Denmark Patent DK3263110 exemplifies a strategic pharmaceutical patent with claims likely centered on specific compounds, formulations, or methods of treatment. Its scope, defined by broad independent claims and narrower dependent claims, navigates the balance between protecting core innovations and maintaining validity. The patent landscape surrounding this patent is competitive, with multiple filings in global jurisdictions aiming to safeguard market share and prevent infringement.

Its strategic value depends on ongoing legal validity, technical breadth, and the evolving patent environment—highlighting the necessity for diligent landscape monitoring, claim drafting precision, and comprehensive freedom-to-operate analyses.


Key Takeaways

  • DK3263110’s scope hinges on the breadth of its independent claims, impacting enforceability and market leverage.
  • Strategic claim language is crucial; broader claims provide extensive protection but risk invalidation, whereas narrow claims offer stronger validity but limited reach.
  • The patent landscape surrounding DK3263110 is dynamic, involving related filings in multiple jurisdictions, necessitating continuous monitoring.
  • Effective use of this patent involves leveraging its rights to deter competitors, licensing, or securing market exclusivity, considering lifecycle and potential challenges.
  • Ongoing patent validity assessments and landscape analytics are vital for informed decision-making in drug development and commercialization.

FAQs

1. What is the typical lifespan of a pharmaceutical patent like DK3263110?
Pharmaceutical patents generally last 20 years from the filing date, subject to maintenance fees. Additional exclusivity can be granted via supplementary protection certificates (SPCs).

2. How does claim language influence patent enforceability?
Broad, open-ended language like “comprising” offers wider protection but can be challenged for lacking novelty. Narrow, specific claims are easier to defend but may limit scope.

3. Can DK3263110 be challenged or invalidated?
Yes. Challenges can be based on prior art, lack of novelty, obviousness, or insufficient disclosure. Patent offices or courts may revoke or limit claims if grounds for invalidity are proven.

4. How does the patent landscape impact potential market entry?
A complex landscape with overlapping patents can restrict freedom-to-operate. Strategic patent landscaping helps identify risks and design-around opportunities.

5. What role do patent claims play in licensing negotiations?
Claims define the scope of protection, influencing licensing terms, royalties, and infringement risks. Clear, enforceable claims are vital for successful licensing agreements.


References

  1. [Patent document DK3263110], Danish Patent Office, 2020.
  2. World Intellectual Property Organization (WIPO), Patent Landscape Reports.
  3. European Patent Office (EPO) patent database and related patent filings.
  4. Patent Scope by the World Intellectual Property Organization (WIPO).
  5. Relevant legal and technical commentary on pharmaceutical patent law.

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.