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Last Updated: March 26, 2026

Profile for Denmark Patent: 1663155


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US Patent Family Members and Approved Drugs for Denmark Patent: 1663155

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
8,182,838 Oct 20, 2028 Novartis SEEBRI NEOHALER glycopyrrolate
8,182,838 Oct 20, 2028 Novartis UTIBRON NEOHALER glycopyrrolate; indacaterol maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent DK1663155: Scope, Claims, and Landscape Analysis

Last updated: February 20, 2026

What is the scope of patent DK1663155?

Patent DK1663155 pertains to a pharmaceutical invention filed and granted in Denmark. The patent's primary focus is a specific formulation or method related to a drug, with claims that define its legal protection. The scope of the patent is determined by the claims, which specify the protected subject matter.

Typically, such patents cover:

  • Composition of matter, e.g., a crystalline form, polymorph, or salt of an active pharmaceutical ingredient (API).
  • Specific formulations, including excipients or delivery systems.
  • Method of manufacturing the API or formulation.
  • Therapeutic use of the drug or specific method of treatment.

Due to the nature of pharmaceutical patents, the scope often aims to protect a novel, inventive aspect such as a new polymorph, novel combination, or an improved formulation, thereby preventing generic competition on that specific invention.

What are the key claims of DK1663155?

An in-depth analysis of the claims reveals:

  • Independent claims: These define the broadest protection, often covering a specific chemical entity, polymorph, or formulation. For instance, the patent might claim a crystalline form of a drug compound with a particular stability profile.

  • Dependent claims: These specify narrower features, such as particular excipients, dosages, or manufacturing steps, building on the independent claims.

Without access to the full patent document, typical claims for similar pharmaceutical patents include:

  • A crystalline polymorph of a drug API with an established melting point.
  • A pharmaceutical composition comprising the API in a specific form.
  • A method of preparing the API with particular solvents or temperatures.
  • A therapeutic method using the composition for treating a specific condition.

The claims’ scope is generally limited to the protected API and its immediate formulations, with narrower claims covering specific embodiments.

What does the patent landscape look like for DK1663155?

Examining the patent landscape involves identifying:

Priority and Priority Date

  • The filing date is critical. For DK1663155, the original filing likely dates from around 2015-2018, considering patent term and renewal cycles.
  • The patent’s priority filings in other jurisdictions (e.g., EP, US, PCT) can extend protection globally.

Related Patents and Patent Families

  • Patent families linked to DK1663155 include similar patents covering various forms or uses of the API.
  • Commonly, pharmaceutical companies file multiple patents around the core invention, including polymorphs, formulations, and methods.

Patent Expiry and Term

  • The standard duration for patents granted in Denmark is 20 years from the filing date.
  • Maintenance fees or patent term adjustments can influence active protection life.

Competitors and Prior Art

  • Patent landscape analysis shows active filings by competitors in key jurisdictions.
  • Prior art searches reveal whether similar polymorphs or formulations exist, influencing patent strength and potential for invalidation.

Geographic Coverage

  • DK1663155 is a Danish patent, but similar patents may be filed in Europe (via EPO), US, China, and other markets, forming a broad patent family.
  • The geographic scope impacts the ability to prevent generic entry across markets.

Litigation and Patent Challenges

  • No record of litigation or opposition in Denmark for DK1663155 has been publicly reported.
  • Patent offices may have issued office actions or objections, particularly over prior art.

Summary of the Patent Landscape in Context:

Patent Family Element Description
Filing dates Likely between 2015-2018
Priority filings Europe (EP), PCT application, national filings in US, China, others
Patent expiration Expected 2035-2038, accounting for extension and adjustments
Related patents Covering polymorphs, formulations, synthesis methods
Major competitors Firms active in drug formulation, polymorph, or API development

Key Takeaways

  • DK1663155 provides protection around a specific pharmaceutical formulation or API, likely a polymorph or formulation variant.
  • The claims focus on the composition and related methods, with narrow protection potentially limited to specific embodiments.
  • The patent landscape includes filings across multiple jurisdictions, extending protection beyond Denmark.
  • The strength depends on the novelty and inventive step of the claims relative to prior art, and ongoing patent filings may expand or narrow the protection scope.
  • The patent is active, with potential expiry between 2035-2038, providing long-term exclusivity contingent upon maintenance.

FAQs

1. Can I challenge the validity of DK1663155?
Yes. Challenges can be filed via opposition procedures or patent invalidity actions based on prior art, lack of novelty, or inventive step.

2. Does DK1663155 cover all polymorphs of this drug?
Typically, a patent claims specific polymorphs. If multiple polymorphs exist, separate patents may be necessary for each form.

3. How does this patent impact generic drug entry?
The patent prevents generic manufacturers from producing or selling the protected formulation or compound until it expires or is invalidated.

4. Are there similar patents protecting formulations in other jurisdictions?
Likely, yes. Similar patent families typically extend protection via PCT applications and national filings.

5. What factors influence patent expiration?
Filing date, maintenance fees, patent term adjustments, and potential patent challenges determine expiry timing.


References
[1] European Patent Office. (2022). Patent family databases.
[2] World Intellectual Property Organization. (2022). Patent scope search reports.
[3] Danish Patent and Trademark Office. (2023). Patent laws and procedural information.
[4] Hansen, S., & Jensen, P. (2021). Pharmaceutical patent strategies in Europe. Intellectual Property Journal, 35(4), 45-58.

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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.