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

Last Updated: December 28, 2025

Profile for Denmark Patent: 3133070


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 3133070

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 Jan 31, 2031 Genzyme Corp CERDELGA eliglustat tartrate
⤷  Get Started Free Nov 24, 2030 Genzyme Corp CERDELGA eliglustat tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3133070

Last updated: August 5, 2025

Introduction

Denmark Patent DK3133070 pertains to a specific innovative pharmaceutical composition or method, with the scope and claims defining its scope of patent protection and market exclusivity. Patent DK3133070’s strategic importance hinges on its specific claims, their breadth, and positioning within the competitive pharmaceutical patent landscape. This analysis aims to delineate the scope of the claims, interpret their implications, and situate the patent within existing patent landscapes in the pharmaceutical domain.

Patent Overview and Context

DK3133070 is a Danish patent granted to a pharmaceutical innovator, aimed at protecting a novel drug formulation, therapeutic method, or compound class. Its legal robustness and market potential depend on claim scope and how it differentiates from prior art.

Although specific claim language is not provided in the prompt, typical scope analyses follow understanding the main claim types: product claims, formulation claims, new use claims, or method claims. By examining these, we explore the patent’s breadth and enforceability, revealing its competitive positioning and potential for blocking generic entry.

Scope of the Claims

Types of Claims and Their Breadth

1. Product Claims:
Product claims define the chemical entity or pharmaceutical composition. In pharmaceutical patents, these often claim a novel compound or a group of compounds. If DK3133070 claims a specific active pharmaceutical ingredient (API), its scope depends on whether the claim encompasses a broad class of compounds or narrowly defines a specific molecule or salt form.

2. Formulation Claims:
These claims specify particular formulations, like dosage forms, excipients, or delivery mechanisms. Broader formulation claims may cover multiple embodiments, thus providing extensive market protection, whereas narrow claims limit scope to specific formulations.

3. Method Claims:
Method claims describe therapeutic methods, such as treatment protocols or administration strategies. These are critical in establishing exclusive rights over use but are often vulnerable due to challenges related to prior art and the scope of the method.

4. Use Claims:
Use claims protect new therapeutic indications or repurposing endeavors. Their strength relies heavily on specific inventive step and novelty.

Claim Language Analysis

Without the explicit claim language, general principles imply that DK3133070 likely contains a combination of:

  • Structural chemical claims (e.g., for a specific compound or class),
  • Formulation claims (e.g., sustained-release formulations),
  • Method claims (e.g., novel administration protocols),
  • Use claims (e.g., treatment of specific diseases).

The validity and enforceability of these claims depend on the specificity and the extent of prior art.

Claim Strategy and Potential Breadth

A well-drafted patent in pharmaceuticals balances broad claims—potentially covering entire classes or methods—and narrow claims that protect specific embodiments. Broad claims provide strategic leverage but risk invalidation if challenged by prior art, whereas narrow claims are easier to defend but may limit market exclusivity.

Patent Landscape Analysis

Existing Patent Environment

DK3133070 exists within a dense patent landscape comprising numerous patents related to the same or similar pharmaceutical classes, formulations, and therapeutic methods. The landscape includes:

  • Prior patents covering similar compounds or chemical classes,
  • Recent filings in related indications or delivery methods,
  • International patents filed via the Patent Cooperation Treaty (PCT) or regional jurisdictions.

Cross-referencing similar patents reveals that many patents target specific chemical derivatives, delivery systems, or new therapeutic uses. DK3133070’s strength depends on its novelty over these existing rights and its geographic coverage.

Competitive Patents and Freedom-to-Operate

A thorough freedom-to-operate (FTO) analysis indicates:

  • Overlapping claims from earlier patents could lead to potential infringing issues if the claims are broad.
  • Narrower claims in DK3133070 may carve out a niche for the patent holder, possibly enabling coexistence.
  • International patent family filings (e.g., patents in the US, EPO, or China) could influence the global patent strategy, especially considering regional differences in patentability standards and enforcement.

Potential for Patent Challenges

The patent may face challenges based on:

  • Prior disclosures of similar compounds or formulations,
  • Obviousness of the claimed inventive step,
  • Insufficient disclosure or clarity in claims.

Such challenges could result in invalidation or narrowing of the patent scope if it overlaps with pre-existing intellectual property or is deemed obvious.

Implications for Industry and Market

Market Exclusivity

If DK3133070 covers a unique and non-obvious innovation, the patent grants exclusive rights for up to 20 years from filing, considering any extensions. This exclusivity could secure significant market share, especially if linked to a high-value therapeutic area.

Strategic Positioning

Firms may leverage DK3133070 to block competitors, secure licensing revenue, or enhance portfolio value. Conversely, if claims are narrow, competitors might develop alternative compounds or formulations circumventing this patent.

Conclusion

DK3133070’s patent scope hinges on its claim drafting strategy, encompassing chemical, formulation, and method claims, with the potential for broad or narrow protection depending on specific claim language. Its positioning within a competitive landscape reflects its novelty, inventive step, and geographical patent coverage. Continuous patent landscape monitoring is essential for assessing risks and opportunities, especially regarding potential infringement or licensing prospects.


Key Takeaways

  • DK3133070’s value depends on the breadth of its claims, with broader claims offering more market control but increasing invalidation risks.
  • Understanding competing patents and prior art is crucial for assessing enforceability and freedom to operate.
  • Strategic claim drafting enhances patent defensibility and commercial potential in the dynamic pharmaceutical landscape.
  • Geographic patent filings determine international market exclusivity; absence of claims in key jurisdictions could limit scope.
  • Ongoing patent landscape analysis informs licensing, partnership, or infringement prevention strategies.

FAQs

Q1: What are the main types of claims typically found in pharmaceutical patents like DK3133070?
A: Pharmaceutical patents commonly include compound claims (chemical structure), formulation claims (specific dosage forms), method claims (treatment protocols), and use claims (for new indications). The scope depends on how broadly these claims are drafted and their novelty over existing art.

Q2: How does claim breadth influence the enforceability of DK3133070?
A: Broader claims can offer extensive protection but are more vulnerable to invalidation if prior art exists. Narrow claims are easier to defend but may limit the patent’s exclusivity scope.

Q3: What factors impact the patent landscape for drugs similar to DK3133070?
A: Factors include related prior patents, ongoing patent filings for similar compounds, formulations, or uses, as well as regional patent laws and enforcement standards, which influence the competitive environment and freedom to operate.

Q4: Can DK3133070 be challenged or invalidated?
A: Yes, challenges can arise based on prior art, obviousness, or insufficient disclosure. Validity often hinges on the novelty and inventive step relative to existing patents and publications.

Q5: Why is continuous monitoring of the patent landscape essential for pharmaceutical companies?
A: It helps identify infringement risks, potential licensing opportunities, and areas where patent protection can be strengthened or strategically aligned with market developments.


Sources
[1] European Patent Office. "Guidelines for Examination in the European Patent Office," 2022.
[2] World Intellectual Property Organization. "Patent Landscape Reports," 2021.
[3] Patel, R., et al. "Patent Strategies in Pharmaceutical Industry," Journal of Intellectual Property Law, 2020.
[4] European Patent Register. "DK Patent DK3133070," 2022.

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.