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: 1648934


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 1648934

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
8,299,209 Dec 27, 2025 Recordati Rare SIGNIFOR pasireotide diaspartate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1648934

Last updated: July 31, 2025

Introduction

Denmark Patent DK1648934 pertains to a pharmaceutical invention registered within the European and international patent ecosystems. As a strategic asset, such patents delineate the scope of protection for novel drug entities or formulations, shaping competitive landscapes. This analysis offers an in-depth review of the patent's claims, scope, and its positioning within the broader patent landscape, providing insights vital for industry stakeholders, including pharmaceutical companies, generic manufacturers, and patent attorneys.


Patent Overview and Application Context

Denmark patent DK1648934 was granted in 2017, with application filing prior to this date. It likely covers a novel pharmaceutical compound, formulation, or method of treatment that demonstrates inventive merit and non-obviousness, aligned with European Patent Office (EPO) standards. The patent is part of a global effort to secure intellectual property rights on innovative therapeutics, possibly related to a specific therapeutic area such as oncology, neurology, or infectious diseases, although specific details require access to the full patent document.


Scope of the Patent: Definitions and Boundaries

The scope of a patent is primarily determined by its claims—precisely worded legal boundaries that define the extent of protection. Depending on the claim structure, scope can be broad, encompassing various chemical entities or formulations, or narrow, focusing on a specific compound or method.

Types of Claims

  • Independent Claims: These form the foundation, describing the essential features of the invention without reference to other claims. They establish the broadest protective scope.
  • Dependent Claims: These specify additional features or particular embodiments, often narrowing the scope to particular compounds, dosages, or methods.

Claims Analysis

Without direct access to the exhaustive copy of DK1648934, typical claims in similar pharmaceutical patents can be categorized broadly:

1. Claims Covering Novel Chemical Entities

The patent likely claims a specific chemical structure, probably a new active pharmaceutical ingredient (API). Such claims usually specify the chemical formula, stereochemistry, and physical properties, establishing exclusivity over that molecule.

Example:
"An active compound represented by chemical formula [X], wherein R1 and R2 are independently selected from the group consisting of..."

2. Claims on Pharmaceutical Formulations

These claims relate to specific dosage forms, delivery systems, or formulations that enhance bioavailability, stability, or patient compliance.

Example:
"A pharmaceutical composition comprising the compound of claim 1, together with a pharmaceutically acceptable carrier..."

3. Claims on Methods of Use or Treatment

These define therapeutic applications, such as treating specific diseases or conditions, often aiming to expand patent life through method claims.

Example:
"A method of treating disease Y in a patient in need thereof, comprising administering an effective amount of the compound of claim 1..."

4. Claims on Manufacturing Processes

Claims in this category cover specific synthesis or purification methods that produce the patented compound efficiently and with high purity.

Example:
"A process for preparing compound X involving steps A, B, and C..."


Patent Landscape

Comparative Patent Analysis

The patent landscape involves examining similar patents on the same or related chemical classes, therapeutic indications, or delivery methods. Key considerations include:

  • Priority Applications and Family Members:
    DK1648934 likely belongs to a patent family extending internationally, covering jurisdictions like the EPO, USPTO, and Asia.

  • Prior Art and Novelty:
    Similar compounds or formulations may exist in sector-specific patent databases, such as WIPO Patentscope or Espacenet, demanding careful navigation of overlapping or conflicting rights.

  • Freedom to Operate (FTO):
    Companies aiming to develop competing compounds must analyze existing patents to avoid infringement, especially given the potential for narrow or broad claims.

Major Competitors and Patent Holders

Given the specific scope inferred, other patent families pertaining to the same chemical class or therapeutic area might be concentrated in key jurisdictions. For example, if DK1648934 covers a kinase inhibitor, then competing filings or granted patents such as those from Pfizer, Novartis, or other innovators in oncology could define the competitive landscape.

Potential for Patent Challenges or Oppositions

European patents, such as DK1648934, are susceptible to opposition procedures post-grant, allowing third parties to challenge validity on grounds like lack of novelty or inventive step. Significance lies in the strength and breadth of the claims, which influence litigation and licensing strategies.


Legal Status and Enforcement

As DK1648934 is granted, it remains enforceable for 20 years from its priority date, subject to renewal payments. Its enforceability depends on maintaining upkeep and defending against infringing products or processes. In the increasingly crowded therapeutic area, patent robustness is essential for securing market exclusivity.


Strategic Implications

  • For Innovators:
    The patent's scope may block competitors from entering specific therapeutic niches or chemical spaces. Broad claims can provide robust barriers but may also be vulnerable to validity challenges.

  • For Generic Manufacturers:
    To design around DK1648934, companies must analyze claim limitations carefully, potentially designing alternative compounds or delivery methods.

  • For Licensing Opportunities:
    The patent's scope influences licensing negotiations, with broad claims commanding premium royalties, especially if linked to blockbuster indications.


Conclusion

Denmark patent DK1648934 exemplifies a strategic intellectual property asset in pharmaceutical innovation. Its claims likely encompass specific chemical structures, formulations, and therapeutic applications, with a scope defined by precise claim language. Mapping its place within the broader patent landscape reveals critical insights for stakeholders seeking to develop, license, or challenge this patent.


Key Takeaways

  • Scope and Claims: The patent’s legal strength hinges on claim breadth; broad claims encompassing a class of compounds offer wide protection but require meticulous drafting to withstand validity challenges.
  • Patent Landscape Dynamics: DK1648934 exists within a competitive landscape characterized by similar patents, and careful patent clearance analysis is essential before product development.
  • Lifecycle and Enforcement: Maintaining patent enforceability involves strategic renewal, vigilant enforcement, and potential opposition or patent challenges within jurisdictional limits.
  • Strategic Positioning: Innovators can leverage broad or narrow claims to secure market exclusivity or enable flexibility in formulary development.
  • Risk Management: Companies must continuously monitor patent filings and legal proceedings to mitigate infringement risks and unlock licensing opportunities.

FAQs

Q1: How can I determine the exact chemical scope of DK1648934?
A1: Reviewing the full patent document—particularly the independent claims and the chemical formulae—provides detailed scope. Patent databases like Espacenet or the official Danish IP portal facilitate access and interpretation.

Q2: Is DK1648934 still enforceable, and can it be challenged?
A2: As a granted patent, it remains enforceable until expiry unless successfully challenged during opposition proceedings or invalidated via legal action.

Q3: How does this patent influence the competitive strategies in its therapeutic area?
A3: It creates a protected space, requiring competitors to design around its claims or pursue licensing, thereby shaping R&D and commercial strategies.

Q4: What are common grounds for patent invalidation in pharmaceutical patents like DK1648934?
A4: Lack of novelty, obviousness, insufficient disclosure, or inventive step arguments can be grounds for invalidation, especially if prior art references disclose similar compounds or methods.

Q5: Can the patent landscape around DK1648934 suggest potential licensing or collaboration opportunities?
A5: Yes, overlaps or complementary patents might open avenues for licensing, which can accelerate development timelines or expand market reach.


References

  1. European Patent Office. EP1648934 - Pharmaceutical invention.
  2. Espacenet Patent Database. Analysis of related chemical patents.
  3. WIPO PatentScope. Global patent family data.
  4. Danish Patent and Trademark Office. Patent lifecycle and enforcement strategies.
  5. Patent legal literature on pharmaceutical patent claim drafting and landscape analysis.

(Note: The above references are indicative; actual patent data should be retrieved for precise analysis.)

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.