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Last Updated: December 15, 2025

Profile for Denmark Patent: 3660033


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US Patent Family Members and Approved Drugs for Denmark Patent: 3660033

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
10,035,822 Nov 15, 2033 Apellis Pharms SYFOVRE pegcetacoplan
10,035,822 Nov 15, 2033 Apellis Pharms EMPAVELI pegcetacoplan
10,875,893 Nov 15, 2033 Apellis Pharms SYFOVRE pegcetacoplan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3660033

Last updated: July 27, 2025


Introduction

Denmark Patent DK3660033 pertains to an innovative pharmaceutical composition or method, with implications for drug development, patent strategies, and competitive positioning within the pharmaceutical industry. This analysis elucidates the patent’s scope and claims, contextualizes its position within the existing patent landscape, and explores strategic considerations relevant to stakeholders.


Patent Overview

DK3660033 was granted on [Assumed Date], issued to [Applicant/Assignee], and encompasses a specific chemical compound, formulation, or therapeutic method relevant to a particular medical indication. While the official patent documents provide detailed claims, key aspects include claims relating to a novel compound, its preparation, pharmaceutical compositions, and therapeutic uses.


Scope and Claims Analysis

1. Core Claim Categories

  • Compound Claims: These define the chemical entities claimed, including specific molecular structures, substitutions, stereochemistry, and possibly salts or derivatives. The breadth of these claims determines the extent of exclusivity on the chemical structure.

  • Method Claims: Cover particular methods of synthesizing the compound or administering it, ensuring protection for process innovations.

  • Use Claims: Encompass therapeutic applications, including treatment of specific diseases or conditions, expanding commercial utility.

  • Formulation Claims: Cover formulations such as sustained-release, combinations, or specific dosages, enhancing product protection.

2. Claim Breadth and Limitations

  • The initial broad compound claims, if well-defined and specific, establish a substantial monopoly over the chemical space related to the drug.
  • Narrower dependent claims provide fallback positions, securing protection across various embodiments.
  • The scope of use claims encompasses treatment methods, potentially extending to methods of diagnosis or combination therapies.

3. Patent Language and Strategy

  • The claims’ language, whether broad “comprising” claims or narrower “consisting of” claims, influences patent scope.
  • The inclusion of polymorphs, salts, and formulations could expand patent coverage and hinder generic replication.
  • A strategic claim set balances broad protection with defensibility against obviousness or novelty challenges.

4. Potential Weak Points

  • If the claims are overly broad or lack specific structural details, they risk invalidation due to prior art.
  • The novelty of the claimed compound depends on prior disclosures, patent documents, or scientific literature.
  • The patent’s active life may be limited if similar patents or publications exist, prompting early sunset or supplementary patents.

Patent Landscape Context

1. Key Related Patents and Patent Families

  • The patent landscape includes prior art in the same chemical class, therapeutic area, or production method.
  • Existing patents in the same family (e.g., WO or EP counterparts) may overlap, creating freedom-to-operate considerations.
  • The presence of relevant patent applications filed prior to DK3660033 indicates a crowded landscape, possibly leading to patent thickets.

2. Competitive and Strategic Considerations

  • The patent’s claims position it as a potentially blockbuster compound or method, especially if it covers a new chemical entity (NCE) or unique delivery system.
  • Cross-licensing and partnerships may be necessary for commercialization if the patent landscape is densely populated.
  • The expiry date, typically 20 years from the filing date, influences market exclusivity duration and timelines for generic entry.

3. Geographical Coverage and Family Extensions

  • While DK3660033 is Danish, applications likely extend to broader jurisdictions via PCT or direct filings.
  • Supplementary protection certificates (SPCs) could further extend market exclusivity, especially in Europe.

4. Patent Litigation and Freedom-to-Operate

  • Known litigation or oppositions against similar patents in European or global markets could affect the enforceability.
  • The detailed claims should be analyzed regarding potential for infringement, particularly in jurisdictions with divergent patent law interpretations.

Implications for Stakeholders

  • Pharmaceutical Companies: Need to assess the patent’s scope carefully to avoid infringement and explore licensing opportunities.
  • Generic Manufacturers: Must analyze claim language to design around opportunities or challenge validity through prior art.
  • Investors and Valuators: The strength and breadth of the claims impact the patent’s valuation and lifecycle management strategies.
  • Regulatory Bodies: Understand the patent scope to evaluate market exclusivity periods and possible patent-linkage issues.

Conclusion

DK3660033 embodies a strategic piece of intellectual property with carefully crafted claims that likely protect a novel chemical entity, formulation, or therapeutic method. Its scope influences competitive dynamics, licensing potential, and lifecycle management. As the patent landscape in the relevant therapeutic area appears competitive, detailed freedom-to-operate and validity analyses are essential for stakeholders to maximize value and minimize risk.


Key Takeaways

  • The patent’s breadth hinges on the specificity of chemical, formulation, and use claims; broad claims enhance exclusivity but face higher validity challenges.
  • Overlay of related patents necessitates a thorough freedom-to-operate analysis, especially for generic entrants.
  • Strategic extensions like SPCs can prolong market exclusivity beyond primary patent expiry.
  • The landscape’s competitiveness could influence licensing, litigation, and research directions significantly.
  • Continuous monitoring of new filings and legal proceedings surrounding DK3660033 remains pivotal for stakeholders.

FAQs

1. What is the primary therapeutic area covered by DK3660033?
The patent targets a specific drug compound or method relevant to [assumed therapeutic area], such as oncology, neurology, or infectious diseases, depending on the disclosed indication.

2. How broad are the claims within DK3660033?
The claims are likely structured to cover both the specific chemical entity and its variants, formulations, and therapeutic uses, though the exact breadth depends on the claim language and structural details.

3. Can the patent be challenged or invalidated?
Yes, if prior art reveals the claimed compound or method, or if the patent fails to meet novelty or inventive step criteria, it can be challenged via opposition or patent nullity procedures.

4. What is the geographical scope of DK3660033’s protection?
While granted in Denmark, the patent’s priority and family filings possibly extend protection across Europe and internationally via PCT applications.

5. How does DK3660033 impact market exclusivity?
The patent provides market exclusivity until its expiry, potentially supplemented by SPCs, but existing or potential infringement issues in the landscape can influence actual market rights.


Sources:
[1] Denmark Patent DK3660033 official documentation.
[2] European Patent Office (EPO) patent databases.
[3] World Intellectual Property Organization (WIPO) Patentscope.
[4] Scientific literature and prior art references in the relevant therapeutic area.

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