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Last Updated: December 12, 2025

Profile for Denmark Patent: 3176170


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US Patent Family Members and Approved Drugs for Denmark Patent: 3176170

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
10,131,667 Jun 12, 2033 Incyte Corp PEMAZYRE pemigatinib
9,611,267 Jan 30, 2035 Incyte Corp PEMAZYRE pemigatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3176170

Last updated: August 7, 2025


Introduction

Denmark Patent DK3176170 pertains to a pharmaceutical invention with potential implications across drug development, generic entry, and patent strategies within the biotech landscape. This report provides an in-depth analysis of the patent’s scope, claims, and the broader patent landscape, equipping stakeholders with insights necessary for strategic decision-making.


Overview of Denmark Patent DK3176170

Patent Number: DK3176170
Filing Date: [Insert Filing Date]
Publication Date: [Insert Publication Date]
Priority Date: [Insert Priority Date]
Status: [Insert status, e.g., granted, pending]
Inventors/Applicants: [Insert Name]
Assignee: [Insert Name]

(Note: Exact dates and owner info are assumed or need confirmation from official patent databases such as EPO or DK Patent Office)


Patent Scope and Claims

Summary of the Invention

While the detailed specification requires direct examination of the patent document, typical pharmaceutical patents of this nature often cover:

  • A specific chemical compound or a class thereof.
  • Pharmaceutical compositions including the compound.
  • Methods of manufacturing the compound.
  • Therapeutic uses for certain medical conditions.

Given the patent’s classification within the pharmaceutical domain, likely claim scope encompasses novel compounds or formulations with claimed efficacy benefits, stability, or enhanced bioavailability.

Claim Analysis

Primary (Independent) Claims:

The core independent claims usually define:

  • A chemical entity with particular structural features.
  • Methods of preparing the compound.
  • Use of the compound for treating specific diseases or conditions.

Dependent Claims:

Dependent claims narrow the scope further, adding limitations such as:

  • Specific substituents or functional groups.
  • Particular dosages or administration routes.
  • Synergistic combinations with other agents.

Note: Without direct claim text, this analysis remains contextual. An example might include claims covering “A compound comprising a core structure of X, Y, with substituents Z, wherein the compound exhibits enhanced selectivity for [target receptor]”.

Legal and Strategic Significance

The scope of claims directly influences patent enforceability and market exclusivity. Broader claims provide wider protection but may face validity challenges via prior art. Narrow claims, while easier to defend, offer limited market control.


Patent Landscape and Competitive Analysis

Key Aspects of the Patent Environment

  • Prior Art Considerations:
    The patent landscape likely includes previous patents on structurally similar molecules, formulations, or methods of use. Overlapping prior art can impact the scope and strength of DK3176170's claims.

  • Related Patents:
    Curating a landscape comprising earlier medicinal chemistry patents, such as those in the same therapeutic class, is critical. For example, if the compound relates to kinase inhibitors, past patents in that category influence freedom-to-operate.

  • Geographical Coverage:
    While this patent pertains to Denmark, similar filings may exist in broader jurisdictions like the EPO, US, China, and Japan, affecting global freedom-to-operate.

Patent Families and Filing Strategy

  • The patent likely belongs to a patent family with counterparts in multiple jurisdictions to secure global rights.
  • Strategic filings may include continuation or divisional applications to extend exclusivity or carve out narrower claims.

Potential Challenges

  • Patent Validity:
    Challenged via prior art, obviousness, or insufficiency of disclosure.

  • Infringement Risks:
    Subsequent patents or publications claiming similar compounds could pose infringement issues.

  • Patent Term and Maintenance:
    Maintenance of the patent requires timely fee payments, with potential to extend via supplementary protection certificates (SPCs), which are often applicable in Europe for pharmaceuticals.


Legal and Commercial Implications

Market Exclusivity:
Granted patent protection extends typically 20 years from the filing date, providing exclusivity for commercial exploitation. The scope of claims determines the breadth of this monopoly.

R&D and Licensing Opportunities:
Robust patent claims can attract licensees or partners for further development, especially if the compound demonstrates a novel or synergistic therapeutic profile.

Patent Litigation Risk:
Similar patents or existing market players may attempt to invalidate or contest the patent based on prior art or claim scope.


Conclusion

Denmark Patent DK3176170 appears to encompass a prioritized chemical compound, optimized formulations, or therapeutic uses within a specific drug class—potentially a novel pharmaceutical compound or a new use thereof. Its claims likely balance broad protection for core inventive features against the necessity to withstand prior art challenges.

Understanding the landscape involves scrutinizing related patents, prior art, and jurisdictional counterparts to assess enforceability and freedom-to-operate. The patent's strategic value hinges on its claim strength, breadth, and scope of protection, significantly impacting commercialization, licensing, and litigation strategies.


Key Takeaways

  • The scope of DK3176170’s claims fundamentally influences its market exclusivity and enforceability.
  • A thorough landscape analysis requires examining related patents, especially in jurisdictions beyond Denmark, to gauge potential patent conflicts.
  • Broader claims provide extended protection but risk validity challenges; narrower claims enhance defensibility but limit scope.
  • Strategic patent filing within a global patent family extends rights and mitigates challenges.
  • Ongoing monitoring of prior art and competitor filings remains essential for maintaining patent robustness.

FAQs

1. What primarily determines the strength of the claims in DK3176170?
The scope and novelty of the chemical compound or therapeutic method defined in the independent claims, along with their technical differentiation from existing prior art, determine core patent strength.

2. Can DK3176170 prevent competitors from developing similar drugs?
If the claims are broad and valid, they can restrict competitors from manufacturing, using, or selling similar compounds within the claim scope, thus providing market exclusivity.

3. How does the patent landscape affect the drug’s commercialization?
A crowded patent landscape with overlapping claims may hinder market entry and increase litigation risk, while clear, strong claims can facilitate licensing and strategic partnerships.

4. What is the significance of patent families in this context?
Patent families offer worldwide protection for the invention, enabling broader market coverage and safeguarding against regional patent challenges.

5. How can patent validity be challenged?
Validity can be contested through opposition procedures, citing prior art, obviousness arguments, or insufficient disclosure, especially if earlier inventions or publications predate the filing.


References

  1. European Patent Office (EPO) Patent Database.
  2. Danish Patent and Trademark Office (DKPTO).
  3. World Intellectual Property Organization (WIPO) Patentscope.
  4. Patent literature analyzing pharmaceutical patent trends.
  5. Relevant patent filings within the drug's therapeutic class.

[Note: Exact data points, application dates, and specifics should be sourced directly from official patent documents upon review.]

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