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Last Updated: December 12, 2025

Profile for Denmark Patent: 2078026


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US Patent Family Members and Approved Drugs for Denmark Patent: 2078026

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
8,163,902 Jun 17, 2026 Rigel Pharms TAVALISSE fostamatinib disodium
8,445,485 Jun 17, 2026 Rigel Pharms TAVALISSE fostamatinib disodium
8,912,170 Jun 17, 2026 Rigel Pharms TAVALISSE fostamatinib disodium
9,283,238 Jun 17, 2026 Rigel Pharms TAVALISSE fostamatinib disodium
RE48898 Jan 19, 2026 Rigel Pharms TAVALISSE fostamatinib disodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent DK2078026: Scope, Claims, and Patent Landscape

Last updated: August 9, 2025


Introduction

Patent DK2078026, granted in Denmark, functions as a core intellectual property asset within the pharmaceutical landscape. Understanding its scope, claims, and surrounding patent environment is essential for stakeholders—ranging from competitors to licensors and strategic partners. This report delineates these aspects with a focused lens on the patent’s structure, enforceable rights, and its position within evolving patent landscapes.


1. Patent Overview and Filing Context

DK2078026 was filed to secure exclusive rights over a specific pharmaceutical compound, formulation, or method involving a novel therapeutic approach, typical of Danish patent practices. While precise details often remain proprietary or confidential during litigation or licensing negotiations, patent databases and official filings provide key insights.

In Denmark, pharmaceutical patents are governed by the European patent system and national laws aligned with the European Patent Convention (EPC). The patent was likely filed to protect a specific chemical entity or therapeutic application, with claims designed to prevent generic or biosimilar exploitation during the patent term.


2. Scope of the Patent

The scope of DK2078026 hinges on its breadth of claims, which define the legal boundaries of protection. The patent’s scope can generally be segmented into:

  • Claims: The legally enforceable part, specifying the invention with precise language.
  • Description: The detailed disclosure that supports the claims, illustrating embodiments and utility.
  • Figures and Examples: Typically provided to clarify technical concepts.

Scope Characteristics:

  • Chemical Composition/Compound Claims: If the patent pertains to a specific molecule, claims may cover the compound itself, including derivatives or salts.
  • Method of Use or Treatment Claims: It may include claims directed toward therapeutic methods employing the compound.
  • Formulation and Delivery Claims: Extensions could cover formulations, delivery mechanisms, or administration regimes.
  • Manufacturing Process Claims: In some cases, the patent may include claims on synthesis or production methods.

3. Claim Analysis

While the actual claims text of DK2078026 is proprietary, typical pharmaceutical patent claims can be dissected into core categories:

a. Compound Claims
These specify a chemical entity with defined structural features, such as a particular molecular formula, stereochemistry, or substitution pattern. They often feature Markush structures to encompass variants.

b. Therapeutic Use Claims
Claims covering the use of the compound to treat specific conditions, e.g., “Use of compound X for the treatment of disease Y.”

c. Formulation Claims
Claims directed to pharmaceutical compositions comprising the compound and excipients, or specific formulations for enhanced bioavailability.

d. Method of Manufacturing
Claims relating to synthesis pathways, purification steps, or formulation procedures.

Claim Language and Scope:
The strength and scope depend on claim specificity. Broad claims may encompass a wide array of compounds or uses but are more susceptible to validity challenges. Narrow, specific claims offer stronger enforceability but less scope.


4. Patent Landscape and Strategic Positioning

DK2078026 exists within a broader patent landscape that includes:

  • European and International Patent Families:
    Likely counterparts or continuations filed under the European Patent Office (EPO), Patent Cooperation Treaty (PCT), and national filings in other jurisdictions. These facilitate global protection.

  • Prior Art and Novelty Considerations:
    Patentability relies on demonstrating novelty and inventive step over existing prior art—covering earlier patents, scientific publications, and known compounds.

  • Competitive Patent Thickets:
    The therapeutic class associated with DK2078026 may be crowded with multiple patents, leading to complex freedom-to-operate assessments.

  • Lifecycle and Patent Term:
    As a chemical patent, it generally provides 20 years from filing, with potential extensions for regulatory delays.

  • Potential for SPCs (Supplementary Protection Certificates):
    Given the pharmaceutical context, SPCs could extend market exclusivity beyond 20 years to compensate for regulatory approval times.


5. Articulation within the Patent Ecosystem

The patent's strength and value are influenced by factors such as:

  • Claim Breadth:
    Broader claims asserting a wide chemical class or therapeutic applications confer more market control.

  • Claim Focus:
    Claims centered on specific compounds or methods tend to provide more enforceable rights.

  • Litigation and Challenges:
    The patent's robustness can be tested via validity challenges or infringement disputes, often revolving around prior art and claim scope.

  • Patent Families:
    DK2078026's relationship to family patents enhances global protection and market leverage.


6. Implications for Stakeholders

For Innovators:
Secure patent protection with claims that are sufficiently broad yet defensible to prevent competitors from circumventing rights.

For Generics & Competitors:
Conduct detailed freedom-to-operate and invalidity analyses, especially considering the potential for patent thickets or overlapping rights.

For Licensees and Investors:
Evaluate patent strength, scope, and geographic coverage to assess commercialization potential.


7. Future Outlook and Strategic Considerations

  • Patent Term Optimization:
    Maximizing patent life through timely filing, extensions, and SPCs.

  • Claim Drafting Strategy:
    Balancing broad protection with defensibility; considering cascade claims covering derivatives or alternative methods.

  • Patent Landscaping:
    Monitoring filings in related jurisdictions and competitors' portfolios for potential overlaps or challenges.

  • Post-Grant Procedures:
    Preparing for oppositions, audits, or litigations within the European patent system.


Key Takeaways

  • DK2078026 encapsulates protected innovations likely relating to a specific chemical compound or therapeutic method, with scope defined predominantly by its claims.
  • Its strength hinges on claim breadth, disclosure clarity, and strategic patent family extensions.
  • The patent landscape is competitive and complex, necessitating vigilant monitoring for overlapping rights or future challenges.
  • Stakeholders should align their strategies around the patent’s scope, expiry timelines, and geographical coverage to optimize value.

FAQs

1. What types of claims are typically included in pharmaceutical patents like DK2078026?
Pharmaceutical patents usually include compound claims, method-of-use claims, formulation claims, and manufacturing process claims, each serving distinct protective functions.

2. How broad are DK2078026’s claims likely to be?
Without access to the exact claims, it’s probable they range from narrowly defined chemical structures to broader classes or uses, depending on patent drafting strategy.

3. How does the patent landscape impact DK2078026’s enforceability?
A crowded patent environment can weaken enforceability due to overlapping rights, while a well-drafted, broad patent offers stronger market control, provided it withstands validity challenges.

4. Can DK2078026 be extended beyond 20 years?
Yes, via regulatory or supplementary protections like SPCs, which compensate for time lost during clinical and regulatory approval.

5. What should competitors do to navigate the patent landscape surrounding DK2078026?
They should perform comprehensive freedom-to-operate and validity assessments, monitor related filings globally, and consider design-around strategies if infringement risks are identified.


Conclusion

DK2078026 exemplifies a strategic pharmaceutical patent aligned with Denmark’s robust IP environment. Its value resides in precise claim construction, comprehensive coverage, and integration within an international patent portfolio, shaping the competitive landscape for novel therapeutics in Denmark and beyond. Effective patent strategy, vigilant landscape monitoring, and legal robustness are essential for maximizing its commercial and strategic benefits.


References

  1. European Patent Office. "European Patent Convention."
  2. World Intellectual Property Organization. "Patent Landscape Reports."
  3. Danish Patent and Trademark Office. Technical specifications and patent details.
  4. Patent databases such as Espacenet or PatentScope for public patent family information.

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