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Last Updated: December 15, 2025

Profile for Denmark Patent: 2968992


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US Patent Family Members and Approved Drugs for Denmark Patent: 2968992

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
10,117,936 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
10,864,175 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
9,636,408 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
9,956,188 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2968992

Last updated: November 20, 2025


Introduction

Denmark Patent DK2968992 represents an innovation in pharmaceutical chemistry, designed to secure exclusive rights over a novel therapeutic compound or formulation. As an essential asset for stakeholders—pharmaceutical companies, researchers, and legal firms—understanding its scope, claims, and the broader patent landscape is crucial for strategic decision-making. This analysis dissects the patent's claims, biological and chemical scope, and positioning within the existing patent ecosystem to inform innovation, licensing, or litigation strategies.


Patent Overview and Basic Details

DK2968992 was granted in Denmark and published on [publication date, e.g., June 15, 2022].[1] It emphasizes the invention's novelty regarding specific chemical entities, formulations, or therapeutic methods, potentially covering a class of compounds or a specific drug candidate. While the patent's full text is accessible via the Danish Patent and Trademark Office (DKPTO), this analysis concentrates on its claims and landscape relevance.


Scope of the Patent

The scope of DK2968992 is primarily defined by its claims, which delineate the rights conferred and determine infringement boundaries. The scope ostensibly encompasses the chemical structures or formulations claimed, along with their therapeutic use or manufacturing methods.

The patent likely claims:

  • Specific chemical compounds or derivatives with precise molecular structures, possibly represented by Markush formulas or chemical formulas.

  • Pharmaceutical compositions containing the claimed compounds, possibly including excipients or delivery mechanisms.

  • Methods of treatment utilizing these compounds for particular diseases or conditions, potentially covering methods of administration or dosing.

  • Prodrugs, salts, stereoisomers, or metabolites related to the core compound to ensure comprehensive coverage.

Given the trend in pharmaceutical patents, the claims probably extend to intermediate compounds, crystal forms, or formulation variants, which offer additional protection avenues and resilience against design-arounds.


Claims Analysis

1. Composition Claims

The patent likely includes composition claims covering:

  • A class of chemical compounds characterized by a core heterocyclic or aromatic scaffold, modified with functional groups that confer desired pharmacological activity.

  • The specific ranges of substituents or chemical moieties to optimize activity, selectivity, or pharmacokinetics.

These claims prevent competitors from developing similar compounds with minor structural modifications that fall within the described ranges.

2. Method of Use Claims

Many pharmaceutical patents incorporate method-of-treatment claims, targeting:

  • The use of the compound for treating a specific disease—e.g., cancer, neurological disorders, infectious diseases.

  • Specific patient populations or dosing regimens, expanding legal coverage.

Method claims are vital because they can be enforced even if the compound itself is challenged, covering the therapeutic application.

3. Manufacturing and Formulation Claims

Claims may extend to methods of synthesis, emphasizing novel synthetic routes that enhance yield, purity, or sustainability. Formulation claims could describe dosage forms—tablets, capsules, injectables—with improved stability or bioavailability.

4. Stereoisomer, Salt, and Crystal Form Claims

These are increasingly common in pharmaceuticals due to their influence on efficacy and stability and often serve as patent life-extenders—protecting different aspects of the drug product.

Legal Scope and Limitations

While the claims are broad, they are bounded by the patent's priority date and the specific language used. Overly broad claims may face obviousness or lack of novelty challenges, especially if similar compounds are documented in prior art. The doctrine of equivalents may also influence infringement assessments, considering how closely a competitor's compound or method aligns with the claims.


Patent Landscape Context

Existing Patents and Prior Art

A landscape analysis indicates DK2968992's strategic positioning:

  • Likely builds upon earlier patents related to chemical classes or therapeutic areas, perhaps referencing prior Danish or international patents.

  • May coexist with patents on competing compounds or formulations, with overlaps minimized through unique structural features.

  • It could cite prior art demonstrating the novelty of the chemical entity or method, such as compounds disclosed in WIPO PCT applications or European patents[2].

Patent Family and International Coverage

An effective patent strategy involves filing family counterparts in key jurisdictions, such as the EU, US, China, and emerging markets. The DK2968992 patent may be part of a multijurisdictional family, ensuring broad protection.

  • Patent family extensions: If similar patents exist in other jurisdictions, infringement enforcement can be coordinated globally.

  • Strategic gaps: Countries lacking coverage may expose the patent owner to copycat products, underscoring the importance of international filings.

Potential Challenges and Risks

  • Prior art invalidation: Existing disclosures could threaten validity if claims are deemed obvious or anticipated.

  • Design-around innovation: Competitors might develop structurally distinct compounds outside the claim scope.

  • Patent expiration: Considering the typical 20-year term, when the patent is granted or filed impacts the horizon for market exclusivity.


Implications for Stakeholders

  • Pharmaceutical Innovators: DK2968992 may serve as a primary patent barrier, allowing exclusive development of specific drugs or formulations, provided claims are robust.

  • Legal and IP Firms: The patent landscape may contain potential challenges or licensing opportunities, requiring ongoing monitoring for patent oppositions or litigation risks.

  • Competitors: Must carefully analyze the claims to design around or challenge its validity via prior art submissions.


Conclusion

Denmark Patent DK2968992 offers a strategic patent right, likely centered on novel chemical entities with specific therapeutic applications. Its claims encompass structural, compositional, and method-based protections vital for maintaining market exclusivity. The patent landscape surrounding it appears actively managed, with potential overlaps and challenges that require continual review.


Key Takeaways

  • Scope of protection hinges on detailed chemical and method claims, designed to cover a broad spectrum of derivatives and uses.

  • Claims specificity and claim breadth influence enforceability; overly broad claims face invalidity risks, while narrow claims may be easier to work around.

  • Patent landscape considerations reveal the importance of international filings and awareness of prior art to sustain robust exclusivity.

  • Active monitoring of legal challenges, overlaps, and potential for patent expiration is crucial for strategic planning.

  • Innovators and competitors must understand the patent claims intricately to defend or challenge their rights effectively.


FAQs

1. What is the primary innovative aspect of Denmark patent DK2968992?
The patent claims revolve around a novel chemical compound or formulation with an asserted therapeutic application, distinguished by unique structural features and methods of use that differentiate it from prior art.

2. How broad are the claims in DK2968992, and what does this mean for competitors?
The claims likely cover specific chemical derivatives, formulations, and treatment methods. Broad claims can impede similar compounds' development, but overly broad claims risk invalidation if prior art discloses similar structures.

3. Can DK2968992 be challenged for validity?
Yes, through legal processes such as opposition or invalidity proceedings, based on prior art disclosures, obviousness, or lack of novelty. A thorough prior art search is essential.

4. What is the significance of patent family and international filings related to DK2968992?
Filing in multiple jurisdictions ensures global protection, preventing competitors from exploiting gaps in coverage. The patent family indicates strategic geographical coverage.

5. How does DK2968992 fit within the overall patent landscape for similar therapeutic compounds?
It likely complements existing patents, extending protection or innovating beyond them. Competitors should analyze overlapping claims to identify potential infringement or areas for innovation.


Sources

[1] Danish Patent and Trademark Office, DK2968992, granted publication details.
[2] Prior art references, including related patents and patent applications in international patent databases.

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