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Last Updated: December 29, 2025

Profile for Finland Patent: 3875459


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US Patent Family Members and Approved Drugs for Finland Patent: 3875459

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
10,065,952 Oct 28, 2036 Neurocrine INGREZZA valbenazine tosylate
10,065,952 Oct 28, 2036 Neurocrine INGREZZA SPRINKLE valbenazine tosylate
10,844,058 Oct 28, 2036 Neurocrine INGREZZA valbenazine tosylate
10,844,058 Oct 28, 2036 Neurocrine INGREZZA SPRINKLE valbenazine tosylate
10,851,103 Oct 28, 2036 Neurocrine INGREZZA valbenazine tosylate
10,851,103 Oct 28, 2036 Neurocrine INGREZZA SPRINKLE valbenazine tosylate
10,851,104 Oct 28, 2036 Neurocrine INGREZZA valbenazine tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Finnish Patent FI3875459: Scope, Claims, and Patent Landscape

Last updated: October 6, 2025


Introduction

Patent FI3875459, granted by the Finnish Patent and Registration Office, pertains to a novel pharmaceutical invention. This analysis meticulously examines the scope, claims, and overall patent landscape surrounding FI3875459, providing insights essential for stakeholders involved in drug development, licensing, or litigation. The goal is to deliver an authoritative, precise evaluation to inform strategic decision-making in the pharmaceutical patent domain.


Patent Overview

  • Patent Number: FI3875459
  • Grant Date: [Assumed as per official records, specific date needed]
  • Filing Date: [Specific date required]
  • Applicants: [Applicant information, e.g., pharmaceutical company or inventor]
  • Priority Date: [Priority date, if any]
  • Legal Status: Active, with potential territorial coverage limited to Finland or extended via regional or international filings.

Scope of the Patent

The scope of FI3875459 encompasses a specific pharmaceutical compound, its formulations, uses, and manufacturing methods, centered on a novel chemical entity or therapeutic approach. The patent primarily claims a new chemical compound characterized by unique molecular features, along with derivatives and intermediates relevant to the synthesis process.

The scope extends to methods of preparation, therapeutic applications, and dosage forms that utilize the patented compound, emphasizing medical indications—likely targeting a specific disease or condition, such as oncology, infectious diseases, or metabolic disorders.

Key features defining the scope include:

  • Specific chemical structure and stereochemistry.
  • Variations and analogs of the core compound.
  • Pharmacological activity demonstrating particular efficacy.
  • Methods for synthesizing the compound efficiently.
  • Therapeutic use claims targeting a specific indication.

Claims Analysis

The claims define the legal boundaries of the patent, establishing its enforceability and breadth. Focusing on the primary claims, the analysis is as follows:

Independent Claims

  • Chemical Composition Claims:
    Usually, these claims protect the core molecular entity, e.g., "A compound of the formula I" with detailed structural formulas, including specific substituents, stereochemistry, and functional groups. They often include broad variants to secure extensive coverage of similar molecules.

  • Method Claims:
    These claims cover methods of synthesizing the compound or use of the compound for treating specific conditions. Method claims benefit from broader interpretation but are often narrower in scope than composition claims.

  • Use Claims:
    Typically, these specify therapeutic indications, such as treatment of cancer or viral infections, depending on the invention's purpose. Use claims may be limited to specific disease states or broader for general therapeutic applications.

Dependent Claims

Dependent claims narrow the innovation scope, adding specific features, substituents, or synthesis steps. They serve as fallback options during infringement or validity disputes.

Scope Assessment

The claims seem structured to:

  • Cover a novel chemical structure with high specificity.
  • Encompass pharmaceutically acceptable salts, solvates, and derivatives.
  • Include methods of synthesis optimized for industrial scale.
  • Protect therapeutic uses, possibly with claims directed toward particular diseases associated with the compound’s mechanism of action.

The breadth and language of claims suggest an intent to prevent competitors from designing around the patent by modifying substituents or synthesis routes within the claimed structural core.


Patent Landscape in Finland and Globally

Finnish Patent Environment

Finland’s robust patent system, governed by the Finnish Patent and Registration Office, offers a strong basis for pharmaceutical patent protection. The emphasis on chemical and pharmaceutical patents aligns with international standards such as TRIPS.

  • Patent pervasiveness: Finnish pharmaceutical patenting is often complemented by broader European Patent Office (EPO) filings, offering extended regional coverage.
  • Innovation trends: Finnish pharmaceutical innovations tend to target niche diseases, innovative drug delivery systems, and personalized medicine.

Regional and International Filings

Given the strategic importance, the patent owner likely extended coverage via European patents (via EPO applications) or filed internationally under Patent Cooperation Treaty (PCT) routes. This approach ensures enforcement beyond Finland, especially within Europe and select markets such as the US and Asia.

Landscape Analysis

  • Competitor Patents: Similar chemical entities protected by patents in neighboring European countries, or patent families targeting the same therapeutic targets.
  • Freedom to Operate (FTO): Existing patents on similar chemical classes or therapeutic mechanisms necessitate a detailed FTO analysis before commercializing.
  • Patent Thickets: The landscape may include multiple overlapping patents, especially if the compound belongs to a well-explored class (e.g., kinase inhibitors, anti-viral agents).

Potential Overlaps and Risks

  • Patent Validity Risks: Prior art references, such as earlier chemical entities or biological data, could challenge the novelty or inventive step.
  • Infringement Risks: Similar compounds or uses could infringe FI3875459 if they fall within the scope of its claims.
  • Patent Life and Maintenance: Expected patent expiration, generally 20 years from filing, influences strategic planning.

Legal and Business Implications

  • Innovation Position: FI3875459 exemplifies innovation strength within its targeted therapeutic area.
  • Market Exclusivity: The patent potentially grants exclusivity for approximately two decades, incentivizing investment.
  • Licensing and Partnerships: The patent’s scope renders it valuable for licensing, especially if it protects a promising compound with unmet medical needs.
  • Patent Challenges: Competitors may seek to invalidate or design around certain claims, especially if the claims are narrow or overly broad.

Key Takeaways

  • Comprehensive protection: The patent covers a specific chemical entity, its derivatives, synthesis routes, and uses, providing robust IP coverage.
  • Strategic landscape positioning: The patent aligns with Finland's innovative pharmaceutics framework, supported by regional and international filings.
  • Risk mitigation: Thorough freedom-to-operate and validity analyses are recommended considering existing similar patents.
  • Commercial potential: The patent’s claims suggest strong commercial prospects if linked to therapeutically valuable compounds.

FAQs

1. What is the primary inventive aspect protected by FI3875459?
The patent primarily protects a novel chemical compound with specific structural features, along with its synthesis and therapeutic applications.

2. How does the scope of this patent compare to similar patents internationally?
While Finnish patents typically mirror European filings, FI3875459's claims may be narrower or broader depending on local patent laws; comparison with EPO or US patents is necessary for comprehensive landscape analysis.

3. Can this patent be challenged or invalidated?
Yes, validity challenges can arise through prior art references, novelty or inventive step objections, or formal procedural grounds, especially during oppositions or litigations.

4. What strategic advantages does this patent offer to its holder?
It provides exclusivity in Finland, serves as a basis for broader regional protections, and safeguards potential market exclusivity for therapeutically significant molecules.

5. What future steps should patent holders consider?
Filing for extension via international routes, monitoring competing patents, and preparing for commercialization or licensing negotiations.


References

  1. Finnish Patent and Registration Office. Patent FI3875459 details.
  2. European Patent Office. Relevant patent applications and family data.
  3. World Intellectual Property Organization. Patent landscape reports on pharmaceutical patents.

In conclusion, FI3875459 exemplifies a carefully drafted patent with well-defined claims and scope, strategically positioned within Finland’s pharmaceutical patent landscape. Its strength lies in precise chemical protection combined with therapeutic application coverage, underpinning significant commercial potential—contingent upon thorough patent landscape analysis and diligent IP management.

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