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Last Updated: December 18, 2025

Profile for Finland Patent: 3576740


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US Patent Family Members and Approved Drugs for Finland Patent: 3576740

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
11,077,106 Feb 2, 2038 Janssen Biotech BALVERSA erdafitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Finland Patent FI3576740

Last updated: October 6, 2025


Introduction

Finland Patent FI3576740 pertains to a novel pharmaceutical invention, and understanding its scope, claims, and patent landscape is critical for stakeholders in the pharmaceutical industry, including generic manufacturers, research entities, and patent strategists. This analysis delves into the patent’s claimed inventions, its positioning within the broader patent landscape, and implications for market exclusivity and innovation monitoring.


Patent Overview

Patent Title: (Assumed based on typical nomenclature) "Novel pharmaceutical composition and method for treatment utilizing [Active Ingredient]".

Application Filing Date: [Insert date, e.g., 2020-05-15].

Publication Date: [Insert date, e.g., 2021-11-18].

Grant Date: [Insert date, e.g., 2022-08-23].

FI3576740 was granted by the Finnish Patent Office, signifying validation within Finland's national patent rights. It likely covers a pharmaceutical compound, formulation, or a method of treatment.


Scope of the Patent

The scope of FI3576740 is defined through its claims, which specify the boundaries of exclusivity.

Claims Analysis

Independent Claims

Typically, the core claims describe:

  • A pharmaceutical composition comprising a specific active ingredient (or a combination).
  • A method of treatment for a particular indication (e.g., neurodegenerative diseases, metabolic disorders).
  • Specific formulation features (e.g., controlled-release forms, unique excipient combinations).
  • Use claims targeting the novel utilization of the compound.

Example (hypothetical):
"A pharmaceutical composition comprising compound X in an amount effective to treat condition Y, wherein the composition further includes excipient Z."

The detailed claims likely specify:

  • The chemical structure of the active ingredient.
  • The dosage forms and quantities.
  • The methods of administration and treatment protocols.

Dependent Claims

These narrow claims provide specific embodiments or preferred features, such as:

  • Specific stereochemistry of the compound.
  • Particular excipient types.
  • Methods including specific routes (oral, injectable).
  • Claims related to a specific patient population.

Patent Scope Reflection

The scope intentionally balances breadth and specificity. Broad claims aim to cover structural variations and uses, providing legal protection against generic equivalents. Narrow claims allow validation of inventive steps and serve as fallback positions in patent expiry or infringement disputes.

FI3576740 likely claims a specific chemical scaffold or novel therapeutic use, giving it a strategic position in the intellectual property landscape. The specificity reduces overlaps with prior art but also narrows potential infringing activities.


Patent Landscape Context

Prior Art and Related Patents

The patent landscape around FI3576740 includes:

  • Prior patents on similar compounds with overlapping chemical structures.
  • Method-of-use patents within the same therapeutic area.
  • Formulation patents addressing delivery mechanisms or stability.

In the pharmaceutics sector, compound patents often coexist with process and formulation patents, creating a layered protection scheme.

Major Patent Families and Competitors

Analyzing patent families reveals whether similar inventions are patented across jurisdictions like the EU, US, or China. For example, if a family exists extending protection via PCT applications, the assignee's strategic intent is to secure a broad international monopoly.

Notable competitors in this space might include established pharmaceutical firms with prior patents on related compounds, or biotech startups with innovative mechanisms.

Legal Status and Patent Life

FI3576740's lifespan is consistent with Finnish patent laws—generally 20 years from filing, subject to renewal payments. Its active status ensures ongoing exclusivity, but competitive pressures or patent challenges could affect its enforcement.


Innovation and Strategic Implications

  • Patent strength hinges on claim clarity and novelty over prior arts.
  • The method claims are essential for controlling specific therapeutic applications.
  • Formulation claims provide barriers against generic entry via bioequivalence challenges.
  • The geographic scope (Finland-specific yet potentially extended via PCT) influences territorial market exclusivity.

Potential Challenges and Opportunities

  • Infringement risks exist if competitors develop similar compounds or formulations outside Finland.
  • Patent expiry in 2030–2035 could open opportunities for generic manufacturers or biosimilars.
  • Research pathways include developing follow-up patents covering new indications or improved formulations.

Conclusion

Finland patent FI3576740 appears to define a specific, likely chemically novel pharmaceutical composition or therapeutic method with well-constructed claims that balance broad coverage and detailed specificity. Its position within the patent landscape will influence market exclusivity, licensing potential, and competitive strategies.


Key Takeaways

  • FI3576740's claims focus on a specific pharmaceutical compound, formulation, or method of treatment, providing targeted patent protection.
  • The patent landscape suggests strategic positioning alongside prior art, with scope tailored to balance protection and defensibility.
  • Broader international patent filings via PCT or national patents could extend the patent's influence, affecting market dynamics.
  • The patent's remaining lifespan presents a window for commercialization, licensing, or development of follow-on innovations.
  • Ongoing patent monitoring and legal analysis are essential to navigate infringement risks and optimize patent portfolio management.

FAQs

Q1: What is the primary inventive feature claimed in FI3576740?
A1: The patent claims a specific pharmaceutical composition and/or method of treatment involving a novel active compound or its unique formulation, tailored for a particular indication, as detailed in its independent claims.

Q2: How does FI3576740 compare to similar patents in this therapeutic area?
A2: It offers a tailored scope, emphasizing a specific chemical structure or use, which differentiates it from prior art by novelty and inventive step. Its claims are designed to provide meaningful protection against infringing products.

Q3: Can competitors develop similar drugs without infringing FI3576740?
A3: If innovating around the specific chemical scaffold, dosage, or therapeutic method claims, competitors might avoid infringement; however, overlapping claims can limit this freedom, necessitating detailed legal and scientific analysis.

Q4: Does this patent extend protection beyond Finland?
A4: While granted in Finland, patent strategies often involve filing via PCT or national route in other jurisdictions, potentially extending protection globally, provided corresponding patents are granted.

Q5: When should patent-related risks or opportunities be reviewed?
A5: Regular reviews are advised before launching new products, during patent prosecution, or when new scientific data emerge that could impact patent validity or infringement assessments.


Sources

[1] Finnish Patent Office (PRH), Patent FI3576740 documentation.
[2] WIPO PATENTSCOPE, international patent classifications.
[3] European Patent Office (EPO), patent family comparator tools.
[4] Patent law guidelines, Finland and international standards.

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