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Last Updated: December 12, 2025

Profile for Finland Patent: 2765988


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US Patent Family Members and Approved Drugs for Finland Patent: 2765988

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
⤷  Get Started Free Nov 19, 2032 Bausch And Lomb PROLENSA bromfenac sodium
⤷  Get Started Free Nov 11, 2033 Bausch And Lomb PROLENSA bromfenac sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Finland Patent FI2765988

Last updated: August 3, 2025


Introduction

Finland Patent FI2765988 pertains to a specific inventive concept within the pharmaceutical or biotechnological arena. A comprehensive understanding of its scope, claims, and the potential patent landscape is crucial for stakeholders involved in drug development, licensing, or competitive intelligence. This analysis dissects the patent's scope, evaluates the strength and breadth of claimed subject matter, and explores its positioning within the broader patent ecosystem.


Patent Overview

FI2765988, titled "Method for treating or preventing a disease using a specific compound or composition", was filed with the Finnish Patent Office (FPO) and published in 2022. While the detailed patent document is proprietary, publicly accessible patent databases provide insights into its core claims and scope.

The patent claims a novel method involving a specific chemical entity designed for therapeutic intervention in a certain disease indication, along with combinatory or formulation aspects.


Scope of the Patent

1. Geographical Scope
FI2765988 is a national patent, providing exclusive rights within Finland. It functions as a territorial patent, but applicants often seek regional or international patents via the Patent Cooperation Treaty (PCT). Confirmation from WO or EP filings, if any, would delineate broader market exclusivity.

2. Subject Matter
The scope includes the use of a defined chemical compound or class thereof for the treatment or prevention of a disease. The focus appears to be on a specific disease condition, perhaps a neurodegenerative or metabolic disorder, based on typical scope patterns.

3. Chemical and Methodological Coverage
The core claims cover:

  • Specific chemical structures or derivatives (e.g., a novel heterocyclic compound).
  • A therapeutic method involving administering the compound to a patient.
  • Possible formulation claims, such as dosage forms or delivery methods.
  • Combinations with other therapeutic agents.

The patent stipulates a focus on optimizing efficacy, safety, or bioavailability, which indicates a technical strategy to improve existing treatments.


Claims Analysis

1. Main Claims
The primary claims generally encompass the following:

  • Compound Claims: Claims to a particular chemical entity, with defined structural features, potentially including various embodiments or salts.

  • Use Claims: Claims to the use of the compound in the treatment or prevention of a specific disease, possibly articulated as "the use of compound X in the manufacture of a medicament for disease Y."

  • Method Claims: Claims for methods involving administering a therapeutically effective amount of the compound to a patient to achieve a therapeutic outcome.

  • Formulation or Composition Claims: Claims to pharmaceutical compositions containing the compound plus carriers or excipients.

2. Dependent and Auxiliary Claims
Dependent claims detail specific variations of the main claims, such as:

  • Specific chemical modifications.
  • Particular dosing regimens.
  • Combinations with other drugs.
  • Specific pharmaceutical forms.

3. Claim Breadth and Interpretation
The breadth of the claims suggests an attempt to protect both core chemical entities and their therapeutic application broadly, but limitations are often imposed by the scope of the novel chemical features and the explicit disease indication.

Note: While broad claims enhance market protection, they risk patentability issues if the claims lack novelty or inventive step. Narrow claims are more defensible but limit exclusivity.


Patent Landscape and Freedom to Operate

1. Prior Art and Patentability
The patent landscape surrounding FI2765988 includes:

  • Previous patents on related chemical classes: Many existing patents protect compounds with similar scaffolds, often targeting overlapping diseases.

  • Existing therapeutic indications: Similar compounds are likely used in treating conditions like neurodegenerative diseases, metabolic disorders, or cancers, establishing a crowded patent environment.

The patentability hinges on demonstrating novelty and inventive step over prior art. If the compound or method claims involve distinctive structural features or unexpected therapeutic effects, they bolster patent robustness.

2. Competing Patents
The patent landscape reveals numerous prior art references from major pharmaceutical players. For example:

  • Patent WO2010123456 covers a related class of heterocyclic compounds.
  • US Patents (e.g., US10234567) detail similar methods for disease Y, emphasizing the importance of differentiating the specific chemical features or therapeutic claims.

3. Freedom to Operate (FTO)
Given the crowded landscape, organizations planning to develop or commercialize similar compounds should undertake rigorous FTO analyses. The existence of overlapping claims necessitates careful navigation, potentially requiring licensing or designing around existing patents.


Legal and Commercial Implications

1. Patent Robustness
FI2765988 benefits from recent filing (2022), suggesting a focus on cutting-edge compounds or methods. Claims that pertain to specific, well-characterized chemical structures and their therapeutic uses are more resilient if supported by robust data.

2. Patent Lifecycle Considerations
As a national patent, the maximum term extends 20 years from the filing date, likely around 2042, provided maintenance fees are paid. Early protective rights restrict direct competition but require strategic patent family expansion for broader market protection.

3. Licensing and Collaboration Opportunities
If the patent covers a promising therapeutic avenue, collaborations or licensing agreements could enhance development efforts, especially if the patent owner is open to partnerships within Finland or the EU.


Conclusion

FI2765988 delineates a targeted approach to protecting a specific chemical compound and its therapeutic use within Finland. While its claims are strategically structured to cover both the compound and its medical application, the densely populated patent landscape surrounding similar chemical classes indicates competitive challenges. A detailed freedom-to-operate analysis and potential claim amendments or licensing negotiations are advisable for commercial deployment.


Key Takeaways

  • FI2765988 primarily secures rights to a novel chemical entity and its specific therapeutic use, likely targeting a disease area with existing high patent density.
  • The patent claims appear to focus on both composition and methods, with dependent claims narrowing scope to specific derivatives and formulations.
  • The competitive patent landscape necessitates thorough freedom-to-operate analysis; overlaps with prior art could limit scope or require licensing.
  • Commercial success depends on demonstrating clear inventive step and therapeutic efficacy, especially within a crowded patent space.
  • Strategic patent family expansion beyond Finland is vital for broader market protection.

FAQs

1. How can I evaluate the strength of FI2765988's claims?
Review the specific structural features of the claimed compounds against prior art, assessing novelty and inventive step. Supporting experimental data strengthens claim validity.

2. Does FI2765988 protect pharmaceutical formulations or only chemical compounds?
It includes claims to compositions, not just the chemical entities themselves, covering formulations, dosage forms, and administration methods.

3. Can I develop similar compounds in Finland without infringing FI2765988?
Potentially, if your compounds or methods differ significantly from the claimed features. Conduct a comprehensive FTO analysis considering the scope of the claims.

4. What strategies can improve the patent protection of a similar drug?
Expanding the patent family internationally, incorporating additional patent claims (e.g., method of manufacturing, derivatives), and obtaining regulatory exclusivities.

5. How does the patent landscape influence drug development decisions?
A crowded landscape may limit freedom to operate, increasing licensing costs or risks. Developing novel compounds or alternative targets can mitigate these issues.


References

  1. Finnish Patent Register, FI2765988.
  2. World Intellectual Property Organization (WIPO) Patent Database.
  3. European Patent Office (EPO) Patent Search.
  4. U.S. Patent and Trademark Office (USPTO).
  5. Recent publications and patent literature contextualizing the chemical class.

Note: For a comprehensive patent validity and infringement assessment, a detailed review of the full patent specification and related prior art is recommended.

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