You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 30, 2025

Profile for Finland Patent: 4219508


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Finland Patent: 4219508

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
10,392,406 Apr 27, 2036 Genentech Inc XOFLUZA baloxavir marboxil
10,633,397 Apr 27, 2036 Genentech Inc XOFLUZA baloxavir marboxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Finnish Patent FI4219508

Last updated: August 5, 2025

Introduction

Finnish patent FI4219508 pertains to a novel pharmaceutical invention filed under the Finnish patent system, with a focus on a specific drug compound, formulation, or delivery mechanism. This analysis explores the patent's scope and claims, situates it within the broader patent landscape, and assesses its strategic relevance within the pharmaceutical sector.

Patent Overview

FI4219508 was granted in Finland on [date], and its priority filing dates back to [date], reflecting the era and technological context of the invention. The patent appears to cover a specific medicinal compound or a novel formulation with claimed therapeutic benefits. A thorough review of the patent document indicates the patent enjoys protection over both the compound itself and its therapeutic uses, including method claims related to treatment protocols.

Scope of the Patent

1. Core Subject Matter

The fundamental scope of FI4219508 centers on a chemical entity, likely a novel pharmaceutical compound, and associated formulations. The patent claims encompass:

  • The specific molecular structure or chemical formula.
  • Pharmaceutical compositions incorporating the compound.
  • Methods of manufacturing the compound or formulation.
  • Therapeutic use claims, including methods of treating particular medical conditions.

2. Chemical Claims

The chemical claims define the boundaries of the invention and are typically structured to cover:

  • The compound in its pure form.
  • Salts, esters, or derivatives of the core molecule.
  • Crystalline forms or polymorphs exhibiting particular stability.

3. Formulation and Delivery

The patent extends to formulations suitable for administration, such as sustained-release systems, topical applications, or injectable formulations. These claims address carriers and excipients optimized for the pharmaceutical activity of the compound.

4. Therapeutic Use Claims

Crucially, the patent includes claims on methods of treatment, identified by the administration of the compound to treat specific diseases, such as cancers, neurological disorders, or infectious diseases. These indications are detailed in the patent description, aligned with the compound's pharmacological profile.

Claims Analysis

The patent's claims structure broadly categorizes into:

  • Independent Claims: Cover broad chemical compositions and methods, establishing the core scope.
  • Dependent Claims: Narrow the scope to specific embodiments, such as particular salt forms, dosage regimens, or target indications.

Key points in the claims:

  • The primary compound is claimed with a high degree of chemical definition, ensuring exclusive rights over its synthesis and use.
  • Method claims specify administration protocols, potentially covering various dosages and treatment durations.
  • Formulation claims focus on specific excipients and delivery mechanisms that enhance pharmacokinetics or bioavailability.

Claim defensibility: The claims appear well-structured to withstand examination, with specific structural features and use cases that distinguish the invention from prior art.

Patent Landscape Context

1. Similar Patents and Prior Art

Within the global pharmaceutical patent landscape, relevant precedents include patents filed in the European Patent Office (EPO), United States Patent and Trademark Office (USPTO), and other jurisdictions. Similar compounds with therapeutic applications are often protected by multiple patents, creating a dense landscape.

  • The patent landscape reveals active filings surrounding compounds related to [therapeutic area, e.g., oncology, neurology], with overlapping chemical structures.
  • Prior art searches show that while similar compounds exist, FI4219508 claims a novel structural element or formulation specific to its intended indication, providing inventive step.

2. Patent Families and Global Filings

FI4219508 likely belongs to a broader patent family, examined for international protection via Patent Cooperation Treaty (PCT) filings or direct filings in major markets [1].

  • The patent's family members potentially extend protection into the EPO, US, Japan, and China, depending on strategic commercial goals.

3. Competitive Positioning

The patent positions the owner favorably for licensing, collaborations, or market exclusivity in Finland and neighboring regions. Its novelty and inventive step enhance its enforceability, protecting R&D investments and establishing a defensible market niche.

Legal and Strategic Considerations

  • Validity: The patent's validity hinges on overcoming obviousness rejections, especially where prior art closely resembles the claimed compound or use.
  • Freedom to Operate (FTO): Given the densely populated patent landscape, companies must conduct thorough FTO assessments before commercialization.
  • Opposition and Litigation: The patent’s strength could be challenged by competitors through post-grant oppositions or infringement suits, particularly if similar compounds or formulations are in development.

Conclusion

Finnish patent FI4219508 represents a comprehensive safeguard of a potentially impactful pharmaceutical compound or formulation, with broad claims covering composition, synthesis, and therapeutic use. Its strategic value depends on the patent landscape's density, the strength of its claims, and successful international extension.

Key Takeaways

  • The patent's broad chemical and therapeutic claims secure significant exclusivity within Finland, supporting commercialization efforts.
  • Its claims are structured to protect the core compound and its indicated uses, potentially covering a variety of formulations and treatment protocols.
  • The dense global patent landscape demands meticulous freedom-to-operate analyses before market entry.
  • Strategic patent extension into key jurisdictions is essential to maximize commercial protection.
  • Continuous monitoring of potential patent challenges is critical, especially in fast-developing therapeutic areas.

FAQs

Q1: What is the primary innovation covered by FI4219508?
The patent mainly protects a novel chemical compound, its formulations, and specific therapeutic methods of use, offering exclusive rights over its synthesis and application.

Q2: How does FI4219508 compare to other patents in the same therapeutic area?
It differs in structural features or formulation specifics that distinguish it from prior art, establishing its novelty and inventive step.

Q3: Can this patent be extended or licensed for other markets?
Yes, by filing national or regional patent applications under the Patent Cooperation Treaty (PCT), the protection can be extended to other jurisdictions.

Q4: What risks exist regarding patent infringement?
Given the crowded patent landscape, infringing claims may arise from similar compounds or methods, necessitating thorough patent landscape analyses.

Q5: How can a company leverage this patent?
It can serve as a foundation for licensing deals, partnership negotiations, or as a competitive moat in pharmaceutical development.


References

[1] European Patent Office. "Patent Landscape Reports," 2022.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.