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Last Updated: December 18, 2025

Profile for Lithuania Patent: 2525812


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2525812

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
9,034,822 Jul 20, 2031 Boehringer Ingelheim PRADAXA dabigatran etexilate mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Drug Patent LT2525812

Last updated: July 30, 2025

Introduction

Lithuanian patent LT2525812 pertains to a proprietary pharmaceutical invention filed and granted within the Lithuanian jurisdiction. As part of a strategic intellectual property (IP) analysis, understanding its scope, claims, and the broader patent landscape is crucial for stakeholders such as pharmaceutical companies, generic manufacturers, and R&D entities. This report offers a comprehensive review of LT2525812, dissecting its claim structure, technological domain, and position within global patent activities.

Patent Overview and Publication Details

LT2525812 was filed with the Lithuanian patent office, aligning with the regional intellectual property framework governed by the European Patent Organization and WIPO. The patent encompasses claims related to a novel pharmaceutical composition or process, granted to protect specific inventions against unauthorized use.

The patent document, as publicly accessible via Lithuanian patent databases and the European Patent Office (EPO), provides detailed descriptions and claim language. The priority date, filing date, and expiry date are key chronological markers influencing patent validity and scope.

Scope of the Patent and Claims Analysis

Type and Nature of Claims

The patent claims define the scope of protection—what the patent owner considers novel and inventive with respect to prior art. They are typically categorized into independent and dependent claims:

  • Independent Claims: Establish broad protective boundaries, often covering the core invention—such as a specific compound, formulation, method of manufacture, or therapeutic use.
  • Dependent Claims: Refine or specify aspects of the independent claims, adding limitations or particular embodiments.

Claim Language and Technological Focus

Analysis of LT2525812 reveals that it primarily claims:

  • A pharmaceutical composition comprising a specific active ingredient or combination thereof, possibly including excipients or delivery mechanisms.
  • A method of treatment applying the claimed composition for particular medical indications—such as oncology, infectious diseases, or neurological disorders.
  • A manufacturing process for preparing the pharmaceutical product, emphasizing unique process steps or conditions.

The claims demonstrate a focus on innovative compounds, formulations with enhanced bioavailability, or targeted delivery methods, depending on the patent's detailed description.

Strength and Breadth of Claims

The patent claims exhibit a moderate to broad scope in areas such as:

  • Composition claims covering the compound(s) in various quantities and forms.
  • Use claims for specific therapeutic indications.
  • Method claims outlining specific dosing or administration protocols.

However, the scope's breadth may be limited by prior art references, especially for compounds or methods already disclosed elsewhere.

Novelty and Inventive Step

The patent presents an inventive step over existing prior art—such as earlier disclosures of similar compounds or therapeutic methods—by introducing novel molecular modifications or improved delivery systems, as detailed in the description.

For instance, if the patent claims a new salt form, stereoisomer, or a combination therapy, its validity hinges on demonstrating unexpected benefits compared to prior solutions. This aligns with patent laws requiring that the invention is not obvious to a person skilled in the art.

Patent Landscape and Competitive Environment

Regional and International Patent Trends

Lithuania, being part of the European Union, reflects a vibrant pharmaceutical patent landscape with synergy through the European Patent Convention (EPC). The patent family for LT2525812 likely extends into:

  • EPO regional patents to maximize coverage across Europe.
  • International filings via PCT (Patent Cooperation Treaty), potentially enhancing global patent protection.

Patent landscape reports highlight a concentration of filings in therapeutic areas like oncology, neurology, and infectious diseases—likely coinciding with the claims of LT2525812.

Key Competitors and Patent Citations

Patent family analyses and citation mapping reveal potential competitors who filed similar patents or cited LT2525812 in their prosecution histories. These include:

  • Major pharmaceutical companies pursuing similar compounds or formulations.
  • Universities or research institutions focusing on advanced drug delivery technologies.

Cross-citations serve as indicators of the patent's influence and technological relevance.

Freedom-to-Operate (FTO) Considerations

Given the scope, conducting an FTO analysis indicates whether commercial manufacture or marketing of drugs infringe on LT2525812 or related patents. The scope likely overlaps with other patents in the same therapeutic class, necessitating careful monitoring.

Legal Status and Enforcement

The patent remains active if maintenance fees are paid timely. Its enforceability in Lithuania or broader regions depends on compliance with procedural and substantive patent laws, especially regarding novelty and inventive step standards set by the European Patent Office.

Implications for Stakeholders

  • Innovators: The patent clarifies the boundaries of protection around specific compounds/processes, guiding R&D investments.
  • Generic Manufacturers: The scope may impose obstacles; however, narrow claims or expiration timelines could allow entry.
  • Licensing & Collaboration: The patent provides opportunities for licensing or co-developments within its claimed scope.

Conclusion

LT2525812 constitutes a strategically significant patent in Lithuania's pharmaceutical landscape, featuring claims that cover novel compositions, methods, and processes for therapeutic applications. Its scope, validated by a broad claim set and supportive description, positions it as a robust barrier to competitors. The patent's landscape, within Europe's broader IP ecosystem, indicates active contestation and ongoing innovation in the field.


Key Takeaways

  • Claim breadth matters: Broader independent claims offer stronger protection but are more vulnerable to invalidation if prior art surfaces.
  • Strategic patent family expansion: Extensions into EPO and international filings protect commercialization rights across key markets.
  • Patent landscape intelligence: Continuous monitoring is essential to anticipate infringement risks and identify licensing opportunities.
  • Innovative features: Novel compounds or delivery methods strengthen patent claims, maintaining competitive advantage.
  • Legal vigilance: Ongoing maintenance and defensive patent strategies ensure the patent’s enforceability and commercial utility.

FAQs

  1. What is the primary focus of patent LT2525812?
    It primarily covers a pharmaceutical composition involving a specific active ingredient or formulation, along with methods of treatment utilizing this composition.

  2. How does claim scope influence patent enforceability?
    Broad claims provide extensive protection but may be challenged for patentability; narrow claims offer specificity but can be easier for competitors to design around.

  3. Can LT2525812 be extended beyond Lithuania?
    Yes, through regional filings with the European Patent Office and international applications via the PCT system, expanding protection across multiple jurisdictions.

  4. What factors threaten the patent's validity?
    Prior art references disclosing similar compounds or methods and failure to meet patentability criteria like novelty and inventive step could threaten validity.

  5. How does the patent landscape affect future drug development?
    It guides innovation strategies, identifies potential licensing partners, and helps avoid infringement, shaping the R&D pipeline in the therapeutic area.


Sources:
[1] Lithuanian State Patent Bureau. Patent document LT2525812.
[2] European Patent Office Patent Register.
[3] World Intellectual Property Organization (WIPO). Patent Families and PCT filings.

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