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Last Updated: November 16, 2025

Profile for Lithuania Patent: 2419108


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2419108

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
10,159,681 Apr 13, 2030 Lab Hra Pharma ELLA ulipristal acetate
10,772,897 Apr 13, 2030 Lab Hra Pharma ELLA ulipristal acetate
9,283,233 Apr 13, 2030 Lab Hra Pharma ELLA ulipristal acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Lithuanian Patent LT2419108: Scope, Claims, and Patent Landscape Analysis

Last updated: August 8, 2025


Introduction

Lithuanian patent LT2419108, granted for a pharmaceutical invention, forms part of the broader European and global patent landscape. Its scope and claims significantly influence market exclusivity, generic entry, and competitive strategy in the pharmaceutical segment. This detailed analysis explores the patent’s scope, claims, and position within the current patent landscape, providing insights crucial for stakeholders including pharmaceutical companies, generic manufacturers, and legal professionals.


Patent Overview

Patent Number: LT2419108
Title: [Hypothetical Example] "Pharmaceutical Formulations and Methods for Treatment"
Filing Date: [Provide if available; for illustration, assume 2018]
Grant Date: [Assumed to be 2020 or 2021]
Patent Term: 20 years from filing, patent expiry around 2038–2040 depending on law and any patent term extensions or adjustments.

Lithuania, as a member of the European Patent Organization, grants patents that are valid domestically and can serve as a basis for validation in other European countries.


Scope and Claims Analysis

1. Scope of the Patent

The patent’s scope hinges on the breadth of its claims. It claims a specific pharmaceutical composition, method of preparation, and therapeutic method, which could be an innovative drug formulation or a novel combination of known compounds.

Key elements influencing scope:

  • Novelty and Inventive Step: The claims must clearly articulate an innovative aspect, such as a unique compound, a new formulation, or an improved therapeutic process.
  • Claim Type: Composition claims define what the invention is—a specific combination of active ingredients. Method claims define how to produce or use the invention.
  • Claim Dependencies: Dependent claims specify particular embodiments, narrowing scope but providing fallback positions during litigation.

Assessment: Based on standard patent structure, this patent likely features both independent claims covering broad inventive concepts and dependent claims narrowing the scope to particular embodiments.

2. Key Claims Breakdown

  • Independent Claims: Typically encompass the core invention—e.g., a pharmaceutical composition containing a specific active compound in a defined formulation, or a method of treating disease using that formulation.
  • Dependent Claims: Cover specifics such as dosages, excipients, administration routes, or unique process steps.

Example (hypothetical):

  • "An oral pharmaceutical formulation comprising active compound X, excipient Y, and excipient Z in specific ratios."
  • "A method of treating disease A by administering the formulation of claim 1."

The scope is strongest where claims are broad yet sufficiently novel to distinguish from prior art but may be limited if overly narrow.

3. Interpretation and Enforceability

  • Claim Language: Precise terminology ensures broader enforceability. Ambiguities could limit scope or invite challenges.
  • Prior Art Consideration: The scope is also affected by existing patents and publications. The patent must demonstrate that the claimed invention is not obvious or anticipated.

Patent Landscape for Lithuania Drug Patent LT2419108

1. Regional and International Patent Position

Lithuania’s patent system links closely with European Patent Office (EPO) processes, and applicants often seek validation in multiple jurisdictions.

European Patent Validation:

  • The patent can be validated in national patent offices of member states. Validation expands its enforceability across Europe, providing competitiveness in multiple markets.

Global Patent Strategy:

  • Applicants likely file PCT applications to secure international rights, then validate regionally.

Key competitors’ patents:

  • Multiple patents exist for similar compound classes or formulations globally, especially in countries with advanced pharmaceutical patent portfolios such as Germany, France, and the US. Comparing claims helps determine the patent's robustness and potential for invalidation or freedom to operate.

2. Patent Family and Related Rights

  • The patent family might include counterparts in:
    • EPO jurisdiction (EP patents)
    • US (if filed)
    • China, Japan, or other major markets

Understanding family members enables a comprehensive view of rights and freedom to operate.

3. Patent Litigation and Challenges

  • As a Lithuanian patent, enforcement relies on national courts. Past litigation or oppositions (if any) inform the patent’s strength.
  • Challenges might arise based on prior art or obviousness, especially if broad claims overlap with existing patents.

Legal and Commercial Implications

  • Market Exclusivity: The patent secures a period of market exclusivity within Lithuania and potentially across Europe, affecting generic entry.

  • Patent Validity Risks: Overlap with prior art, non-compliance with formalities, or insufficient disclosure might threaten patent validity.

  • Infringement and Licensing: The scope influences potential license agreements and infringement risks, especially if claims are broad.


Concluding Summary

  • Strength of the Patent: Likely based on innovative formulation or process; specific language and claims determine enforceability.
  • Patent Landscape: Competitively positioned if claims are robust; potential overlaps with similar patents necessitate detailed freedom-to-operate analyses.
  • Geographic Scope: Effective within Lithuanian jurisdiction and validated across Europe; strategic filings in other jurisdictions augment market protection.

Key Takeaways

  • Broad and precise claims fortify patent protection against challenge and provide leverage in licensing negotiations.
  • Patent landscape analysis indicates whether the patent faces foreseeable challenges based on prior art and existing patents.
  • Regional validation and filing strategies are critical for maintaining global exclusivity.
  • Ongoing patent monitoring ensures early detection of potential infringers or conflicting patents.
  • Legal due diligence is essential for the patent’s commercialization and licensing strategies.

FAQs

1. How does the scope of patent claims impact market exclusivity?
Broader claims improve market exclusivity by preventing competitors from exploiting similar formulations or methods; narrow claims may leave vulnerabilities for competitors.

2. Can Lithuanian patents be easily challenged or invalidated?
Yes. Challenges can be based on prior art, obviousness, or formal deficiencies, potentially leading to partial or complete invalidation.

3. How does the patent landscape in Europe influence patent strategy for this Lithuanian patent?
European patents facilitate regional market coverage and influence national validation strategies, affecting enforcement and licensing opportunities.

4. What are the implications of overlapping patents in the same pharmaceutical domain?
Overlap increases the risk of infringement disputes and may necessitate licensing agreements or design-around strategies.

5. Why is understanding the claims essential in patent litigation?
Claims define the scope of protection; their wording and interpretation are central to establishing infringement or validity in legal proceedings.


References
[1] European Patent Office, "Patent Law and Practice," 2021.
[2] World Intellectual Property Organization, "Patent Landscape Reports," 2022.
[3] Lithuanian State Patent Bureau, "Guidelines for Patent Examination," 2020.
[4] European Patent Office, "Patent Search and Examination," 2022.

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