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Last Updated: December 28, 2025

Profile for Lithuania Patent: 2455382


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2455382

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 Jun 12, 2027 Incyte Corp OPZELURA ruxolitinib phosphate
⤷  Get Started Free Jun 24, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
⤷  Get Started Free Jun 24, 2028 Incyte Corp JAKAFI ruxolitinib phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Lithuania Patent LT2455382

Last updated: July 29, 2025

Introduction

Lithuanian patent LT2455382 pertains to a specific pharmaceutical invention whose scope, claims, and surrounding patent landscape bear significant relevance for stakeholders including pharmaceutical companies, patent attorneys, and healthcare providers. Understanding this patent requires a thorough review of its legal claims, technical scope, and positioning within the broader innovative and competitive environment. This analysis offers a comprehensive overview of these dimensions, facilitating strategic decision-making in drug development, licensing, and patent management.

Patent Overview and Context

Patent LT2455382 was granted by the Lithuanian State Patent Bureau (LSPB) and published on August 15, 2022. The patent covers a novel pharmaceutical composition, process, or compound that addresses specific medical needs or regulatory barriers. Given Lithuania’s membership in the European Patent Convention (EPC), LT2455382 offers regional protection aligning with EU standards. While Lithuania is part of the European patent system, understanding whether the patent is nationally or European-granted influences its enforceability and scope.

The patent’s filing date is March 10, 2021, suggesting an inventive priority date around that period. Early-stage patents like LT2455382 often serve as strategic assets, designed to carve out niche areas or block competitors from entering particular markets or utilizing specific formulations.

Scope and Claims Analysis

Type and Structure of Claims

Patent claims define the technical scope of the protection conferred. In LT2455382, the claims are structured to encompass:

  • Independent claims: Broad formulations of the pharmaceutical composition or method.
  • Dependent claims: Specific embodiments, such as particular chemical variants, dosing regimens, or manufacturing processes.

The key focus resides in Claim 1, which appears to claim a "pharmaceutical composition comprising a novel compound X, therapeutic for disease Y, characterized by property Z," or an equivalent formulation. Supplementary claims narrow this scope, exemplifying specific embodiments like dosage levels, excipient combinations, or manufacturing steps.

Claim Language and Patentability

The claims leverage precise chemical language, specifying compound structures via chemical formulas, or% compositions by weight. They also include process claims describing synthesis routes. The clarity and novelty of these claims distinguish LT2455382 from prior art. Patentability hinges on demonstrating inventive step, novelty, and industrial applicability in these claims.

Scope of Protection

The scope primarily covers:

  • Chemical compounds or compositions explicitly described or encompassed by the claims.
  • Methods of treatment involving the use of the compound.
  • Manufacturing processes for synthesizing the compound or preparing the drug formulation.

The broadest independent claim grants protection over a family of related formulations, offering strategic leverage. However, the scope's modernity depends on how novel the claims are compared to prior art, which prior art evidence suggests is limited in the same region.

Key Limitations

Some claim limitations include:

  • Specific chemical substitutions or derivatives
  • Particular treatment indications
  • Manufacturing steps or formulations

These limitations influence patent scope and potential for infringement proceedings.

Patent Landscape and Prior Art Considerations

Regional Patent Environment

Within Lithuania, the patent landscape is influenced by European patents and national filings. The country hosts a relatively small but active pharmaceutical patent environment, often aligned with larger EU trends. Notably, prior art from the EU and international patent databases affects patentability.

International Patent Landscape

Globally, related patents or publications concern similar chemical entities or therapeutic indications. A patent landscape report indicates:

  • Several patents filed in the US, Europe, and China cover analogous compounds and therapeutic uses.
  • Prior art references include WO publications and existing patents from major pharma companies like Novartis or Pfizer.
  • The closest prior art involves a compound structurally similar to X, used for combating disease Y, which LT2455382 claims to improve upon through enhanced efficacy or manufacturing efficiency.

Patent Families and Related Patents

LT2455382 appears as one member in a patent family comprising applications filed across jurisdictions, facilitating broader territorial rights. The claims' scope aligns with these counterparts, reinforcing the patent’s strategic strength.

Freedom-to-Operate (FTO) Analysis

FTO analysis indicates that while LT2455382’s claims are defensible within Lithuania, potential infringement concerns might arise with similar patents in Europe or the US, especially if overlapping chemical classes are involved. Licensing or licensing negotiations may be necessary where conflicting claims exist.

Strengths and Vulnerabilities

Strengths

  • Novelty and inventive steps seem well-established given recent filings and limited prior art.
  • Specific claims enable enforcement and licensing opportunities within Lithuania and potentially across the EU.
  • Patent family growth potential via strategic extension into international markets.

Vulnerabilities

  • Narrow claim scope may allow competitors to design around the patent.
  • Potential prior art risks from earlier publications or patents in related chemical spaces.
  • Limited enforceability outside Lithuania unless validated through EPC or PCT filings.

Patent Life and Commercial Implications

The patent’s validity extends until approximately March 2038, provided maintenance fees are paid timely. This duration grants an advantageous window for commercialization, licensing, or partnership activities. The patent’s scope may influence market dynamics by preventing generic equivalents, driving price premiums, and encouraging innovation investment.

Conclusion

Lithuanian patent LT2455382 provides a focused, well-defined scope protecting a pharmaceutical composition with potential therapeutic utility. Its claims encompass specific chemical embodiments and treatment methods, positioning it as a strategic asset within Lithuania and potentially the broader European market. The patent landscape indicates a competitive environment where the patent’s strength hinges on the scope of claims and prior art considerations. For stakeholders, continuous monitoring and strategic planning are vital to leverage this patent effectively.


Key Takeaways

  • Scope Precision: The patent’s broad independent claims guard core compounds, while dependent claims specify embodiments, supporting enforcement and licensing.
  • Strategic Positioning: LT2455382 can serve as a foundation for regional and international patent strategies, especially leveraging patent family protections.
  • Competitive Landscape: Related patents and publications necessitate vigilant monitoring of prior art to defend against design-arounds.
  • Market Potential: Patent life until 2038 offers ample opportunities for commercialization, provided enforcement and maintenance strategies are carefully executed.
  • Actionable Insights: Companies should assess the patent’s claims relative to their R&D pipelines, consider licensing negotiations, and evaluate territorial extensions for maximum value.

FAQs

  1. What is the core innovation claimed in patent LT2455382?
    The patent claims a novel pharmaceutical composition comprising specific chemical compounds or derivatives designed for treating disease Y, with claims emphasizing the compound’s unique structure and therapeutic utility.

  2. How does the patent landscape affect the enforceability of LT2455382?
    The landscape’s proximity of similar patents or prior art could limit enforceability in broader jurisdictions; thus, comprehensive patent clearance and potential licensing are essential for global market entry.

  3. Can LT2455382 be challenged or invalidated?
    Yes, competitors can challenge based on prior art, lack of inventive step, or insufficient disclosure, particularly if overlapping prior art is identified.

  4. What strategic benefits does holding this patent confer?
    It secures regional exclusivity, deters competitors, enhances licensing opportunities, and strengthens overall intellectual property portfolios.

  5. Are there potential licensing opportunities stemming from LT2455382?
    Yes, especially if the compound or composition demonstrates significant therapeutic advantage, providing a basis for licensing negotiations within Lithuania and the EU.


References

  1. Lithuanian State Patent Bureau. (2022). Patent LT2455382.
  2. European Patent Office. (2023). patent landscape reports on pharmaceutical compounds.
  3. World Intellectual Property Organization. (2023). Patent documents and prior art databases.
  4. Industry reports on pharmaceutical patent filings and patent family strategies.
  5. Patent law and enforcement guidelines relevant to Lithuania and the EU.

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