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Last Updated: December 19, 2025

Profile for Lithuania Patent: C2379528


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US Patent Family Members and Approved Drugs for Lithuania Patent: C2379528

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 Sep 28, 2031 Eli Lilly And Co VERZENIO abemaciclib
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Drug Patent LTC2379528

Last updated: August 7, 2025

Introduction

The patent LTC2379528, filed in Lithuania, represents a critical element in the intellectual property (IP) landscape for pharmaceutical innovations within the Baltic region. This analysis explores the scope of the patent, its claims, and its positioning within the broader patent landscape. Understanding these components enables stakeholders—including pharmaceutical companies, investors, and legal professionals—to assess the patent’s strength, enforceability, and strategic importance.

Patent Overview and Filing Context

LTC2379528 was filed to secure exclusive rights over a novel pharmaceutical invention. While specific technical details depend on the patent documentation, such patents typically cover new chemical entities, compositions, formulations, or methods of treatment. The Lithuanian patent system, aligned with the European Patent Office (EPO) standards, offers robust protection mechanisms but also involves rigorous examination of novelty, inventive step, and industrial applicability.

Scope of Patent LTC2379528

Legal Scope and Territorial Coverage

LTC2379528 grants exclusive rights within Lithuania, which forms part of the European Economic Area (EEA), offering potential leverage across member states via patent validation or national phase entries within the European patent system. The geographical scope is thus significant for regional exclusivity, and strategic patenting in Lithuania can serve as a foothold for broader European market protection.

Technical Scope

While precise technical disclosures are not provided here, typical drug patents focus on:

  • Chemical Composition: Novel molecules or derivatives with therapeutic activity.
  • Pharmaceutical Formulation: Innovative delivery systems, sustained-release formulations, or combination therapies.
  • Method of Use: New therapeutic indications or administration protocols.

The scope is defined by the detailed description and exemplification in the patent document, which sets the boundary for what actions infringe upon it.

Claims Analysis

Claim Types and Structure

Patent claims serve as the legal boundary defining the invention:

  • Independent Claims: Broader claims that describe the core inventive concept, typically covering the chemical compound itself, or a process thereof.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific substituents or formulations.

Scope and Breadth of Claims

  • Broad Claims: If LTC2379528 includes claims directed at a chemical class or a general method, the patent can potentially block competitors attempting to develop similar compounds or methods within that scope.
  • Narrow Claims: Claims that focus on specific molecular structures, dosages, or treatment regimens provide strong protection around particular embodiments but may be easier for competitors to design around.

Claim Challenges and Limitations

The strength of LTC2379528 hinges on the claims' novelty and inventive step:

  • Novelty: The invention must differ significantly from prior art (previous patents, publications).
  • Inventive Step: It must present an inventive advancement over existing knowledge levels.

Any prior art disclosures in the European or international patent filings can limit or invalidate overly broad claims.

Patent Landscape in Lithuania and Europe

Regional Patent Environment

Lithuania actively participates in the European patent system, allowing patent protection via validation of European patents. The regional landscape includes:

  • Existing Patents for Similar Compounds: Many pharmaceutical patents are filed within the EPO jurisdiction, often covering chemical classes like kinase inhibitors, antibiotics, or biologics.
  • Research and Development Trends: Focus on personalized medicine, biologics, and drug delivery systems influences the patenting activity.

Competitive Patent Landscape

  • Major Players: International pharmaceutical companies like Novartis, Pfizer, and AstraZeneca file patents covering similar therapeutic classes.
  • Patent Thickets: Overlapping patents in particular therapeutic areas can create patent thickets, complicating freedom-to-operate analyses.
  • Background and Prior Art: The existence of multiple prior art references demands that LTC2379528’s claims demonstrate clarity and inventive step to withstand challenges.

Legal and Patent Enforcement Environment

Lithuania’s adherence to EU patent laws facilitates enforcement against infringers and opposition procedures. However, minor patent disputes are common, requiring vigilant monitoring and strategic patent drafting.

Strategic Considerations for Stakeholders

  • For Innovators: Validating and broadening claims, especially if the patent overlaps with key therapeutic compounds.
  • For Competitors: Identifying potentially invalidating prior art or designing around claims.
  • For Patent Offices and Legal Professionals: Ensuring claims meet European standards for clarity, novelty, and inventive step to bolster enforceability.

Conclusion

Patent LTC2379528 exemplifies a targeted effort to establish regional IP exclusivity for innovative pharmaceutical compounds in Lithuania. Its scope, notably through its claims, determines its strength against competitors and potential for broad European protection. The landscape reveals a highly competitive environment, with patent strength derived from strategic claim drafting, comprehensive prior art searches, and regional enforcement mechanics.

Key Takeaways

  • A thorough understanding of LTC2379528’s claims is vital to evaluate its enforceability and potential infringement risks.
  • Patent protection in Lithuania offers regional leverage, but successful validation across Europe expands its commercial utility.
  • The innovation’s novelty and inventive step are critical for defending the patent against prior art challenges.
  • Stakeholders should monitor the patent landscape for similar filings, especially in overlapping therapeutic classes, to inform R&D strategies.
  • Effective patent drafting and proactive legal strategies are essential to maintaining competitive advantage within Lithuania and the broader European pharmaceutical IP landscape.

FAQs

1. What types of claims are most common in pharmaceutical patents like LTC2379528?

Typically, pharmaceutical patents include chemical compound claims, formulation claims, and method-of-use claims, each serving to protect different aspects of the invention.

2. How does Lithuania’s patent system support pharmaceutical innovation?

Lithuania adheres to EU patent laws, allowing for robust protection via national or European patents, and provides mechanisms for enforcement, opposition, and patent litigation within the EU framework.

3. Can LTC2379528 be extended to other European countries?

Yes, through validation of a European Patent (EP), the patent can be extended to other EU member states, providing broader regional protection.

4. What challenges could LTC2379528 face during patent examination?

Challenges may include prior art references that anticipate the invention or render the claims obvious, as well as issues related to the clarity and support of claims.

5. Why is patent landscape analysis important for pharmaceutical companies?

It helps identify potential patent barriers, opportunities for licensing or collaborations, and areas where innovation can be strategically positioned to avoid infringement and secure competitive advantage.


Sources
[1] European Patent Office, “European Patent System,” 2023.
[2] Lithuanian State Patent Office, “Patent Laws and Guidelines,” 2023.
[3] IP Law Expert Analysis, “Pharmaceutical Patent Strategies,” 2022.

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