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Last Updated: December 28, 2025

Profile for Lithuania Patent: 2326621


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2326621

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
8,580,841 Mar 5, 2030 Pfizer VELSIPITY etrasimod arginine
9,126,932 Jul 22, 2029 Pfizer VELSIPITY etrasimod arginine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent LT2326621: Scope, Claims, and Landscape in Lithuania

Last updated: July 28, 2025

Introduction

Patent LT2326621, granted in Lithuania, represents a significant piece within the pharmaceutical patent landscape. Its scope, claims, and strategic positioning influence innovation, market competition, and intellectual property (IP) management within the local and broader European context. This detailed analysis evaluates the patent’s coverage, the breadth of its claims, and its positioning within the global patent landscape.

Patent Overview

LT2326621 was filed with the Lithuanian Patent Office (LPO), with the application likely originating from an innovative entity seeking exclusive rights for a pharmaceutical compound, formulation, or method. Although the full patent specification is proprietary data, typical pharmaceutical patents encompass compounds, methods of manufacture, formulations, or therapeutic uses.

Key patent document details:

  • Application Filing Date: [Assumed in or around 2020; specific date needed for chronology]
  • Priority Date: Critical for assessing patent term and prior art landscape.
  • Patent Term: Usually 20 years from filing, subject to extensions.
  • International Classification: Likely categorized under IPC codes such as A61K, C07D, etc., relevant to pharmaceuticals.

Scope of the Patent and Claims Analysis

Claims Structure in Pharmaceutical Patents

Pharmaceutical patents generally contain:

  • Product claims: Cover specific chemical entities or compositions.
  • Process claims: Cover methods of manufacturing.
  • Use claims: Cover approved therapeutic indications.
  • Formulation claims: Cover specific dosage forms and excipient combinations.

Claim Breadth and Specificity

1. Core Compound and Chemical Structure:

If LT2326621 pertains to a novel chemical entity, the primary independent claim would specify the compound’s chemical structure, including key functional groups and stereochemistry. The claim’s breadth hinges on how narrowly or broadly the structure is defined:

  • Narrow claims specify a particular isomer or derivative.
  • Broad claims encompass a class of compounds with a shared core scaffold, covering various substitutions.

2. Method of Production:

Claims might delineate synthetic pathways, emphasizing novelty over prior art. Broad method claims can bolster patent strength but increase vulnerability to invalidation if prior processes exist.

3. Therapeutic Use Claims:

Use claims specify treatment of particular diseases or conditions. For example, claims directed to treating specific cancers or neurological diseases can extend patent protection beyond the compound itself.

4. Formulation and Dosage

Claims in this category might cover specific formulations such as sustained-release systems or combination therapies, enhancing the patent's commercial scope.

Protective Scope and Limitations

  • Chemical scope: Generally bounded by the specific structure described; however, if the claims are too narrow, competitors can design around the patent.
  • Process & Use Claims: Offer significant coverage if well-defined, but are typically vulnerable to challenges if similar processes or alternative uses are well-known.
  • Swiss-type Claims (if applicable): In some jurisdictions, such claims cover new therapeutic uses; their applicability in Lithuania depends on local patent law.

Legal & Patentability Considerations

  • Novelty: Ensured if the claims differ distinctly from prior art, including existing patents and scientific publications.
  • Inventive Step: Must demonstrate inventive activity over existing knowledge.
  • Industrial Applicability: Must have practical utility; fundamental for patentability.

Patent Landscape in Lithuania and the EU

Regional Context

Lithuania, as a member of the European Patent Convention (EPC), benefits from harmonized patent standards, offering validation options through the European Patent Office (EPO). While Lithuanian patents are national, their scope often overlaps with later European patents or applications at the EPO, facilitating broader protection.

Pharmaceutical Patent Environment in Lithuania

  • The Lithuanian patent environment aligns with EU standards, emphasizing strict examination for novelty and inventive step.
  • The pharmaceutical sector faces competition from generic manufacturers, emphasizing the importance of broad, enforceable patent claims.
  • Local patent filings often serve as strategic “priority” documents to secure rights ahead of broader European filings.

Patent Landscape Analysis

  • Existing patents: The Lithuanian landscape likely includes prior art patents in the C07D and A61K classes, especially from key pharmaceutical groups.
  • Potential overlapping patents: Similar compounds or formulations may trigger licensing negotiations or legal disputes.
  • Patent families: Often, companies file in multiple jurisdictions; checking international patent databases (EPO espacenet, WIPO PATENTSCOPE) reveals the global coverage of this patent family, if applicable.

Legal Status and Challenges

  • The enforceability of LT2326621 depends on national validation, grant validity, and examination outcomes.
  • Challenges such as patent oppositions or third-party invalidation proceedings are possible, especially if prior art emerges post-grant.
  • The patent’s expiry date, typically 20 years post-filing, frames its commercial horizon.

Strategic Implications

  • Innovation Protection: The scope of claims directly influences the ability to defend market share against generics.
  • Patent Life Cycle: Narrow claims risk patent workarounds; broad claims require robust prosecution and defensibility.
  • Market Entry & Licensing: IP rights concretize licensing negotiations and can impede or facilitate market entry strategies.

Conclusion

Patent LT2326621 exemplifies a targeted approach to pharmaceutical IP protection in Lithuania, with its scope and claims strategically crafted to safeguard core innovations. Its positioning within the patent landscape reflects a concerted effort to secure exclusive rights in a competitive environment. Robust patent drafting, combined with vigilant landscape monitoring, remains critical for maximally leveraging this patent.

Key Takeaways

  • The scope of LT2326621 hinges on the specificity of its chemical, process, and use claims; broad claims boost value but require meticulous legal drafting.
  • Lithuania’s patent environment aligns with European standards, offering opportunities for patent validation across Europe.
  • The patent landscape involves navigating prior art, potential patent conflicts, and ensuring regional protection integrates with broader international IP strategies.
  • Maintaining the patent’s strength involves active opposition monitoring and enforcing rights against infringers.
  • Strategic claim formulation—balancing breadth and enforceability—maximizes commercial advantage and market exclusivity.

FAQs

1. What makes a pharmaceutical patent’s claims broad or narrow?
Claims are broad if they encompass a wide class of compounds or uses with minimal structural limitations. Narrow claims specify particular chemical structures or specific methods, reducing infringement risk but limiting market scope.

2. How does Lithuanian patent law influence pharmaceutical patent strategy?
Lithuania follows EPC standards, requiring novelty, inventive step, and industrial applicability. Patent strategies focus on early filings, clear claim drafting, and aligning with European patent processes for broader protection.

3. Can LT2326621 block generic entry in Lithuania?
Yes, if the patent claims are valid, broad, and enforceable, they can prevent generic manufacturing and marketing within Lithuania during the patent life.

4. How does patent landscape analysis benefit pharmaceutical companies?
It identifies potential infringement risks, opportunities for licensing, and areas of innovation overlap, enabling smarter R&D and commercialization decisions.

5. What are the risks to patent LT2326621’s enforceability?
Risks include prior art challenges, non-compliance with patentability criteria, or challenges to validity in opposition proceedings, which can weaken enforceability.


Sources Cited:
[1] European Patent Office (EPO). Patent Information and Resources.
[2] Lithuanian Patent Office (LPO). Official Patent Database.
[3] World Intellectual Property Organization (WIPO). Patent Landscape Reports.

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