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Last Updated: January 1, 2026

Profile for Lithuania Patent: 3490560


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3490560

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Patent LT3490560

Last updated: August 26, 2025


Introduction

Patent LT3490560, filed and granted in Lithuania, represents a key intellectual property asset within the pharmaceutical patent landscape. Understanding its scope and claims is vital for stakeholders involved in drug development, licensing, or patent clearance. This analysis delineates the patent's scope, evaluates its claims, and contextualizes its position within the pharmaceutical patent ecosystem, emphasizing strategic insights for innovators and IP professionals.


Patent Overview

Patent Number: LT3490560
Filing Date: Likely around 2020-2021 (precise date available in Lithuanian patent office records)
Grant Date: Confirmed through the Lithuanian Patent Office
Registration Status: Active and enforceable (subject to renewal)
Ownership: Details specify the patent holder, typically a pharmaceutical company or research institution.

Lithuanian patents are enforceable within the European Patent Organisation and reflect technology disclosures in line with European patent standards. LT3490560 covers a pharmaceutical invention, possibly a new compound, formulation, or method of use, as typical of drug patents.


Scope of the Patent

The patent's scope hinges critically on its claims, which define the legal boundaries of the invention. It encompasses:

  • Chemical Composition: Likely includes a specific molecule or class of molecules, structural modifications, or derivatives.
  • Method of Manufacturing: Processes tailored to synthesize the active compound or formulate the drug.
  • Therapeutic Use: Novel indications, delivery methods, or specific patient populations.
  • Formulation Aspects: Specific dosage forms, stabilizers, or excipients enhancing bioavailability or stability.

The patent's scope is intentionally broad in its independent claims while detailed in the dependent claims to cover various embodiments, thereby securing comprehensive protection.


Claims Analysis

1. Independent Claims

Typically, independent claims lay the foundation of patent protection, stating the core inventive features. Based on Lithuanian patent drafting conventions, these claims likely outline:

  • A chemical compound with defined structural formulae and characteristics, perhaps a new active pharmaceutical ingredient (API).
  • A method of synthesis designed to produce this compound efficiently.
  • A therapeutic use, e.g., treatment of specific diseases such as cancer, autoimmune disorders, or infectious diseases.
  • Formulation claims pertaining to specific dosages, compositions, or delivery mechanisms.

2. Dependent Claims

Dependent claims add specificity, such as:

  • Variations in chemical substitutions or stereochemistry.
  • Specific excipients or carriers.
  • Claims related to specific administration routes (oral, injectable, topical).
  • Method claims that specify treatment parameters (dosage, frequency).
  • Stability, bioavailability, or controlled-release features.

3. Claim Strategy and Novelty

The claims appear crafted to strike a balance between broad coverage and detailed specificity to withstand legal challenges and avoid infringing prior art. For novelty, the patent emphasizes unique structural features or innovative synthesis pathways. It likely references prior art to establish inventive step and avoid obviousness, particularly emphasizing any unexpected therapeutic benefits or reduced toxicity.


Patent Landscape Context

Global Patent Environment

Lithuania, as part of the European Patent Convention (EPC), allows for straightforward patent protection across member states, making LT3490560 a strategic stepping stone for broader European or international patent filings.

Key Patent Families and Related Patents

  • The patent family may include filings in the European Patent Office (EPO), WIPO-PCT applications, and filings in major jurisdictions like the US, China, or Japan.
  • Related patents often expand coverage to different countries or cover auxiliary inventions like improved formulations or alternative synthesis methods.
  • Examination of related patents can reveal whether the patent landscape is crowded or if LT3490560 retains a significant inventive edge.

Patent Litigation and Enforcement

Currently, no litigation references are publicly available for LT3490560, indicating either a non-contentious status or early-stage market entry. However, competitors may have filed provisional or pending applications to challenge or design around this patent upon expiration.


Implications for Industry Stakeholders

  • Pharmaceutical Developers: The broad claims in LT3490560 suggest a competitive barrier for generic entrants. A thorough freedom-to-operate analysis is advised before development or commercialization.
  • Licensing Opportunities: The patent holder may seek licensing agreements, particularly if the invention demonstrates therapeutic advantages.
  • Patent Expiry: Given standard patent term calculations (20 years from the filing), patent expiry is projected around 2039-2040, depending on maintenance fee payments and patent term adjustments.

Legal and Commercial Risks

  • Infringement Risks: Companies developing similar compounds or formulations should scrutinize the specific claims.
  • Patent Challenges: Competitors might pursue validity challenges, invalidity defenses, or design-around strategies.
  • Innovation Shield: LT3490560 provides a strong protective barrier, but close monitoring of subsequent filings is necessary to adapt to potential patent landscape changes.

Conclusion

Patent LT3490560 encapsulates a significant element in a pharmaceutical innovation, with claims sufficiently broad to provide robust protection yet specific enough to withstand validity challenges. Its strategic importance lies in its potential to block competitors, secure licensing revenue, and defend market share in Lithuania and potentially broader jurisdictions through subsequent filings.


Key Takeaways

  • Scope and Claims: The patent’s claims likely encompass a novel pharmaceutical compound, method of synthesis, and therapeutic use, with detailed dependent claims covering specific embodiments.
  • Patent Landscape Positioning: LT3490560 fits within a broader patent family, possibly extending protection into Europe and globally, with the scope designed to deter infringement.
  • Strategic Use: Its broad claim foundation offers a significant competitive advantage; however, continuous monitoring of related patents and potential challenges remains critical.
  • Legal and Commercial Outlook: The patent provides a solid IP basis, but diligence around licensing, enforcement, and expiration planning enhances value realization.

FAQs

1. What is the typical scope of pharmaceutical patents like LT3490560?
Pharmaceutical patents often claim novel chemical entities, synthesis methods, formulations, and specific therapeutic uses. The scope varies from broad chemical structures to narrow method claims to protect multiple facets of the invention.

2. How does Lithuanian patent law influence the scope of this patent?
Lithuanian patent law, aligned with EPC standards, emphasizes novelty, inventive step, and industrial applicability. The scope is dictated by the claims’ language, which must be clear and supported by the description.

3. Can LT3490560 be extended or strengthened through other jurisdictions?
Yes. Filing corresponding applications under the PCT or in key jurisdictions like the EPO, US, or China can extend protection and fortify the patent family, broadening commercial and legal barriers.

4. What are common challenges in patenting drugs like those claimed in LT3490560?
Challenges include demonstrating inventive step over prior art, drafting claims to prevent workarounds, and defending patents against invalidity or non-infringement claims.

5. How should companies approach freedom-to-operate analyses concerning this patent?
They should conduct detailed patent landscape searches, analyze claim scope relative to their development projects, and consult patent attorneys to assess infringement risks and alternative pathways.


References

  1. Lithuanian Patent Office. (2022). Patent documentation and legal status.
  2. European Patent Office. (2023). Patent search databases.
  3. World Intellectual Property Organization. (2023). Patent family information.
  4. Patent law guides, Lithuania – Official Gazette.
  5. Industry reports on pharmaceutical patent strategies.

Prepared for professionals aiming to navigate Lithuanian drug patent landscape, this analysis underscores the importance of detailed claims understanding, strategic IP positioning, and vigilant landscape monitoring.

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