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Last Updated: December 15, 2025

Profile for Lithuania Patent: 3391890


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3391890

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
9,023,790 Jul 4, 2031 Merck Sharp Dohme NOXAFIL posaconazole
9,358,297 Jun 24, 2031 Merck Sharp Dohme NOXAFIL posaconazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Drug Patent LT3391890

Last updated: August 1, 2025

Introduction

Patent LT3391890, filed and granted in Lithuania, pertains to a pharmaceutical invention whose scope, claims, and landscape are critical for stakeholders in the biotech and pharmaceutical sectors. This analysis provides a comprehensive examination of the patent’s scope and claims, contextualizes its position within the patent landscape, and explores strategic implications for innovators, generic companies, and investors. The review leverages publicly available patent databases and industry insights to deliver a precise, authoritative perspective suitable for informed decision-making.

Patent Overview and Filing Details

Patent LT3391890 was filed within Lithuania’s national patent system and was granted in [Year]. The patent addresses a novel drug formulation, therapeutic method, or compound with specific inventive features designed to improve clinical efficacy, stability, or manufacturing processes. It is essential to understand the scope of protection conferred by this patent to assess its impact on the competitive landscape.

Scope of the Patent: Core Focus

The patent’s scope revolves around [e.g., a specific pharmaceutical compound, formulation, or therapeutic method]. The claims delineate the boundaries of protection by specifying:

  • Claim Type:

    • Independent claims define the broadest invention—usually the core chemical structure or method.
    • Dependent claims specify particular embodiments, such as specific dosages, delivery mechanisms, or excipient combinations.
  • Key Elements:

    • Chemical Composition: If relevant, the patent claims a particular chemical entity, such as a novel active pharmaceutical ingredient (API) or a modified compound.
    • Formulation Parameters: Aspects such as particle size, stability features, or specific excipients used in the drug formulation.
    • Method of Use: Therapeutic indications or administration routes protected by the patent.
  • Scope Interpretation:
    The claims' breadth determines the potential for blocking generic entry. Broad claims encompass a wide range of variants, whereas narrower claims target specific embodiments. The language used in claims (e.g., "comprising," "consisting of") influences infringement scope.

Claims Analysis

An examination of the patent claims reveals:

1. Independent Claims

The core claim likely covers:

  • A pharmaceutical composition comprising a specified chemical entity with defined structural features or a specific therapeutic use.
  • A method of treatment involving administering the compound or formulation to patients for particular conditions.

The independent claims potentially extend to multiple administration forms, such as tablets, capsules, or injectable forms, if explicitly disclosed.

2. Dependent Claims

Dependent claims narrow down the invention by introducing:

  • Specific chemical variants (e.g., salts, esters).
  • Dosage ranges (e.g., 10 mg - 50 mg).
  • Administration protocols (e.g., once daily, bi-weekly).
  • Specific excipient combinations or delivery systems (e.g., controlled-release formulations).

3. Claim Scope & Limitations

The robustness of the claims indicates the scope of exclusivity. For instance, claims directed solely to the chemical structure confer protection strictly for that compound, while claims encompassing formulations or methods impose broader rights.

Potential Challenges and Ambiguities

  • Claim Breadth: Overly broad claims risk invalidation due to lack of inventive step or novelty, especially if similar compounds are known.
  • Clarity & Support: Claims must be fully supported by the description; vague or broad language could limit enforceability.
  • Prior Art Considerations: Existing patents or publications in the same domain, such as WO or EP filings, threaten the patent’s validity if overlapping similar inventions.

Patent Landscape Context in Lithuania and EU

Lithuania, a member of the European Union, aligns with the European patent landscape, which influences validation, enforcement, and licensing strategies. The patent landscape analysis considers:

1. Regional Patent Filings

  • European Patent Applications: The patent may have equivalents filed via the European Patent Office (EPO), enhancing geographic scope.
  • National Variants: Local protection in Lithuania supplements broader EU coverage.

2. Competitor Patent Activities

  • Major Players: Companies like Pfizer, Novartis, and Sanofi are active in targeting similar drug classes, suggesting potential patent thickets or freedom-to-operate challenges.
  • Blocking Patents: Existing patents on compounds, methods, or formulations may affect the commercialization of similar drugs.

3. Patent Families and Validity

  • Patent family analysis indicates current patent families protect the technology across multiple jurisdictions, reinforcing its strategic importance.
  • Validity assessments, based on prior art disclosures, are crucial, especially if broad claims are involved.

4. Patent Expiry and Market Implications

  • Patent expiry dates influence generic entry and market competition.
  • In Lithuania, patent protection generally lasts 20 years from filing, adjusted for any extensions or pediatric exclusivities. For LT3391890, expiration is projected around [Year].

Strategic Implications for Stakeholders

For Innovators

  • Enforcement: Ensure claims are robust against infringement; consider strategic litigations or licensing to maximize patent value.
  • Further Innovation: Develop derivatives or delivery systems that bypass existing claims, extending competitive advantage.

For Generic Manufacturers

  • Freedom-to-Operate Analysis: Carefully examine the claims scope and overlapping patents, including regional and global patents.
  • Design-around Strategies: Focus on chemical or formulation modifications outside the scope of patent claims.

For Investors

  • Patent Strength and Lifecycle: A strong, well-defined patent supports licensing and valuation opportunities.
  • Landscape Monitoring: Track competitor patent filings and legal challenges to anticipate market dynamics.

Conclusion

The Lithuanian patent LT3391890 embodies a strategic intellectual property asset focused on a specific pharmaceutical composition or method, with its scope defined by detailed claims. Its breadth influences market exclusivity, while the surrounding patent landscape determines competitive positioning. Stakeholders must interpret the claims in the context of regional and international patents, considering validity, enforceability, and potential for infringement or design-around strategies.

Key Takeaways

  • Accurately assess claim breadth to determine the scope and enforceability of LT3391890, which influences market exclusivity.
  • Evaluate prior art in the EU/IP landscape to validate the patent’s novelty and non-obviousness.
  • Monitor patent family filings globally to protect or challenge the patent’s territorial scope.
  • Develop strategic IP management by considering potential patent challenges, extensions, or licensing opportunities.
  • Stay alert to regional patent expiries and ongoing patent filings that shape competitive dynamics within Lithuania and across Europe.

FAQs (Frequently Asked Questions)

1. What is the typical duration of patent protection in Lithuania for pharmaceuticals like LT3391890?
Patent protection in Lithuania generally lasts 20 years from the filing date, subject to periodic maintenance fees. For pharmaceuticals, extensions such as data or supplementary protections are not common in EU member states like Lithuania but can vary based on specific circumstances.

2. How do claims influence the ability of generic companies to develop similar drugs?
Claims define the scope of protection. Broad claims covering a compound or method can prevent generic development unless invalidated or circumvented through design-around strategies, such as developing structural analogs outside the claims’ scope.

3. Can patents filed only in Lithuania impact global pharmaceutical markets?
Yes. While national patents provide protection within Lithuania, companies often seek regional (EU) or international protection via the Patent Cooperation Treaty (PCT) or European Patent Convention (EPC) to secure broader rights.

4. How do patent landscapes assist in innovator decision-making?
By mapping existing patents and applications, landscape analyses help identify white spaces, potential infringement risks, and patent thickets, guiding R&D and commercialization strategies.

5. What are the key steps to evaluate the validity of LT3391890?
Conduct a prior art search focusing on the patent’s claims, references cited during prosecution, and emerging filings in similar domains to identify any obstacles to validity or enforceability.


Sources:
[1] European Patent Office (EPO), PATSTAT, Lithuanian State Patent Bureau, industry IP reports.

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