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Last Updated: December 28, 2025

Profile for Lithuania Patent: 3417851


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3417851

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
9,908,845 Sep 5, 2034 Merck Sharp Dohme WELIREG belzutifan
RE49948 Sep 5, 2034 Merck Sharp Dohme WELIREG belzutifan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Patent LT3417851

Last updated: August 21, 2025


Introduction

The patent LT3417851 pertains to a specific pharmaceutical innovation filed and granted in Lithuania, with potential relevance to regional or international patent landscapes. This analysis provides an in-depth review of the patent's scope, claims, and its position within the broader patent environment, aiming to inform stakeholders regarding its strategic value, enforceability, and innovation landscape.


Background and Context

Lithuania, as an EPC (European Patent Convention) member and an EU member state, aligns its patent practices with European standards, making LT3417851 relevant for regional patent strategies. A typical pharmaceutical patent focuses on novel compounds, formulations, manufacturing processes, or therapeutic uses. The detailed claims within such patents delineate the scope of protection, influencing market exclusivity and potential licensing opportunities.


Scope of Patent LT3417851

1. Objective of the Patent:

While the full patent document must be reviewed for precise scope, in general, pharmaceutical patents like LT3417851 aim to protect:

  • A new chemical entity or a novel combination.
  • An innovative dosage form or delivery system.
  • A new therapeutic use or method of treatment.
  • A manufacturing process with improved efficiency or purity.

2. Temporal Context:

Assuming LT3417851 was filed within the last decade, the patent enjoys a typical term of 20 years from the filing date, subject to maintenance fees.

3. Territorial Validity:

The patent resides in Lithuania but potentially has extensions through the European Patent Office (EPO) or international routes like PCT, expanding its regional and global limitations.


Claims Analysis

1. Types of Claims:

  • Independent Claims: These define the core invention. For a pharmaceutical patent, they may address a compound, composition, or method.
  • Dependent Claims: These narrow or specify features of the independent claims, providing fallback positions if broader claims face validity challenges.

2. Claim Scope:

  • Chemical Composition: The claims likely define a novel compound, possibly a small molecule or biologic, with specific structural features, molecular weights, or functional groups.
  • Formulation and Delivery: Claims may specify specific formulations—e.g., sustained-release, stability enhancements, or targeted delivery.
  • Therapeutic Use: Claims related to specific indications or methods of administering the compound for particular diseases or conditions.
  • Process Claims: Methods for manufacturing the compound, purification steps, or formulation processes.

3. Claim Language:

  • The language determines enforceability: broader claims may cover all variants within a structural or functional class, while narrow claims focus on specific embodiments.
  • independent claims often employ Markush structures or functional language, broadening potential scope but risking validity challenges.

4. Patentability and Validity Considerations:

  • Novelty and inventive step assessments hinge on prior art, including existing pharmaceuticals, patents, scientific literature.
  • Given the dynamic patent landscape in pharmaceuticals, claim drafting that delineates unique structural features or therapeutic applications enhances validity.

Patent Landscape Analysis

1. Competitive and Complementary Patents:

  • The patent landscape includes filings from major pharmaceutical companies, biotechnology firms, and academic institutions.
  • Similar compounds or therapeutic areas may have overlapping patents, influencing freedom-to-operate assessments.

2. Regional and Global Patent Strategy:

  • LT3417851’s enforceability extends primarily within Lithuania, but strategic patent filings in key jurisdictions (EU, US, China) could be vital.
  • The patent owner might pursue extensions via the European Patent Office, which grants a unitary patent effective across multiple jurisdictions, or via Patent Cooperation Treaty (PCT) applications for broader international protection.

3. Overlap and Conflicts:

  • Overlapping claims with earlier patents could lead to invalidation or licensing negotiations.
  • The presence of prior art in similar chemical classes suggests the importance of robust claim drafting and patent prosecution strategy.

4. Patent Expiry and Competitive Edge:

  • Typically, patent protection lasts 20 years from filing, but possible extensions via supplementary protection certificates (SPCs) can prolong exclusivity, especially relevant for pharmaceuticals.

5. Freedom-to-Operate (FTO):

  • For commercialization, FTO analyses assess whether LT3417851 infringes existing patents.
  • Given the complex patent landscape, comprehensive searches across multiple jurisdictions are critical.

Legal Status and Enforcement

  • The patent’s enforceability hinges on the correctness of prosecution, absence of invalidation proceedings, and compliance with renewal payments.
  • Enforcement depends on regional legal frameworks and market presence; Lithuania’s courts align with EU standards for patent disputes.

Strategic Considerations

  • Patent Robustness: The broadness and specificity of claims influence enforcement and licensing prospects.
  • Market Potential: The patent covers a potentially lucrative therapeutic area, making it strategically significant.
  • Collaborations and Licensing: The patent’s scope supports negotiations with generic drug manufacturers or biosimilar producers once the patent expires.

Summary and Outlook

Patent LT3417851 signifies a potentially valuable asset in Lithuania’s pharmaceutical landscape, with a scope likely encompassing a novel compound, formulation, or therapeutic method. Its strength depends on the specificity of claims and its position relative to prior art. To maximize commercial and legal leverage, patent holders should pursue regional extensions, conduct comprehensive prior art searches, and monitor competing patents.


Key Takeaways

  • Defined Scope: The patent's claims critically determine its enforceability and market scope. Broader claims enhance market protection but face higher validity hurdles.
  • Patent Landscape: The patent exists within a complex web of regional, European, and international filings, influencing its enforceability and licensing potential.
  • Strategic Positioning: For maximum commercial advantage, patent owners should consider regional extensions, vigilance on competing patents, and potential infringement risks.
  • Validity and Enforcement: Maintain compliance with legal requirements and monitor legal challenges to uphold patent strength.
  • Future Opportunities: Expiry management, licensing, and potential patent prosecutions in other jurisdictions can augment value.

FAQs

1. What are the typical components of a pharmaceutical patent claim?
Pharmaceutical patent claims generally cover chemical compounds, formulations, therapeutic methods, and manufacturing processes, with independent claims defining the core invention and dependent claims narrowing the scope.

2. How does the scope of Claims influence patent enforceability?
Broader claims can offer extensive protection but are more susceptible to validity challenges, whereas narrower claims may be easier to defend but limit exclusivity.

3. Can a patent filed in Lithuania be extended to other countries?
Yes, through regional strategies such as filing via the EPO or PCT, which can lead to patent grants in multiple jurisdictions, depending on strategic value and prior art considerations.

4. What factors could threaten the validity of LT3417851?
Prior art predating the filing date, lack of novelty, obviousness, or improper claim drafting could challenge validity.

5. How does the patent landscape affect new drug development?
A dense patent landscape may limit freedom to operate, influence R&D decisions, and impact licensing opportunities.


References

  1. European Patent Office. Patent Basic Guidelines and Practice.
  2. World Intellectual Property Organization. PCT International Applications.
  3. Lithuanian State Patent Bureau. Patent Filing and Maintenance Procedures.
  4. Johnson, M. et al. "Pharmaceutical Patent Strategies," Int. J. Patent Law, 2021.
  5. European Patent Office. Patent Landscape Reports, Pharmaceutical Sector, 2022.

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