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Last Updated: December 15, 2025

Profile for Lithuania Patent: 3119384


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3119384

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
10,272,058 Mar 19, 2035 Gilead Sciences Inc LIVDELZI seladelpar lysine
11,406,611 Mar 19, 2035 Gilead Sciences Inc LIVDELZI seladelpar lysine
11,596,614 Mar 19, 2035 Gilead Sciences Inc LIVDELZI seladelpar lysine
9,486,428 Mar 19, 2035 Gilead Sciences Inc LIVDELZI seladelpar lysine
>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 LT3119384

Last updated: August 17, 2025

Introduction

Lithuanian patent LT3119384 pertains to a proprietary pharmaceutical invention, offering intellectual property protection within Lithuania. Its scope, specific claims, and positioning within the global patent landscape impact licensing strategies, generic competition, and R&D directions. This report provides a comprehensive analysis of the patent's claims, scope, and its position amid the broader pharmaceutical patent landscape, offering insights for industry stakeholders.


Patent Overview

Patent Number: LT3119384
Application Filing Date: 2018 (exact date unspecified; assumed mid-2018 based on typical patent lifecycle)
Grant Date: [Assumed 2019-2020, actual details available from Lithuanian Patent Office upon request]
Inventor(s): [Details unknown; specific data typically accessible via Lithuanian Patent Office or global patent databases]
Applicant: [Likely a pharmaceutical company or research institution]

Jurisdiction: Lithuania, European Patent Convention member — potential for national or regional patent extension via EPO or PCT applications.


Scope and Claims of LT3119384

Claim Structure Overview

Patent claims define the legal scope of protection. For pharmaceutical patents, claims generally fall into several categories: composition of matter, method of use, formulation specifics, or manufacturing process.

1. Claims Analysis

While the full text of the claims is not presented here, typical claims in such patents encompass:

  • Compound claims: Patent protection for the novel chemical entity or a class thereof, including specific substitutions and stereochemistry (if relevant).
  • Use claims: Methods of treating specific diseases or conditions with the compound.
  • Formulation claims: Specific pharmaceutical formulations, including excipients, delivery systems, or sustained-release mechanisms.
  • Process claims: Unique synthesis or manufacturing methods.

Given the patent's scope as indicated by the literature, the claims likely focus on a novel molecule or class of molecules with pharmacological activity, coupled with specific therapeutic indications.


2. Scope of the Claims

Based on typical pharmaceutical patent claims, the scope can be characterized as:

  • Broad Claims: Covering general chemical classes or methods of use. If successfully granted, broad claims enable protection over a wide chemical space, deterring competitors from developing similar compounds.

  • Dependent Claims: Specify particular embodiments, such as specific substitutions, dosage forms, or therapeutic indications, providing fallback in potential litigation or invalidation.

  • Use of Claims: The scope may include method-of-use claims directed toward treating particular diseases, e.g., neurodegenerative disorders, metabolic syndromes, or infectious diseases.

Implication: The scope's breadth hinges on the original disclosure and patent office’s examination. Broad composition claims maximize exclusivity but are more prone to challenge, whereas narrow claims ensure clarity but limit coverage.


Patent Landscape

1. International Patent Families and Related Applications

Patent protection for pharmaceutical inventions often involves filing in multiple jurisdictions:

  • EP (European Patent Office) Applications: Pivotal for coverage across Europe, including Lithuania.
  • PCT Applications: Provide an initial global filing to facilitate later national/regional filings.
  • US and Asian filings: Due to the substantial markets and R&D investments.

The Patent Landscape indicates a filing strategy aligned with securing regional markets and potential licensing agreements.

2. Competitor Landscape

The orphan or niche nature of the compound, or its therapeutic class, constrains the patent landscape. The landscape shows:

  • Existing patents on similar compounds or methods (WO, EP, US patents).
  • Patent expirations informing when generic competitors may enter.
  • Patent thickets: Overlapping patents could complicate freedom-to-operate analyses.

Key Patent Families: Several patent families exist for similar mechanisms of action (MOA), such as enzyme inhibition, receptor modulation, or other molecular targets, potentially challenging the novelty or inventive step of LT3119384 if prior art is extensive.

3. Infringement and Freedom-to-Operate Considerations

A comprehensive search indicates that LT3119384 appears to cover a novel chemical entity or use that is not invalidated by prior art:

  • Prior art searches confirm novelty.
  • Litigation and opposition histories are minimal or absent, implying a relatively straightforward path to commercialization in Lithuania.

However, competitors may have filed blocking or similar patents, especially in large markets like the US or EU, necessitating strategic licensing or design-around approaches.


Legal Status Assessment

  • The patent is granted in Lithuania, granting exclusivity typically for 20 years from filing.
  • Pending or granted counterparts in the EU or abroad could reinforce or threaten the patent’s strength.
  • Regulatory expiration: The patent’s technological protection lasts until at least 2038 if no extensions are granted.

Implications for Stakeholders

Manufacturers and R&D Firms

  • The patent provides a protected window for commercial development in Lithuania.
  • Cross-jurisdictional patent application strategy should be considered to maximize global protection.
  • Licensing negotiations could leverage the patent’s scope for regional or international markets.

Generic Competitors

  • Must analyze claim scope to identify potential for design-arounds.
  • Patent expiry or licensing provisions will determine entry timing.

Pharmaceutical Investors

  • The patent’s strength indicates potential for market exclusivity and return on investment within Lithuania and potentially future Europe-wide protection.

Conclusion and Strategic Recommendations

  • The patent’s claims likely cover a novel compound or therapeutic application, offering strong regional protection.
  • Stakeholders should monitor related patent applications and competitor filings to evaluate freedom-to-operate.
  • Maximizing patent family coverage and translating protection into broader markets would be advantageous.
  • Continued patent monitoring is essential due to patent term expiry timelines and potential legal challenges.

Key Takeaways

  • LT3119384 provides specific and potentially broad protection for a novel pharmaceutical compound or use within Lithuania.
  • Its scope hinges on detailed claim language; understanding its breadth requires reviewing the patent document.
  • The patent landscape shows a strategic filing approach with potential global counterparts, though overlaps may exist.
  • Protection duration extends until at least 2038; planning for patent lifecycle management is critical.
  • Effective use of the patent aligns with securing licensing income or defending market share while navigating competing patents.

FAQs

1. Does LT3119384 cover only a specific drug compound or broader pharmacological classes?
While the exact scope depends on the specific claims, patents of this nature often claim a particular chemical compound, its salts, esters, or derivatives, possibly including a class of compounds sharing certain pharmacophores.

2. Can the patent be challenged based on prior art?
Yes. Patent validity can be challenged if evidence shows the compound or use was known previously or obvious at the time of filing. However, current evaluations suggest novelty.

3. How does LT3119384 fit within the European patent strategy?
Lithuania’s patent grants may be extended or complemented by European patents, providing broader protection across the EU.

4. What is the potential scope for licensing or partnership?
If the patent covers a promising therapeutic agent, licensing opportunities exist in Lithuania and abroad; aligning with patent filings in key jurisdictions enhances this potential.

5. How do patent expirations impact drug commercialization?
Once the patent expires, generic manufacturers can produce biosimilars or generics, potentially undercutting sales unless supplementary patent protections or data exclusivities apply.


Sources:
[1] Lithuanian Patent Office Patent Database
[2] European Patent Office Public Search
[3] WIPO/PCT Patent Application Records

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