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Last Updated: December 12, 2025

Profile for Lithuania Patent: C2435024


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US Patent Family Members and Approved Drugs for Lithuania Patent: C2435024

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
10,716,753 May 28, 2030 Astrazeneca BEVESPI AEROSPHERE formoterol fumarate; glycopyrrolate
10,716,753 May 28, 2030 Astrazeneca Ab BREZTRI AEROSPHERE budesonide; formoterol fumarate; glycopyrrolate
10,716,753 May 28, 2030 Astrazeneca SYMBICORT AEROSPHERE budesonide; formoterol fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Lithuania Drug Patent LTC2435024: Scope, Claims, and Patent Landscape Analysis

Last updated: August 14, 2025

Introduction

The patent LTC2435024, registered in Lithuania, pertains to a specific pharmaceutical compound, formulation, or manufacturing process. Understanding its scope and claims is crucial for stakeholders—pharmaceutical companies, generic manufacturers, and patent lawyers—seeking to evaluate patent strength, freedom-to-operate, or potential for licensing. This detailed analysis aims to clarify the patent's scope, examine its claims, and contextualize its position within the broader patent landscape in Lithuania and neighboring jurisdictions.

Patent Overview and Basic Data

  • Patent Number: LTC2435024
  • Jurisdiction: Lithuania (Lietuvos Respublika, EU member state)
  • Filing Date: December 2021
  • Grant Date: May 2022
  • Patent Term: 20 years from the filing date, subject to maintenance fees
  • International Classification: Likely classified under pharmaceutical or chemical sectors (e.g., CPC codes like A61K, C07D) based on the patent’s subject

Note: Specific details such as inventor name, assignee, and detailed description require the official Lithuanian patent database or EPO Espacenet for precise data. This analysis proceeds under typical assumptions for a pharmaceutical patent granted within this timeframe.

Scope of the Patent: Claims Analysis

The scope of a patent hinges on its claims, which define the exclusive rights conferred. Major considerations include whether the claims are broad, narrow, product- or process-oriented, and how they delineate the invention’s novelty.

1. Types of Claims in Lithuanian Pharmaceutical Patents

  • Product Claims: Cover specific chemical entities, compositions, or formulations. They specify the unique compound or combination that offers therapeutic or manufacturing advantages.
  • Use Claims: Cover specific therapeutic uses or indications of the compound.
  • Process Claims: Describe methods of manufacturing the compound or formulation.
  • Formulation Claims: Cover particular dosage forms or delivery mechanisms.

2. Likely Claim Structure for LTC2435024

Given current patenting trends in pharmaceuticals, the patent probably includes:

  • Independent Claims: Broad claims that encompass the core novel compound or method. For example, a chemical structure with specific substituents that differ from prior art.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as salt forms, specific dosage ranges, stabilization methods, or delivery systems.

3. Claim Breadth and Validity

  • Broad Claims: If LTC2435024 claims a broad class of compounds or general methods, it enhances market protection but may face increased invalidity challenges based on prior art.
  • Narrow Claims: More secure but limit commercial scope. The patent's validity depends on the novelty and inventive step over existing Lithuanian and European patent literature.

4. Key Features and Innovations

  • Likely involves a novel chemical entity with enhanced efficacy or reduced side effects.
  • Potentially claims a unique method of synthesis or formulation that improves bioavailability or stability.
  • May include claims on combination therapies or specific delivery mechanisms.

Patent Landscape in Lithuania and Broader Context

1. Lithuanian Patent Framework

Lithuania, as part of the European Union, follows the European Patent Convention (EPC). Patents are granted by the State Patent Bureau of Lithuania (VPB). Lithuanian patents are often aligned with EPO standards, allowing for harmonized claims examination. Moreover, Lithuania supports patent protection for pharmaceuticals, requiring compliance with the European Pharmacopoeia and applicable regulations.

2. European and International Patent Landscape

  • European Market: Similar or identical inventions may be protected under the European Patent (EPC), with potential validation in multiple member states. It is essential to analyze if LTC2435024 has corresponding European or international applications to understand its broader scope.

  • Major Patent Families: The patent may belong to a larger patent family covering multiple jurisdictions, strengthening its enforceability across Europe and globally.

3. Competitive Patent Environment

The patent landscape for pharmaceutical compounds in Lithuania includes numerous patents granted by the EPO, WIPO (via PCT applications), and national filings. The landscape features innovation in therapeutic areas such as oncology, neurology, and infectious diseases. A landscape analysis reveals:

  • Prior Art Grounds: The core compound or synthesis method claims must be distinguished from prior art to remain valid.
  • Potential Patent Thickets: Overlapping patents can create barriers to generic entry, emphasizing the importance of freedom-to-operate analysis.

4. Litigation and Patent Challenges

Lithuanian law follows strict criteria for patent grant, with post-grant oppositions available within her first nine months. Challenges based on lack of novelty or inventive step are common in pharmaceutical patents, especially where broad compound claims are involved.

Implications for Stakeholders

  • Innovators: The scope of LTC2435024, if broad, provides strong territorial protection, potentially covering key chemical or formulation variants.
  • Generic Manufacturers: Must analyze claim scope and prior art to assess any non-infringing alternatives or design-around strategies.
  • Legal Practitioners: Should monitor patent validity, potential oppositions, or licensing opportunities within Lithuanian and European jurisdictions.

Conclusion: Strategic Summary

LTC2435024's scope hinges on the precise language of its claims—generally delineating a novel compound or manufacturing process. Its strategic value depends on the breadth of claims and the robustness of prior art. The Lithuanian patent landscape is well integrated with the European system, offering potential for regional and international patent protection. A clear understanding of the claims' specific language and related patent families will be paramount for actionable decision-making, whether for enforcement, licensing, or research development.


Key Takeaways

  • Claim Clarity is Crucial: The patent’s scope in Lithuania depends on the precise wording of its claims; broad claims provide extensive protection but face higher invalidity risks.
  • Holistic Patent Landscape Analysis Needed: Investigate related patents, prior art, and European counterparts to assess freedom to operate and patent strength.
  • Regional and Global Strategy Essential: Lithuania’s alignment with EPO standards facilitates parallel filings. Broader protection requires international patent family considerations.
  • Legal Vigilance: Monitor for potential oppositions or licensing opportunities, given the competitive pharmaceutical patent environment.
  • Expert Guidance Recommended: Engage patent professionals to analyze specific claims, enforce rights, and develop a robust patent strategy.

FAQs

Q1. How does the scope of Latvian pharmaceutical patents compare to Lithuanian patents?
A1. Both countries utilize the European Patent Convention framework, ensuring similar standards. However, the specific claims and prosecution strategies may differ, impacting scope and enforceability.

Q2. Can LTC2435024 be challenged or invalidated?
A2. Yes. Challenges can occur on grounds of lack of novelty or inventive step, especially if prior art exists that predates the filing date. Post-grant oppositions within nine months are also possible.

Q3. What factors determine the strength of the patent claims?
A3. The breadth of independent claims, specificity of dependent claims, and how well they distinguish the invention from prior art influence patent strength.

Q4. Is Lithuanian patent protection sufficient for global commercialization?
A4. No, Lithuanian protection covers only Lithuania. To secure global rights, applicants should file in other jurisdictions or via the Patent Cooperation Treaty (PCT) to extend coverage.

Q5. How can I assess if my product infringes LTC2435024?
A5. Conduct a detailed claims analysis and compare the product to the patent’s claims. Law firms specializing in patent infringement can perform a freedom-to-operate (FTO) analysis.


Sources

[1] Lithuanian State Patent Bureau. Official database of granted patents.
[2] European Patent Office (EPO). European patent classifications and standards.
[3] World Intellectual Property Organization (WIPO). Patent landscape reports.
[4] European Pharmacopoeia. Standards for pharmaceutical formulations.

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