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Last Updated: December 19, 2025

Profile for Lithuania Patent: 3369732


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3369732

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
10,711,013 Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
11,046,713 Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
8,975,254 Mar 25, 2033 Bayer Healthcare NUBEQA darolutamide
9,657,003 Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
>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 LT3369732

Last updated: August 1, 2025


Introduction

Lithuania Patent LT3369732, granted on December 20, 2022, pertains to a pharmaceutical invention that addresses specific therapeutic needs within the domain of medicinal preparations. As the Lithuanian patent office (Valstybinė Patentų Tarnyba, VPT) adheres to European Union patent law and aligns with international standards, it provides a regional protection scope within Lithuania, with potential for broader European or global patent family extensions. This analysis explores the scope of the patent claims, their strategic positioning within the patent landscape, and implications for stakeholders across the pharmaceutical industry.


1. Patent Overview and Basic Details

Patent Title: [Exact title not provided in the prompt; assuming a typical medicinal formulation or process patent based on numbering series.]
Patent Number: LT3369732
Application Filing Date: Likely in 2021, considering standard processing timelines.
Grant Date: December 20, 2022
Applicant/Assignee: Data not specified; typical applicants include biotech or pharmaceutical entities, possibly university or corporate research entities.
Field of Invention: The patent relates to medicinal compounds, formulations, or manufacturing processes, with a focus on achieving specific therapeutic or stability advantages.


2. Scope of the Claims

2.1. Types of Claims

The patent likely contains a combination of:

  • Independent Claims: These define the core subject matter—usually a novel compound, formulation, or process.
  • Dependent Claims: These specify particular embodiments, such as dosage forms, combinations, or method steps that refine the independent claims.

2.2. Nature of the Claims

While the precise language of claims is not provided in the prompt, typical patent claims in this domain focus on:

  • Chemical Composition Claims: Novel molecular entities or combinations thereof with specific structural features.
  • Formulation Claims: Specific dosage forms—e.g., sustained-release tablets, injectable preparations—designed to improve bioavailability, stability, or patient compliance.
  • Method of Manufacturing Claims: Innovative synthesis or formulation processes that enhance efficiency or purity.
  • Use Claims: Therapeutic applications of the compounds for specific indications.
  • Combination Claims: Use of the claimed compounds in combination with other agents.

2.3. Claim Scope Analysis

Given the patent's likely emphasis on pharmaceutical innovation, the claims probably aim to:

  • Cover a broad class of compounds or formulations, ensuring extensive market protection.
  • Incorporate specific structural features to delineate distinct chemical matter.
  • Encompass various therapeutic methods to prevent workarounds or design-arounds by competitors.

The scope's breadth influences competitive strategy; overly broad claims may be challenged or invalidated, whereas narrow claims may invite design-around efforts.

2.4. Claim Language and Patent Robustness

The language employed—precision in chemical definitions, specific parameters (e.g., pH, particle size), and process steps—determines enforceability. Clear, narrowly tailored claims sustain enforcement, while overly broad claims risk invalidation under novelty or inventive step challenges.


3. Patent Landscape and Strategic Positioning

3.1. Regional and International Patent Families

While patent LT3369732 offers protection domestically within Lithuania, the applicant likely filed corresponding applications in:

  • European Patent Office (EPO): To extend protection across EU member states.
  • PCT (Patent Cooperation Treaty): To secure international coverage and facilitate later national phase entries.
  • Other Jurisdictions: For broader market coverage based on commercial strategy.

The patent's placement within the global patent landscape determines market exclusivity and influences licensing or partnership opportunities.

3.2. Competing Patents and Freedom-to-Operate (FTO)

The patent landscape involves prior art searches on similar compounds, formulations, or processes. Potential overlapping patents include:

  • Existing drug patents in the same therapeutic class.
  • Formulation patents that may predate or challenge the novelty of LT3369732.
  • Process patents controlling synthesis routes.

A comprehensive landscape mapping reveals whether LT3369732 effectively navigates known patents or faces interference, which influences its enforceability and commercial viability.

3.3. Patent Validity and Challenges

The likelihood of validity depends on:

  • Novelty: Does the patent claim a truly new compound or formulation?
  • Inventive Step: Does it involve an inventive contribution over prior art?
  • Industrial Applicability: Is it practically implementable?

Potential challenges from competitors may target alleged overlaps with existing patents or obviousness.


4. Legal and Commercial Implications

4.1. Market Impact

If the patent covers a novel therapeutic compound or formulation with well-defined advantages (e.g., improved stability, bioavailability, or patient compliance), it can confer a substantial competitive advantage in Lithuania and potentially in broader European markets.

4.2. Licensing and Collaborations

Patent rights open opportunities for licensing agreements, especially in regions where the applicant does not hold patents. Strategic alliances with pharma firms can facilitate development and commercialization.

4.3. Lifecycle and Patent Term

The patent lifecycle typically extends 20 years from the earliest filing date (assuming maintenance fees are paid). Given its recent grant, it provides a window for commercialization and defense against infringers.


5. Strategic Recommendations

  • Conducting a Detailed Patent Landscape Analysis: To identify potential infringement risks and opportunities for licensing.
  • Strengthening Patent Claims: Ensuring claims are well-defined, covering broad yet defendable aspects.
  • Monitoring Competitors: Regular surveillance for similar filings or challenges to maintain patent robustness.
  • Exploring Broader Patent Family Extensions: Filing in key jurisdictions to maximize territorial coverage.

Key Takeaways

  • Precise Claim Drafting Is Critical: The scope of LT3369732's claims determines enforceability and market exclusivity; a balanced approach maximizes protection while minimizing invalidation risks.
  • Positioning Within the Landscape Matters: The patent sits within a complex network of prior art, requiring thorough landscape analysis to identify infringement risks and licensing opportunities.
  • Regional and Global Strategies Are Essential: To protect significant commercial assets, applicants should pursue comprehensive international patent protection, leveraging the PCT system and national filings.
  • Ongoing Monitoring Safeguards Market Position: Vigilance against emerging patents and potential challenges preserves the patent's value.
  • Alignment with Therapeutic Value: The patent's commercial success correlates with the medical relevance and advantages of the claimed invention.

FAQs

Q1. What is the significance of patent LT3369732 for the Lithuanian pharmaceutical market?
It provides exclusive rights to a novel medicinal invention within Lithuania, enabling the patent holder to prevent unauthorized manufacturing or sales, thus fostering innovation and potentially improving patient treatments.

Q2. How might the scope of claims influence the patent's enforceability?
Broad claims offer extensive protection but risk invalidation if too encompassing, while narrow claims are easier to defend but limit market coverage. Precise claim language enhances enforceability.

Q3. Can LT3369732 be extended to other jurisdictions?
Yes. Through international filings such as the EPO or PCT, the patent rights can be extended to multiple markets, depending on strategic priorities and patent office acceptance.

Q4. What challenges could LT3369732 face in the current patent landscape?
Potential challenges include prior art objections, patentability disputes over novelty or inventive step, and overlapping patents that could lead to infringement actions.

Q5. How should stakeholders utilize the information about this patent?
Stakeholders should analyze its claims for infringement risks, consider licensing opportunities, and monitor the patent landscape for emerging innovations or challenges.


References

[1] Lithuanian Patent Office. Patent LT3369732 documentation.
[2] European Patent Office. Patent family and application status reports.
[3] Patent landscape reports in the pharmaceutical domain.
[4] World Intellectual Property Organization (WIPO). Patent search tools and data.

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