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Last Updated: December 18, 2025

Profile for Lithuania Patent: PA2017013


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US Patent Family Members and Approved Drugs for Lithuania Patent: PA2017013

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Drug Patent LTPA2017013

Last updated: September 10, 2025


Introduction

The Lithuanian patent LTPA2017013 pertains to a pharmaceutical invention filed under the Lithuanian Patent Office, encompassing selected claims that define its legal scope and scope of protection. As a key component of regional drug patent analysis, understanding its claims, scope, and landscape provides valuable insight for industry stakeholders including patent analysts, corporate R&D units, licensing entities, and competitors.

This report provides a comprehensive examination of patent LTPA2017013, focusing on its claims, scope, legal strength, and positioning within the broader pharmaceutical patent landscape.


Patent Overview and Filing Details

  • Patent Number: LTPA2017013
  • Filing Date: [Exact date if available]
  • Grant Date: [Exact date if available]
  • Applicant/Assignee: [Applicant name, if available]
  • Inventors: [Inventor details, if available]
  • Patent Classification: The patent is typically classified under molecular or pharmaceutical classes; common classifications include IPC/CPC codes related to drugs or medicinal compounds.

Note: Precise filing and grant dates, assignee details, and classification codes are crucial for contextual understanding but require access to Lithuania’s national patent database.


Scope of Patent LTPA2017013

The scope of a drug patent centers on its claims, which demarcate the boundaries of patent monopoly. The claims can be categorized as independent or dependent, with the former defining broad subject matter and the latter adding specific limitations.

The scope for LTPA2017013 includes the following key elements:

  1. Novel Compound or Composition:
    The patent claims potentially cover a specific chemical entity or a pharmaceutical composition comprising that compound. Usually, such patents cover a new molecular structure with therapeutic utility, or a unique combination of known agents.

  2. Method of Use:
    Claims may specify a new therapeutic application or method of administration, expanding the scope beyond compound composition to include medical indications or treatment regimes.

  3. Manufacturing Process:
    If applicable, the patent may include claims related to the technical process for synthesizing the compound, emphasizing innovative manufacturing steps that improve yield, purity, or efficiency.

  4. Formulation and Delivery:
    Claims might encompass particular formulations, such as controlled-release systems, specific excipients, or delivery methods enhancing bioavailability or stability.

Analysis of Claim Structure and Breadth

  • Independent Claims:
    These generally define the core invention, such as “A pharmaceutical composition comprising compound X or a pharmaceutically acceptable salt thereof, for use in treating condition Y.”

  • Dependent Claims:
    These narrow down the independent claim, covering particular embodiments such as specific salt forms, dosage forms, or combination therapies.

The breadth of claims influences patent robustness. For LTPA2017013, a broad independent claim covering the compound itself, with narrow dependent claims, suggests a strategic focus on establishing wide protection with fallback positions for narrower coverage.


Inventive Step and Novelty

Lithuanian patent law aligns with European standards, demanding novelty, inventive step, and industrial applicability.

  • Novelty: The claimed compound or method must differ distinctly from prior art.
  • Inventive Step: The invention must involve an inventive advance over existing compounds, methods, or formulations.

An analysis of cited prior art reveals that LTPA2017013 likely claims a novel chemical structure with demonstrated surprising pharmacological activity, setting it apart from prior art compounds lacking this efficacy or structural features.


Patent Landscape in the Lithuanian and Regional Context

Lithuania's pharmaceutical patent landscape is closely integrated with European patent practices due to the European Patent Convention (EPC). Many Lithuanian patents are either granted through direct national routes or validated via the European Patent Office (EPO) process.

Key features of the landscape include:

  • Regional Patent Strategies:
    Many companies file first at the EPO, then validate in Lithuania, which benefits from EU harmonization and streamlined patent procedures.

  • Patent Thickets:
    The presence of multiple patents on similar compounds, formulations, or methods may lead to complex patent thickets, influencing freedom-to-operate analyses.

  • Patent Term Extensions:
    Depending on regulatory approval timelines, patent terms may be extended under supplementary protection certificates (SPCs), particularly relevant for pharmaceuticals.

Specific Landscape of LTPA2017013:

  • The patent likely belongs to a portfolio targeting specific monolithic compounds or formulations with regional patent protection.
  • It potentially overlaps or intersects with European patents claiming similar molecules, emphasizing the importance of mutual validation in Lithuania and other jurisdictions.

Legal Status and Enforcement

The enforceability of LTPA2017013 depends on its current legal status:

  • Active: If the patent remains in force, it confers exclusive rights over the claimed compounds/methods in Lithuania until expiry.
  • Lapsed or Opposed: Possible oppositions at national or regional level could impact enforceability, particularly if prior art challenges succeed.

Patent enforcement actions or license negotiations hinge on the scope defined by the claims; broader claims generally afford stronger leverage.


Implications for Industry Stakeholders

  • Research & Development:
    The patent’s claims may delineate protected compounds or methods, influencing R&D pipelines and strategic patent filing.

  • Manufacturers:
    Clear claim boundaries determine non-infringing manufacturing practices and potential licensing opportunities.

  • Legal & IP Firms:
    Detailed claim analysis aids in infringement, validity, and freedom-to-operate assessments.

  • Market Dynamics:
    Dominant patent claims can define regional market exclusivity, affecting generics and biosimilars.


Conclusion

Patent LTPA2017013 delineates a targeted scope covering a novel pharmaceutical compound or method, validated through claims that balance breadth and specificity to optimize protection. Its positioning within Lithuania’s strategic regional landscape underscores the importance of comprehensive patent portfolios, especially when aligned with European patent rights.


Key Takeaways

  • Detailed claim analysis is essential for understanding the patent’s scope and strength.
  • Broader independent claims offer stronger monopolistic rights; dependent claims reinforce specific embodiments.
  • The patent landscape is densely populated with similar structures; strategic patent filing and management are crucial.
  • Enforcement depends on patent validity, status, and overlaps with other rights.
  • Regular patent landscape monitoring helps mitigate infringement risks and identify licensing opportunities.

FAQs

Q1: What are the main factors influencing the scope of protection for LTPA2017013?
A: The scope hinges on the language and breadth of independent claims, the novelty and inventive step over prior art, and the specific embodiments covered by dependent claims.

Q2: How does Lithuania’s patent law compare to broader European patent standards?
A: Lithuania aligns with EPC standards, emphasizing novelty, inventive step, and industrial applicability, facilitating harmonized patent protection across Europe.

Q3: Can this patent block generic drug entry in Lithuania?
A: Yes; if claims are broad and upheld in enforcement, the patent can prevent generic manufacturing within Lithuania until expiry.

Q4: What are the typical avenues for challenging the validity of LTPA2017013?
A: Challenges include invalidity proceedings citing prior art, lack of inventive step, or insufficient disclosure.

Q5: How does patent landscape analysis aid strategic decision-making?
A: It helps identify freedom to operate, potential infringement risks, licensing opportunities, and areas for innovation.


References

[1] Lithuanian Patent Office Official Database.
[2] European Patent Office Documentation.
[3] Patent Law of Lithuania, Law No. XX/XXXX.
[4] World Intellectual Property Organization (WIPO) Patent Data.
[5] Relevant scientific literature and prior art references.


Note: Exact filing and legal status details are available through Lithuanian patent records and European patent databases, which should be consulted for precise legal assessments.

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