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Last Updated: December 16, 2025

Profile for Lithuania Patent: PA2021010


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US Patent Family Members and Approved Drugs for Lithuania Patent: PA2021010

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
11,827,646 Jan 25, 2036 Genentech Inc EVRYSDI risdiplam
9,969,754 May 11, 2035 Genentech Inc EVRYSDI risdiplam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Lithuania Drug Patent LTPA2021010

Last updated: August 20, 2025


Introduction

Lithuania's LTPA2021010 patent represents a strategically significant patent within the pharmaceutical landscape of the Baltic region. This patent, filed and granted in Lithuania, contributes to the broader intellectual property (IP) landscape in the pharmaceutical sector. An in-depth analysis of its scope, claims, and related patent environment offers valuable insights for pharmaceutical companies, investors, and legal professionals navigating the regional and global patent landscapes. This review synthesizes available patent documentation, elucidates the patent's coverage, and situates it within the global pharmacological patent context.


Patent Overview and Technical Field

LTPA2021010 pertains to pharmaceuticals, specifically to a novel compound, formulation, or method of use related to a therapeutic agent. While comprehensive details from the official patent document are absent, typical Lithuanian patent filings for drugs relate to innovative chemical entities or specific therapeutic applications.

The patent likely addresses one or more of the following:

  • A novel chemical compound with therapeutic efficacy.
  • An innovative formulation that enhances bioavailability or stability.
  • A unique method of administration or use in treating specific conditions.

Given the strategic position of Lithuania within the European patent system, it is probable that this patent incorporates claims aligned with European Patent Office (EPO) standards, providing a basis for potential regional or international patent extensions.


Scope and Claims Analysis

1. Claims Structure and Hierarchy

Lithuanian pharmaceutical patents usually contain a series of independent and dependent claims delineating distinct aspects:

  • Independent claims: Broadly cover the compound, formulation, or method without further limitations.
  • Dependent claims: Narrowed embodiments, such as specific chemical derivatives, dosages, or application scenarios.

The scope of LTPA2021010 hinges on the specificity and breadth of its independent claims; broader claims can cover variations of the compound or method, while narrower claims safeguard specific embodiments.

2. Determining Patent Scope

  • Chemical Composition or Compound Claims: If the patent covers a chemical entity, claims likely define the molecular structure, including core scaffolds, substitutions, or stereochemistry.
  • Method of Use or Treatment Claims: Could encompass therapeutic methods, such as treating particular diseases or conditions.
  • Formulation Claims: Might cover pharmaceutical compositions, including excipients, delivery systems, or sustained-release formulations.

The scope's strength depends on claim novelty, inventive step, and the language's breadth—broad claims provide extensive protection but are more vulnerable to invalidation if found obvious or not novel.

3. Novelty and Inventive Step

The novelty of LTPA2021010 primarily relies on the uniqueness of its chemical structure or therapeutic method vis-à-vis prior art. Lithuania's patent examination standards align with European regulations, requiring that claims demonstrate an inventive step beyond known compounds or methods.

4. Specific Versus Broad Claims

  • If the patent emphasizes a particular chemical substitution pattern, its claims are likely narrow but highly defensible.
  • Broader claims encompassing a class of compounds or methods are riskier but offer extensive market protection if granted.

Patent Landscape Context

1. Regional and Global Patent Environment

Lithuania, as part of the European Union, adheres to the European Patent Convention (EPC) standards, allowing for regional patent filings that can be validated across member states. LTPA2021010 could be part of an extended patent family, possibly corresponding to broader European or international patent applications (e.g., PCT applications).

2. Competitor Patent Mapping

Assessment of the patent landscape requires identifying similar patents filed within the EU, neighboring countries, and internationally. Competitor patents may focus on similar chemical classes or therapeutic methods, creating potential infringement or freedom-to-operate considerations.

For instance, if similar compounds are patented by competitors in the U.S. or China, this could influence market entry and licensing strategies within Lithuania and broader Europe.

3. Patent Life and Extension Opportunities

The initial patent term typically lasts 20 years from the filing date, subject to maintenance fees. Given the pharmaceutical development timeline, patent life extension mechanisms such as SPC (Supplementary Protection Certificate) may be relevant for additional exclusivity.


Legal and Commercial Implications

  • Protection of Innovation: The scope determines how effectively the patent prevents competitors from entering the market with similar compounds or methods.
  • licensing and Collaboration: A well-defined patent scope facilitates licensing negotiations and strategic partnerships.
  • Infringement Risks: Broad claims must be balanced with the risk of invalidation, especially if prior art is asserted against it.

Conclusion

LTPA2021010 appears to encompass a strategic patent with claims likely centered on chemical structure, formulation, or therapeutic method, aligned with European standards. Its scope, dictated by claim breadth and specificity, determines its strength and market coverage within Lithuania and beyond. Understanding its position amidst the existing patent landscape allows stakeholders to assess risks, opportunities, and potential for commercialization or licensing.


Key Takeaways

  • Scope is dependent on claim breadth: Broader claims offer extensive protection but face higher invalidation risks.
  • Alignment with European standards enhances regional patent enforceability**: Lithuania’s adherence to EPC makes the patent relevant across the EU.
  • Intellectual property positioning is crucial for market exclusivity: Properly drafted claims can safeguard R&D investments.
  • Patent landscape analysis is vital: Identifying similar patents informs freedom-to-operate and infringement strategies.
  • Patent term extensions can maximize commercial rights: Lifecycle management through SPCs is essential for competitiveness.

FAQs

Q1: What is the typical scope of a Lithuanian pharmaceutical patent like LTPA2021010?
A1: It generally covers specific chemical compounds, formulations, or medical methods with claims defined to balance broad protection against prior art and enforceability.

Q2: How does the patent landscape impact the commercialization of drugs in Lithuania?
A2: A well-mapped patent landscape helps identify potential infringement risks, licensing opportunities, and areas for innovation, shaping strategic decisions.

Q3: Can this Lithuanian patent be extended or validated elsewhere?
A3: Yes, through regional filings within the EU or international routes like PCT, providing broader geographical protection beyond Lithuania.

Q4: What factors influence the strength of the patent claims?
A4: Novelty, inventive step, claim clarity, and alignment with prior art are key determinants; narrower claims are easier to defend but less protective.

Q5: How does Lithuania’s patent system compare with other jurisdictions for drug patents?
A5: Lithuania’s system follows European standards, facilitating regional patent protection, similar to other EPC member countries, but with local nuances in examination practices.


References

[1] European Patent Convention (EPC), 1973.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT).
[3] Lithuanian State Patent Bureau. Patent regulations and procedures.
[4] European Patent Office (EPO) Guidelines for Examination.

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