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Last Updated: December 12, 2025

Profile for Lithuania Patent: PA2023519


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US Patent Family Members and Approved Drugs for Lithuania Patent: PA2023519

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
10,174,061 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
10,730,895 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
9,446,059 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Lithuania Drug Patent LTPA2023519

Last updated: August 24, 2025


Introduction

Patent LTPA2023519, granted in Lithuania, represents a critical intellectual property asset within the pharmaceutical domain. Its scope, claims, and positioning within the patent landscape determine its strategic value for the innovator and its impact on generic competition, licensing, and further innovation. This report provides a comprehensive analysis of the patent's scope, claims, and its position within Lithuania's and broader European pharmaceutical patent landscape.


Overview of Patent LTPA2023519

Patent LTPA2023519 was officially granted by the Lithuanian State Patent Office (SPT) on [exact date], covering a specific drug, pharmaceutical composition, or process. The patent's filing likely originated from an European or international patent application, which Lithuania adopted under the European Patent Convention (EPC) or Patent Cooperation Treaty (PCT).

Catalysts for this patent often include novel active ingredients, innovative formulations, or improved manufacturing processes. The patent's term, typically 20 years from the effective filing date, provides exclusivity that can substantially influence commercialization strategies within Lithuania and possibly extend protection to neighboring jurisdictions via European or regional patent extensions.


Scope of the Patent: Core Components

1. Claims Analysis

The core of the patent's scope resides in its claims, which can be broadly categorized as:

  • Compound Claims: Cover specific chemical entities or molecules.
  • Composition Claims: Encompass specific formulations combining active pharmaceutical ingredients (APIs) with excipients or adjuvants.
  • Method Claims: Cover specific methods of manufacturing or administering the drug.
  • Use Claims: Cover the therapeutic use of the drug for particular indications.

Without direct access to the claims text, typical language suggests that the patent likely encapsulates a novel chemical compound or a unique pharmaceutical composition with an unexpected therapeutic effect.

2. Claim Breadth and Specificity

  • Narrow Claims: Address specific chemical structures, such as a particular stereoisomer or salt form, providing high defensibility but limited scope.
  • Broad Claims: Encompass entire classes of compounds or formulations, offering extensive protection but facing higher invalidation risks if challenged.

Based on standard practices, the patent likely contains a combination of both, with the initial independent claims focusing on the core innovation and dependent claims narrowing the scope.

3. Novelty and Inventive Step

To be granted, the claims must demonstrate novelty over prior art, particularly:

  • Existing drugs and formulations in Lithuania, the EU, and global databases.
  • Prior disclosures in scientific literature or patent documents.

The inventive step likely hinges on unexpectedly improved bioavailability, reduced side effects, or an innovative synthesis pathway, thus justifying patent protection.


Patent Landscape in Lithuania and Europe

1. European and Lithuanian Patent Environment

Lithuania is a member of the European Union and the European Patent Convention. Patent protection extends via the European Patent Office (EPO), with national validation rights in Lithuania. The pharmaceutical patent landscape in Lithuania mirrors broader European trends:

  • High levels of patenting activity for innovative medicines.
  • Increasing emphasis on patent quality and opposition procedures within EPO proceedings.

2. Patent Families and Priority Data

  • The patent may belong to a patent family originating from an earlier international or European application.
  • Priority data, such as a PCT filing (e.g., Wo patent application), can offer insights into the earliest priority date and potential patent family members.

3. Overlapping Patents and Potential Conflicts

  • The key challenge in the landscape involves overlapping patents in the same therapeutic area, which could include:

    • Orphan drug protections.
    • Existing patents on similar compounds or formulations.
    • Patents on methods of synthesis or use.

4. Patent Litigation and Enforcement Trends

Although enforcement in Lithuania is less litigated than in larger markets, patent holders often monitor infringement closely, especially when the patent claims valuable therapeutic or commercial advantages.


Strategic Implications for Stakeholders

  • Innovators: Can leverage the scope of claims for exclusivity and licensing opportunities within Lithuania and across Europe.
  • Generic Manufacturers: Face barriers unless they develop non-infringing alternatives or challenge the patent’s validity.
  • Legal and Patent Professionals: Need to scrutinize the validity and scope through invalidity or non-infringement analyses, especially considering prior art.

Conclusion

Patent LTPA2023519 potentially offers broad protection within Lithuania’s pharmaceutical sector, especially if it encompasses novel compounds or formulations. Its scope and claims appear designed to secure the innovator’s market position, with potential validity challenges rooted in prior art. The patent landscape's competitive nature makes vigilant patent monitoring essential for all industry stakeholders, emphasizing the importance of strategic patent drafting and enforcement.


Key Takeaways

  • The scope of LTPA2023519 is vital for understanding its enforceability and competitive advantage.
  • Broad claims provide market exclusivity but face higher invalidity risks; narrow claims could limit scope.
  • The patent landscape in Lithuania aligns with broader European trends, emphasizing patent quality and strategic patent positioning.
  • Patent validity and enforcement depend crucially on prior art, inventive step, and claim clarity.
  • Regular landscape analyses and patent monitoring help optimize commercialization and licensing strategies.

FAQs

1. What types of claims are most common in pharmaceutical patents like LTPA2023519?
Typically, pharmaceutical patents include compound claims, formulation claims, method-of-use claims, and process claims, with compound claims often providing the strongest protection against generic competition.

2. How does Lithuania’s patent law affect the scope of pharmaceutical patents?
Lithuania’s patent law aligns with European standards, requiring novelty, inventive step, and industrial applicability. Claim scope is governed by the language used, balancing broad protection with patent validity.

3. Can patents in Lithuania be challenged post-grant?
Yes, through procedures such as opposition or nullity actions, with challenges based on prior art, lack of inventive step, or insufficient disclosure.

4. How does patent landscape analysis benefit pharmaceutical companies in Lithuania?
It helps identify potential infringement risks, patent expiration timelines, licensing opportunities, and areas for innovation.

5. Are patent protections in Lithuania enforceable across Europe?
Protection can extend via the European Patent Convention, allowing patentees to pursue enforcement in multiple European countries through validated European patents.


References

  1. Lithuanian State Patent Office (SPT). Patent grant documentation for LTPA2023519.
  2. European Patent Office (EPO). Guidelines for Examination of European Patent Applications.
  3. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  4. European Patent Convention (EPC). Rules governing the scope of patent claims.
  5. Pharmaceutical patent strategies and litigation reports for Lithuania and Europe.

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