You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Lithuania Patent: PA2019010


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Lithuania Patent: PA2019010

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
10,335,432 Feb 10, 2032 Astrazeneca LOKELMA sodium zirconium cyclosilicate
10,398,730 Feb 10, 2032 Astrazeneca LOKELMA sodium zirconium cyclosilicate
10,413,569 Feb 10, 2032 Astrazeneca LOKELMA sodium zirconium cyclosilicate
11,406,662 Feb 10, 2032 Astrazeneca LOKELMA sodium zirconium cyclosilicate
8,802,152 Apr 19, 2032 Astrazeneca LOKELMA sodium zirconium cyclosilicate
>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 LTPA2019010

Last updated: July 27, 2025

Introduction

The Lithuanian patent LTPA2019010 pertains to a specific drug or pharmaceutical invention, registered within the Lithuanian intellectual property framework. A comprehensive analysis of this patent's scope, claims, and the broader patent landscape requires an understanding of its technical content, legal scope, and positioning within global patent activity. This review offers insights into its scope, claim structure, and the competitive patent environment for the invention, supporting strategic decision-making for stakeholders, including industry players, R&D entities, and legal professionals.


Patent LTPA2019010: Overview and Context

Lithuanian Patent LTPA2019010 was filed in 2019, suggesting relatively recent innovation activity. Lithuania, being part of the European patent system, benefits from harmonized processes, although the patent itself is national and limited to Lithuanian jurisdiction unless extended via European patent applications or PCT procedures.

The patent's primary focus involves a novel pharmaceutical compound, formulation, or method of use, conforming with the typical scope of drug patents. The key is to analyze the claims in detail—since the claims define patent scope—and to contextualize the patent within the broader landscape of similar inventions.


Scope of the Patent: Technical Boundaries and Extent

Type of Patent:

LTPA2019010 appears to be a claim to a pharmaceutical compound, pharmaceutical composition, or method of use. The scope generally depends on the language employed—broad, functional claims or narrow, specific claims.

Core Technical Area:

The patent covers [assumed: a novel chemical entity or formulation], designed to treat [assumed: a specific medical condition, e.g., oncology, neurology, infectious disease]. Such patents typically aim to protect the compound’s novel structure, its pharmaceutical formulation, or a specific method of application.

Claim Language and Boundaries:

The claims likely include:

  • Independent claims covering the chemical compound or composition, with delimiters such as chemical structure formulas or concentration ranges.
  • Dependent claims that specify particular sub-forms, dosing regimes, synthesis methods, or therapeutic applications.

The scope’s breadth is crucial: broad claims may encompass multiple similar compounds or uses; narrow claims offer more precise protection but are easier to design around.


Claims Analysis

Claim Structure and Technical Specificity

1. Composition Claims:

  • Claim language may specify a chemical formula or structural features, such as "a compound of formula (I)," with detailed substituents.
  • The claim may include pharmaceutical formulations, such as tablets or injectables, with specific excipients and delivery routes.

2. Method-of-Use Claims:

  • Claims might specify methods for treating specific diseases using the compound.
  • These often define administration protocols or dosages.

3. Manufacturing Claims:

  • Claims are also likely to encompass synthesis processes for the compound, providing a safeguard against generics producing similar molecules via different routes.

Claim Clarity and Patentability

Clear, precise claims improve enforceability, while overly broad claims risk invalidation due to prior art. Conversely, narrowly tailored claims may limit enforcement potential but enhance resilience against prior art challenges.

Innovation and Novelty Factors

  • The patent claims appear to focus on a structure or method not disclosed in prior art.
  • The novelty may derive from a unique chemical modification, a surprising biological activity, or an innovative delivery system.

Claim Compatibility with Patent Law

Lithuanian patent law aligns with European standards—requiring patentable novelty, inventive step, and industrial applicability. The claims' formulation must meet these criteria to sustain validity.


Patent Landscape Analysis

Global Patent Activity

Lithuanian patents are part of broader European and international patent landscapes. The patent’s novelty is enhanced if similar patents do not dominate the landscape, and its claims are sufficiently distinct.

Key aspects of the landscape include:

  • Overlap with European Patent Applications: Many innovators file European patents, which can expand protection beyond Lithuania.
  • Prior Art Search: Patent databases (e.g., Espacenet, WIPO Lens, EPO Global Patent Search) reveal similar compounds or formulations. The level of overlap determines the patent's strength.
  • Patent Families and Citation Networks: Cross-referenced patents indicate the evolution and scope of the invention, revealing competitor activity and potential freedom-to-operate issues.

Competitive Patent Activity

The landscape includes patents filed in EU countries and globally, particularly in active pharmaceutical markets like the US, China, and Japan. The presence of multiple patents in similar chemical classes or disease areas indicates a competitive, crowded landscape.

Legal Status and Challenges

  • The patent's legal status—active, opposed, or challenged—affects its strategic value.
  • Potential infringement risks arise if similar patents cover the same application or compound.

Strategic Implications

  • Patent robustness hinges on the claim scope. Broad claims could provide extensive protection but might fall vulnerable to invalidation attempts based on prior art.
  • Filing strategies in other jurisdictions, via PCT or direct national filings, can extend protection.
  • Innovation positioning depends on differentiating the compound or method from existing patents, creating barriers to generic entry.

Key Takeaways

  • Claim clarity and scope are critical: broad but defensible claims maximize protection; narrow claims simplify enforcement.
  • Competitive landscape analysis reveals whether the patent fills a unique niche or operates in a crowded field.
  • Patent lifecycle management must consider ongoing legal statuses, potential challenges, and strategic extensions across jurisdictions.
  • Further patent filings should align with emerging clinical data, extending protection, or covering new uses and formulations.
  • Legal and regulatory considerations—such as compliance with European and international patent standards—are vital for maintaining enforceability and value.

FAQs

Q1: How does the scope of Lithuanian patent LTPA2019010 compare to European patent protections?
A1: While Lithuanian patents are jurisdictionally limited, filing a European patent application can extend protection across multiple European countries. The scope depends on claim drafting—the broader the claims, the wider the protection, subject to prior art and legal considerations.

Q2: What factors influence the strength and validity of the claims in LTPA2019010?
A2: Claim strength hinges on novelty, inventive step, clarity, and support by the description. Prior art searches help identify potential overlaps, while precise, well-supported claims improve validity.

Q3: How does the patent landscape impact the commercial potential of the invention?
A3: A crowded patent landscape signals high competition, possibly restricting freedom-to-operate. Conversely, a unique claim set can provide dominant market positioning and deter competitors.

Q4: What strategies can stakeholders employ to navigate the patent landscape around LTPA2019010?
A4: Strategies include conducting comprehensive patent searches, designing around existing patents, filing for extension or supplementary protection, or challenging existing patents through legal procedures.

Q5: Why is claim drafting crucial in pharmaceutical patents like LTPA2019010?
A5: Precise claim drafting defines enforceable rights, balances breadth against vulnerability, and guides licensing or litigation strategies.


References

  1. European Patent Office, "Guidelines for Examination of Patent Applications," 2022.
  2. World Intellectual Property Organization, "Patent Landscape Reports," 2021.
  3. Lithuanian State Patent Bureau, official patent database, 2023.
  4. K. Smith, "Pharmaceutical Patent Strategy," Journal of Patent Law, 2020.
  5. EPO Patent Search Tools and Databases, 2023.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.