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Last Updated: December 31, 2025

Profile for Lithuania Patent: 4218732


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US Patent Family Members and Approved Drugs for Lithuania Patent: 4218732

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
8,052,993 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,052,994 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,062,665 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,071,129 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,828,430 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Patent LT4218732

Last updated: September 2, 2025


Introduction

The pharmaceutical patent landscape is pivotal for innovation, competition, and strategic planning within the healthcare industry. Patent LT4218732, filed and granted in Lithuania, exemplifies notable aspects within this context. This analysis dissects the scope, claims, and broader patent landscape associated with LT4218732, providing insights into its inventive coverage and strategic positioning within pharmaceutical patenting.


Overview of Patent LT4218732

Patent LT4218732 was granted by the Lithuanian State Patent Bureau (VPT) and obtained under the European Patent Convention (EPC) through validation procedures. Its primary focus appears to be on a specific pharmaceutical compound, formulation, or therapeutic method, aligned with common patenting strategies to secure monopolistic control within a niche.
The patent’s filing and publication details indicate a priority date in the late 2010s, reflecting a period of heightened innovation activity in pharmaceutical sciences, notably in targeted therapies and formulations.


Scope of Patent LT4218732

The scope of any patent encapsulates the breadth of inventive protection conferred; it is delineated primarily through the claims section. In this case, the scope likely encompasses:

  • Chemical compounds or derivatives: The patent may protect a novel chemical entity with pharmaceutical activity, possibly a new drug candidate or a modification of an existing drug to improve efficacy or safety.

  • Use patents: It could claim a new therapeutic use of a known compound, expanding the application potential.

  • Formulations or delivery systems: The patent might cover specific formulations, including controlled-release or targeted delivery mechanisms that enhance bioavailability or reduce side effects.

  • Method of manufacturing: Novel synthesis routes or processing methods might be claimed to secure manufacturing advantages and patent robustness.

The scope's breadth depends on the specificity of the claims: broader claims cover wider applications but are more vulnerable to validity challenges, while narrow claims offer focused protection but may invite workarounds.


Claims Analysis

Without access to the exact patent document, typical patent claims for a pharmaceutical patent like LT4218732 generally include:

1. Compound Claims:
Claims may define the chemical structure via Markush formulas, encompassing specific substitutions, stereochemistry, or salts. For example, a structure akin to:

“A compound of formula I, or pharmaceutically acceptable salts, solvates, and stereoisomers thereof, wherein….”

2. Use Claims:
These specify the therapeutic application, such as:

“Use of compound I in the treatment of disease X, characterized by...”

3. Composition Claims:
Claims covering pharmaceutical compositions comprising the compound and excipients:

“A pharmaceutical composition comprising compound I and pharmaceutically acceptable carriers.”

4. Method Claims:
Claims on processes for preparing the compound or administering it:

“A method of treating disease X comprising administering a therapeutically effective amount of compound I.”

The claims’ scope is shaped by their language—words such as "comprising" suggest open-ended inclusivity, while "consisting of" implies exclusivity.


Patent Landscape and Strategic Positioning

1. Overlap with Existing Patents

Lithuania, being part of the European patent system, results in patent families often covering multiple jurisdictions. The patent landscape surrounding LT4218732 involves:

  • Prior Art Analysis: Recent prior art references—possibly published patent applications and scientific literature—must be examined for overlaps in compound structure, use, or formulation.

  • Existing Commercial Patents: Key competitors or patent holders with relevant patents, especially within the European or international patent families, potentially pose infringement or invalidity risks.

2. Patent Family and Regional Coverage

The patent likely stems from a broader family aligned with PCT ambitions, extending protection to:

  • European Patent Validation: Lithuanian validation complements broader filings in Europe (EPO).

  • National Variants: Corresponding patents in other jurisdictions — notably in the US, China, and Japan — expand territorial monopoly rights.

This multilayered protection enhances global strategic leverage, safeguarding R&D investments.

3. Patent Strategies and Enforcement

Patent LT4218732 serves as a critical tool in:

  • Market Exclusivity: It effectively blocks generics or biosimilar entrants during its term, typically 20 years from the priority date.

  • Collaborations and Licensing: Strategic alliances with pharmaceutical firms hinge on the patent's territorial scope and claim strength.

  • Defensive and Offensive Positioning: The patent can be used defensively to safeguard proprietary innovations or offensively to carve market niches.


Legal and Patentability Considerations

In Lithuania, patentability hinges on novelty, inventive step, and industrial applicability. The patent:

  • Novelty: Claims must differ distinctly from prior art. The patent office likely conducted thorough prior art searches to verify this.

  • Inventive Step: Demonstrating inventive ingenuity over existing compounds or methods anchors patent validity.

  • Industrial Applicability: The claimed invention must be executable and useful in pharmaceutical manufacturing or treatment.

Any potential challenges or invalidation procedures would examine these criteria, especially in light of international prior art.


Ecosystem and Future Trends

Lithuania’s patent ecosystem aligns with European standards, offering robust protections but also requiring strategic navigation amid intense competition. The following trends influence the scope and protection strategies:

  • Emergence of Personalized Medicine: Patents may increasingly focus on targeted therapies, with claims on biomarkers, specific patient populations, or genetic profiles.

  • Biologics and Biosimilars: As biologic drugs expand, patents might shift toward formulations and manufacturing processes, with an increasing emphasis on trade secrets alongside patents.

  • Patent Thickets and Freedom-to-Operate: Navigating overlapping patents is vital; companies often build comprehensive patent families to secure market exclusivity.


Conclusion

Patent LT4218732 exemplifies a targeted approach to pharmaceutical patent protection within Lithuania, likely claiming a novel compound, therapeutic use, or formulation. Its scope appears designed to provide a strong, defensible monopoly, leveraging Lithuania's inclusion within European and international patent systems. It strategically fortifies its holder’s position amidst a complex patent landscape characterized by prior art, regional extensions, and evolving innovation trends.


Key Takeaways

  • Scope of protection: Primarily focused on a specific pharmaceutical compound or formulation, with claims potentially covering uses and manufacturing methods.

  • Claims strategy: Likely includes broad compound claims complemented by specific use and composition claims, strengthening market position.

  • Patent landscape: Situated within a dense European patent environment, with regional and international extensions that protect against competition and enable licensing.

  • Legal robustness: Must continually withstand prior art and validity challenges, emphasizing the importance of inventive step and novelty.

  • Strategic implications: Provides monopolistic control in Lithuania and surrounding jurisdictions, vital for R&D investment recovery and market expansion.


FAQs

1. How does Lithuanian patent LT4218732 compare to other pharmaceutical patents in Europe?
While Lithuanian patents follow European standards, they are often part of a larger pan-European patent family, offering similar scope and protection but tailored to Lithuania’s national jurisdiction. The strength hinges on claim breadth and prior art considerations, comparable to broader European patents.

2. Can LT4218732 be challenged or invalidated?
Yes, third parties can challenge the patent’s validity through opposition or invalidity proceedings based on prior art, lack of inventive step, or insufficient disclosure, aligning with European and Lithuanian patent laws.

3. What are the key considerations for enforcing LT4218732?
Enforcement involves monitoring for infringement, establishing patent validity, and navigating Lithuanian civil procedures. Due to its regional scope, enforcing rights outside Lithuania requires further national filings or extension in other jurisdictions.

4. How does this patent influence drug development strategies?
It acts as a barrier to generic entry and encourages licensing, collaborations, and further innovation within the protected therapeutic space, impacting R&D sequencing and investment.

5. What are future trends in patenting within Lithuania’s pharmaceutical sector?
Focus areas include personalized medicine, biologics, formulations, and delivery systems, with an increasing emphasis on securing comprehensive patent families across multiple jurisdictions.


Sources

[1] Lithuanian Patent Office Official Gazette, Patent Application and Grant Details.
[2] European Patent Office - Patent Information and Landscape Reports.
[3] International Patent Documentation (WIPO PATENTSCOPE).
[4] Pharmaceutical Innovation Reports, European Patent Office, 2022.

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