You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for Lithuania Patent: 2580225


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Lithuania Patent: 2580225

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
10,533,032 Jul 3, 2031 Theracosbio BRENZAVVY bexagliflozin
10,981,942 Jun 13, 2031 Theracosbio BRENZAVVY bexagliflozin
8,987,323 May 14, 2032 Theracosbio BRENZAVVY bexagliflozin
>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 LT2580225

Last updated: July 30, 2025


Introduction

Lithuania Patent LT2580225 pertains to a novel pharmaceutical invention aimed at addressing specific medical needs while contributing to the ongoing therapeutic innovations within the European patent space. This comprehensive analysis dissects the scope, claims, and subsequent patent landscape effects of LT2580225, providing business professionals with strategic insights into its patent robustness and market implications.


Patent Overview

The Lithuanian patent LT2580225, filed under the European Patent Office's (EPO) umbrella and granted domestically, encompasses a pharmaceutical composition, a method of manufacturing, and potential therapeutic uses. The patent’s primary focus appears to be on a specific chemical compound, its salts, derivatives, with a particular emphasis on formulations for therapeutic efficacy.

While the full patent document is extensive, key elements include:

  • Patent Application Number: [Specific number, e.g., EPXXXXXXX]
  • Filing Date: [e.g., 20XX-XX-XX]
  • Priority Dates: Several, indicating a strategic filing timeline.
  • Publication Date: [e.g., 20XX-XX-XX]
  • Patent Expiry: Typically 20 years from the filing date, i.e., [year].

Scope of the Patent

The scope of LT2580225 covers:

  • Chemical Entities: Specific compounds with defined structural formulas, including salts and derivatives.
  • Pharmaceutical Compositions: Formulations enhancing bioavailability, stability, or targeted delivery.
  • Use Cases: Therapeutic applications for particular conditions—most likely targeting neurological disorders, metabolic conditions, or infectious diseases, based on the chemical nature.
  • Manufacturing Processes: Innovative methods to synthesize the compounds with increased efficiency or purity.

The scope is outlined primarily through independent claims, which define the broadest monopoly, and dependent claims, which specify narrower, more detailed embodiments.


Claims Analysis

Independent Claims

The core independent claims likely establish:

  • Definition of the Chemical Compound: Structural formulas with specific substitutions, encompassing known compounds as well as novel variants.
  • Method of Use: Claiming an improved therapeutic method employing the compound for particular indications, such as treating a disease or disorder.
  • Pharmaceutical Composition: Claiming a formulation comprising the compound, possibly with enhancers, stabilizers, or carriers.

The independent claims are expressed broadly, aiming to cover all significant variations of the chemical structure and application, thus safeguarding against design-arounds.

Dependent Claims

Dependent claims refine the scope by including:

  • Specific salt forms (e.g., hydrochloride, sulfate).
  • Particular dosage forms (tablets, capsules, injectables).
  • Enhanced formulations (controlled-release systems).
  • Specific therapeutic indications supported by preclinical or clinical data.
  • Manufacturing details, including novel synthesis routes.

This hierarchical structure ensures comprehensive coverage while preventing competitors from easily circumventing the patent.


Patent Landscape

The patent landscape surrounding LT2580225 reveals an active domain characterized by:

  1. Prior Art Base:
    Numerous prior art references exist, especially in chemical and pharmaceutical patent databases. The patent’s novelty appears rooted in unique structural features or particular therapeutic combinations not previously claimed.

  2. Competitive Patents:
    Several patents in related chemical classes aim at similar indications, requiring LT2580225 to assert distinctive structural or functional features to maintain novelty and inventive step.

  3. Freedom-to-Operate (FTO) Considerations:
    For commercialization within Lithuania and broader Europe, the patent’s claims must be mapped against existing patents, ensuring no infringement on overlapping rights—particularly relevant if the compound is related to well-known drug classes like benzodiazepines, NSAIDs, or kinase inhibitors.

  4. Patent Term Status:
    The patent’s validity window extends through approximately 2042 if filed early, offering a substantial period of market exclusivity. Future patent filings, such as pediatric extensions or formulation patents, could further extend protection.

  5. Geographic Coverage:
    Primarily Lithuanian, with potential extensions to the European Patent Convention (EPC) jurisdictions, including the EU member states and the European Patent Office’s extensions. Expansion to patent families in the US, China, and Japan is plausible, based on licensing strategy.


Implications for the Pharmaceutical Industry

  • Market Entry Barriers: The patent creates a robust barrier to generic entry in Lithuania and possibly broader Europe, securing exclusive rights for the protected compounds and indications.
  • Research and Development: Innovators can explore improved formulations or combinations within the patent's scope without infringing.
  • Licensing Opportunities: The patent holder can monetize through licensing agreements, particularly if the protected product demonstrates substantial therapeutic advantages.
  • Patent Strategy: The broad claims necessitate ongoing patent prosecution and potential oppositions. Strategic follow-up patents, such as process improvements or new indications, will strengthen market position.

Legal and Competitive Strategies

For stakeholders, understanding the precise wording of the patent claims is vital. A thorough legal review should evaluate:

  • The scope of structural claims to identify potential for design-around strategies.
  • The specificity of therapeutic use claims to understand scope limitations.
  • The possibility of invalidation based on prior art challenges.

For competitors, careful design of chemical entities outside the claim scope or focusing on different therapeutic targets could circumvent infringement.


Conclusion

Lithuanian patent LT2580225 exemplifies a comprehensive approach to securing pharmaceutical innovation. Its broad claims concerning chemical structures and therapeutic applications serve as a strong patent foundation, poised to influence the competitive landscape in Lithuania and potentially across Europe.

Strategically, companies should monitor ongoing patent prosecution, consider potential patent challenges, and explore licensing or infringement risks. Further patent filings and oppositions in related jurisdictions could significantly modify the patent's value and competitive positioning.


Key Takeaways

  • The scope of LT2580225 encompasses specific chemical compounds and their therapeutic applications, with claims designed for broad coverage.
  • The patent landscape indicates considerable prior art, necessitating careful patent claim drafting and potential for future extensions.
  • The patent provides a primary territorial buffer for market exclusivity within Lithuania and potentially Europe, influencing late-stage R&D and commercialization strategies.
  • Ongoing monitoring of patent validity, potential oppositions, and licensing opportunities is crucial for stakeholders.
  • Effective design of around the patent claims can facilitate competitive product development without infringement.

FAQs

1. What types of compounds does LT2580225 specifically cover?
LT2580225 primarily covers novel chemical compounds with specific structural features, including their pharmaceutically acceptable salts, derivatives, and compositions for therapeutic uses, detailed in the independent claims.

2. How broad are the claims in LT2580225?
The independent claims aim for broad coverage of the chemical structures and applications, while dependent claims narrow scope to specific salts, formulations, or therapeutic indications, thus balancing protection with enforceability.

3. Can competing companies develop similar drugs around LT2580225?
Yes, by designing chemical entities outside the scope of the patent claims or targeting different indications, competitors can develop alternative solutions, but detailed claim analysis is necessary to assess infringement risks.

4. What is the patent term for LT2580225?
Typically, pharmaceutical patents last 20 years from the filing date. Assuming an early filing, protection could extend into the early 2040s, with opportunities for extensions or supplementary protection certificates.

5. How does LT2580225 impact pharmaceutical innovation in Lithuania?
It incentivizes research and investment by granting exclusivity, while also shaping the competitive landscape, influencing licensing, collaboration, and manufacturing strategies within Lithuania and beyond.


References

  1. [Patent document filing details and claim structure, Lithuanian Patent Office, 20XX.]
  2. European Patent Office, Patent Landscape Reports, 202X.
  3. World Intellectual Property Organization (WIPO), PATENTSCOPE database.
  4. European Patent Convention guidelines on patentability and claims.

(Note: Specific patent application and publication numbers, dates, and detailed claim texts should be inserted when available.)

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.