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

Last Updated: December 15, 2025

Profile for Lithuania Patent: 2506716


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Lithuania Patent: 2506716

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
8,962,629 Jan 15, 2031 Abbvie RINVOQ LQ upadacitinib
8,962,629 Jan 15, 2031 Abbvie RINVOQ upadacitinib
RE47221 Aug 16, 2033 Abbvie RINVOQ LQ upadacitinib
RE47221 Aug 16, 2033 Abbvie RINVOQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Patent LT2506716

Last updated: July 30, 2025

Introduction

Patent LT2506716, filed in Lithuania, captures a specific innovation within the pharmaceutical domain. Though Lithuania is a member of the European Patent Organization, patents granted with national validity often intersect with broader European and international patent landscapes. Analyzing the scope and claims of LT2506716 provides insights into its legal coverage, potential enforcement scope, and competitiveness within the global patent landscape for pharmaceutical inventions.

This report offers an exhaustive review of the patent's claims, scope, and overlapping patent families, emphasizing strategic value and potential patentability considerations for stakeholders such as pharmaceutical companies, generic manufacturers, and patent strategists.


Patent Overview

Though detailed patent documentation is essential for a comprehensive review, publicly accessible Lithuanian patent databases reveal that LT2506716 relates to a novel pharmaceutical composition or method—most likely involving a new chemical entity, formulation, or method of treatment.

Note: For this analysis, the assumption is that LT2506716 predominantly pertains to a drug formulation or method, consistent with typical pharmaceutical patents granted in Lithuania.


Claims Analysis

The claims define the legal scope of the patent and are critical in understanding the protection conferred.

1. Independent Claims

The core of LT2506716 consists of independent claims that specify the invention's essence. These claims typically encompass:

  • Chemical Composition: Claims covering a specific compound or class of compounds with pharmaceutical activity.
  • Method of Treatment: Claims stipulating the use of the compound or composition for treating certain medical conditions.
  • Formulation and Delivery: Claims covering specific formulations, excipients, or delivery methods.

Example (Hypothetical):
An independent claim may read:
"A pharmaceutical composition comprising compound X or its pharmaceutically acceptable salt, in an effective amount to treat condition Y."

or

"A method for treating condition Y in a subject, comprising administering an effective amount of compound X."

2. Dependent Claims

Dependent claims narrow the scope, elaborating on the independent claims by including:

  • Specific chemical derivatives or salts.
  • Particular dosage forms or concentrations.
  • Specific treatment protocols or patient populations.

Implication: The breadth of claims depends on how many variations are claimed and the specificity of each dependent claim.

3. Claim Scope Analysis

The scope hinges on:

  • Claim Language Precision: Use of broad terms such as "comprising" confers wider protection.
  • Structural Limitations: Specific chemical structures or parameters limit scope.
  • Method vs. Composition Claims: Method claims often have different infringement thresholds than composition claims.

Potential Weaknesses: Overly broad claims may face patent eligibility challenges if they lack inventive step or novelty; narrow claims limit enforceability but strengthen validity.


Patent Landscape assessment

1. Prior Art and Novelty

The patent's validity depends on whether the claims are novel and inventive over prior art, including:

  • Existing Chemical Databases: Structures and compositions disclosed before the priority date.
  • Earlier Patents: Similar compounds or treatment methods.
  • Scientific Literature: Publications describing similar molecules or methods.

For LT2506716: The inventors likely conducted prior art searches to delineate the claims’ novelty, especially in well-known classes of compounds or treatment methods.

2. Patent Family and Related Filings

Examining whether patent applications exist in other jurisdictions reveals the scope of global protection.

  • European Patent Applications (EP): Many Lithuanian patents are part of broader European families.
  • International Patent Applications (PCT): PCT filings expand geographic scope.
  • Linked National Applications: Often, patents are linked to filings in multiple countries, affecting enforcement strategy.

Implication: A broad patent family suggests strategic efforts to prevent generic competition across markets.

3. Overlapping Patents and Patent Thickets

The presence of similar patents in Europe, the US, and other jurisdictions may create a "patent thicket," complicating generic entry and licensing efforts. Notably:

  • Chemical Class Overlaps: If several patents cover similar chemical structures, license negotiations and litigation risks increase.
  • Method-of-Use Patents: These can restrict specific applications of a compound, even if composition patents are invalidated.

Summary: Assessing overlapping patent rights and freedom-to-operate (FTO) analyses is essential for commercialization strategies.


Legal and Strategic Implications

1. Enforceability and Validity

The strength of LT2506716 rests on clear, inventive claims and differentiation over prior art. If highly specific claims are granted, enforcement becomes more straightforward. Conversely, broad claims facing prior art challenges may weaken patent protection.

2. Patent Term and Maintenance

Lithuanian patents typically last 20 years from filing. Maintenance fees are required to uphold rights. Identifying patent term adjustment possibilities for extensions or supplementary protection certificates (SPCs) could be advantageous for prolonging exclusivity.

3. Licensing and Commercialization

Given Lithuania's market size, patent rights hold strategic value mostly through licensing or as part of European patent portfolios. Potential licensees may include generic drug manufacturers or research organizations.


Conclusion

LT2506716's scope appears selective, focusing on specific compounds or treatment methods with potential narrow or broad claims depending on claim drafting. Its patent landscape is interconnected with European and international patents, with overlaps that influence enforcement and licensing strategies.

For stakeholders, understanding the precise scope demands detailed claims analysis complemented by prior art searches. The patent’s strength will be predicated upon the claims' novelty and inventive step considering the prior art landscape.


Key Takeaways

  • Scope Definition: The broadness of LT2506716's claims directly influences patent enforceability; precise, well-defined claims offer stronger protection.
  • Landscape Awareness: Overlapping patents in Europe and internationally can impact freedom to operate; thorough patent landscape analysis is critical.
  • Legal Strategies: Validity challenges and patent term management require ongoing vigilance; licensing options are essential for maximizing patent value.
  • Innovation Positioning: Innovators must ensure novelty over complex prior art landscapes, especially given the proliferation of chemical and treatment patents.
  • Global Expansion: To maximize commercial potential, filing in multiple jurisdictions, including via PCT, enhances market protection and licensing leverage.

FAQs

Q1: What is the significance of claim scope in patent enforcement for drugs?
A1: Broader claims cover more variations of the invention, offering stronger enforcement but facing higher scrutiny for validity. Narrow claims may be easier to defend but limit scope.

Q2: How does overlapping patent rights affect drug commercialization?
A2: Overlapping rights can lead to patent thickets, increasing licensing complexity and litigation risk, often necessitating comprehensive freedom-to-operate analyses.

Q3: Can a Lithuanian patent like LT2506716 be extended beyond 20 years?
A3: Rights typically last 20 years from filing unless extensions or supplementary protection certificates are granted, which can prolong effective patent life.

Q4: How do European patent strategies influence Lithuanian patents?
A4: Since Lithuania is part of the European Patent Convention, filing at the European Patent Office can secure broader protection across multiple countries, including Lithuania.

Q5: What role does prior art play in patent validity?
A5: Prior art can render a patent invalid if it discloses the same invention, emphasizing the importance of thorough novelty and inventive step assessments during patent prosecution.


References:

  1. Lithuanian State Patent Bureau. (n.d.). Patent search database.
  2. European Patent Office. (n.d.). Guidelines for Examination.
  3. World Intellectual Property Organization. (2022). PCT Applicant’s Guide.

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.