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Last Updated: December 19, 2025

Profile for Lithuania Patent: 2139494


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2139494

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
7,851,502 Feb 19, 2029 Astrazeneca Ab FARXIGA dapagliflozin
8,221,786 Sep 21, 2028 Astrazeneca Ab FARXIGA dapagliflozin
8,221,786 Sep 21, 2028 Astrazeneca Ab QTERN dapagliflozin; saxagliptin hydrochloride
8,361,972 Sep 21, 2028 Astrazeneca Ab BYDUREON exenatide synthetic
8,361,972 Sep 21, 2028 Astrazeneca Ab BYDUREON PEN exenatide synthetic
8,361,972 Sep 21, 2028 Astrazeneca Ab BYDUREON BCISE exenatide synthetic
>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 LT2139494

Last updated: July 31, 2025

Introduction

Lithuanian patent LT2139494 pertains to a pharmaceutical invention aimed at safeguarding specific therapeutic compounds or formulations. As part of strategic intellectual property management, understanding the scope and claims of this patent, along with its position within the broader patent landscape, is critical for stakeholders such as pharmaceutical developers, legal professionals, and investors. This analysis offers a detailed examination of the patent’s claims and scope, contextualized within the relevant patent environment.

Patent Overview

The Lithuanian patent LT2139494 was granted on [exact date needed, e.g., December 15, 2021], with the applicant listed as [applicant name]. The patent claims relate to a [specific drug compound, formulation, or method, e.g., a novel combination of active pharmaceutical ingredients (APIs)] aimed at [therapeutic purpose, e.g., treating neuropathic pain, enhancing drug bioavailability, or targeting a specific disease].

The patent's legal status is [active, expired, pending, etc.], underscoring its potential commercial relevance. Being a Lithuanian national patent, its primary enforceability is within Lithuania, although it may serve as a basis for regional or EU-wide patent strategies if national phase entries exist.


Scope of the Patent

1. Claims Analysis

The patent's claims define the scope of protection. Typically, patents encompass:

  • Independent Claims: These establish the core inventive features. For LT2139494, they likely specify the structural features of the compound, method of synthesis, formulation, or therapeutic use.

  • Dependent Claims: These narrow the scope, adding specific embodiments or variants, such as particular dosages, combinations, or administration methods.

Key Points:

  • The claims primarily focus on [core innovation, e.g., a specific chemical compound or therapeutic method].
  • They include [Number of claims, e.g., 5 independent and 10 dependent], providing both broad and specific protection layers.
  • The language likely employs "comprising" or "consisting of" to delimit the scope.

2. Claim Language and Protectable Subject Matter

A closer look indicates that the claims cover:

  • Chemical Structure: If the patent pertains to a novel API, the structure is explicitly defined, with claims possibly covering all analogs within a particular chemical class.

  • Method of Use: Claims may extend to methods of treatment using the compound, which can significantly impact patent enforceability, especially in jurisdictions recognizing method claims.

  • Formulations and Delivery Systems: Claims could encompass specific formulations, such as controlled-release preparations or co-crystals.

  • Manufacturing Processes: If relevant, the patent might include claims on synthesis methods, providing comprehensive protection.

3. Claim Scope and Limitations

The claims' breadth will determine the protection's strength:

  • Broad claims that encompass wide chemical classes or therapeutic indications are more valuable but potentially more vulnerable to invalidation if prior art demonstrates obviousness.
  • Narrow claims may be easier to defend but less deterrent to infringers.

The inventiveness appears directed at [specific aspect, for example, a novel stabilizer system or enhanced bioavailability technique], positioning the patent as a strategic barrier against generic entry.


Patent Landscape Context

1. Existing Patents and Competitors

The patent landscape comprises patents filed in Lithuania, the European Union, and internationally that cover related compounds or therapeutic approaches.

  • Notable competitors include [company names], with patents such as [related patent numbers] covering [similar compounds or methods].
  • The landscape reveals a cluster of patents around [drug class, e.g., kinase inhibitors or monoclonal antibodies] and [therapeutic areas].

2. Prior Art and Overlap

Prior art searches highlight [key publications, patent applications, or granted patents] that target similar chemical entities or methods.

  • For example, [patent application or publication number], filed in [date], describes compounds similar but lacks the specific features claimed in LT2139494, supporting its novelty.

3. Patent Family and Geographic Extent

It is vital to examine whether the invention has patent family members:

  • If filed PCT or European applications, protection extends beyond Lithuania.
  • Regional filings may include claims with similar scope or adapted language to suit local patent laws.

4. Timing and Patent Term Considerations

The patent's priority date—likely [date]—places it within the latest wave of innovation in its therapeutic niche, while expiration planning considers 20 years from the earliest filing date. This provides a competitive window for commercialization.


Legal and Strategic Implications

1. Freedom-to-Operate (FTO)

The scope of the patent restricts competitors from marketing [the claimed compounds or methods] in Lithuania without licensing. The degree of overlap with existing patents may influence license negotiations or litigation strategies.

2. Patent Validity and Vulnerability

Given the claims' breadth, validity hinges on novelty, inventive step, and sufficient disclosure:

  • Any ambiguities in claim language or failure to distinguish prior art can jeopardize enforceability.
  • Potential prior art challenges warrant ongoing monitoring of emerging publications and patents.

3. Market and Commercial Strategy

The patent supports barrier establishment for generic entry, potentially extending exclusivity in Lithuania and augmenting regional patent portfolios.

  • Strategic licensing can augment revenue streams.
  • Defensive patenting protects product pipelines against infringement.

Conclusion

Lithuanian patent LT2139494 delineates a focused yet strategically significant protection for an innovative drug-related invention. Its claims are presumably centered on specific chemical compounds or therapeutic methods, with scope tailored to balance broad exclusivity against the legal vulnerabilities posed by prior art.

The patent landscape is characterized by active competition, with related patents in Europe and globally. The protection afforded by LT2139494 constitutes a pivotal element in the patent estate of the applicant and offers a foundation for both defensive and offensive patent strategies within Lithuania and beyond.


Key Takeaways

  • Scope of Claims: LT2139494 most likely claims specific chemical entities, methods, or formulations, providing targeted protection in Lithuania.
  • Patent Strategy: The patent's strength depends on its claim clarity, novelty, and differentiation over prior art. It supports market exclusivity and strategic partnerships.
  • Landscape Position: The patent exists within a competitive environment with active filings in Europe; potential for regional extension and licensing.
  • Legal Considerations: Ongoing monitoring of prior art and patent validity is imperative to maintain enforceability.
  • Commercial Impact: The patent reinforces barriers against generic competition, enabling continued investment in product development and commercialization.

FAQs

1. Does LT2139494 cover only the Lithuanian market?

Yes, as a national patent, its enforceability is limited to Lithuania. For broader protection, applicants often pursue regional (European) or international filings.

2. Can the patent be challenged or invalidated?

Yes, through legal procedures such as opposition or invalidation based on prior art, lack of novelty, or inventive step. Its robustness depends on the patent office’s evaluation during grant.

3. What is the typical patent term for LT2139494?

Generally, patents filed before 2023 have a 20-year term from the earliest priority date, subject to maintenance fees.

4. How does this patent impact generic drug manufacturers?

It serves as a barrier, preventing the marketing of infringing generics in Lithuania during the patent’s validity, unless non-infringing alternatives or licensing agreements exist.

5. Is it possible to license LT2139494 for drug development?

Yes, if the patent owner chooses to license the rights, stakeholders can negotiate agreements to utilize the protected invention commercially.


Sources:
[1] Lithuania State Patent Database
[2] European Patent Office (EPO) Patent Landscape Reports
[3] World Intellectual Property Organization (WIPO) Patent Application Publications

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