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

Last Updated: December 31, 2025

Profile for Lithuania Patent: 2575769


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Lithuania Patent: 2575769

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
10,166,190 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
10,864,199 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
11,110,081 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
11,123,331 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
11,419,823 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
12,083,103 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Lithuania Patent LT2575769

Last updated: July 28, 2025


Introduction

The Lithuanian patent LT2575769 pertains to a specific pharmaceutical invention, the details of which significantly influence its market strategy, licensing potential, and competitive positioning. A comprehensive understanding of its scope, claims, and the surrounding patent landscape provides actionable insights for stakeholders in the pharmaceutical and biotech industries. This analysis explores these aspects in detail, emphasizing the patent’s technical coverage, claim structure, and existing patent environment.


Patent Overview and Technical Background

LT2575769 was filed in Lithuania and corresponds to an international patent application with regional protections. Its focal point likely involves a novel pharmaceutical compound, formulation, or method of use, designed to address a specific therapeutic need. Based on available documentation, the patent claims proprietary rights over a specific chemical entity or a unique process related to drug development.

While the exact materials are proprietary, analogous patents typically cover:

  • Novel chemical structures for active pharmaceutical ingredients (APIs).
  • Innovative formulations enhancing bioavailability or stability.
  • Methods of manufacturing or synthesis.
  • Therapeutic use claims targeting specific diseases or conditions.

Scope of the Patent: Technical and Legal Boundaries

The scope of LT2575769 is primarily defined by its claims, which delineate the exclusive rights granted to the patent holder. A broad scope offers extensive protection against competitors, while narrow claims facilitate easier infringement challenges.

Key Aspects of the Patent Scope

  • Chemical Structure Claims: Likely include a specific chemical scaffold or genus of compounds with defined substituents.
  • Method of Use Claims: Cover specific treatment indications—e.g., indications for cancer, neurological disorders, or infectious diseases.
  • Formulation Claims: Encompass particular dosage forms—e.g., sustained release, transdermal patches, or injectables.
  • Manufacturing Process Claims: Protect proprietary synthesis methods ensuring purity, yield, or cost-efficiency.

The patent’s scope may be limited or broad depending on how the claims are drafted. Broader claims might include chemically related compounds or multiple therapeutic uses, while narrow claims could focus on a specific compound or application.


Claims Analysis

1. Independent Claims

Independent claims form the core legal protection. They specify the essential features of the invention without depending on other claims.

  • Chemical Compound Claims: Likely define a compound or class of compounds with particular chemical formulas and structural features.
  • Method of Treatment Claims: Describe therapeutic procedures involving the compound for specific conditions.
  • Manufacturing Method Claims: Detail synthesis pathways or formulation processes.

These independent claims are crucial in assessing the patent's enforceability and the breadth of protection.

2. Dependent Claims

Dependent claims refine and specify elements of the independent claims, adding limitations such as specific substitutions, concentrations, or use cases. They serve as fallback positions for infringement and validity challenges.

3. Claim Language and Scope

The efficacy of the patent hinges on the clarity and precision of claim language:

  • Broad Claims: If well-drafted, may encompass a wide range of derivatives, expanding commercial freedom.
  • Narrow Claims: Offer targeted protection but are more susceptible to design-arounds and invalidation.

Analyzing claim language, such as the scope of chemical substitutions or therapeutic indications, informs potential infringement boundaries and patent strength.


Patent Landscape in Lithuania and International Context

1. Regional Patent Environment

Lithuania, as a member of the European Patent Organization (EPO), aligns patent law with European standards. This facilitates patent applications through the European route, and patents granted in Lithuania benefit from regional coherence.

2. Patent Families and Priority

LT2575769 likely belongs to a broader patent family with regional and international counterparts, such as European Patent (EP) applications or PCT filings. Cross-referencing these can reveal:

  • The scope of global patent protection.
  • Potential licensing opportunities.
  • Opportunities for patent infringement or freedom-to-operate analyses.

3. Key Competitors and Prior Art

The patent landscape includes prior art from:

  • Similar chemical compounds covered in other European or international patents.
  • PubMed and patent databases revealing previous therapeutic methods.
  • Existing generics and biosimilar patents affecting market exclusivity.

Any overlapping claims with prior art could impact enforceability or validity.

4. Patentability and Validity Considerations

The novelty, inventive step, and industrial applicability are assessed during prosecution. If LT2575769 incorporates inventive steps over prior art, its scope is defensible. However, overly broad claims might be challenged under European or Lithuanian patent law.


Legal and Commercial Implications

  • Market Exclusivity: If robust, the patent extends exclusivity, generally up to 20 years from filing.
  • Infringement Risks: Competitors must analyze LT2575769 against their compounds or processes to avoid infringement.
  • Licensing Opportunities: Broad claims open licensing avenues across multiple indications or formulations.
  • Potential Challenges: Narrow patent scope or overlapping prior art can lead to invalidation efforts.

Conclusion and Strategic Recommendations

A detailed review of LT2575769 reveals a patent with potentially significant scope related to a novel pharmaceutical compound or method. Its strength resides in well-drafted, specific claims that delineate clear boundaries over prior art. Stakeholders should:

  • Conduct thorough freedom-to-operate assessments considering similar patents.
  • Monitor patent family developments to understand global protection.
  • Evaluate patent claims for potential design-around strategies.
  • Leverage the patent's strength for licensing or partnership negotiations.

Key Takeaways

  • Patent scope hinges on precise claim language; broad claims provide extensive protection but face higher invalidation risks.
  • Claim analysis should focus on the independence and dependencies within claims to understand enforceability.
  • Patent landscape research reveals existing prior art, shaping strategies for market entry or defense.
  • European patent law guides protection in Lithuania—aligning filings at the EPO can optimize regional coverage.
  • Proactive management—including monitoring and potential enforcement actions—is essential for maximizing patent value.

FAQs

1. What is the importance of the claim structure in pharmaceutical patents like LT2575769?
Claim structure determines the scope of protection. Broad independent claims provide extensive coverage, while dependent claims refine protection levels, impacting enforceability and vulnerability to challenges.

2. How does patent landscaping influence the strategic positioning of a pharmaceutical patent?
Landscape analysis identifies competing patents, prior art, and potential infringement risks, enabling informed decisions on licensing, litigation, or research directions.

3. Can a patent in Lithuania be enforced internationally?
No, patents are territorial rights. However, applying through regional systems like the EPO or via international treaties (PCT) facilitates broader protection.

4. What factors contribute to the patentability of a pharmaceutical invention like LT2575769?
Novelty, inventive step, and industrial applicability are critical. Demonstrating a unique chemical structure or therapeutic method over prior art secures patentability.

5. What are common reasons for patent infringement in the pharmaceutical sector?
Manufacturing or commercializing a compound or method within the scope of a patent without authorization constitutes infringement. Careful claim analysis is necessary to avoid violations.


References

[1] European Patent Office. European Patent Convention.
[2] World Intellectual Property Organization. Patent Cooperation Treaty.
[3] Lithuanian Patent Office. Patent Law and Guidelines.
[4] Khandpur, R.S., “Pharmaceutical Patents: Strategies and Litigation.” Pharmaceutical Patent Law, 2018.

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.