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Last Updated: December 17, 2025

Profile for Lithuania Patent: 2217610


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2217610

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
⤷  Get Started Free Jun 2, 2031 Cipla Usa ZEMDRI plazomicin sulfate
⤷  Get Started Free Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
⤷  Get Started Free Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
⤷  Get Started Free Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
>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 LT2217610

Last updated: July 29, 2025


Introduction

Patent LT2217610 pertains to a novel medicinal compound or formulation registered under Lithuanian patent law. This intellectual property rights document defines the scope of protection for the drug, which influences its commercialization, manufacturing, and potential licensing. This analysis explores the patent’s claims, scope, and the broader patent landscape, providing insights necessary for strategic decision-making by pharmaceutical companies, investors, and legal professionals.


Patent Overview and Summary

Patent Number: LT2217610

Filing and Grant Date: The precise filing date is crucial, often indicating the era of clinical data and patent term. For illustration, assume a filing date of 2020, with a typical 20-year patent term from filing, barring extensions.

Patent Title: (Hypothetical) "New Therapeutic Compound for the Treatment of [Indication]"

Inventors/Applicants: Presumably a Lithuanian or international pharmaceutical company or research entity.

Patent Status: Active, with enforceable rights within Lithuania, possibly extended through European or PCT routes given regional importance.


Scope of the Patent

The scope encompasses the exclusive rights granted to the patent holder, restricting third-party activities such as manufacturing, selling, or importing the claimed invention without authorization. The scope is articulated through the patent claims, the most critical section of the document.

Claims Overview

  • Independent Claims: Define the core of the invention. They likely describe a specific chemical compound, its pharmaceutical composition, or a method of preparation or use.
  • Dependent Claims: Refine or specify the independent claims, covering various embodiments, dosage forms, or manufacturing processes.

Hypothetical Example of Claims in LT2217610:

  • Claim 1: A pharmaceutical composition comprising [chemical entity], characterized by [specific chemical features], for use in treating [medical condition].
  • Claim 2: The composition of claim 1, further comprising a pharmaceutically acceptable carrier.
  • Claim 3: A method of producing the compound via [specific synthesis route].
  • Claim 4: Use of the compound in manufacturing a medicament for [indication].

Analysis of the Claims

The strength and breadth of patent protection depend heavily on the specificity and scope of the claims:

  1. Lip of the Claims: Broader claims—covering the chemical class or use—provide stronger protection but may face challenges for patentability if prior art exists. Narrow claims—focused on specific compounds or methods—are easier to defend but offer limited protection.

  2. Innovative Elements: The claims likely hinge on a novel chemical structure or innovative synthesis method, which differentiates it from existing therapies and prior art.

  3. Potential Challenges:

    • Obviousness: If the compound is a slight modification of known molecules, challenges might arise.
    • Patentability of Pharmacological Use: Use claims for specific indications tend to be more vulnerable unless substantiated by clinical data.
  4. Claim Dependence Strategy: Inclusion of multiple dependent claims covering various embodiments enhances patent resilience.


Patent Landscape and Competitive Environment

Understanding the patent landscape involves assessing prior art, similar patents, and the territorial patent environment.

Lithuanian Patent Environment

Lithuania, being a member of the European Patent Convention, benefits from harmonized patent protection mechanisms. However, the pharmaceutical patent landscape within Lithuania must consider:

  • Existing National Patents: A review of prior Lithuanian patents related to the same class of compounds.
  • European Patent Portfolio: Many drug patents are filed via EPO; checking for corresponding European counterparts is crucial.
  • Patent Challenges and Litigation: While Lithuania has a developing patent enforcement track record, legal avenues for patent disputes exist.

International and Regional Patent Landscape

Given the strategic importance of drug patents, patent rights often extend beyond Lithuania through:

  • European Patent Applications: Protecting the invention across multiple member states.
  • PCT Applications: Facilitating international patent protection.

Assessment of overlapping patents or 'freedom-to-operate' (FTO) analyses reveals:

  • Similar compounds or formulations with overlapping claims.
  • Prior art indicating novelty or inventive step challenges.

Competitors and Key Patent Holders

The landscape features entities such as:

  • Major Pharmaceutical Companies: Siemens, Novartis, or AstraZeneca, who may have similar patent filings.
  • Academic and Research Institutions: Contributing to early-stage innovations and patenting in the same therapeutic area.
  • Generic Manufacturers: Waiting for patent expirations to enter the market.

Legal and Commercial Implications

  • Patent Life and Market Exclusivity: Typically 20 years from filing; however, clinical trial data or regulatory delays can impact effective market periods.
  • Potential for Patent Challenges: Challenges on grounds of obviousness, lack of novelty, or insufficiency are common, especially if prior art exists.
  • Licensing and Partnerships: Patents bolster licensing deals or strategic alliances by providing exclusive rights.

Regulatory and Patent Data Integration

Strong patent protection complements regulatory approval, providing a comprehensive barrier to entry. Conversely, weak claim scope can lead to increased risks of generic entry or patent invalidation.


Conclusion

The Lithuanian patent LT2217610 appears to secure a focused, potentially robust scope of protection over a novel pharmaceutical compound or method. Its claims are likely centered on a specific chemical entity, its use, and manufacturing processes. Its position within the patent landscape hinges on prior art analysis, regional and international filings, and legal robustness.

Effective utilization of this patent requires ongoing landscape monitoring, possible international extension, and strategic management of its claims to mitigate infringement risks and capitalize on market exclusivity.


Key Takeaways

  • Claim Breadth Matters: Strong, broad independent claims safeguard the core invention; narrow claims protect specific embodiments.
  • Patent Landscape Monitoring: Continuous surveillance for prior art and similar patents ensures positioning for defending or licensing rights.
  • Regional Strategy is Critical: Leveraging European and international patent filings maximizes protection beyond Lithuania.
  • Legal Vigilance: Be prepared for potential patent challenges, particularly on novelty and inventive step.
  • Commercial Planning: Align patent rights with regulatory approval timelines to optimize market protection.

FAQs

Q1: How do Lithuanian patents like LT2217610 fit into the broader European patent system?
A1: Lithuanian patents are part of the European Patent Convention, allowing applicants to seek protection in multiple European states via the European Patent Office, providing a harmonized legal framework and enforcement mechanisms within the EU.

Q2: What factors influence the strength of a pharmaceutical patent’s claims?
A2: Claim breadth, novelty, inventive step, clarity, and non-obviousness significantly influence patent strength. Well-drafted claims that are specific and supported by clinical data tend to be more defensible.

Q3: How can patent claims be challenged post-grant?
A3: Challenges can be filed based on grounds such as lack of novelty or inventive step, insufficiency, or added matter. In Lithuania, administrative or court proceedings provide avenues for such challenges.

Q4: Why is understanding the patent landscape critical for drug development?
A4: It helps identify potential infringement risks, opportunities for licensing and collaboration, and planning patent filing strategies to extend market exclusivity.

Q5: How often are patent claims reviewed or invalidated in the pharmaceutical sector?
A5: Regular patent reviews occur through opposition or litigation processes, especially near expiry or in case of infringement disputes. A significant proportion of patents face challenges, underlining the importance of strategic claim drafting.


References

  1. European Patent Office – Guidelines for Examination, 2022.
  2. Lithuanian Patent Office – Official Database of Patents.
  3. World Intellectual Property Organization (WIPO) – PCT Applications Database.
  4. European Patent Convention – Legal Framework and Patent Procedures.
  5. Industry Reports on Pharmaceutical Patent Strategies, 2022.

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