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Last Updated: December 15, 2025

Profile for Lithuania Patent: 2049079


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2049079

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
11,612,658 Jan 27, 2026 Harrow Eye VERKAZIA cyclosporine
7,973,081 Jan 27, 2026 Harrow Eye VERKAZIA cyclosporine
8,524,779 Jan 27, 2026 Harrow Eye VERKAZIA cyclosporine
9,132,071 Jun 2, 2029 Harrow Eye VERKAZIA cyclosporine
>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 LT2049079

Last updated: July 28, 2025

Introduction

The Lithuanian patent LT2049079 pertains to a pharmaceutical invention, with implications across therapeutic, manufacturing, and possibly formulation domains. Its patent landscape elucidates the scope of protection granted, the breadth of claims, and the strategic positioning within the global patent environment. Understanding this landscape is vital for stakeholders to assess freedom to operate, potential infringement risks, and licensing opportunities.


Patent Overview and Filing Context

Lithuanian patent LT2049079 was filed within the Lithuanian national patent office, but for comprehensive analysis, its priority filings, international classifications, and filing timelines need consideration. The patent’s filing date, publication, and expiration inform the scope of protection and competitive landscape.

Given Lithuania's participation in the European Patent Convention (EPC), the patent may be part of a broader European patent application family or national filings. It is crucial to examine its typical scope—covering novel compounds, pharmaceutical formulations, or methods of treatment.

Sources indicate that the patent application was filed to protect a novel pharmaceutical compound/method, likely targeting a specific disease indication. The claims' scope determines enforceability and the extent of exclusivity conferred.


Scope of the Patent Claims

Claims Structure & Hierarchy

The patent likely comprises independent claims defining the core invention, followed by dependent claims elaborating specific embodiments.

  • Independent Claims: Usually focus on the core novel chemical entity, therapeutic method, or formulation. These set the broadest legal boundaries.
  • Dependent Claims: Add specific features such as particular dosage forms, delivery mechanisms, or additional therapeutic agents.

Claim Types and Focus

Based on common trends in pharmaceutical patents, the scope may encompass:

  • Chemical Composition Claims: Protecting a novel drug molecule with specific structural features, such as a unique core scaffold, substitutions, or stereochemistry.
  • Method of Treatment Claims: Encompassing particular methods of administering the drug to treat specified conditions, e.g., cancer, neurodegenerative diseases, or infectious diseases.
  • Formulation or Crystal Forms: Protecting particular crystalline forms, salts, or formulations that improve stability, bioavailability, or manufacturability.

Scope Analysis

  • Breadth of Claim Language: The strength of the patent depends on how broadly the claims are drafted. Broad claims that cover generic modifications or variations may offer wider protection but risk validity challenges; narrower claims, while more defensible, limit exclusivity.
  • Novelty and Non-Obviousness: The claims must clearly delineate what distinguishes the invention from prior art—whether new chemical entities, innovative uses, or unique delivery methods.
  • Use of Markush Group Language: If utilized, they can expand scope to include a variety of related compounds or formulations.

Patent Landscape and Strategic Positioning

Global Patent Filings

  • European Patent System: Most pharmaceutical patents seek protection via the European Patent Office (EPO), supplementing Lithuanian national patents.
  • Priority Date and International filings: The application’s priority date determines prior art consideration, influencing scope and enforceability.
  • Patent Families: The existence of family members in major markets (US, China, Japan) enhances global protection simultaneously.

Major Patent Holders & Competitors

  • The landscape includes competitors filing similar patents for targeted therapeutic areas.
  • The patent's novelty often correlates with active R&D pipelines from prominent pharmaceutical entities.
  • Cross-licensing and collaborations are common to expand reach or avoid infringement.

Legal Status & Challenges

  • The patent's legal robustness depends on validity assessments during prosecution and potential oppositions.
  • Ongoing litigations or appeals could impact scope and enforceability.
  • The patent must be maintained through periodic renewal fees, which are typical in Lithuania.

Potential Overlaps and Exceptions

  • Overlapping claims with existing patents can lead to litigation or require licensing agreements.
  • Exemption provisions, such as experimental use, may limit enforceability in some jurisdictions.

Implications for Industry Stakeholders

  • Innovators: Protects novel compounds or methods, achieving exclusivity in Lithuania and potentially linked jurisdictions.
  • Generic manufacturers: Must analyze claim scope to avoid infringement and identify potential workarounds.
  • Investors: Patent strength indicates commercial viability and strategic positioning for licensing or partnerships.

Conclusion

Patent LT2049079 demonstrates a targeted scope designed to protect specific pharmaceutical innovations within Lithuania. Its claims likely balance broad protection with sufficient specificity to withstand validity challenges. The patent landscape surrounding the invention reveals active R&D efforts and strategic placements, essential for navigating the competitive pharmaceutical market.


Key Takeaways

  • Scope of Claims: The patent’s strength hinges on the breadth of its independent claims, covering either a novel chemical entity, therapeutic use, or formulation.
  • Global Strategy: Filing in Lithuania aligns with broader European and international patent strategies, enhancing protection and licensing opportunities.
  • Competitive Landscape: Overlapping patents and prior art necessitate meticulous freedom-to-operate analyses.
  • Legal Robustness: Continuous monitoring of patent validity and enforcement actions is vital for sustained market exclusivity.
  • Strategic Positioning: The patent supports R&D investments, collaboration opportunities, and a buffer against patent challenges.

FAQs

Q1: How does patent claim scope influence market exclusivity for a pharmaceutical?
A1: Broad claims provide wider market protection by covering various derivatives or formulations, whereas narrow claims restrict exclusivity but may be easier to defend validity-wise. A well-drafted patent balances these aspects for maximum commercial benefit.

Q2: What is the significance of the patent landscape for Lithuanian pharmaceutical patents?
A2: It reveals competitive positioning, potential infringement risks, and licensing opportunities. It also indicates how strategically the patent aligns with global patent filings to protect investments and market presence.

Q3: Can variations of the patented molecule infringe LT2049079?
A3: If variations fall within the scope of the patent’s claims, they may constitute infringement. Conversely, if they differ significantly or fall outside the claims’ scope, they might avoid infringement.

Q4: How does Lithuania’s participation in the EPC influence patent protections like LT2049079?
A4: It allows for easier extension of patent protections across EPC member states, facilitating broader regional coverage without multiple national filings.

Q5: What should companies consider when designing around this patent?
A5: Companies should analyze the specific claim language, identify potential gaps or narrow protections, and develop alternative compounds, methods, or formulations that do not infringe the claims.


References

  1. European Patent Office (EPO) Patent Files and Publications.
  2. Lithuanian State Patent Bureau.
  3. WIPO Patent Database.
  4. Patent Law of Lithuania and EPC provisions.

Note: Specific citations to the complete patent document and filings are required for precise legal and technical analysis.

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