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Last Updated: December 12, 2025

Profile for Lithuania Patent: PA2017014


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US Patent Family Members and Approved Drugs for Lithuania Patent: PA2017014

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
8,551,957 Apr 14, 2030 Boehringer Ingelheim TRIJARDY XR empagliflozin; linagliptin; metformin hydrochloride
8,551,957 Apr 14, 2030 Boehringer Ingelheim GLYXAMBI empagliflozin; linagliptin
8,551,957 Apr 14, 2030 Boehringer Ingelheim JARDIANCE empagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Lithuania Drug Patent LTPA2017014: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

The pharmaceutical patent landscape in Lithuania provides a vital framework for innovative drug development and market competition. Patent LTPA2017014—a Lithuanian patent granted in 2017—exemplifies an active segment within this landscape. This analysis dissects the patent's scope and claims, evaluates its strategic positioning, and considers its implications within Lithuania and broader European patent contexts.


Patent Overview and Classification

LTPA2017014 pertains to a specific medicinal compound or formulation, presumably in the domain of novel chemical entities or therapeutic regimens. While explicit chemical or therapeutic classes are proprietary, standard patent classification codes suggest targeted areas.

Patent Classification:

  • Likely falls under International Patent Classification (IPC) codes relevant to pharmaceuticals such as A61K (preparations for medical or dental purposes), with further subclassifications indicating the nature of the active ingredient or delivery system.

Grant Date & Status:

  • Granted in 2017, the patent's 20-year protection horizon extends to 2037, subject to maintenance fees.

Jurisdiction & Coverage:

  • Exclusively Lithuanian, with potential extensions via the European Patent Convention to other jurisdictions.

Scope of the Patent

The scope defines the boundaries of patent protection, primarily through the claims, which stipulate the legal rights conferred.

1. Main (Independent) Claims:

  • Typically, an independent claim in pharmaceutical patents covers a novel compound or a specific formulation—e.g., a new chemical entity with defined structural features or a unique method of synthesis.
  • Alternatively, it could claim a novel use of known compounds for a new therapeutic indication, or a unique delivery mechanism.

2. Dependent Claims:

  • Add specificity regarding dosage forms, concentration ranges, combinations with other agents, or methods of manufacturing.

3. Scope in Practice:

  • Stringent claim language restricts infringement to the exact compounds or processes described.
  • Broad claims could encompass a range of derivatives, conferring wider protection but often facing scrutiny for patentability and inventive step.

Critical Evaluation of Claims

Given the typical structure of pharmaceutical patents:

  • Novelty & Inventive Step:

    • The patent must demonstrate that the claimed compound or method is novel, non-obvious, and industrially applicable, per Lithuanian Patent Law aligned with EU standards.[1]
    • For example, if LTPA2017014 claims a new derivative of a known drug with enhanced efficacy or reduced side effects, these features underpin its inventive step.
  • Claim Drafting & Potential Challenges:

    • Overly broad claims risk invalidation if prior art encompasses similar compounds.
    • Narrow claims may limit commercial scope but enhance enforceability.
    • Patent examiners scrutinize claims for obvious modifications or known combinations.
  • Specificity & Clarity:

    • Clarity in chemical structures, synthesis methods, and therapeutic uses are essential for enforceability.
    • Ambiguous language can lead to litigation or invalidation.

Patent Landscape in Lithuania and Europe

1. Lithuanian Patent Environment:

  • Lithuania's patent system aligns with EU directives, offering robust protection for pharmaceuticals.[2]
  • The national patent office (VTEK) examines applications for novelty, inventive step, and industrial application.

2. European Patent Considerations:

  • Since Lithuania is a member of the European Patent Organisation, patent protection can often be extended via the European Patent Office (EPO).
  • Patent families for LTPA2017014 likely exist, with equivalents filed in other jurisdictions to extend commercial rights.

3. Competitive Landscape & Patent Clusters:

  • The patent landscape includes both local and multinational pharmaceutical innovators.
  • Key players may include Lithuanian biotech firms and regional subsidiaries of global pharmaceutical giants.

4. Patent Litigation & Freedom-to-Operate:

  • Lithuanian patent law supports enforcement and infringement proceedings, but a thorough freedom-to-operate (FTO) analysis is critical, considering existing patents, especially within the EU.

Strategic Implications

  • Innovator’s Perspective:

    • Secure comprehensive claims covering compounds, uses, and formulations.
    • Leverage national protection with European extensions to maximize market exclusivity.
  • Follow-on & Generic Manufacturers:

    • Analyze the claims to identify potential design-arounds.
    • Monitor prior art and patent expirations to plan entry strategies.
  • Regulatory & Market Impact:

    • Patent protection influences regulatory approval, pricing, and market share.
    • For Lithuanian market entry, compliance with EU pharmaceutical regulations complements patent strategies.

Legal & Patent Lifecycle Considerations

  • Maintenance & Lifespan:

    • Ongoing maintenance fees are essential to uphold patent rights until 2037.
    • Patent term extensions, if applicable due to regulatory delays, could be considered under EU rules.
  • Potential Challenges & Patent Terminations:

    • Invalidity actions can arise from prior art, insufficient disclosure, or obvious claims.
    • Oppositions, common within the EU patent system, could impact the patent's enforceability.

Conclusion & Final Thoughts

LTPA2017014 exemplifies a strategically crafted pharmaceutical patent within Lithuania's evolving IP framework. Its scope, centered on novel claims pertinent to specific drug compounds or formulations, offers a robust foundation for commercial monopoly and R&D incentives. However, its strength ultimately hinges on precise claim drafting, thorough prior art searches, and strategic extensions across jurisdictions.

For stakeholders, understanding the nuances of this patent enriches decision-making—whether for licensing, developing similar compounds within the legal boundaries, or planning patent expiration-related market strategies.


Key Takeaways

  • Scope Management: Precise, well-drafted claims that balance breadth with enforceability are vital for maximizing patent protection.
  • Landscape Awareness: Regularly monitor Lithuanian and European patent filings to avoid infringement and identify licensing opportunities.
  • Strategic Extensions: Leverage Lithuania's EU membership to extend patent protection via European patents, increasing market exclusivity.
  • Legal Vigilance: Maintain ongoing patent maintenance and prepare for possible patent challenges to secure long-term rights.
  • Holistic Approach: Combine patent strategies with regulatory planning to optimize market entry and profitability.

FAQs

1. Can the scope of LTPA2017014 be expanded post-grant?
No, amendments to claims are generally limited after grant. However, patent owners can file divisional applications or patent extensions to broaden protection scope within legal limits.

2. How does Lithuanian patent law compare to other EU countries for pharmaceuticals?
Lithuanian patent law closely aligns with EU standards, providing similar protection and procedural efficiencies, but local examination and procedural specifics vary.

3. What are the main challenges in defending a pharmaceutical patent like LTPA2017014?
Challenges include prior art invalidation, claim interpretation disputes, and patent expiry or licensing disputes.

4. Is patent LTPA2017014 likely to cover a broad class of compounds or a specific molecule?
Without detailed claim language, it is unclear; however, pharmaceutical patents often aim for a balance, claiming both specific molecules and broader classes if supported by data.

5. How can a company effectively utilize this patent landscape for drug development?
By conducting comprehensive patent landscape analyses, securing strategic patent filings, and planning lifecycle management, companies can maximize protection and market opportunities.


Sources

  1. Lithuanian Patent Law and EU Patent Regulations.
  2. WIPO. "Lithuania – Patent Laws and Procedures."

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