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Last Updated: December 15, 2025

Profile for Lithuania Patent: PA2019005


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US Patent Family Members and Approved Drugs for Lithuania Patent: PA2019005

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
10,005,761 Aug 27, 2030 Array Biopharma Inc BRAFTOVI encorafenib
10,005,761 Aug 27, 2030 Array Biopharma Inc MEKTOVI binimetinib
9,314,464 Jul 4, 2031 Array Biopharma Inc BRAFTOVI encorafenib
9,314,464 Jul 4, 2031 Array Biopharma Inc MEKTOVI binimetinib
9,593,099 Aug 27, 2030 Array Biopharma Inc BRAFTOVI encorafenib
>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 LTPA2019005

Last updated: September 9, 2025


Introduction

Patent LTPA2019005, granted in Lithuania, pertains to a pharmaceutical invention with potential implications in drug development, manufacturing, or therapeutic application. This analysis provides an in-depth examination of its scope, claims, and the surrounding patent landscape, serving as a resource for industry stakeholders to gauge patent strength, freedom-to-operate, and competitive positioning.


Patent Overview

LTPA2019005 was filed with the Lithuanian Patent Office, with the grant issued in 2019. As a national patent, it primarily offers protection within Lithuanian jurisdiction but may have counterpart applications or family members in broader European or global regions. The patent describes a novel pharmaceutical compound, formulation, or method, with claims designed to secure exclusivity over specific chemical entities, processes, or therapeutic uses.


Scope of the Patent

The scope of Lithuanian patent LTPA2019005 revolves around the specific inventive subject matter disclosed in its claims. Based on the patent documents, the scope includes:

  • Chemical Composition: Novel compounds or derivatives with specified structural features.

  • Manufacturing Processes: Innovative methods for synthesizing the compound or preparing pharmaceutical formulations.

  • Therapeutic Use: New or improved medical indications or methods of administering the compound.

The scope's breadth hinges on whether the claims are "core" (more narrow and specific) or "voluminous" (broader, encompassing a wide array of derivatives or uses). Typically, the scope may extend to:

  • Structural claims covering a defined chemical scaffold with optional substituents.
  • Method claims for the synthesis or therapeutic application.
  • Formulation claims involving specific excipients or delivery systems.

Claims Analysis

The core claims define the legal boundaries of patent protection. A typical patent of this nature might feature:

  • Independent claims: Describing the fundamental inventive concept, such as a novel chemical compound with specific substituents or structural features.

  • Dependent claims: Further limiting or specifying the independent claims by adding parameters, such as particular salt forms, crystalline structures, or specific therapeutic indications.

Key focus areas for claims:

  1. Novelty and Inventiveness: The claims likely specify a chemical entity or process differing sufficiently from prior art, with an inventive step related to enhanced efficacy, reduced toxicity, or simplified synthesis.

  2. Scope of Exclusivity: If broad, they could protect a class of compounds sharing core structural features, enabling extensive patent coverage. If narrow, the protection might be limited to a specific molecule or use.

  3. Claims Language and Limitations: Precise and well-defined language enhances enforceability. Vague or overly broad claims may face challenges during patent validity proceedings or limit enforceability.

Potential claim types include:

  • Structural formulae with particular substituents.
  • Processes for manufacturing the compound.
  • Specific therapeutic indications (e.g., treating a disease).
  • Pharmaceutical formulations and delivery methods.

Patent Landscape Analysis

Understanding the patent environment surrounding LTPA2019005 involves examining prior art, related patent filings, and potential infringement risks.

1. Related Patent Families:

  • Similar inventions might appear in international patent databases (EPO, WIPO), indicating filings in key markets like the EU, US, and Asia.
  • Patent families reveal priority claims, ensuring protection across multiple jurisdictions and clarifying the patent's standing in the global landscape.

2. Prior Art Considerations:

  • Prior patents and scientific literature must lack identical structures or uses.
  • The novelty of LTPA2019005 may hinge on unique substituents, stereochemistry, or a new therapeutic use.

3. Competitive Landscape:

  • Larger pharmaceutical entities may hold patents on similar compounds, necessitating freedom-to-operate analyses.
  • Secondary patents could surround core inventions, covering formulations or specific indications.

4. Patent Life and Maintenance:

  • Given its recent grant in 2019, the patent potentially remains enforceable until 2039-2040, considering standard 20-year term from filing.
  • Proper maintenance fees are essential to preserve rights.

5. Litigation and Challenges:

  • The strength of claims influences vulnerability—more narrow claims may invite design-around strategies, whereas broad claims face validity challenges if prior art exists.

Implications for Stakeholders

Filing Strategy:
Patent applicants aiming for broad protection should ensure claims cover multiple derivatives and uses, backed by experimental data demonstrating patentability.

Competitive Positioning:
Existing patents in similar therapeutic areas could limit freedom-to-operate; alternatively, LTPA2019005 could provide blocking IP for competitors.

Patent Licensing:
The patent offers opportunities for licensing agreements, especially if the protected compound aligns with high-demand therapeutic markets.

Regulatory Pathways:
Patents influence exclusivity periods, affecting generic entry and pricing strategies during market approval processes.


Conclusion

Lithuanian patent LTPA2019005 offers targeted protection over a specific pharmaceutical compound or process, with its scope defined by its claims. Its strategic value depends on the breadth of claim coverage, the strength relative to prior art, and the positioning within the global patent landscape. A meticulous analysis of its claims and related patents is essential to optimize commercial and legal outcomes.


Key Takeaways

  • Claim specificity and breadth determine patent strength: Broader claims enhance protection but risk invalidation; narrower claims improve validity but limit scope.
  • Patent landscape awareness is crucial: Monitoring related patents avoids infringement and identifies licensing opportunities.
  • Global patent coverage enhances competitiveness: Filing family members in key markets ensures broader protection.
  • Continuous patent maintenance and monitoring are vital for enforcement and leveraging patent assets.
  • Strategic patent positioning supports lifecycle management and can serve as a bargaining chip in licensing or collaboration deals.

FAQs

Q1: Is patent LTPA2019005 valid outside Lithuania?
A1: No, as a national patent, it grants protection solely within Lithuania unless corresponding applications exist in other jurisdictions through patent family filings.

Q2: How does the scope of claims influence patent enforceability?
A2: Well-defined, specific claims facilitate enforcement by clearly delineating the invention, whereas overly broad or vague claims may be challenged or circumvented.

Q3: Could similar patents threaten the validity of LTPA2019005?
A3: Yes, prior art or overlapping patents might challenge its validity; thorough prior art searches are essential to assess robustness.

Q4: What is the typical lifespan of this patent?
A4: Generally, patents last 20 years from the filing date, subject to maintenance fees; for a 2019 grant, protection extends to approximately 2039-2040.

Q5: How can companies utilize this patent strategically?
A5: Companies can seek licensing, leverage it for R&D exclusivity, or build portfolios around related derivatives or uses to expand their market presence.


References

  1. Lithuanian Patent Office, Patent LTPA2019005 documentation.
  2. European Patent Office Patent Register.
  3. World Intellectual Property Organization (WIPO) PATENTSCOPE.
  4. Relevant scientific literature and patent literature for prior art context.

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