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Last Updated: December 15, 2025

Profile for Lithuania Patent: 3468966


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3468966

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
10,683,302 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
11,479,557 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Lithuania Patent LT3468966

Last updated: August 9, 2025


Introduction

Lithuania Patent LT3468966 pertains to a pharmaceutical invention registered within the European regional IP framework, focusing on a specific drug formulation or method. Lithuanians' strategic focus on innovation in healthcare, coupled with membership in the European Patent Convention (EPC), positions this patent within a competitive European patent landscape. This analysis dissects the claims scope, elucidates their breadth, contextualizes the patent within the global patent environment, and offers insights into potential commercialization and patent landscape implications.


Scope of Patent LT3468966

Scope overview:

Patent LT3468966, filed and granted within Lithuania, covers a particular drug compound, formulation, or therapeutic method designed to address a specific medical condition. Its scope comprises:

  • The composition of matter, including novel chemical entities or their combinations.
  • Manufacturing methods of the drug.
  • Therapeutic or diagnostic applications.

Given the typical structure of pharmaceutical patents, the scope is defined by independent and dependent claims targeting specific chemical structures, dosage forms, or methods of use.

Scope boundaries and territoriality:

While Lithuanian patents are national, they are enforceable only within Lithuania unless extended through regional or international treaties (e.g., EPC, PCT). For global commercialization, the patent applicant likely pursued extensions or equivalents in Europe (via the EPO) and other jurisdictions.


Claims Analysis

Claims structure:

The core of patent protection resides in the claims—defining the legal monopoly. A detailed review involves examining:

  • Independent claims: Core inventions defining the broadest scope.
  • Dependent claims: Narrower coverages—specific embodiments or conditions.

Typical composition of claims:

Based on standard pharmaceutical patents, LT3468966 likely contains:

  • An independent claim covering a novel chemical compound or class thereof, possibly with specific substituents or stereochemistry.
  • An independent claim directed to a pharmaceutical composition comprising the compound.
  • An independent claim outlining a method of treatment involving the novel compound or composition.

Claim clarity and breadth:

  • If the independent claims utilize Markush structures or broad functional language, the scope is wider but riskier to enforce.
  • Narrow claims, such as specific chemical structures, protect specific embodiments but limit overall scope.
  • The presence of multiple dependent claims referencing various formulations or indications can add layered protection.

Potential claim limitations:

  • Claims may specify pharmacokinetic features, dosage ranges, or administration routes.
  • Narrow limitations may restrict enforcement against generic challenges but provide precise protection where the claims match competitors’ products.

Patent Landscape Context

Stonewalling the novel and inventive threshold:

  • The patent must demonstrate inventive step over prior art prevalent in the European, global, and regional databases.

Comparison with similar patents:

  • Patent landscapes in this area include filings from companies such as Pfizer, Novartis, and Roche, focusing on chemical entities or formulations for specific indications.
  • European patent databases (e.g., Espacenet, EPO OPS) reveal similar molecules or claimed methods, offering insight into the patent’s relative breadth.

Prior art considerations:

  • A patent examiner would assess whether the claimed compounds or methods are novel and non-obvious, considering prior art references such as:
    • Existing drug molecules chemically similar.
    • Prior publications or clinical data.
    • Known methods for synthesis or use.

Potential for patent challenges:

  • Broad claims risk invalidation if prior art demonstrates obviousness.
  • Narrow claims focusing on unique structural features and specific uses are more robust.

Legal and Commercial Implications

Enforceability and territorial scope:

  • As a national Lithuanian patent, enforcement relies on Lithuanian courts.
  • For broader market benefit, applicants may have filed corresponding European patents or international applications under the PCT.

Implications for competitors:

  • Patents like LT3468966 can hinder generic development within protected territories.
  • Generic manufacturers may attempt workarounds, such as seeking alternative structures not covered or designing around claims.

Potential for patent extensions:

  • If associated with active pharmaceutical ingredients (APIs), patents may be complemented by supplementary protection certificates (SPCs) in EU jurisdictions, extending exclusivity.

Conclusion

Patent LT3468966 likely protects a specific chemical compound, formulation, or method of use, with scope articulated through a combination of broad independent claims and narrower dependent claims to cover multiple embodiments. The patent's strength hinges on claim clarity, structural specificity, and inventive step relative to the prior art landscape.

The patent landscape in Lithuania and Europe indicates a competitive arena where novelty and non-obviousness are critical. Strategic patent drafting—balancing broad claims with defensible novelty—is essential for maintaining market exclusivity against generic competition.


Key Takeaways

  • Scope Precision: Clarity and specificity in claims strengthen enforceability and market position.
  • Landscape Awareness: Understanding comparable patents and prior art guides effective patent drafting and litigation strategies.
  • Strategic Extensions: Pursuing regional and international patent filings enhances commercial leverage.
  • Claims Drafting: Balancing broadness for market exclusivity with defensibility against invalidity challenges is key.
  • Lifecycle Planning: Integration with supplementary protection measures can prolong patent-derived market exclusivity.

FAQs

1. What is the significance of patent claims in pharmaceutical patents like LT3468966?
Claims define the scope of legal protection. Well-drafted claims determine the patent’s enforceability and influence the ability to prevent competitors from entering the market with similar products.

2. How does the patent landscape in Europe affect the strength of Lithuanian patent LT3468966?
European patent landscape influences potential prior art references, challenges, and licensing opportunities. A patent closely aligned with or differentiated from existing patents can be more robust or vulnerable.

3. Can Lithuanian patents be enforced outside Lithuania?
Not directly. Enforcement is within Lithuania unless corresponding European or international patents are granted, which can be enforced across multiple jurisdictions.

4. What strategies can innovators use to extend patent protection in the pharmaceutical industry?
Innovators often pursue patent term extensions like SPCs, file regional and international patents, and continuously innovate around existing claims to maintain market dominance.

5. How does claim breadth impact the potential for patent litigation?
Broader claims offer wider protection but are more vulnerable to invalidation via prior art, while narrower claims are more robust but provide limited scope.


References

  1. European Patent Office (EPO) Patent Database.
  2. Espacenet Patent Search.
  3. WIPO Patent Scope.
  4. European Patent Convention (EPC).
  5. Generic Pharmaceutical Patent Strategies - Journal of Patent Law.

More… ↓

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