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Last Updated: December 17, 2025

Profile for Lithuania Patent: 3184523


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3184523

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
10,245,269 Apr 11, 2033 Epizyme Inc TAZVERIK tazemetostat hydrobromide
10,821,113 Apr 11, 2033 Epizyme Inc TAZVERIK tazemetostat hydrobromide
11,491,163 Apr 11, 2033 Epizyme Inc TAZVERIK tazemetostat hydrobromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Lithuania Drug Patent LT3184523: Scope, Claims, and Patent Landscape Analysis

Last updated: August 23, 2025


Introduction

The pharmaceutical patent landscape involves complex legal frameworks that govern the protection, commercialization, and innovation associated with medicinal compounds. Lithuania’s patent system, aligned with European Union directives and the European Patent Convention, plays a strategic role in safeguarding intellectual property rights within its jurisdiction. The focus herein is on patent LT3184523, examining its scope, claims, and the broader patent landscape in Lithuania and the EU concerning similar pharmacological inventions.


Patent Overview: LT3184523

LT3184523 is a Lithuanian national patent granted or filed with the European Patent Office (EPO), which Lithuania follows as a member of the European patent system. Although specific technical disclosures are not publicly detailed here, typically, such patents in the pharmaceutical domain cover novel compounds, formulations, methods of manufacturing, or therapeutic applications.


Scope of Patent LT3184523

The scope of any pharmaceutical patent hinges on its claims, which define the legal boundaries of exclusivity. In the case of patent LT3184523, the scope likely encompasses:

  • Innovative Medicinal Compounds: Possibly a new chemical entity or a novel derivative, with specified structural components and unique pharmaceutical activity.
  • Therapeutic Methods: Claims may extend to methods of treatment employing the compound, including indications such as oncology, neurology, or infectious diseases.
  • Formulation Claims: Encompassing specific compositions, delivery mechanisms, or combination therapies that enhance efficacy or bioavailability.
  • Manufacturing Processes: Claims could include synthesis routes, purification steps, or formulation techniques proprietary to the inventor.

The patent's scope is ultimately constricted by the explicit language of its claims; broad claims cover extensive uses or compounds, while narrow claims focus on specific embodiments. A common strategy in pharmaceutical patents is to balance broad claims for strategic monopoly with narrower, more defensible embodiments.


Claims Analysis

1. Composition and Structural Claims:
If the patent claims a new chemical compound, these will define the molecular structure, substitution patterns, stereochemistry, and purity standards. For example, a claim might state:

"A compound having the structure of Formula I, characterized by substitutions at positions X, Y, and Z..."

These structural claims underpin the novelty and inventive step, which are critical for patent validity.

2. Method of Use Claims:
Often, patents in the pharmaceutical sector include claims for therapeutic methods, such as:

"A method of treating [disease], comprising administering an effective amount of compound X..."

Such claims extend the patent's protection to specific medical applications, vital in the residual patent life post-patient market entry.

3. Formulation and Delivery Claims:
Claims may specify:

"A pharmaceutical composition comprising compound X, a pharmaceutically acceptable carrier, and excipients, in a formulation suitable for oral delivery."

This scope covers proprietary delivery systems that improve stability, absorption, or patient compliance.

4. Manufacturing Process Claims:
Claims might describe synthesis routes, purification steps, or process conditions, such as:

"A process for preparing compound X involving steps A, B, and C..."

These protect against generic manufacturing techniques that could circumvent the patent.


Patent Landscape Context in Lithuania and Europe

1. National and Regional Patent Systems:
Lithuania, as a member of the European Union, accepts European patents validated locally. The jurisdiction’s patent landscape is influenced by EU patent directives, emphasizing robust patent examination standards meant to prevent the grant of overly broad or invalid patents.

2. Existing Patent Families and Prior Art:
The novelty of LT3184523 depends on the state of prior art, including:

  • European Patent Applications: similar compounds or therapeutic claims filed elsewhere.
  • Patent Families: related patents filed in multiple jurisdictions.
  • Scientific Literature: prior publications on similar compounds or methods.

An analysis of patent offices such as EPO, USPTO, and other jurisdictions can reveal whether LT3184523 enjoys freedom to operate or faces potential infringement risks.

3. Competitive Patent Landscape:
In the pharmaceutical sector, patent thickets often exist around blockbuster molecules or platform technologies. The scope of LT3184523 may overlap with patents owned by competitors, especially if it falls within a well-explored chemical class like kinase inhibitors or monoclonal antibodies.

4. Patent Term and Supplementary Protection:
Pharmaceutical patents typically last 20 years from filing, with possible extensions via Supplementary Protection Certificates (SPCs) in Europe, potentially protecting LT3184523 until around 2033-2035, depending on the filing date and delays.


Legal and Strategic Considerations

1. Validity and Enforceability:
For patent claims to be enforceable, they must satisfy novelty, inventive step, and industrial applicability criteria. Patent examiners in Lithuania and the EPO rigorously scrutinize these aspects, especially for pharmaceuticals, given the high stakes.

2. Dealings and Litigation Risks:
Patent holders must monitor potential infringement and defend their patent rights through opposition processes if challenged. The patent's strength hinges on its claim breadth, clarity, and prior art considerations.

3. Post-Grant Strategies:
Filing divisional patents, supplementary protections, or licensing arrangements within the EU could extend rights and market exclusivity, influencing the competitive landscape.


Conclusion

LT3184523 represents a strategically valuable patent in Lithuania’s pharmaceutical patent landscape, likely aiming to protect a novel drug candidate or therapeutic method. Its scope, defined primarily by its claims, covers a targeted chemical compound or treatment modality, with potential extensions to formulations and manufacturing processes. The patent landscape in Lithuania and broader Europe is highly competitive, demanding careful navigation of prior art and strategic patent filing practices to sustain exclusivity.


Key Takeaways

  • The scope of LT3184523 is primarily dictated by its claims, which likely encompass structural, therapeutic, and process innovations.
  • A robust patent landscape analysis is essential to identify potential infringement risks or opportunities for licensing.
  • Strategic patent protection, including broader claims and supplementary protections, enhances market exclusivity.
  • Ongoing monitoring of patent opposition and market activities ensures sustained patent strength.
  • Aligning Lithuanian patent protection within the wider European jurisdiction maximizes commercial potential and legal enforceability.

Frequently Asked Questions

1. What makes a pharmaceutical patent claim broad or narrow?
Claims are broad if they encompass a wide range of compounds, uses, or formulations, providing extensive protection. Narrow claims specify particular structures or uses, offering limited but more defensible protection.

2. How does Lithuania’s patent system compare to the broader EU?
Lithuania follows the European Patent Convention, ensuring harmonization with EU standards. The patent examination process emphasizes novelty and inventive step, similar to other EU member states.

3. Can a patent like LT3184523 be challenged or invalidated?
Yes, through opposition proceedings, challenges based on prior art, or courts if invalidity is proven due to lack of novelty, inventive step, or other legal grounds.

4. What strategies can extend a patent’s effective life in the pharmaceutical industry?
Filing divisional patents, obtaining SPCs, developing new formulations or methods, and patenting secondary indications can prolong market exclusivity.

5. How important is prior art searching in patent application and enforcement?
Crucial. It determines patent validity and helps identify potential infringement or freedom-to-operate concerns, informing both patent drafting and litigation strategies.


References

  1. European Patent Office. Guidelines for Examination.
  2. Lithuanian Patent Office. Patent Laws and Procedures.
  3. World Intellectual Property Organization. Patent Landscape Reports.
  4. European Patent Convention. Articles on patentability and claims.
  5. Recent legal analyses and industry reports on pharmaceutical patent strategies.

This detailed analysis provides a foundation for understanding the strategic importance of Lithuanian patent LT3184523 within the pharmaceutical landscape, equipping stakeholders with insights to make well-informed decisions.

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