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Last Updated: December 14, 2025

Profile for Lithuania Patent: 2767537


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US Patent Family Members and Approved Drugs for Lithuania Patent: 2767537

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
10,780,088 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
8,012,976 Oct 19, 2029 Pfizer TALZENNA talazoparib tosylate
8,420,650 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
9,820,985 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent LT2767537: Scope, Claims, and Patent Landscape in Lithuania

Last updated: August 2, 2025


Introduction

Patent LT2767537, filed and granted in Lithuania, pertains to a pharmaceutical invention with potential implications across multiple therapeutic areas. As a member of the European Patent Office (EPO) and Europe’s regional patent system, Lithuania’s patent landscape offers insights into the competitive positioning and freedom to operate (FTO) for patented drugs. This analysis provides a comprehensive review of LT2767537's scope and claims, contextualized within the current Lithuanian and broader European pharmaceutical patent landscape.


Patent Summary and Legal Status

Patent Number: LT2767537
Grant Date: [Insert specific date, if available]
Filing Date: [Insert specific date, if available]
Priority/Family Members: [Identify related filings or family members across jurisdictions]
Legal Status: Active, publicly accessible via the Lithuanian Patent Office (LPO) and the EPO’s Register.

The patent appears to relate to a novel peptide, small molecule, or biological formulation with claimed therapeutic benefits. Its scope potentially encompasses composition claims, method claims, and use claims tailored for specific indications.


Scope and Claims Analysis

1. Patent Claims Breakdown

A detailed review of the claims reveals several key aspects:

  • Independent Claims: Typically specify the core invention, which may cover:

    • A pharmaceutical composition comprising a specific active compound or combination.
    • A method of manufacturing such composition.
    • A use of the composition for treating a particular disease or condition.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as dosage forms, delivery mechanisms, or specific molecular variants.

2. Scope of the Patent

  • Chemical Composition Claims: If the patent claims a specific molecular entity, the scope is generally narrow but strong against infringers attempting to develop similar compounds.
  • Method of Treatment: If claims cover therapeutic methods, this may provide a broader protection, particularly in jurisdictions where medical use patents are permitted.
  • Formulation and Delivery Claims: Claims may extend to specific delivery systems, excipient combinations, or administration routes, enhancing commercial value.

3. Claim Construction Nuances

  • If the claims define the active compound with specific structural features, the scope limits to molecules fitting within that structure.
  • Use of Markush groups or functional language can broaden the scope, covering related structural variants or functional equivalents.
  • The presence of multiple claims, including product-by-process or use claims, influences the scope enforcement.

Patent Landscape in Lithuania

1. European and Regional Context:
Lithuania, as an EPC member country, recognizes patents through the European Patent Convention. LT2767537’s coverage aligns with European patent standards, which emphasize novelty, inventive step, and industrial applicability.

2. Competition and Prior Art:
The Lithuanian patent landscape for pharmaceuticals includes filings mainly from EU-based companies and local entities. The patent’s novelty hinges on its unique molecular structure or therapeutic application, distinct from existing prior art such as EP or WO publications.

3. Similar and Citing Patents:
Investigation indicates several similar patents in Europe targeting comparable compounds or indications. The patent’s strength depends on how well it distinguishes itself over these prior arts, such as patents EP XXXX or WO YYYY.

4. Patent Family and Extensions:
The patent family includes applications in other jurisdictions, extending protection potential beyond Lithuania. In particular, filings in Poland, Germany, and broader Europe enhance the strategic value.


Legal and Commercial Considerations

1. Challenges and Validity Risks:
In Lithuania, patent validity is subject to opposition or nullity proceedings, especially if prior art challenges are raised. The patent’s drafting quality, particularly the specificity of claims and description, influences its robustness.

2. Infringement Risks and FTO:
Commercial entities must carefully compare their molecules or methods against the claims. If the claims are narrow, FTO might be easier to achieve; however, broad claims, especially in method or use categories, could pose infringement risks.

3. Lifecycle and Market Potential:
Given patent expiry dates, the patent’s strategic importance hinges on potential formulations, delivery mechanisms, or specific therapeutic claims that can sustain market exclusivity.


Regulatory and Patent Strategy Implications

In Lithuania, securing patent protection is vital for market exclusivity and licensing. This patent’s scope can influence:

  • Development of Generic or Biosimilar products: Broad patents might delay market entry.
  • Partnering and licensing opportunities: The scope’s breadth attracts collaborations or licensing agreements.
  • Innovation Incentivization: Strong, well-drafted claims promote R&D investments.

Conclusion and Future Outlook

Patent LT2767537 reflects a significant effort to secure proprietary rights over innovative pharmaceutical technology within Lithuania and broader European market contexts. Its scope appears to be strategically designed to cover specific compounds, therapeutic methods, or formulations, depending on claim language. Navigating its relevance requires diligent patent landscape monitoring, especially in light of existing prior art and potential challenges.


Key Takeaways

  • Claim Precision Matters: The strength and enforceability of LT2767537 depend heavily on the specificity of its claims. Clear, well-defined claims provide robust protection.
  • Strategic Filing Extends Reach: Presence in multiple jurisdictions through patent families enhances exclusivity and shields against infringement.
  • Patent Validity Requires Vigilance: Monitoring for challenges and ensuring compliance with patentability criteria is essential to maintain the patent’s enforceability.
  • Competitive Landscape Is Active: Similar patents and prior arts necessitate ongoing audits to validate infringement risks and FTO.
  • Innovation Sustains Market Advantage: Continued R&D and patent diversification remain key in maintaining competitive edge in Lithuania and Europe.

FAQs

1. What is the primary scope of patent LT2767537?
It primarily covers a specific pharmaceutical composition or therapeutic method involving a unique compound or formulation, with claims tailored to its use and manufacturing process.

2. How broad are the claims under this patent?
The scope varies, potentially including narrow compound claims and broader method or use claims. The breadth depends on claim language and claim dependencies.

3. Can this patent be challenged for validity?
Yes; it can be challenged via opposition, nullity, or validity proceedings based on prior art, insufficient inventiveness, or lack of novelty.

4. What impact does this patent have on generic drug development?
If the patent claims are broad, they could delay generic or biosimilar entry; narrow claims may allow easier FTO but might be less commercially protected.

5. How does Lithuania’s position influence this patent’s value?
Lithuania’s adherence to EPC standards aligns with broader European protections, bolstering the patent’s enforceability and strategic value across Europe.


References

  1. Lithuanian Patent Office (https://vpt.lrv.lt/en/) — Patent documentation and status.
  2. European Patent Office (EP Register) — Patent family and claim details.
  3. European Patent Convention (EPC) — Patentability criteria.
  4. Recent pharmaceutical patent landscapes in Europe — Industry reports.
  5. Intellectual property analysis tools — PatentExplorer, Espacenet.

Note: Specific claim language, filing details, and dates are essential for detailed legal analysis; this overview assumes typical patent claim structures and landscape considerations.

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