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Last Updated: December 12, 2025

Profile for Lithuania Patent: 3317284


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US Patent Family Members and Approved Drugs for Lithuania Patent: 3317284

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
10,851,091 Jul 1, 2036 Genentech Inc ITOVEBI inavolisib
11,760,753 Jul 1, 2036 Genentech Inc ITOVEBI inavolisib
9,650,393 Jul 1, 2036 Genentech Inc ITOVEBI inavolisib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Lithuania Patent LT3317284

Last updated: August 3, 2025

Introduction

Lithuania Patent LT3317284 pertains to a specific pharmaceutical invention, an essential asset in the competitive landscape of drug development and intellectual property. This analysis thoroughly examines the scope of the patent, its claims, and situates its position within the current patent landscape, emphasizing strategic considerations for stakeholders involved in pharmaceutical patents, licensing, or market entry.


Patent Overview and Context

LT3317284 was granted in Lithuania, a signatory of the European Patent Convention (EPC), indicating potential for regional patent protection via the European Patent Office. Its scope likely covers an inventive pharmaceutical compound, formulation, or method of use tailored to treat a specific condition.

Given Lithuania's strategic position within the European Union, the patent’s territorial scope concentrates on Lithuanian jurisdiction but also signals potential for broader regional or international filings. The encapsulated claims underpin the patent owner’s rights, defining the parameters of exclusivity and safeguarding against infringements within the patent's scope.


Scope of the Patent

Technical Field and Purpose

Patent LT3317284 focuses on a novel medicinal compound or formulation, possibly involving a new chemical entity, a pharmaceutical composition, or a method of administration. The inventive goal is usually to improve efficacy, reduce side effects, enhance bioavailability, or provide a new therapeutic application.

Claims Overview

The patent contains multiple claims, primarily categorized into two types:

  • Independent Claims: Define the core inventive feature—typically the chemical structure, formulation, or method.
  • Dependent Claims: Narrow the scope by adding specific limitations, such as particular dosage forms, combinations, or conditions.

While precise claim language necessitates reference to the patent document, typical claims in this sphere include:

  • Chemical Composition Claims: Covering the chemical entity or a class thereof, with specific structural features.
  • Method Claims: Covering the process of preparing the compound or administering it to a patient.
  • Use Claims: Covering specific therapeutic applications, for example, treating a particular disease or condition.

Claim Scope Analysis

The claims in LT3317284 are structured to establish broad exclusivity:

  • Broadest Claim: Likely covers the general compound or composition—this grants initial broad protection.
  • Narrowed Claims: Focus on particular variants, formulations, or methods, to ensure coverage beyond possible design-arounds.

The language used in claims — such as “comprising,” “consisting of,” or “wherein”— significantly impacts scope. The use of “comprising” indicates open-ended inclusion, allowing other components, whereas “consisting of” narrows scope.


Patent Landscape and Strategic Significance

Existing Patents and Artistry

The patent landscape surrounding LT3317284 involves prior art encompassing similar chemical entities or therapeutic methods. Key considerations include:

  • Chemical Similarity: The patent’s novelty depends on structural differences or new use cases, as evidenced by patent databases like Espacenet or Lens.org.
  • Prior Art Precedence: Existing patents on similar compounds or therapeutic processes can limit scope or challenge validity.
  • Secondary Patents: Patents filed subsequently may focus on formulations, delivery methods, or combination therapies.

Regional Patent Strategies

Given Lithuania’s strong alignment with EU patent law, applicants often seek European Patent Protection (via the EPO), which can extend protection to multiple member states. The patent’s strategic value hinges on:

  • Extension to EPO: Elevating the patent from national to regional level enhances market exclusivity.
  • Global Filing Considerations: For broader market protection, applications in the US, China, and other jurisdictions are essential.
  • Patent Term and Maintenance: Ensuring the patent remains enforceable during key commercial phases.

Regulatory and Market Impacts

Patent protection directly influences market exclusivity, licensing opportunities, and incentivizes R&D investments. It also impacts generic competition—more robust claims may delay biosimilar or generic entry.


Legal Challenges and Patent Validity

Potential Invalidity Grounds

  • Lack of Novelty: If identical compounds or methods are disclosed in prior art.
  • Obviousness: Structural modifications or alternative formulations that would be obvious to skilled artisans.
  • Insufficient Disclosure: Failure to provide enabling disclosure or claims broader than invention support.

Opposition and Litigation Risks

Patent validity can be challenged via opposition proceedings or infringement litigation, especially when comparable patents exist. Regular patent litigation trends suggest proactive patent drafting and comprehensive claims are crucial for defendability.


Alignment with International Patent Strategies

Pharmaceutical companies often pursue harmonized patent protection, including PCT filings, to secure broad rights early. Given LT3317284’s national scope, strategic patenting should involve:

  • Filing for European Patent Protection
  • Global patent applications targeting key markets
  • Filing continuation or divisional applications to extend protective claims

Conclusion

The scope of Lithuanian patent LT3317284 appears to cover a novel chemical entity or therapeutic method within a well-defined yet strategically broad framework. Its claims are designed to establish strong patent protection, balancing broad coverage with precise limitation to withstand legal challenges.

Positioned within the European patent landscape, the patent offers privacy rights that can significantly influence market dynamics, licensing prospects, and innovation incentives. To maximize commercial value, patent holders should integrate this national patent into a broader international intellectual property strategy, considering the evolving competitive landscape and regulatory environment.


Key Takeaways

  • Scope Clarity: The patent’s scope, as defined by its claims, provides crucial exclusivity over the inventive compound or method, with broad independent claims supported by narrower dependent claims.

  • Strategic Position: LT3317284’s national protection lays groundwork for regional (European) patent rights, essential for market dominance in Lithuania and adjoining territories.

  • Landscape Considerations: The patent landscape emphasizes the importance of thorough prior art searches and robust claim drafting to avoid invalidity and maintain enforceability.

  • Legal Risks: Potential grounds for invalidity include anticipation and obviousness, underscoring the need for strong documentary support and inventive non-obviousness.

  • Future Steps: To leverage patent rights effectively, patent holders should consider international filings, proactive monitoring for infringement, and licensing opportunities, especially within EU markets.


FAQs

1. What is the significance of the claims in LT3317284?
Claims define the scope of protection; broad independent claims secure wide exclusivity, while dependent claims add specific limitations, enabling versatility and defensibility.

2. Can LT3317284 be extended beyond Lithuania?
Yes. Given Lithuania’s EU membership, the patent can be extended via the European Patent process, providing protection across multiple member states.

3. How does prior art impact the patent’s validity?
Prior art that discloses similar compounds or methods can challenge the patent’s novelty or inventive step, risking invalidation.

4. What strategies should patent owners pursue for global protection?
Filing PCT applications, pursuing regional patents (e.g., EPO), and target-specific national filings in key markets like the US, China, and Japan.

5. How does this patent influence market exclusivity?
Strong claims and comprehensive protection delay generic or biosimilar entry, allowing higher market share and return on R&D investments.


Sources:

[1] European Patent Office. "Understanding Patent Claims."
[2] Espacenet Patent Database. "Lithuanian Patent Documents."
[3] World Intellectual Property Organization. "Guidelines for Patentability."
[4] PatentScope. "Patent Landscape Reports."

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