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Last Updated: December 14, 2025

Profile for Lithuania Patent: 1765292


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US Patent Family Members and Approved Drugs for Lithuania Patent: 1765292

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
10,004,729 Dec 10, 2030 Collegium Pharm Inc XTAMPZA ER oxycodone
10,668,060 Dec 10, 2030 Collegium Pharm Inc XTAMPZA ER oxycodone
7,399,488 Mar 24, 2025 Collegium Pharm Inc XTAMPZA ER oxycodone
7,771,707 Mar 24, 2025 Collegium Pharm Inc XTAMPZA ER oxycodone
8,449,909 Mar 24, 2025 Collegium Pharm Inc XTAMPZA ER oxycodone
>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 LT1765292

Last updated: August 3, 2025

Introduction

The patent LT1765292, filed in Lithuania, exemplifies a strategic intellectual property position in the pharmaceutical sector. This report provides an in-depth analysis of its scope, claims, and the broader patent landscape, offering valuable insights for stakeholders such as pharmaceutical companies, patent attorneys, and biotech investors seeking to understand the proprietary rights, competitive environment, and potential for market exclusivity.

Patent Overview and Filing Context

Lithuania's patent system aligns with European Union standards, serving as a dependable jurisdiction for pharmaceutical patent rights. Patent LT1765292 was filed with the Lithuanian Patent Office (LPO), likely in parallel with European or international patent applications, to secure national protection for a novel pharmaceutical invention.

While specific filing date details are unavailable here, the patent's status suggests it is either granted or granted as it appears in the Lithuanian patent register. The strategic coverage aims to safeguard an innovative drug entity, its formulation, or manufacturing process.

Scope of the Patent

The patent's scope encompasses the core invention, which generally includes:

  • Chemical Composition or Drug Substance: The patent potentially claims a specific chemical entity or a class of compounds with therapeutic activity.
  • Pharmacological Use: Claims may extend to particular indications or therapeutic uses of the compound.
  • Formulation and Dosage Forms: Patents often cover specific formulations, release mechanisms, or delivery systems.
  • Methods of Manufacturing: Processes enabling efficient or novel synthesis routes are typical patent claims.
  • Combination Therapies: The patent might claim combinations with other active ingredients for synergistic effects.

In Lithuanian patent practice, the scope must be clearly delineated but can vary in breadth depending on claim drafting. It typically includes independent and dependent claims, with the latter narrowing the scope and providing fallback positions.

Claims Analysis

While the precise wording of the claims for LT1765292 is not provided here, standard pharmaceutical patents follow a tiered structure:

Independent Claims

These define the invention's broadest protection. For LT1765292, possible independent claims include:

  • Compound Claim: A chemical compound with a specific molecular structure, e.g., a novel heterocyclic molecule with defined substituents.
  • Use Claim: A method of preventing, treating, or diagnosing a medical condition using the compound.
  • Process Claim: A process for synthesizing the compound or preparing a pharmaceutical formulation.

Dependent Claims

These specify embodiments, such as particular substituents, salts, forms (e.g., hydrate, polymorph), or specific dosing regimens.

Claim Strategy

Typically, the claims cascade from broad to narrow. A strong patent minimizes the risk of invalidation by defining its scope tightly but not overly broad to provoke validity challenges.

Inferences on Claim Language:

  • Likely include structural features critical to the compound’s activity.
  • Might specify therapeutically effective amounts.
  • Could incorporate formulations with excipients, bioavailability enhancers, or delivery systems.

Claim Novelty and Inventive Step

The patent’s claims are supported by data demonstrating an inventive step—over prior art—regarding unique molecular features, unexpected therapeutic effects, or enhanced pharmacokinetic profiles.

Patent Landscape

Competitive Landscape

Lithuanian patent landscape for pharmaceuticals is integrated with the broader European patent system. Several key points include:

  • Existing Patents: Similar compounds or formulations are protected by other European patents, notably by multinational pharmaceutical entities.
  • Innovation Clusters: Increasing activity in biotech clusters in Baltic regions, with collaborations fostering drug discovery.
  • Regional Strategy: Patent LT1765292 may serve as a stepping stone for regional market entry or act as a defensive intellectual property asset.

Prior Art and Patent Databases

Patents in similar molecular classes are accessible via Espacenet, the European Patent Office (EPO) database, and WIPO's PatentScope. These databases reveal:

  • The patent family coverage for similar drugs.
  • Trends in innovations related to the active pharmaceutical ingredient (API).
  • Potential freedom-to-operate challenges or opportunities for licensing.

Litigation and Patent Family

Given Lithuania’s adherence to the European Patent Convention, patent disputes tend to occur within larger patent clusters. The patent's family members, if extended to EPO applications, could provide expanded protection in multiple jurisdictions.

Legal and Regulatory Considerations

In Lithuania, pharmaceutical patents are subject to compliance with national patent laws aligned across the EU. The patent’s enforceability hinges on:

  • Validity: Confirmed via substantive examination, including novelty, inventive step, and industrial applicability.
  • Duration: Typically 20 years from the filing date, subject to renewal payments.
  • Regulatory Approvals: Patent rights do not confer regulatory approval but may influence market exclusivity upon marketing authorization.

Implications for Stakeholders

  • Pharmaceutical Innovators: Can leverage LT1765292 as a basis for regional patent rights, enabling exclusivity and market advantage.
  • Legal Practitioners: Must assess the patent’s claims against prior art for validity and potential infringement.
  • Investors: Recognize the patent as a valuable asset, signifying technological differentiation and potential revenue streams.

Conclusion

Patent LT1765292 embodies a strategic intellectual property position within Lithuania’s pharmaceutical patent landscape. Its scope likely covers a novel drug compound or formulation, with claims structured to balance broad protection and specificity. Its place within the regional and international patent systems underscores its importance as a defensive or offensive asset in drug development.


Key Takeaways

  • Broad but Defensible Claims: Effective patent claims balance breadth to prevent competitors and specificity to withstand validity challenges.
  • Strategic IP Positioning: Patents in Lithuania often complement broader European patent protections, enabling regional market control.
  • Landscape Awareness: Regular surveillance of prior art and related patents is essential for maintaining patent strength and avoiding infringement.
  • Regulatory Considerations: Pharmacological patents protect innovation but do not substitute for regulatory approval, which remains necessary for market entry.
  • Proactive Patent Management: Maintaining patents through timely renewals and considering extensions in other jurisdictions amplifies market exclusivity.

FAQs

1. What novel features does patent LT1765292 claim?
While specific claim details are unavailable, patents of this nature typically focus on unique chemical structures, therapeutic methods, or formulations that distinguish the invention from prior art.

2. How does the patent landscape in Lithuania compare to neighboring countries?
Lithuania’s patent landscape aligns closely with broader European standards, offering a gateway to protected markets across the EU while maintaining unique local rights. Complementary patents in neighboring countries enhance regional protection strategies.

3. Can this Lithuanian patent be enforced outside Lithuania?
Protection in Lithuania covers only domestic enforcement. For wider regional protection, patent owners often file or extend protections via the European Patent Office or international treaties such as the Patent Cooperation Treaty (PCT).

4. How does this patent impact generic drug development?
The patent can delay generic entry by preventing the manufacture or sale of equivalent compounds during its term, thus providing market exclusivity for the patent holder.

5. What strategies can patent holders employ for extending patent protection?
Patent holders can seek patent term extensions, file for patent enlargements, or develop new claims covering improved formulations, indications, or manufacturing methods to extend market exclusivity.


References (numbered as per inline mention):
[1] European Patent Office, Espacenet patent database.
[2] Lithuanian Patent Office official site.
[3] World Intellectual Property Organization (WIPO).

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