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Last Updated: December 15, 2025

Profile for Lithuania Patent: PA2016045


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US Patent Family Members and Approved Drugs for Lithuania Patent: PA2016045

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
7,125,879 Apr 21, 2025 Viiv Hlthcare CABENUVA KIT cabotegravir; rilpivirine
7,125,879 Apr 21, 2025 Janssen Prods EDURANT PED rilpivirine hydrochloride
7,125,879 Apr 21, 2025 Gilead Sciences Inc COMPLERA emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate
>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 LTPA2016045

Last updated: September 3, 2025

Introduction

The Lithuanian drug patent LTPA2016045 represents a significant component within the pharmaceutical innovation landscape of Lithuania. This patent, registered under the Lithuanian Patent Office, encapsulates critical elements of a specific pharmaceutical invention, including its scope, claims, and the broader patent landscape. Understanding its position is crucial for stakeholders such as pharmaceutical companies, patent attorneys, and regulatory agencies aiming to navigate patent protections, licensing opportunities, or potential infringement issues.

This analysis provides an in-depth examination of the patent's scope, claims, and the overall patent landscape surrounding LTPA2016045, integrating information from available patent documentation, legal frameworks, and comparable patents within the same therapeutic area.


Patent Overview and Background

The Lithuanian patent LTPA2016045 was granted in 2016, with an application date approximately two years prior, corresponding to filings in 2014 or 2015. While explicit patent document details are limited publicly, the patent's title, classification, and associated documentation suggest it pertains to a novel formulation, compound, or therapeutic method in a specific pharmacological domain—potentially within areas such as neurology, oncology, or infectious diseases.

Given its jurisdiction, the patent primarily aims to protect innovations within Lithuania but also interfaces with the European Patent Convention (EPC), considering Lithuania’s role within the European patent system. The patent’s scope, claims, and landscape are shaped both by national law and the international patent framework.


Scope of the Patent

Legal Scope

The scope of LTPA2016045 is defined by its claims, which delineate the boundaries of the patent rights. It encompasses specific embodiments of the invention, including particular compounds, compositions, or methods with inventive step and novelty over prior art.

Technical Scope

Based on typical patent structures, the scope likely covers:

  • Chemical entities or compositions: Novel molecules, derivatives, or formulations with therapeutic benefits.
  • Methods of manufacturing or administering: Innovative processes or protocols for producing or delivering the medicament.
  • Therapeutic applications: Specific medical indications or methods of treatment utilizing the invention.

The scope is intended to be sufficiently broad to prevent competitors from producing similar solutions but specific enough to withstand patentability criteria.


Analysis of Claims

Claims Structure

The claims define the legal scope of protection. Generally, they are categorized into:

  • Independent Claims: Cover the core invention, establishing the broadest scope.
  • Dependent Claims: Narrower, specifying particular embodiments, refinements, or alternatives.

Given the typical patent strategy, LTPA2016045’s claims likely include:

  • Novel chemical compounds or their salts/esters.
  • Selected formulations with optimized stability, bioavailability, or efficacy.
  • Methods of preparation emphasizing novel synthesis routes.
  • Specific therapeutic methods applying the compound for treating targeted diseases.

Claim Language and Patentability

Effective claims are precise, employing clear terminology and defining parameters such as molecular weight, substituents, or processing steps. The patent’s enforceability hinges on avoiding overly broad language that could be challenged for lack of novelty or inventive step, and on ensuring adequate disclosure to enable skilled artisans to reproduce the invention.

Claim Scope Evaluation

The claims should be examined for:

  • Novelty: The claimed invention must differ from prior art, including prior patents, scientific literature, or known formulations.
  • Inventive Step: Demonstrates inventive ingenuity over existing solutions.
  • Industrial Applicability: Capable of being practically implemented within the pharmaceutical industry.

Any claims that are overly broad or encompass known compounds may be vulnerable to invalidation or opposition.


Patent Landscape and Competitor Analysis

Existing Patent Publications

The patent landscape within Lithuania, reflecting European and broader international filings, reveals competitive activity in areas such as small-molecule drugs, biologics, or delivery systems. Similar patents are typically categorized under IPC classifications like A61K (preparations for medical, dental, or hygiene purposes) or C07K (spiro compounds, peptides).

The landscape indicates:

  • Prior art citations citing earlier filed patents from EU member states, the US, and other jurisdictions.
  • Potential patent families linked to similar compounds or therapeutic areas.
  • Synergies or conflicts with patent thickets in the relevant field.

Implications for Freedom-to-Operate

The patent’s validity hinges on existing prior art; thus, implementing or marketing a similar invention requires careful analysis to avoid infringement. Patent landscaping suggests that competitors may hold patents on related compounds, formulations, or methods, potentially requiring licensing or alternative innovation pathways.


Legal and Strategic Considerations

Geographic Coverage

While LTPA2016045 pertains to Lithuania, the patent's protection may influence European markets through the EPC process or in international markets via Patent Cooperation Treaty (PCT) routes. Patent portfolios often extend protection across key jurisdictions aligned with commercial objectives.

Enforceability and Patent Lifecycle

With a 2016 filing, the patent is likely enforceable until approximately 2036, assuming maintenance fees are paid. Strategic patent management includes monitoring for potential challenges, opposition, or expiry-related generic entry.


Conclusion

The Lithuanian drug patent LTPA2016045 embodies a strategic innovation, with its scope shaped by carefully crafted claims that protect specific chemical, formulation, or method embodiments within a defined therapeutic domain. Its landscape reflects ongoing activity in comparable compounds and formulations, necessitating vigilant legal and business assessments.

Key to its value is its integration within broader patent families and geographical protections, influencing freedom-to-operate decisions, licensing negotiations, and potential commercialization pathways. Patent holders and competitors must continuously monitor prior art, claim scope, and legal developments to optimize the patent’s strategic utility.


Key Takeaways

  • Scope Precision: The patent’s claims define its enforceable protection, emphasizing specific chemical or methodological embodiments integral to its competitive advantage.
  • Landscape Awareness: Similar patents in Lithuania and Europe highlight a dense innovation field requiring thorough freedom-to-operate and invalidity analyses.
  • Legal Strategy: The patent’s longevity likely extends to 2036, with ongoing maintenance and potential patent challenges impacting its strategic value.
  • Regional Significance: While focused on Lithuania, the patent's influence extends through regional and international patent frameworks, necessitating aligned IP strategies.
  • Innovation Outlook: Innovations in drug compositions or methods in Lithuania are closely linked to European developments; patent robustness and scope are critical for market success.

FAQs

  1. What is the typical scope of a Lithuanian pharmaceutical patent like LTPA2016045?
    The scope usually covers specific chemical compounds, formulations, or methods of treatment, defined by its claims, aiming to block competitors from producing similar inventions within the territory.

  2. How does the patent landscape influence the value of LTPA2016045?
    The presence of related patents and prior art can restrict the scope, impact licensing opportunities, or necessitate design-around strategies, thereby directly affecting the patent's commercial potential.

  3. Can a patent filed in Lithuania be enforced in other European countries?
    Not directly. However, through the European Patent Convention, a validated European patent can be enforced across member states, including Lithuania, once granted.

  4. What factors determine if the claims of LTPA2016045 are sufficiently broad?
    Patent claims must balance breadth with specificity; overly broad claims risk invalidation, while overly narrow claims might limit commercial scope.

  5. What strategies can patent holders employ to protect innovations like those in LTPA2016045?
    Strategies include filing continuations, expanding regional protections, monitoring prior art, enforcing rights against infringers, and maintaining lifecycle management.


References

[1] Lithuanian Patent Office. (2016). Patent document LTPA2016045.
[2] European Patent Office. (2022). Guidelines for Examination.
[3] WIPO. (2022). Patent Landscape Reports on Pharmaceutical Innovations.

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