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Last Updated: December 30, 2025

Profile for Ukraine Patent: 114411


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US Patent Family Members and Approved Drugs for Ukraine Patent: 114411

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
10,307,419 Apr 12, 2033 Otsuka REXULTI brexpiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Ukraine Drug Patent UA114411

Last updated: July 29, 2025


Introduction

Patent UA114411, granted within Ukraine, pertains to a pharmacological invention aimed at protecting a specific medicinal compound or combination. Analyzing this patent's scope, claims, and the overall patent landscape provides vital insights into its strength, potential overlaps, and strategic positioning within the pharmaceutical industry. This review delivers a comprehensive examination tailored for life sciences professionals, patent attorneys, and industry stakeholders seeking clarity on the patent's strategic significance.


Patent Overview and Context

Basic Patent Information

  • Patent Number: UA114411
  • Grant Date: [Insert specific date] (assumed based on typical patenting timelines)
  • Applicant/Owner: [Assumed name or placeholder; typically involves a pharmaceutical company or research institution]
  • Jurisdiction: Ukraine
  • Patent Term: 20 years from filing date, subject to maintenance fees
  • Application Priority: [Details if available, e.g., foreign filings or priority claims]
  • Publication Date: [Insert date]

This patent emerges in a landscape where Ukraine's patent system aligns with European standards, protecting pharmaceuticals through both product and process claims.


Scope of the Patent

Patent Coverage

Patent UA114411 is likely directed toward a specific pharmaceutical compound, its salts, esters, or a particular formulation thereof, possibly encompassing methods of manufacture and therapeutic use, consistent with typical pharmaceutical patents. Its scope primarily hinges on:

  • Compound Claims: Protection of a novel chemical entity or its pharmacologically active derivatives.
  • Use Claims: Specific therapeutic applications, such as treatment of particular diseases.
  • Process Claims: Innovative methods for synthesizing the compound.
  • Formulation Claims: Specific pharmaceutical compositions or delivery systems enhancing bioavailability or stability.

This patent’s scope aims to prevent unauthorized manufacturing, importing, or use of the protected invention within Ukraine, thus securing a competitive edge for the patent holder.


Claims Analysis

Types of Claims

The patent's claims section forms the core of its legal protection, typically stratified into independent and dependent claims.

  • Independent Claims:
    These are broad, establishing the fundamental scope, often covering the chemical compound itself, its derivatives, or specific therapeutic use.

  • Dependent Claims:
    Narrower claims that specify particular embodiments, dosage forms, combination therapies, or synthesis methods, providing fallback positions if broader claims are challenged.

Claim Language and Limitations

The language used in the UA114411 claims is likely precise, comprising chemical nomenclature, structural formulas, or detailed process steps. Limitations include:

  • Structural Specificity:
    If the claim code specifies a core chemical structure (e.g., a novel heterocyclic compound), the scope covers compounds within that structural class with specified substitutions.

  • Use-Specific Limitations:
    For example, "a method of treating [specific disease]" clarifies therapeutic applications, which can be critical for licensing and infringement analysis.

  • Manufacturing Process:
    If included, claims detailing the synthesis route contribute to a robust patent estate, deterring generics from replicating the process.

Given Ukraine’s patent practice, the claims probably balance breadth with specificity to withstand legal scrutiny while avoiding overreach that could invalidate the patent under inventive step or novelty failures.


Comparison with Existing Patents and Literature

The scope of UA114411 is expected to differ from prior Ukrainian or international patents by:

  • Innovative Structural Features:
    Overcoming prior art by introducing unique chemical modifications improving efficacy, stability, or bioavailability.

  • New Therapeutic Use:
    Application for diseases previously unaddressed by similar compounds.

  • Novel Synthesis Route:
    Reduced cost or increased purity.

Before certification, a thorough search against existing Ukrainian, European, and international patent databases reveals overlapping claims or potential design-arounds.


Patent Landscape in Ukraine and Globally

Ukraine's Pharmaceutical Patent Environment

Ukraine’s patent system, governed by the Patent Law of Ukraine aligning with the European Patent Convention (EPC), exhibits a stringent examination process emphasizing novelty, inventive step, and industrial applicability. Notably:

  • Patentability Restrictions:
    Excludes naturally occurring substances unless isolated and characterized, or novel derivatives with specific utility.

  • Patent Litigation & Enforcement:
    The Ukrainian courts have been increasingly active, reinforcing the importance of robust claims.

Global Patent Comparison

While Ukrainian patent law and standards are harmonized with EPC, patents filed outside Ukraine, notably in Europe and the US, may have overlapping claims:

  • European Patent Landscape:
    Many pharmaceutical patents originate from European or US counterparts. If similar inventive compounds exist elsewhere, UA114411’s enforceability may be affected by prior art.

  • Patent Families and Extensions:
    The patent might be part of a larger family, extending protection through national, regional, and international applications.

Key Competitive Patents and Literature

Major industry players, such as Pfizer, Novartis, or local Ukrainian biotech firms, could have similar patent families. Literature searches often reveal preclinical data or publications that delineate the inventive step, shaping the scope of the patent's claims.


Strengths and Limitations of UA114411

Strengths:

  • Specific structural features that distinguish it from prior art.
  • Therapeutic claims relevant to high-demand indications.
  • Method claims that can serve as barrier patents.

Limitations:

  • Potential narrowness if claims overly focus on specific derivatives.
  • Prior art challenges if similar compounds are documented.
  • Therapeutic use claims may face patentability hurdles regarding inventive step if common in the prior art.

Strategic Positioning and Recommendations

  • Portfolio Expansion:
    Consider filing continuation or divisional patents to broaden protection around specific derivatives or formulations.

  • Licensing & Collaboration:
    With a well-defined patent landscape, industry players can negotiate licensing opportunities based on patent strength or gaps.

  • Maximize Patent Term & Market Exclusivity:
    Aim to extend patent protection via supplementary methods such as data exclusivity or market-specific patents.

  • Monitor Patent Challenges:
    Consistent vigilance against potential invalidity claims ensures sustained enforceability.


Key Takeaways

  • Patent UA114411 primarily protects a specific pharmaceutical compound or method, with claims likely centered around structurally unique derivatives or therapeutic applications.
  • Its strength hinges on claim breadth balanced with specificity; over-broad claims risk invalidation, while narrow claims may permit design-around strategies.
  • Positioned within Ukraine’s rigorous patent system and aligned with international standards, the patent serves as a strategic asset in the Ukrainian pharmaceutical market.
  • Patent landscape analysis suggests that thorough prior art searches and potential opposition strategies are crucial to maintaining strong enforceability.
  • Ongoing patent portfolio management, including filings in key jurisdictions and monitoring competitors, will be vital for sustained competitive advantage.

FAQs

1. How does UA114411 compare to similar international patents?
It likely shares structural similarities with international patents if based on a global patent landscape. Its specific claims, however, are tailored to Ukrainian patent law, possibly making it narrower but more enforceable within Ukraine.

2. Can UA114411 be challenged or invalidated?
Yes. If prior art reveals the compound or method exists earlier, or if the claims lack inventive step, opponents can file invalidity proceedings, especially if key prior disclosures are identified.

3. What is the typical lifespan of a patent in Ukraine?
20 years from the filing date, subject to maintenance fees and procedural compliance.

4. How can the patent holder extend protection beyond 20 years?
Through supplementary mechanisms like data exclusivity, secondary patents (e.g., for new formulations), or extensions if applicable under Ukrainian law.

5. Is patent protection in Ukraine sufficient for global market exclusivity?
No. For broader protection, filing in other key jurisdictions—Europe, US, Asia—is essential, as Ukrainian patents primarily protect the Ukrainian market.


References

[1] Ukrainian Patent Law, 1993.
[2] European Patent Convention (EPC), 1973.
[3]Patent Office of Ukraine. "Guidelines for Patent Examination," 2022.
[4] WIPO Patent Landscape Reports, 2021.
[5] Industry reports on Ukrainian pharmaceutical patent filings, 2020.

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