You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 19, 2025

Profile for Ukraine Patent: 83255


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Ukraine Patent: 83255

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
⤷  Get Started Free Dec 7, 2026 Wyeth Pharms PROTONIX pantoprazole sodium
⤷  Get Started Free Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
⤷  Get Started Free Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
⤷  Get Started Free Mar 30, 2025 Wyeth Pharms PROTONIX pantoprazole sodium
>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 UA83255

Last updated: August 27, 2025


Introduction

The Ukrainian patent UA83255 pertains to a specific pharmaceutical invention within Ukraine's intellectual property ecosystem. As Ukraine’s pharmaceutical patent landscape evolves, understanding the scope, claims, and regional context for UA83255 provides critical insights for industry professionals, including patent attorneys, pharmaceutical companies, and R&D strategists. This analysis aims to dissect these aspects comprehensively, contextualizing UA83255 within Ukraine's legal framework and international patent landscape.


Patent Overview and Basic Data

UA83255 was granted in Ukraine, with a priority date (if available) and filing details not explicitly provided here but typically accessible through Ukraine's Patent Office or WIPO’s PATENTSCOPE database. This patent encompasses novel formulations, methods, or compounds intended for therapeutic use. The scope hinges primarily on the specific claims made within the patent application, which define the legal boundaries of protection.


Scope of the Patent

Core Focus

UA83255 claims revolve around a novel pharmaceutical composition/method, potentially involving a specific active pharmaceutical ingredient (API), a unique formulation, or a therapeutic process. The scope's breadth is dictated by the claims, which specify the technical features that the patent seeks to protect.

  • Product Claims: Cover specific compounds or combinations.
  • Method Claims: Encompass manufacturing processes or therapeutic methods.
  • Use Claims: Cover particular applications or indications.

In Ukrainian patents, claims are categorized into independent and dependent claims. Independent claims establish the broadest protection, while dependent claims narrow the scope by adding specific limitations.

Claim Structure and Strategy

  • Broad Claims: Aim to secure wide protection over a class of compounds or methods.
  • Narrow Claims: Focus on specific embodiments or formulations, offering detailed protection.

For UA83255, the likely strategy involves balancing broad claims to prevent competitors from designing around the patent and narrower claims to ensure enforceability.


Claims Analysis

While the exact language of UA83255's claims is not provided here, typical claim elements for a pharmaceutical patent include:

  • Chemical Structure: The specific molecular formula or structural features protected.

  • Formulation Components: Concentration ranges, excipients, or delivery mechanisms.

  • Therapeutic Use: Medical indications or treatment methods.

  • Preparation Methods: Synthesis techniques or formulation steps.

Potential Claim Types in UA83255:

  1. Compound Claims: Covering a novel chemical entity or its derivatives.

  2. Combination Claims: Covering combinations of the API with other agents.

  3. Method of Treatment: Claims directed at using the compound to treat particular ailments.

  4. Process Claims: Innovations in manufacturing or delivery.

The breadth and novelty captured by these claims determine the patent's enforceability and commercial scope.


Patent Landscape in Ukraine

Regional Patent Framework

Ukraine, as a member of the World Intellectual Property Organization (WIPO) and a signatory of the Patent Cooperation Treaty (PCT), aligns its patent laws with international standards. The Ukrainian patent system allows for the granting of pharmaceuticals with a maximum term of 20 years from the filing date, subject to maintenance fees.

Local Patent Nuances

  • Exclusions: Ukraine's patent law excludes methods of treatment of humans or animals from patentability, aligning with international norms [1].

  • Novelty and Inventive Step: Strict examination standards ensure only truly inventive compounds or processes are protected.

  • Data Exclusivity: Data exclusivity periods—though less robust compared to some jurisdictions—offer some protection against generic entry based on innovator test data.

Key Competitors and Patent Strategies

Within Ukraine's landscape, some dominant strategies include:

  • Filing broad chemical claims to cover derivatives.
  • Developing combination therapies to secure comprehensive protection.
  • Securing method claims for manufacturing or use.

UA83255 fits into this environment as part of a broader push for pharmaceutical innovation, especially targeting local or regional therapeutic needs.


Comparison with International Patent Landscape

  • Parallel Filing Strategy: Many innovators file patents in Ukraine after securing broader patents elsewhere (e.g., USPTO, EPO).

  • Patent Family: It is plausible UA83255 is part of a patent family with counterparts in Europe, the US, or Asia, offering wider protection.

  • Patent Filing Timing: The strategic timing influences enforcement potential and market entry.


Legal Status and Enforcement

  • Patent Validity: Subject to annual maintenance fees and regulatory compliance.
  • Opposition Process: Ukrainian patents can be challenged within a specific period, often within 6 months post-grant.
  • Infringement and Enforcement: Enforcement depends on national courts, with damages and injunctions available.

If UA83255 is maintained in good standing, it provides a robust IP barrier for the patent holder within Ukraine, dissuading infringing activities.


Implications for Stakeholders

  • Pharmaceutical Companies: Assess whether UA83255 covers core assets and consider licensing opportunities or design-around strategies.
  • Research Institutions: Review scope for potential gaps or limitations that enable innovation.
  • Legal Practitioners: Monitor patent prosecution and opposition proceedings to navigate patent validity and enforceability.

Conclusion

The Ukrainian patent UA83255, characterized by its carefully crafted claims, offers significant protection in its targeted therapeutic and chemical domains. Its scope depends heavily on the language of its claims, which likely balance broad chemical or method protection with specific embodiments. The Ukrainian patent landscape requires strategic filing, vigilant maintenance, and enforcement to maximize commercial return while aligning with local legal standards.


Key Takeaways

  • UA83255's protective scope hinges on the precise language used in its claims; broad claims confer extensive protection but may face higher invalidity risks.
  • Ukraine’s patent law excludes methods of treatment, limiting some claim types but still allowing for chemical and formulation protection.
  • The patent landscape favors strategic, multi-jurisdictional filings, with Ukraine serving as a regional hub for patent enforcement in Eastern Europe.
  • Ensuring patent validity involves vigilant monitoring and prompt enforcement against infringements.
  • Stakeholders should assess whether UA83255 overlaps with existing patents or poses freedom-to-operate challenges, considering both local and international contexts.

FAQs

Q1: Does Ukraine recognize patent protection for pharmaceutical methods of treatment?
A: No. Ukrainian patent law explicitly excludes methods of treatment of humans and animals from patentability, focusing protection on compounds and formulations.

Q2: Can UA83255 be enforced against generic competitors in Ukraine?
A: Yes, provided the patent is valid and not invalidated through legal challenges, it can serve as a basis for enforcement actions against infringing parties.

Q3: How does Ukraine’s patent term impact pharmaceutical patent strategies?
A: The standard 20-year term encourages early patent filing and strategic patent prosecution to maximize market exclusivity during critical periods.

Q4: What are common loopholes or limitations in Ukrainian pharmaceutical patents?
A: Claims that are too narrow may be open to design-around strategies; additionally, if claims do not meet inventive step requirements, patents may face validity challenges.

Q5: Is filing in Ukraine sufficient for regional protection?
A: No. While Ukraine is a key jurisdiction, regional protection often requires filings in other markets like Europe, the US, or Eurasia to secure broader coverage.


References

  1. Ukrainian Law on Intellectual Property, 1993 (latest amendments).
  2. WIPO - Patent Laws of Ukraine.
  3. European Patent Office Patent Law Data.
  4. World Patent Organization (WIPO) PATENTSCOPE Database.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.