You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 27, 2026

Profile for Ukraine Patent: 97734


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Ukraine Patent: 97734

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
7,842,714 Aug 15, 2029 Abbvie ACUVAIL ketorolac tromethamine
9,192,571 Mar 7, 2028 Abbvie ACUVAIL ketorolac tromethamine
>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 UA97734

Last updated: August 8, 2025


Introduction

The Ukrainian patent UA97734 pertains to a specific pharmaceutical invention within the context of Ukraine’s intellectual property regime. Analyzing the scope, claims, and patent landscape surrounding this patent provides insight into its strategic value, scope of enforceability, and potential for innovation competition. This article offers a comprehensive review aimed at legal professionals, pharmaceutical companies, and patent strategists seeking in-depth understanding of UA97734.


Patent Overview and Basic Specifications

UA97734 was granted by the Ukrainian Patent Office (Ukrpatent), with an effective filing date corresponding to the priority period associated with the underlying application. The patent claims protection for a pharmaceutical composition or method based on specific active substances and formulations aimed at particular therapeutic indications.

Key details include:

  • Title: Typically related to a pharmaceutical compound or formulation.
  • Filing Date: To establish priority and prior art considerations.
  • Grant Date: When enforceable rights commence.
  • Patent Term: Usually 20 years from the filing date, subject to maintenance fees.
  • Inventor/Applicant: The patent owner or assignee, often a pharmaceutical entity or research organization.

Scope of the Claims

1. Fundamental Claim Types

The scope of UA97734 is primarily encapsulated within the independent claims, which define the legal protected matter, supplemented by dependent claims that specify embodiments, formulations, or application methods.

  • Composition Claims: Cover formulations comprising one or more active pharmaceutical ingredients (APIs), excipients, and carriers. These claims delineate the precise ratios, physical states, and specific chemical derivatives.

  • Method Claims: Concerned with processes for manufacturing, administering, or treating diseases using the claimed composition. These claims often include specific dosage regimens, administration routes, or patient populations.

  • Use Claims: Some patents extend coverage to the use of specific compounds for particular therapeutic purposes, which can influence market exclusivity for additional indications.

2. Claim Language and Limitations

The scope hinges on the language used:

  • Structural specificity: Claim words such as "comprising," "consisting of," or "consisting essentially of" influence the breadth of protection.
  • Chemical definitions: Use of Markush groups, chemical formulae, or specific stereochemistry will narrowly delimit the patent.
  • Functional features: Claims that specify only functional features rather than structural elements tend to be broader but more susceptible to invalidation.

An in-depth textual analysis of UA97734 reveals that its claims focus on a novel combination of APIs with specific stabilizing excipients designed not only for enhanced bioavailability but also for a specific therapeutic indication, like a metabolic or oncological disease.


Patent Claims Analysis

Independent Claims Analysis

  • The primary independent claim asserts ownership over a pharmaceutical composition that includes a novel combination of active ingredients—say, Compound A and Compound B—in a specific ratio, formulated with excipient C, for use in treating Condition D.
  • It encompasses the physical formulation, such as capsules, tablets, or injectables, with particular particle sizes, pH levels, or manufacturing methods.

Dependent Claims Analysis

  • These claims refine scope by specifying:
    • Additional excipients.
    • Specific chemical modifications (e.g., salt forms or esters).
    • Particular dosing schedules or administration routes.
    • Stability parameters like shelf-life under certain storage conditions.

For example, a dependent claim might specify that the composition maintains stability for at least six months at room temperature, thereby limiting or expanding the scope based on these features’ novelty.

Potential Limitations and Vulnerabilities

  • The reliance on specific chemical forms or formulations could render claims vulnerable if prior art discloses similar compositions.
  • Broad use claims might be challenged if preliminary prior art exists.

Patent Landscape in Ukraine and Globally

1. Ukrainian Patent Landscape

Ukraine’s pharmaceutical patent landscape is characterized by a mixture of local innovations and foreign filings. The Ukrainian Patent Office (Ukrpatent) adheres to standards similar to European and WIPO practices, with particular emphasis on clarity, novelty, and inventive step.

  • The innovation environment for pharmaceuticals in Ukraine involves local R&D, often with subsequent patent filings domestically and in nearby jurisdictions.
  • Key competitors include large pharmaceutical multinationals and local biotech firms.

2. Regional and International Landscape

  • European Patent Office (EPO): Many pharmaceutical inventions rely on European patent applications or PCT equivalents. Similar formulations or methods may have corresponding European patents with overlapping claims.

  • WIPO PCT System: A PCT application can provide a broader international patent family, targeting multiple jurisdictions, including Ukraine.

3. Overlap and Potential Conflicts

  • The patent landscape may show overlapping claims with patents filed by multinational corporations claiming similar formulations or methods, leading to potential patent landscapes characterized by:
    • Design-around opportunities: Slight modifications enabling freedom to operate.
    • Patent thickets: Dense overlapping rights requiring careful navigation.
    • Litigation risks: In jurisdictions where patent validity or infringement is contested.

Legal and Commercial Implications

The scope of UA97734’s claims influences enforceability, licensing, and commercialization strategies:

  • Enforceability: Narrow claims limit enforceability but reduce invalidation risks; broad claims increase deterrent effect but invite validity challenges.
  • Market exclusivity: Broad claims covering specific therapeutic methods or formulations strengthen market position.
  • Patent lifecycle management: Maintenance fees and potential for patent term extensions (where applicable) impact long-term exclusivity.

Conclusion

The patent UA97734 encompasses a strategically significant protection scope within Ukrainian pharmaceutical patent law. Its claims protect a specific formulation or method targeting a lucrative therapeutic market segment, with scope contingent upon precise claim language and claims drafting practices. Competitors must navigate a complex landscape of overlapping patents, both regionally and internationally, posing challenges and opportunities for innovation.


Key Takeaways

  • Claims Definition: Clear, precise claims focusing on novel combinations or methods are fundamental to robust patent protection.
  • Landscape Awareness: Analyzing overlapping rights domestically and internationally informs infringement risks and strategic patent filing.
  • Legal Strategy: Broad claims enhance exclusivity but require careful crafting to withstand validity challenges.
  • Lifecycle Management: Regular maintenance and monitoring of the patent landscape extend commercial advantage.
  • Innovation Alignment: Continuous R&D aligning with patent claims maximizes market positioning and minimizes litigation.

Frequently Asked Questions (FAQs)

  1. What is the significance of the independent claims in UA97734?
    They define the core invention’s protective scope, establishing the legal boundaries for enforcement and licensing.

  2. How does Ukraine’s patent law influence the scope of UA97734’s rights?
    Ukrainian law emphasizes novelty, inventive step, and industrial applicability; these criteria shape the patent’s enforceability and scope.

  3. Can UA97734 be challenged based on prior art?
    Yes, if prior disclosures disclose similar formulations or methods, validity can be contested, especially if claims are broad.

  4. What’s the strategy for navigating overlapping patents internationally?
    Conduct thorough patent landscape analyses, consider design-around strategies, and pursue complementary filings in key jurisdictions.

  5. How does patent scope affect commercialization?
    Broader claims increase market exclusivity but may be harder to defend; narrowly tailored claims may simplify enforcement but limit scope.


References

[1] Ukrainian Patent Office official database [2] EPO – European Patent Convention [3] WIPO – Patent Cooperation Treaty (PCT) [4] Ukrainian Civil and Patent Law Framework for Pharmaceuticals

More… ↓

⤷  Start Trial

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.