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Last Updated: December 16, 2025

Profile for Ukraine Patent: 109172


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US Patent Family Members and Approved Drugs for Ukraine Patent: 109172

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
8,546,436 Feb 29, 2032 Ironwood Pharms Inc DUZALLO allopurinol; lesinurad
8,546,436 Feb 29, 2032 Ironwood Pharms Inc ZURAMPIC lesinurad
9,956,205 Dec 28, 2031 Ironwood Pharms Inc DUZALLO allopurinol; lesinurad
9,956,205 Dec 28, 2031 Ironwood Pharms Inc ZURAMPIC lesinurad
>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 UA109172

Last updated: August 13, 2025

Introduction

Patent UA109172, filed in Ukraine, pertains to a pharmaceutical compound or formulation designed to address specific medical needs. Analyzing this patent's scope, claims, and overall landscape offers insights into its competitive position and the innovation's novelty within the broader pharmaceutical sector. This assessment provides pharmaceutical companies, legal professionals, and investors with a comprehensive understanding of UA109172's strategic importance in Ukraine and potentially in other markets.

Patent Scope and Claims

Patent Title and Abstract

Although explicit details of UA109172 are not publicly available, typical patent documents disclose an innovative pharmaceutical compound, a novel formulation, or an improved method of synthesis. The abstract generally summarizes the invention's essence—either a new chemical entity, dosage form, or manufacturing process. For pharmacological patents, the scope usually includes the compound's chemical structure, pharmaceutical composition, and therapeutic method of use.

Claims Drafting

The claims define the legal boundaries of patent protection. For UA109172, the claims likely encompass:

  • Independent Claims: Core features of the claimed invention, such as the chemical structure of the drug, specific synthesis methods, or unique formulations.

  • Dependent Claims: Refinements or specific embodiments, such as dosage specifics, combinations with other compounds, or particular manufacturing conditions.

Scope of the Claims

The typical scope of a pharmaceutical patent like UA109172 is designed to protect:

  • Chemical Structure: If the patent pertains to a novel chemical entity, claims will specify the compound's molecular formula, defining the scope of chemical protection.

  • Method of Use: Claims may cover methods of treating certain medical conditions using the compound, expanding the patent's scope to therapeutic applications.

  • Formulation and Dosage Forms: Claims may extend to specific formulations, such as sustained-release preparations or combinations with adjuvants.

  • Synthesis Routes: Innovative manufacturing processes can also be protected, safeguarding cost-effective or more sustainable synthesis methods.

The breadth of these claims typically balances protecting genuine innovation while avoiding overly broad claims that risk invalidation or non-patentability.


Patent Landscape Context

Ukraine's Pharmaceutical Patent Environment

Ukraine’s patent framework aligns with European norms, governed by the Law of Ukraine "On Patents for Inventions." The patent term is 20 years from the filing date, with specific stipulations for pharmaceutical inventions, particularly regarding data exclusivity and patentability (novelty, inventive step, industrial applicability).

Legal and Regulatory Considerations

Pharmaceutical patents in Ukraine are scrutinized for compliance with national and international standards. The Ukrainian Patent Office (Ukrpatent) evaluates novelty and inventive step rigorously, especially given recent amendments aligning with European UPOV and WTO TRIPS agreements.

Patent Family and Related Applications

UA109172 likely belongs to a broader patent family, including counterparts filed in the European Patent Office (EPO), Eurasian Patent Organization (EAPO), and potentially in other jurisdictions such as the US or China. These family members strengthen patent protection strategy across multiple markets.

Competitive Patent Environment

The Ukraine patent landscape for pharmaceuticals is competitive, with several patents filed for similar chemical classes, therapeutic methods, or formulations. Notably, generic manufacturers seek patents to infringe upon or develop around innovative compounds, emphasizing the importance of robust patent claims and legal enforcement.

Patent Enforcement and Challenges

Patent enforcement in Ukraine faces challenges posed by local manufacturing practices, patent life cycles, and potential patent oppositions or litigations. Successful enforcement depends on clear claim language, maintenance of patent validity, and strategic litigation.


Significance of the Patent

Protection of Innovation

UA109172’s claims potentially fortify the innovation against generic entry, providing a period of market exclusivity that incentivizes R&D investments. The patent's scope directly correlates with the strength of market position and licensing opportunities.

Market Implication

If formulated for a high-demand medical indication, the patent can guide marketing and commercialization strategies within Ukraine, especially if aligned with regulatory approvals. It may also serve as a bargaining chip in licensing negotiations or partnerships.

Strategic Positioning

A strong patent portfolio, including UA109172 and related filings, enhances a company’s competitive advantage, deters infringement, and provides leverage in patent disputes, especially against generic challengers post-expiry.


Conclusion and Recommendations

  • Patent Claims Analysis: Careful review of both independent and dependent claims is essential to evaluate the breadth and enforceability of protection. Focus on whether claims cover both the chemical entity and its therapeutic uses.

  • Landscape Monitoring: Continuous tracking of pharmaceutical patent filings both in Ukraine and internationally ensures the protection of innovations and identification of potential infringements.

  • Legal Validation: Regular patent validity assessments can safeguard against invalidation risks, especially considering Ukraine’s evolving patent laws.

  • Licensing and Commercialization: Leveraging the patent’s protection can facilitate licensing agreements, especially given Ukraine’s strategic position as a gateway to Eastern European markets.


Key Takeaways

  • Patent UA109172 likely covers a novel chemical compound, formulation, or therapeutic method with strategic significance within Ukraine’s pharmaceutical IP landscape.

  • The scope of claims determines the extent of protection; precise claim drafting is critical for defending against infringement and enabling licensing.

  • Ukraine’s patent environment emphasizes strict novelty and inventive step audits, aligning with European standards, which underpins the patent’s validity and enforceability.

  • A comprehensive patent landscape analysis reveals competition, guides infringement avoidance strategies, and supports expansion into global markets.

  • Proactive monitoring and legal validation underpin the patent’s strategic value and commercial potential.


FAQs

1. What is the typical scope of pharmaceutical patents like UA109172?

Pharmaceutical patents generally cover the chemical structure of a drug, pharmaceutical compositions, methods of use, and manufacturing processes. The scope depends on how broadly the claims are drafted, balancing coverage and legal validity.

2. How does Ukraine’s patent law influence the protection of pharmaceutical patents?

Ukraine’s patent law aligns with international standards, requiring novelty, inventive step, and industrial applicability. Patent protection lasts 20 years, with specific provisions for pharmaceuticals, including data exclusivity, impacting patent enforcement.

3. Can UA109172 be extended or supplemented in other jurisdictions?

Yes. The patent family may include filings in EPO, US, China, or other markets, allowing patent protection beyond Ukraine. These filings can extend the geographic scope and commercial reach.

4. What are common challenges to pharmaceutical patent validity in Ukraine?

Invalidation can arise from prior art disclosures, lack of inventive step, or insufficient disclosure. Ensuring that the claims are novel, inventive, and clearly supported improves robustness against legal challenges.

5. How does the patent landscape impact generic drug competition?

Strong, well-drafted patents delay generic entry, prolonging exclusivity and revenue. Conversely, weak or challenged patents can facilitate generic filings, impacting market share and profitability.


Sources:

[1] Ukrainian Patent Law, Law of Ukraine “On Patents for Inventions”
[2] European Patent Office Guidelines for Examination
[3] World Intellectual Property Organization (WIPO) Patent Database
[4] Ukrainian Patent Office official publications
[5] Industry reports on pharmaceutical patent trends in Eastern Europe

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