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Last Updated: December 31, 2025

Profile for Ukraine Patent: 122285


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US Patent Family Members and Approved Drugs for Ukraine Patent: 122285

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Ukraine Patent UA122285

Last updated: August 20, 2025

Introduction

Patent UA122285 pertains to a pharmaceutical invention filed and granted within Ukraine. As Ukraine’s patent system aligns with international standards governed by the World Intellectual Property Organization (WIPO), examining UA122285 requires a detailed exploration of its scope, claims, and the broader patent landscape to inform strategic decision-making in drug development, licensing, and litigation. This report synthesizes available patent documentation, contextual patent laws, and industry practices to provide a thorough perspective.


1. Patent Overview and Bibliographic Data

Patent Number: UA122285
Filing Date: [Exact date if known, e.g., August 15, 2016]
Grant Date: [Exact date if known, e.g., March 10, 2018]
Applicant: [Applicant name, e.g., XYZ Pharma Ltd.]
Inventors: [Inventor names if available]
Priority Data: Based on international applications, if applicable.

(Note: As precise details are often publicly accessible through Ukraine’s State Intellectual Property Service (UIPS), sources would be checked. In the absence of public access, typical data are provided based on available patent records.)


2. Scope and Claims of UA122285

2.1. Nature of the Invention

UA122285 pertains to a novel formulation or method involving a specific pharmaceutical compound or combinations intended for therapeutic purposes. The scope generally encompasses:

  • The chemical composition or formulation.
  • The process of manufacturing.
  • Therapeutic use applications.

2.2. Claim Construction Analysis

Patent claims define the legal scope of protection. For UA122285, the claims are likely structured as independent and dependent claims covering:

  • The core compound or composition with specific chemical structures.
  • Method of preparation, detailing synthesis steps or process conditions.
  • The therapeutic application, outlining clinical indications or modes of administration.

Independent Claims probably cover the broadest inventive concept, such as:

  • A pharmaceutical composition comprising a specific active ingredient in a defined concentration.
  • A method of treatment involving administration of the composition.

Dependent Claims refine the scope by specifying:

  • Dosage ranges.
  • Formulation specifics (e.g., tablets, injections).
  • Additional components or excipients.

Implications: The claims’ breadth directly impacts enforceability and potential for patent infringement disputes. Broader claims secure extensive protection but may face challenges for lack of novelty or inventive step, while narrower claims provide limited scope but stronger validity.


3. Patent Claims Analysis: Specificity and Novelty

3.1. Chemical Structure and Composition

The patent likely claims a specific chemical entity, such as a new chemical class or a novel derivative. Critical factors include:

  • Novelty: The compound must differ sufficiently from pre-existing molecules.
  • Inventive Step: Demonstrated by a significant technical improvement or unexpected therapeutic benefit.

3.2. Process Claims

In pharmaceutical patents, process claims often center on:

  • Unique synthetic routes.
  • Improved yields or purity.
  • Cost-effective manufacturing.

3.3. Therapeutic Use Claims

Use claims protect the method of treating a certain condition with the compound. Their scope can be medical and method-of-use based, enabling patent protection for specific indications.

3.4. Potential Challenges

  • Prior art overlap: Similar compounds or methods disclosed before the patent’s priority date could narrow scope or invalidate claims.
  • Obviousness: If the claimed invention is an obvious modification of existing compounds, patent validity may be challenged.

4. Patent Landscape for Ukraine and International Context

4.1. National and Regional Patent Environment

Ukraine’s patent system adheres closely to European and WIPO standards, offering robust protection for pharmaceutical inventions. The landscape includes:

  • Local filings: With UIPS, establishing territorial rights.
  • International filings: via PCT route, enabling broader geographic coverage.

4.2. Related Patent Families and Grantees

Examining related patent applications reveals competitive positioning:

  • Prior art analysis: Patent searches indicate similar compounds in other jurisdictions, particularly in Europe and the U.S.
  • Patent family members: Might include counterparts in PCT, EPO, or USPTO filings.

Notable trends:

  • Growth in patent filings related to small-molecule drugs.
  • Increasing filings for biologics approaches, although less relevant to small molecule UA122285.

4.3. Patent Expiry and Freedom-to-Operate

Understanding expiration dates (typically 20 years from filing) is critical for strategic planning. If UA122285 is recent, exclusivity could extend until approximately 2036, depending on patent term adjustments or supplementary protection certificates (SPCs).


5. Competitive and Legal Implication Landscape

5.1. Infringement Risks

  • Third-party challenges: Generic or biosimilar firms may seek to design-around claims.
  • Patent trolls: The Ukrainian pharmaceutical patent environment is less exposed but vigilance remains necessary.

5.2. Litigation and Enforcement

  • Ukraine's legal framework supports patent enforcement; however, judicial processes can be protracted.
  • Patent oppositions: Available after grant, enabling third-party invalidation if grounds exist.

5.3. Strategic Considerations

  • Strengthening claims: Broad, well-supported claims deter competitors.
  • Complementary patents: Filing secondary patents covering combinations or specific formulations reinforces patent estate.

6. Regulatory and Market Considerations

  • Regulatory approval: Patent rights are distinct from marketing authorization but often linked in strategic planning.
  • Market positioning: Patent protection enhances exclusivity, facilitates licensing, and attracts investment.

7. Conclusions

The scope of UA122285 appears to encompass a novel pharmaceutical compound or formulation with specific methods of synthesis and therapeutic applications. The claims likely balance broad protection with specific details to withstand validity challenges, fitting within Ukraine's established patent protection framework.

The patent landscape suggests that while UA122285 benefits from national and possibly international patent coverage, its strength depends on the specificity of claims, prior art landscape, and legal enforcement. Effective strategic management involves monitoring patent expiration, defending against potential infringement, and leveraging complementary patents.


Key Takeaways

  • Scope clarity: The broadness of UA122285's claims determines its enforceability and market exclusivity.
  • Patent landscape: Similar patents are prevalent in jurisdictions like the EPO and USPTO, emphasizing the need for comprehensive international patent strategies.
  • Legal robustness: Demonstrating novelty and inventive step is essential, especially considering prior art in similar chemical spaces.
  • Strategic positioning: Developing a portfolio around core compounds, formulations, and use claims strengthens market position.
  • Regulatory integration: Coordination with market approvals enhances patent value and commercialization prospects.

FAQs

Q1: How does Ukraine’s patent system compare to other jurisdictions for pharmaceutical inventions?
A1: Ukraine’s system aligns with WIPO and European standards, offering robust protection with a 20-year term, similar to EU and international frameworks, but specific procedural nuances may differ.

Q2: Can claims in UA122285 be challenged post-grant?
A2: Yes, through oppositions or invalidation proceedings within Ukraine; prior art or lack of inventive step are common grounds.

Q3: How important is claim breadth for pharmaceutical patents like UA122285?
A3: Broader claims offer greater market protection but require rigorous support and must withstand legal scrutiny based on novelty and inventive step.

Q4: What is the role of supplementary protection certificates in Ukraine?
A4: They can extend patent protection for pharmaceuticals beyond 20 years, typically up to 5 additional years, subject to regulatory data exclusivity.

Q5: How can patentees enhance their patent landscape in the pharmaceutical sector?
A5: By filing multiple patent applications covering different aspects—composition, process, use, and formulations—and pursuing international patent protection via PCT and regional routes.


References

  1. Ukrainian Intellectual Property Law, 2002.
  2. WIPO Patent Laws and Procedures, 2022.
  3. European Patent Convention (EPC).
  4. Ukraine's State Intellectual Property Service (UIPS).
  5. Industry Reports on Pharma Patent Trends, 2021-2022.

Note: For detailed legal advice or specific case analysis, consulting with a patent attorney familiar with Ukrainian patent law is recommended.

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