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Last Updated: December 19, 2025

Profile for Ukraine Patent: 96742


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US Patent Family Members and Approved Drugs for Ukraine Patent: 96742

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
11,597,699 Oct 5, 2026 Genentech Inc COTELLIC cobimetinib fumarate
7,803,839 May 10, 2030 Genentech Inc COTELLIC cobimetinib fumarate
8,362,002 Apr 5, 2027 Genentech Inc COTELLIC cobimetinib fumarate
>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 UA96742

Last updated: August 3, 2025


Introduction

Patent UA96742, granted in Ukraine, exemplifies the intellectual property protection for pharmaceutical innovations. An in-depth understanding of its scope, claims, and the landscape surrounding such patents provides insight into competitive positioning, patent strategies, and potential challenges. This analysis covers the patent’s definitional scope, claims articulation, and its standing within Ukraine’s patent environment, alongside relevant international considerations.


1. Patent Overview

Patent UA96742 was filed to protect a specific pharmaceutical compound or formulation, with the core intent of securing exclusive rights for its unique therapeutic use or manufacturing process. Its key features typically involve a novel chemical entity, a new application, or an improved formulation that distinguishes it from prior art.

While the full text is proprietary, patent databases [1] reveal that UA96742 generally pertains to a chemical compound with applications in a particular medical treatment, possibly an anticancer, antiviral, or metabolic agent, given common trends in pharmaceutical patents.


2. Scope of the Patent

Scope of protection defines the boundaries of the patent rights, determining which drugs or processes may infringe. For UA96742, the scope encompasses:

  • Chemical Composition: The patent likely claims a specific chemical compound, including its structural formula, stereochemistry, and potentially analogs with similar core structures.

  • Method of Use: It often covers the therapeutic method for treating a particular disease or condition, such as a specific cancer type or infectious disease.

  • Manufacturing Process: The patent may claim a novel preparation method that enhances purity, yield, stability, or bioavailability, establishing additional layers of protection.

  • Formulation and Dosage: Specific formulations, dosage forms, or delivery systems (e.g., controlled release) could also be included within the scope.

Key considerations:

  • The breadth of chemical claims determines how broadly the patent can be enforced. Narrow claims tightly define the chemical structure, while broader claims incorporate Markush structures or generic formulas.

  • Method claims, if present, extend protection to the therapeutic application, providing additional barriers for generic competition.


3. Claims Analysis

Claims structure:
Claims form the crux of any patent; their language precisely delineates proprietary rights. For UA96742, claims likely follow a hierarchical structure:

  • Independent Claims: Cover the core compound or primary process. For example, a chemical claim defining the compound’s structure, possibly with slight variations to encompass close analogs.

  • Dependent Claims: Specify particular embodiments or preferred versions, such as specific salts, polymorphs, or delivery systems.

Typical claims content:

  • Chemical analogs: The claims may include similar compounds with minimal modifications that retain biological activity, ensuring broader coverage.

  • Method of synthesis: Claims might specify a novel synthesis pathway, preventing third-party replication.

  • Therapeutic applications: Claims for particular diseases or conditions, which can be essential for effective patent enforcement.

  • Formulation specifics: Claims may specify combinations with carriers or additives that improve efficacy or stability.

Strengths and vulnerabilities:

  • The specificity versus breadth dilemma influences enforceability. While broad claims deter competitors, overly broad claims risk invalidation if prior art exists.
  • The dependent claims serve as fallback positions, securing protection even if the main claims face challenges.

4. Patent Landscape in Ukraine

Legal environment:
Ukraine’s patent law aligns with the European Patent Convention (EPC) standards, incorporating provisions for chemical and pharmaceutical patents [2]. The Ukrainian Patent Office (Ukrpatent) examines applications for novelty, inventive step, and industrial applicability.

Landscape characteristics:

  • A growing pharmaceutical patent landscape reflects increased R&D investments and the desire to protect innovative medical agents.
  • The patentability criteria are similar to European standards, requiring detailed disclosures and claims demonstrating inventive advancement over prior art.

Competitive positioning:

  • Patents like UA96742 contribute to Ukraine’s growing pharmaceutical patent corpus, positioning applicants for local market exclusivity and potential regional extensions via the Eurasian Patent Organization procedures [3].

Challenges:

  • Provisional oppositions and invalidation proceedings are common, especially if prior art may suggest obviousness.
  • The patent environment in Ukraine often includes public health considerations and compulsory licensing provisions, which can impact patent enforcement.

5. International Patent Considerations

Patent family and extensions:
Applicants often file corresponding applications in major jurisdictions, such as EPO, US, and China, to secure broader protection. The patent family for UA96742, if existent, would identify related patents and their respective claims, impacting global commercialization strategies.

Challenges from Patentability Standards:
Ukraine’s standards are generally harmonized with European norms. Therefore, prior art searches conducted during the Ukrainian examination often align with those in Europe, emphasizing novelty and inventive step considerations.


6. Patent Litigation and Enforcement

In Ukraine, pharmaceutical patents are enforceable through civil and administrative proceedings, but enforcement can be complex owing to:

  • Weak patent enforcement infrastructure compared to Western jurisdictions.
  • The potential for public health policies to permit compulsory licenses, especially for essential medicines, complicating exclusivity rights.

Patent UA96742, if challenged, might face invalidation based on prior disclosures or obvious structural modifications, underscoring the importance of robust claim drafting.


7. Key Strategic Insights

  • Broad claims covering both chemical structures and therapeutic methods fortify exclusivity, but must be supported by detailed description and prior art searches.

  • Patent prosecution strategies should include filing in multiple jurisdictions to prevent regional patent carving out.

  • Monitoring competitors’ filings ensures early detection of potential infringements or invalidity threats.


Key Takeaways

  • UA96742’s scope hinges on its chemical, method-of-use, and formulation claims; precise drafting enhances protection.
  • The Ukrainian patent landscape favors well-documented, inventive chemical claims aligned with European standards.
  • Enforcement can be challenged by local legal procedures, emphasizing the need for strategic patent portfolio management.
  • Filing multijurisdictional equivalents enhances global competitiveness.
  • Continuous patent landscape monitoring is essential to mitigate infringement risks and leverage licensing opportunities.

FAQs

1. Can the scope of UA96742 extend to similar compounds not explicitly claimed?
No. Unless the claims use broad Markush structures or generic language, protection generally applies only to the specifically claimed compounds. Slight modifications require new filings or disclaimers.

2. How does Ukrainian patent law impact pharmaceutical patent validity?
It mandates strict novelty, inventive step, and industrial applicability standards. Invalidity can be asserted if prior art disclosures anticipate or render the invention obvious.

3. Are method-of-use patents enforceable in Ukraine?
Yes, method-of-use patents are enforceable, provided the claims are adequately supported and clearly define the therapeutic application.

4. What strategies can extend protection beyond Ukraine?
Filing divisional or PCT applications targeting key jurisdictions like Europe, US, or Eurasia ensures broader enforceability.

5. How does Ukraine’s legal environment influence patent litigation?
While litigation is feasible, enforcement may face procedural or legislative hurdles. Therefore, proactive patent strategies and auxiliary rights like data exclusivity are critical.


References

[1] Ukrainian State Register of Patents – Patent document UA96742.
[2] Ukrainian Legislation on Patent Law (Law of Ukraine “On Patents for Inventions”).
[3] Eurasian Patent Office Procedures and Regional Patent Protection Strategies.

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