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Last Updated: December 16, 2025

Profile for Eurasian Patent Organization Patent: 202090659


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 202090659

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
10,786,489 Oct 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
12,138,250 Oct 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Scope, Claims, and Patent Landscape for Eurasian Patent Organization Patent EA202090659

Last updated: August 7, 2025


Introduction

Eurasian Patent Organization (EAPO) patent EA202090659 pertains to a drug patent held within the Eurasian patent system, which consolidates patent rights across member states including Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan. This analysis examines the scope of the claims, their individual components, and positions this patent within the broader landscape of pharmaceutical innovation in Eurasia.

Understanding this patent's scope and claims is essential for stakeholders involved in drug development, licensing, litigation, or market entry strategies in Eurasia. It also offers insight into the innovation trends in the region and how this patent fits into existing patent landscapes.


Patent Overview and Basic Details

While the full patent document's content is proprietary, available public records provide key insights:

  • Patent Number: EA202090659
  • Filing/Publication Date: October 2020 (assumed based on number and typical timeline)
  • Applicant: [Data Not Provided]
  • Inventor/Owner: [Data Not Provided]
  • Priority Date: [Likely 2019 or earlier, based on Eurasian patent process timelines]
  • Patent Family: Likely linked to filings in individual Eurasian member states as well as possibly in WIPO (PCT) or other jurisdictions.

The patent generally focuses on a novel pharmaceutical compound or composition with therapeutic utility. The exact chemical structure or formulation is essential for detailed analysis but assumes pharmaceutical innovation related to the treatment of specific diseases.


Scope of the Patent

Claims Analysis

Patent EA202090659, like typical pharmaceutical patents, likely contains multiple claims divided into independent and dependent claims:

  • Independent Claims: These define the core invention, such as a novel chemical entity, method of synthesis, or medical use.
  • Dependent Claims: These specify particular embodiments, formulations, dosage forms, or application methods.

Given standard practices, the scope probably includes:

  • Novel Chemical Compound: A specific chemical structure with desirable pharmacological activity.
  • Pharmaceutical Composition: A formulation comprising the compound, possibly with carriers or excipients.
  • Method of Use: A treatment method for a particular disease or medical condition, e.g., cancer, infectious disease, or metabolic disorder.

The core independent claim might define:

"A compound of formula [X], or a pharmaceutically acceptable salt thereof, capable of [desired biological activity], characterized by..."

This broad language aims to encompass the compound's chemical variations and therapeutic uses, providing extensive patent protection.

Claim Scope Considerations

  • Breadth and Specificity: Broad claims protect a wide chemical space but risk invalidity if deemed obvious or lack novelty. Narrow claims focus on specific compounds or uses but limit scope.
  • Scope of Protection: If the patent claims cover a broad chemical class, they could block generic competitors' access. Conversely, narrower claims provide a safer legal armor but less extensive market monopoly.
  • Use Claims: Claims for specific medical indications extend protection into therapeutic methods, often highly valued.

Legal and Technical Limitations

  • The claims' validity depends on demonstrating novelty, inventive step, and industrial applicability.
  • Possibility of overlaps with prior art, especially if similar compounds or uses exist.

Patent Landscape in Eurasia

Regional Patent Environment

The Eurasian patent system strives to harmonize patent rights, but notable differences exist compared to other jurisdictions:

  • Patentability Criteria: Similar to Europe and Russia — novelty, inventive step, industrial applicability.
  • Pharmaceutical Patent Challenges: Strict scrutiny on inventive step and prior art, especially concerning known compounds with minor modifications.
  • Compulsory Licensing and Patent Term: Following TRIPS, patents grant 20-year protection, with some flexibility in Eurasia.

Competitor and Innovation Landscape

  • The landscape features both domestic firms and multinational pharmaceutical companies.
  • Key areas include oncology, infectious diseases, and rare diseases.
  • Patent filings often cluster around chemical modifications, delivery systems, and therapeutic methods.

Patent Families and Infringement Risks

This patent likely forms part of a broader family, with filings in Russia, Kazakhstan, etc., emphasizing the importance of intra-regional patent coordination. Infringement analysis must consider local enforcement mechanisms and potential patent challenges.


Related Patents and Prior Art

Review of prior patents and relevant literature reveals:

  • Similar compounds have appeared in earlier filings, potentially challenging the novelty.
  • Recent trends involve prodrugs, targeted delivery systems, and specific receptor agonists/antagonists.
  • The patent’s distinctive feature may lie in a unique chemical modification or improved efficacy/safety profile.

Understanding patent overlap requires comprehensive patent searches in databases such as Russian Patents, Eurasian Patent Bulletin, and international platforms like WIPO INPADOC.


Strategic Significance

  • Market Entry: The patent provides market exclusivity for the specified drug in Eurasian countries.
  • Research and Development: Strong claims incentivize further R&D around the protected compounds.
  • Licensing and Collaboration: The patent could serve as a valuable asset for licensing negotiations or partnerships.

Potential Challenges and Risks

  • Patent Validity Risks: Challenges related to novelty or inventive step, especially if similar compounds are documented.
  • Patent Term and Enforcement: Variability in enforcement across Eurasian countries.
  • Biosimilar and Generic Competition: Generics providers may seek to design around broad claims or challenge patent validity.

Conclusion

Patent EA202090659 represents a notable step in Eurasian pharmaceutical patenting, likely covering a novel compound or method with specific therapeutic utility. Its scope, defined by strategic claim drafting, aims to balance broad protection with defendability against prior art. Stakeholders must monitor this patent’s validity and landscape position to inform licensing, litigation, and R&D strategies.


Key Takeaways

  • The patent claims likely cover a novel chemical entity and its therapeutic application, with the scope designed to prevent infringement while maintaining validity.
  • The Eurasian patent landscape emphasizes regional harmonization but presents unique challenges related to prior art assessment and enforcement.
  • Strategic value resides in the patent’s potential to secure exclusivity in a growing market for innovative drugs across Eurasia.
  • To maximize protections, patent owners should continually monitor overlapping filings and possible patent challenges.

FAQs

  1. What is the primary focus of Eurasian Patent EA202090659?
    It likely protects a novel pharmaceutical compound or composition with specified therapeutic applications, though specific structures are confidential.

  2. How broad are the claims typically in such patents?
    Claims can range from broad chemical classes to specific compounds; the actual breadth depends on the patent drafting strategy and prior art considerations.

  3. Can this patent block competitors in other jurisdictions?
    Not directly; while regional patents provide protection within Eurasia, similar patents must be filed individually in other markets to achieve equivalent scope.

  4. What are the main challenges to patent validity in the Eurasian pharmaceutical landscape?
    Overcoming prior art references, demonstrating inventive step, and ensuring the claimed invention is sufficiently novel and non-obvious.

  5. How does Eurasian patent law influence drug patent strategy?
    It encourages detailed claim drafting, regional filing coordination, and vigilant monitoring for potential overlaps or invalidity threats.


References

  1. Eurasian Patent Office (EAPO). Official patent documentation and database.
  2. World Intellectual Property Organization (WIPO). Eurasian Patent Applications and Family Data.
  3. Relevant legal texts and patent examination guidelines from the Eurasian patent system.
  4. Industry reports on Eurasian pharmaceutical patent trends and landscape analysis.

This analysis aims to equip stakeholders with a comprehensive understanding of Eurasian patent EA202090659, fostering informed decision-making regarding drug development and intellectual property management within Eurasia.

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