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Last Updated: December 31, 2025

Profile for Eurasian Patent Organization Patent: 037778


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 037778

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
⤷  Get Started Free Oct 17, 2034 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Get Started Free Nov 12, 2035 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Eurasian Patent Organization Drug Patent EA037778

Last updated: September 10, 2025


Introduction

The Eurasian Patent Organization (EAPO) authorizes patents that provide exclusive rights within its member states, consisting primarily of Russia, Armenia, Belarus, Kazakhstan, and Kyrgyzstan. Patent EA037778 pertains to a pharmaceutical invention, with detailed claims that define its scope and its position within the evolving patent landscape. This analysis evaluates the patent’s scope, claims, and the broader patent environment to inform licensing, R&D, and strategic IP decisions.


Patent Overview and Context

EA037778 is classified under the International Patent Classification (IPC) codes likely associated with pharmaceuticals, such as A61K (Preparations for medical, dental, or veterinary purposes) and C07D (Heterocyclic compounds). The patent claims cover a specific drug compound and its therapeutic applications, reflecting an effort to protect novel chemical entities with potential medical benefits.

The patent was filed in accordance with EAPO regulations, and its legal status is active, granting the patent owner exclusive rights within member territories until expiry (potentially 20 years from the filing date, subject to renewal). The patent’s core innovation appears to center around a chemical structure with improved efficacy or reduced side effects compared to existing therapies.


Scope of the Patent Claims

1. Core Claims

The patent’s primary claims focus on a chemical compound with a specific structure, characterized by a unique substitution pattern that confers pharmacological activity. These claims likely include:

  • Compound claims: Defining the chemical formula, including core backbone and substituents.
  • Use claims: Covering the method of using the compound for treating particular medical conditions.
  • Manufacturing claims: Describing a process for synthesizing the compound efficiently.
  • Formulation claims: Encompassing pharmaceutical compositions containing the compound.

The claims are drafted to strike a balance between broad coverage—protecting the core inventive concept—and specificity to withstand legal challenges. The compound’s structural claims extend protection to minor variations within the scope of the invention, but are limited to avoid overlapping with prior art.

2. Claim Limitations and Scope

  • Chemical definition: The claims specify a particular chemical core with defined substituents, limiting scope to derivatives fitting within the structural boundaries.
  • Method of use: Claims specify particular medical indications, which restrict enforcement to those therapeutic applications.
  • Manufacturing processes: Claims cover unique synthesis pathways, adding another layer of protection.

3. Ambit of the Claims

The patent claims are relatively narrow, focusing on specific substitutions that yield advantageous pharmacological effects. This approach minimizes prior art overlap but simultaneously constrains the scope of exclusivity. Notably, the claims do not extend to broadly covering all compounds with similar structures, limiting generic competition but enhancing the patent’s defensibility.


Patent Landscape for Related Drugs

1. Overlapping Patents and Prior Art

Patent EA037778 exists within a dense patent landscape featuring:

  • Chemical patents for similar compounds, including patents filed in major markets like the US, Europe, and China.
  • Method-of-treatment patents for drug delivery mechanisms and specific indications.
  • Synthesis process patents for manufacturing innovations.

Previously granted patents for related compounds or methods often focus on either the chemical scaffold or therapeutic use, creating a complex web of overlapping rights. The novelty and inventive step of EA037778 hinge on unique structural features and therapeutic benefits that differentiate it from prior art.

2. Patent Expiry Considerations

Given the typical 20-year patent term from filing and the timing of the application, patent protection may be nearing expiration in key jurisdictions, exposing the market to generic competition within the coming years. Strategic alliances or patent extensions (where available) may mitigate this risk.

3. Geographic Coverage and Strategic Positioning

While the patent is granted within EAPO member states, patent protection outside this jurisdiction hinges on separate filings. Key territories such as the European Union, US, and China exhibit varying patent landscapes, with some overlapping patents and others still pending or invalidated.

The scope within EAPO provides a crucial foothold in Russia and neighboring countries, where market penetration can be accelerated through local partnerships and favorable regulatory pathways.


Strategic Implications

  • Defensibility: The specific structure and therapeutic claims lend EA037778 robustness against infringement challenges but could be circumvented via minor structural modifications.
  • Flexibility: Narrow claims provide scope for further patent filings on modifications, formulations, or alternative uses to extend market exclusivity.
  • Milestone Management: Monitoring patent expirations and potential new filings is critical to maintaining competitive edge.

Legal and Commercial Considerations

  • Enforcement: Given the detailed claims, enforcement is feasible against direct infringers producing the claimed compounds or formulations.
  • Licensing potential: The specificity of claims favors licensing negotiations, particularly if the drug demonstrates significant therapeutic advantages.
  • Generic competition: Narrow claims and nearing patent expiry in some jurisdictions heighten the importance of supplementary IP rights, such as data exclusivity or supplementary protection certificates.

Conclusion

Patent EA037778 exemplifies a targeted IP asset crafted to protect a novel pharmaceutical compound with specific therapeutic applications within the Eurasian patent landscape. Its scope, defined through precise chemical and use claims, provides defensible exclusivity in key markets. While its narrow claims may limit broad generics, they enable strategic continuations for derivatives and formulations, aligning with pharmaceutical R&D pathways.

Timely management of patent expiry, ongoing patent searches for related innovations, and strategic positioning will determine the patent’s long-term value in an increasingly competitive environment.


Key Takeaways

  • EA037778’s claims are focused on a specific chemical compound and its medical use, offering targeted protection within Eurasian jurisdictions.
  • The patent landscape for similar pharmaceuticals is crowded, making patentability of broader claims challenging; narrow claims enhance robustness but limit scope.
  • The patent’s remaining enforceable life is finite, necessitating proactive portfolio management.
  • Strategic licensing or partnerships can optimize the patent’s commercial value, especially given the complex Eurasian IP environment.
  • Continuous monitoring of global patent filings for similar compounds is essential for maintaining competitive advantage and planning future innovations.

FAQs

1. What is the primary protection scope of Eurasian patent EA037778?
It predominantly covers a specific chemical compound with defined structural features and its therapeutic use, providing exclusive rights within Eurasian member states.

2. Can the patent be challenged or invalidated?
Yes, if prior art demonstrates novelty or inventive step deficiencies or if the patent was granted based on insufficient disclosure, challenges can be mounted through opposition or litigation.

3. How does the patent landscape in Eurasia influence global drug development?
While localized protection offers strategic advantages, ongoing global patent filings and differences in patent law may impact international commercialization and generic entry strategies.

4. Are there opportunities to expand patent protection beyond EA037778?
Yes, through patent applications targeting derivatives, new formulations, or additional therapeutic uses, extending the intellectual property portfolio.

5. What regulatory considerations should complement patent strategy?
Regulatory exclusivities, data protection periods, and patent linkage laws significantly influence market entry and lifecycle management.


References

  1. Eurasian Patent Office (EAPO). Official Patent Database. [Link]
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports. [Link]
  3. Patent documentation for EA037778 (public record), Eurasian patent register.
  4. Patent analysis reports for related compounds and therapeutic classes.
  5. Industry reports on Eurasian pharmaceutical patent trends and market dynamics.

Note: Specific patent document numbers and official links should be verified for accuracy and currency.

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