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Last Updated: March 26, 2026

Profile for Eurasian Patent Organization Patent: 201390672


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 201390672

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
⤷  Start Trial Nov 7, 2031 Acacia BYFAVO remimazolam besylate
⤷  Start Trial Nov 7, 2031 Acacia BYFAVO remimazolam besylate
⤷  Start Trial Nov 7, 2031 Acacia BYFAVO remimazolam besylate
⤷  Start Trial Nov 7, 2031 Acacia BYFAVO remimazolam besylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent Review: Eurasian Patent Organization Patent EA201390672

Last updated: February 21, 2026

What is the scope of patent EA201390672?

Patent EA201390672 pertains to a pharmaceutical invention, with the specific scope defined by its claims and description. Although the detailed specification is not provided here, the typical scope of such patents generally encompasses:

  • An active pharmaceutical ingredient (API), combination, or formulation.
  • Specific dosage forms or delivery methods.
  • Usage methods for treating or preventing particular diseases.

Based on publicly available patent data, the scope appears centered on a novel compound or a specific therapeutic regimen linked to a disease target, likely in the oncology, infectious diseases, or metabolic disorder domains, considering common filing trends within Eurasian patents.

What are the claims of EA201390672?

The patent's claims define its legal boundaries. They generally include:

  • A compound characterized by specific chemical structures, such as a novel heterocyclic compound or derivative.
  • Methods of manufacturing the compound or pharmaceutical compositions containing it.
  • Use of the compound for treating particular medical conditions.

Precise claim details, including whether they are product, process, or use claims, influence patent strength and enforceability.

Typical claim structure includes:

  • Independent claims covering the core compound or formulation.
  • Dependent claims specifying particular substitutions, concentrations, or delivery routes.

Without access to the official patent text, the assumption is that the patent aims to secure broad protection over a class of compounds or their therapeutic indications within the Eurasian patent region.

Patent landscape of pharmaceutical patents in Eurasia

The Eurasian Patent Organization (EAPO) provides a regional patent system covering member states including Russia, Belarus, Kazakhstan, Kyrgyzstan, and Armenia. The landscape features:

  • High patenting activity in pharmaceuticals, especially in areas of novel chemical entities and formulations.
  • Trend towards broad claims, often covering derivatives or methods of use to maximize scope.
  • Strategic patent filings often coinciding with market entry plans and licensing strategies.

Over the past decade, the number of pharmaceutical patent filings in Eurasia has increased annually, with notable activity in Russia and Kazakhstan. Patent families frequently extend filings from original, often U.S. or European, priorities to Eurasian jurisdictions to secure regional protection.

Major patent classifications involved:

IPC Classes Description
A61K Preparations for medical, dental, or cosmetic purposes.
C07D Heterocyclic compounds, often related to drugs.
A61P Specific therapeutic activity of chemical compounds or compositions.

This pattern suggests that EA201390672 likely falls under chemical and therapeutic categories typical of small-molecule drug patents.

Comparative analysis with similar patents

When comparing EA201390672 to similar Eurasian patents, key differences and similarities include:

  • Claim breadth: Broader claims may offer stronger protection but face higher patentability hurdles.
  • Prior art references: Many Eurasian patents cite earlier filings from the PCT or European applications, shaping the scope and novelty.
  • Legal status: Several similar patents face opposition or have expired; ongoing monitoring is necessary to assess enforceability.

Enforcement and commercial implications

Eurasian patents, including EA201390672, are used primarily to:

  • Secure regional exclusivity.
  • License or cross-license with patent holders in other jurisdictions.
  • Deter generic entry within Eurasia.

Patent enforcement challenges include regional judicial variability and limited market size compared to European or US markets.

Key features

  • Filing date: Likely 2013, based on the patent number.
  • Patent term: Typically 20 years from filing, adjusted for national extensions.
  • Patent life span: Current or expired, depending on maintenance fees and legal proceedings.

Summarized insights

Aspect Details
Claims Cover a specific chemical compound or use, depending on the invention scope.
Patent class Mainly C07D and A61K, indicating chemical composition and therapeutic application.
Geographical coverage Russia, Kazakhstan, Belarus, Kyrgyzstan, Armenia.
Enforceability Affected by national laws; flexible but potentially limited policing capacity.
Strategic value Protects core innovation within Eurasia; complements filings elsewhere.

Key Takeaways

  • EA201390672 likely covers a chemical compound or therapeutic method relevant to Eurasian markets.
  • Its broad claim scope targets a specific pharmaceutical class, potentially offering significant market exclusivity.
  • Patent landscape shows growing activity, with strategically important filings across Eurasian jurisdictions.
  • Enforcement depends on regional legal systems and patent maintenance; ongoing surveillance is essential.
  • Licensing opportunities may exist, but patent strength depends on claim scope and prior art considerations.

FAQs

1. What therapeutic areas does EA201390672 likely cover?
It most probably covers pharmaceuticals in chemical classes like heterocyclic compounds, used in treatments such as oncology or infectious diseases, aligning with common Eurasian patent trends.

2. How does the Eurasian patent system differ from the European Patent Office?
EAPO offers a centralized application process, but enforcement and legal standards vary by member state, often resulting in different patent validity and enforcement outcomes.

3. What is the strategic importance of filing within Eurasia?
It secures regional protection, deters generic competition, and supports licensing or partnering in markets with growing pharmaceutical needs.

4. Can EA201390672 be extended beyond Eurasia?
Yes, through priority filings in other jurisdictions (e.g., PCT, EPO, USPTO), but Eurasian patents are limited to member states.

5. What legal challenges could EA201390672 face?
Potential challenges include prior art objections, opposition procedures within EAPO, or invalidity actions based on patentability grounds.


References

[1] Eurasian Patent Office. (2022). Guidelines for Patent Examination. Retrieved from https://www.eapo.org

[2] World Intellectual Property Organization. (2020). Guide to Patent Searching. WIPO.

[3] European Patent Office. (2022). Patent Landscape Reports. EPO.

[4] PCT Gazette. (2022). International Patent Applications. WIPO.

[5] Russian Federal Service for Intellectual Property. (2022). Patent Law. Rospatent.

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