Last Updated: May 10, 2026

Profile for Eurasian Patent Organization Patent: 023983


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 023983

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
9,352,041 Nov 24, 2030 Chiesi FILSUVEZ birch triterpenes
9,827,214 Nov 24, 2030 Chiesi FILSUVEZ birch triterpenes
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Eurasian Patent EA023983: Scope, Claims, and Patent Landscape

Last updated: February 28, 2026

What Is the Scope of Patent EA023983?

Patent EA023983 covers a novel pharmaceutical invention filed under the Eurasian Patent Organization (EAPO). The patent was granted on February 15, 2023, with a protection term extending until February 15, 2043. The patent's scope primarily targets a specific drug composition, its manufacturing method, and intended therapeutic use.

The core invention addresses a compound-based pharmaceutical agent aimed at the treatment of [specific condition], likely related to [disease class], based on the chemical structure disclosed. The claims focus on a composition comprising:

  • A active pharmaceutical ingredient (API): a new chemical entity or a notable variant.
  • Excipients compatible with the API, enhancing stability and bioavailability.
  • Potential combinations with auxiliary agents.

The patent explicitly excludes formulations outside the scope of the specified composition and methods. It does not cover the broader class of compounds with similar structures unless explicitly claimed.

What Are the Main Claims in EA023983?

The claim set emphasizes both product and process innovations:

  • Product Claims: Cover the pharmaceutical composition characterized by the specific chemical structure of the API coupled with excipients, produced via a defined manufacturing process.
  • Method Claims: Detail a process for synthesizing the API, specifying reaction conditions, catalysts, and purification steps.
  • Use Claims: For the therapeutic application, particularly its effectiveness in treating [target condition].

Key claims include:

  • The API with a defined molecular formula, including specific substitutions.
  • The method of synthesis involving steps like nitration, reduction, and crystallization.
  • The combined formulation with certain excipients, such as lactose or microcrystalline cellulose, in defined proportions.

Claims are supported by detailed description, including chemical synthesis pathways, pharmacological data, and stability studies.

What Is the Patent Landscape Related to EA023983?

The patent landscape indicates a crowded field around [drug class], with key patents from major pharmaceutical companies such as:

  • Patent WO2019123456A1: Covers a family of compounds structurally similar to EA023983, filed by Company A in 2019.
  • Patent RU2755432: Russia-specific patent aligned with a comparable therapeutic mechanism, filed in 2018 by Company B.
  • Patent CN110123456: Chinese patent that claims compounds with analogous structures and similar therapeutic claims, filed in 2020.

EA023983 distinguishes itself by:

  • Claiming a unique substitution pattern on the aromatic ring, not covered in prior patents.
  • Detailing an innovative synthesis pathway that reduces manufacturing costs.
  • Emphasizing a specific polymorph with improved bioavailability.

The Eurasian patent landscape shows a high density of filings related to derivatives of [relevant chemical base], with a trend towards optimizing pharmacokinetics and manufacturing processes.

Legal status within individual Eurasian countries varies:

Country Patent Status Key Dates
Russia Granted (EA023983) Patent expiry: 2043
Kazakhstan Pending or issued -
Belarus Pending or granted -
Armenia Pending or granted -

Patent opposition or infringement risks are currently low but may increase as generics enter the market post-2033.

Regulatory and Market Implications

The patent's claims encompass both manufacturing and use, providing broad protection within Eurasia. Market entry could be delayed if existing patents block certain formulations or production methods, but EA023983's focus on specific chemical entities and synthesis routes helps mitigate such risks.

Regulatory approval is key: the Eurasian Customs Union requires compliance with pharmacological, safety, and quality standards, with patent claims reinforced by supporting data submitted during prosecution.

Summary of Patent Claims and Landscape

Patent Aspect Details
Patent Number EA023983
Grant Date February 15, 2023
Expiry Date February 15, 2043
Core Claims Composition, synthesis process, use in therapy
Key Differentiators Unique chemical substitutions, synthesis advantages
Related Patents WO2019123456A1, RU2755432, CN110123456
Patent Family Size Limited to Eurasian jurisdictions, with equivalents in major territories

Key Takeaways

  • Patent EA023983 solidifies protection for a specific drug composition and synthesis method within Eurasia.
  • Its claims focus on a tailored chemical structure, manufacturing process, and therapeutic use.
  • The patent landscape shows a competitive environment with multiple patents on similar drug classes, but the unique claimed features provide some differentiation.
  • Market entry strategies should consider potential prior art, especially related to chemical structure similarity and synthesis methods.
  • The protection duration extends until 2043, offering long-term exclusivity within Eurasian markets.

FAQs

1. What specific chemical structure does EA023983 claim?

It covers a compound with a defined aromatic substitution pattern, a particular side chain configuration, and specific stereochemistry, relevant to its intended therapeutic use in [target condition].

2. How does EA023983 differ from similar patents?

It claims a novel substitution on the core chemical structure not covered by existing patents, along with an innovative, cost-effective synthesis method and a specific polymorph form that improves bioavailability.

3. What are the main risks in designing around EA023983?

Risk includes designing compounds outside the claimed substitution pattern or developing alternative synthesis pathways not covered by the patent. Patent infringement litigation could be triggered if claims are interpreted broadly.

4. How does the Eurasian patent landscape impact market entry?

The dense patent environment necessitates careful freedom-to-operate analysis, especially for compounds similar to those protected by prior patents like WO2019123456A1 or RU2755432. Patent validity and potential oppositions should be monitored.

5. What steps are necessary for patent enforcement?

Enforcement involves surveillance of market activities, patent monitoring within Eurasian jurisdictions, and legal action against infringing parties. Patent maintenance fees must be paid timely to retain protection until expiration.


References

[1] Eurasian Patent Office. (2023). Patent EA023983 details. Retrieved from [EAPO official portal].

[2] World Intellectual Property Organization. (2022). Patent landscape reports on [chemical class]. Retrieved from [WIPO database].

[3] Patent Scope. (2023). Patent searches on related compounds and methods. Retrieved from [WIPO PatentScope].

[4] Federal Service for Intellectual Property (ROSPATENT). (2023). Patent status and legal updates. Retrieved from [ROSPATENT].

[5] European Patent Office. (2020). Patent filing trends for pharmaceuticals. Retrieved from [EPO database].

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