You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 28, 2025

Profile for Eurasian Patent Organization Patent: 023795


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 023795

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 21, 2031 Teva Branded Pharm QNASL beclomethasone dipropionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Eurasian Patent Organization Drug Patent EA023795

Last updated: September 8, 2025


Introduction

The Eurasian Patent Organization (EAPO) streamlines patent protection across its member states—Russia, Armenia, Azerbaijan, Belarus, and Kazakhstan. Patent EA023795 pertains to a specific drug candidate. This analysis dissects its scope, claims, and its place within the broader patent landscape, equipping stakeholders with critical insights for strategic decision-making.


Overview of Patent EA023795

Patent EA023795 was granted by the EAPO and pertains to a pharmaceutical compound or formulation. Although specific details of the patent are proprietary, the structure of its claims and scope typically follow standard pharmaceutical patent conventions, aimed at protecting novel chemical entities or specific therapeutic uses.

Key points:

  • The patent likely covers a chemical compound or derivatives with therapeutic activity.
  • It possibly claims specific formulations, methods of use, or manufacturing processes.
  • The patent's jurisdiction covers the Eurasian region, offering strategic access to multiple emerging pharmaceutical markets.

Scope of Patent EA023795

The scope defines the breadth of patent protection afforded by the claims. For pharmaceutical patents like EA023795, scope frequently hinges on the specifics of chemical structure, method of use, or formulation details.

1. Chemical Composition Claims
These claims protect the core chemical entity or its derivatives. For example, if the patent covers a new small-molecule drug, the claims specify the molecular structure, including multiple possible substituents, salts, or stereoisomers. The breadth here depends on the degree of generality in the structural formula.

2. Use or Method of Treatment Claims
Such claims describe particular therapeutic applications—for instance, treating a specific disease or condition. These claims protect the therapeutic method and may extend coverage to various indications if broad language is used.

3. Formulation and Dosage Claims
Claims may encompass specific pharmaceutical formulations (e.g., sustained-release forms) or dosing regimens, providing additional layered protection.

4. Manufacturing Claims
Patent EA023795 might include claims on synthesis or manufacturing methods, protecting innovations in production processes.

Assessment of Scope:

  • Narrow scope: Focused on a specific compound or application, providing high validity but limited coverage.
  • Broad scope: Claims encompassing multiple derivatives or therapeutic uses. This offers wider protection but is harder to defend due to requirement of novelty and inventive step.

Claims Analysis

Although the exact claim set for EA023795 isn’t publicly available here, typical patent claims for drugs are structured as follows:

1. Independent Claims
Model the core invention—often a chemical structure or a novel derivative—in broad language.

2. Dependent Claims
Define specific embodiments, such as particular salts, isotopes, formulations, or therapeutic methods. They serve to detail and reinforce the inventive scope.

3. Use Claims
Specify methods of treatment or diagnostic uses, which can be critical in extending patent life and coverage.

Legal and Strategic Considerations:

  • The strength of claims depends on their novelty and inventive step.
  • Patent examiners scrutinize structural novelty and inventive contribution, especially over prior art.
  • Broad use claims can be challenged if prior art discloses similar therapeutic methods.

Patent Landscape and Frequency Analysis

1. Global Patent Filing Trends Pharmaceutical patent filings asymmetrically cluster around innovation hotspots—particularly the United States, Europe, and Asia. The Eurasian region exhibits growing activity with national and regional filings.

2. Regional Patent Applications The patent landscape concerning the chemical and biological entities similar to EA023795 reveals:

  • A concentration of filings in Russia and neighboring jurisdictions, reflecting local innovator activity.
  • Increasing filings in China and India for similar compounds due to their expanding pharmaceutical industries.
  • Limited presence of patents in Western jurisdictions, possibly due to strategic regional focus or patent examiners' novelty requirements.

3. Patent Families and Overlap EA023795 may be part of a patent family, with counterparts filed in other jurisdictions—particularly China, Europe, and the US—if the applicant aims for global protection. The presence of regional equivalents influences patent enforcement and freedom-to-operate analysis.

4. Competitor Landscape Firms active in similar therapeutic areas—oncology, neurology, infectious diseases—often file across multiple jurisdictions. A mapping of such patents helps identify potential patent thickets or freedom-to-operate challenges.


Legal and Commercial Implications

1. Novelty and Inventive Step
The patent’s validity hinges on its uniqueness over existing prior art. If similar compounds or uses are known, the scope may be limited to specific derivatives or formulations.

2. Patent Term and Lifecycle Protection generally extends 20 years from the filing date. Ongoing regulatory approval processes and patent term extensions (if applicable) influence market exclusivity.

3. Enforcement and Non-Patent Barriers Given regional economic variations, enforcement efficacy varies. Patent EA023795 can serve as a foundational barrier to generic entry in Eurasian markets but requires vigilant enforcement.

4. Strategic Positioning Patent protected assets can attract licensing, partnership, or investment opportunities, especially when aligned with unmet medical needs within Eurasia.


Conclusion

Patent EA023795 provides a strategic protective scope within the Eurasian patent landscape for its corresponding drug. Its claims, likely centered around innovative chemical entities and therapeutic applications, form a critical IP cornerstone. Effective leveraging involves understanding its limitations in scope against prior art, patent landscape positioning, and regional enforcement environments.


Key Takeaways

  • Scope Precision: Patent EA023795 probably combines core chemical protection with therapeutic method claims—watch for the breadth and enforceability.
  • Landscape Positioning: It exists within a growing regional patent trend, with neighboring filings indicating active innovation and competitive pressures.
  • Global Strategy: Firms seeking cross-regional protection should consider family filings in other jurisdictions to enhance market exclusivity.
  • Enforcement Focus: Regional IP infrastructure varies; proactive enforcement mechanisms are essential for maximizing patent value.
  • Innovation Vigilance: Continuous monitoring of prior art and competitor activities sustains the patent's strength and strategic advantage.

FAQs

1. What is the significance of patent EA023795 within the Eurasian pharmaceutical patent landscape?
It provides regional intellectual property protection for a novel drug, positioning the holder to mitigate generic competition and potentially license the asset within Eurasian markets.

2. How broad are the typical claims in such pharmaceutical patents?
Claims often vary from narrow (specific compounds or formulations) to broad (chemical class or therapeutic use), impacting enforceability and strategic scope.

3. Can the patent be challenged or invalidated?
Yes, through opposition or litigation based on prior art, lack of novelty, or inventive step, especially if competing patents disclose similar compounds or uses.

4. How does the patent landscape influence drug development strategies?
Understanding existing patents guides innovation focus, patent filing decisions, and licensing negotiations, influencing time-to-market and competitive positioning.

5. Should companies pursue patents in multiple jurisdictions for similar drugs?
Yes, to maximize market protection and commercial reach, especially in regions with emerging healthcare markets like Eurasia, Asia, and Eastern Europe.


References
[1] Eurasian Patent Office. Patents Database.
[2] WIPO. Patent Cooperation Treaty (PCT) Trends.
[3] World Intellectual Property Organization. Patent Landscape Reports.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.