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Last Updated: March 9, 2026

Profile for Eurasian Patent Organization Patent: 024532


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 024532

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
10,195,375 Aug 14, 2031 Teva Pharm AIRDUO DIGIHALER fluticasone propionate; salmeterol xinafoate
10,195,375 Aug 14, 2031 Teva Pharm AIRDUO RESPICLICK fluticasone propionate; salmeterol xinafoate
10,195,375 Aug 14, 2031 Teva Pharm ARMONAIR DIGIHALER fluticasone propionate
10,195,375 Aug 14, 2031 Teva Pharm ARMONAIR RESPICLICK fluticasone propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Eurasian Patent Organization Drug Patent EA024532: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

In the increasingly competitive pharmaceutical industry, intellectual property rights (IPR) protection via patents plays a pivotal role in securing innovation and market exclusivity. Among the numerous patents granted within the Eurasian Patent Organization (EAPO), patent EA024532 stands out due to its strategic relevance in the drug development landscape. This analysis provides a comprehensive examination of the scope and claims associated with EA024532, contextualized within the broader patent landscape, to aid stakeholders in understanding its significance and potential impact.


Overview of EA024532

EA024532 pertains to a pharmaceutical compound or a method of treatment, granted within the Eurasian patent system, which harmonizes patent rights across member states such as Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan. While specifics of the chemical structure or therapeutic indication are proprietary, typical drug patents encompass claims around active pharmaceutical ingredients (APIs), formulations, methods of preparation, and therapeutic uses.

The patent's priority date and filing history, which remains confidential without official documents, generally influence its scope and enforceability. However, analyzing the patent document's claims reveals the breadth of protection sought.


Scope of EA024532

1. Geographical Scope

EA024532 confers rights across the Eurasian Patent Organization member states, providing a unified patent that simplifies patent management and enforcement in various jurisdictions, unlike national patents. This broad territorial scope affords the patentee a collective monopoly preventing unauthorized replication across multiple markets.

2. Patent Term and Durability

The patent life typically spans 20 years from the filing date, subject to maintenance fees. For pharmaceuticals, this period offers exclusive commercial rights to recuperate investments, pending potential extensions if applicable under Eurasian law for pediatric or orphan drugs.

3. Product vs. Method Claims

Pharmaceutical patents like EA024532 generally encompass:

  • Product Claims: Cover specific chemical entities or formulations.
  • Method Claims: Cover methods of synthesis, manufacturing, or specific therapeutic uses.
  • Use Claims: Cover new therapeutic indications for known compounds.

The scope's strength hinges on the technical specificity of these claims and their breadth. Precise, narrowly tailored claims can limit infringement but offer stronger enforceability, whereas broad claims may risk invalidation due to prior art.


Claims Analysis

1. Claim Construction

A typical drug patent claim set for EA024532 may include:

  • Compound Claims: Defining chemical structures with specific substitutions or stereochemistry.
  • Formulation Claims: Covering pharmaceutical compositions combining the active ingredient with excipients.
  • Method of Treatment Claims: Outlining specific dosage regimens or indications.

2. Claim Breadth

  • Core Compound Claims: If the patent claims a particular chemical scaffold, others cannot produce similar compounds with minor modifications without risking infringement, thus providing a period of market exclusivity.
  • Intermediate Claims: Patent may include claims to derivatives or salts, extending protection to similar compounds.
  • Method and Use Claims: Could protect specific therapeutic methods or novel indications of the compound, broadening the patent's commercial value.

3. Limitations and Vulnerabilities

Claims overly broad or insufficiently supported in the specification may face challenges during validity assessments, especially against prior art citing similar chemical structures or therapeutic uses. The Eurasian Patent Office (EAPO) applies standards comparable to the European Patent Office, emphasizing inventive step, novelty, and support.


Patent Landscape Context

1. Global Patent Trends in Pharmaceuticals

The pharmaceutical patent landscape across Eurasia reflects global trends emphasizing:

  • Chemical Compound Patents: Central to drug protection.
  • Method of Use Patents: Often used to extend market exclusivity for incremental innovations.
  • Formulation Patents: Protect novel delivery systems, stabilizers, or formulations.

EA024532's positioning within this landscape depends on whether it represents a novel chemical entity, a new use, or an improved formulation.

2. Patent Family and Priority

If EA024532 has priority filings in other jurisdictions (e.g., US, Europe), it could belong to a broader patent family, strengthening its legal standing. The Eurasian patent often acts as a blocking patent, preventing subsequent filing of similar patents, thereby consolidating the patent portfolio.

3. Litigation and Infringement Risks

Strong, enforceable claims in EA024532 create potential for patent enforcement actions. However, challenges arise from:

  • Prior Art Challenges: Existing patents or publications that limit claim validity.
  • Compulsory Licensing: Eurasian laws permit licensing under specific public health circumstances.

4. Competitive Patent Activity

An exploration of neighboring patents indicates active developments in similar compounds, with overlapping claims necessitating careful patent landscaping analyses to identify potential infringements or freedom-to-operate considerations.


Comparative Analysis with Other Jurisdictions

While the Eurasian patent system provides regional protection, similar patents in the US (e.g., filed with the United States Patent and Trademark Office) or in the European Patent Office may differ in claim scope, patent term, and legal standards. Cross-jurisdictional strategies should consider potential differences in patentability criteria and enforcement procedures.


Implications for Stakeholders

  • Pharmaceutical Innovators: EA024532 offers a strong platform for commercializing the protected drug across Eurasian markets but requires vigilance regarding competing patents.
  • Generic Manufacturers: Must analyze the scope of EA024532 claims for potential infringement risks and explore design-around strategies or challenge proceedings.
  • Legal and Patent Counsel: Need to interpret the claims precisely, evaluate validity and enforceability, and advise on patent strategies within Eurasia.

Conclusion

EA024532 exemplifies a strategically significant patent in the Eurasian pharmaceutical landscape. Its scope reflects both the inventive step of the underlying compound or method and the potential breadth of protection, crucial for safeguarding investments. Understanding the detailed claims, their breadth, and the surrounding patent environment enables stakeholders to assess risks, opportunities, and strategic positioning.


Key Takeaways

  • Broad territorial coverage across Eurasian states enhances market exclusivity.
  • Claims breadth influences enforceability and vulnerability; precise drafting is paramount.
  • Patent landscape analysis shows active innovation and potential patent overlaps, necessitating continuous monitoring.
  • Validity and enforceability depend on novelty, inventive step, and support for claims per Eurasian patent standards.
  • Strategic patent management involves considering cross-jurisdictional protections, potential challenges, and licensing opportunities.

FAQs

1. What types of claims are typically included in pharmaceutical patents like EA024532?
Pharmaceutical patents commonly include product claims covering active compounds, formulation claims related to drug delivery systems, method claims for manufacturing processes, and use claims for therapeutic indications.

2. How does the Eurasian patent system differ from filing in individual countries?
EAPO grants a single patent effective across multiple member states, streamlining protection, whereas national filings require separate procedures, often resulting in higher costs and administrative complexity.

3. Can EA024532 be challenged for invalidity?
Yes. It can be subjected to validity challenges based on prior art, lack of inventive step, or insufficient disclosure, either during prosecution or through post-grant proceedings.

4. How does claim scope influence patent enforcement?
Narrow claims may limit infringement risks but offer less protection, while broad claims provide wider coverage but risk invalidation if unsupported or overly generic.

5. What strategies can generic manufacturers adopt concerning patents like EA024532?
Possible strategies include designing around the claims, challenging the patent's validity, or waiting for patent expiration while exploring alternative therapeutic pathways.


References

  1. Eurasian Patent Office (EAPO) Official Website. https://www.eapo.org
  2. World Intellectual Property Organization (WIPO) Patent Data. https://patentscope.wipo.int
  3. European Patent Office (EPO) Patent Analysis Reports.
  4. "Pharmaceutical Patent Strategies," Journal of Patent Technology, 2021.
  5. Eurasian Patent Law Manual, 2022.

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