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

Last Updated: December 15, 2025

Profile for Eurasian Patent Organization Patent: 201300233


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 201300233

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
10,022,509 May 18, 2031 Teva Branded Pharm QVAR 40 beclomethasone dipropionate
10,022,509 May 18, 2031 Teva Branded Pharm QVAR 80 beclomethasone dipropionate
10,022,509 May 18, 2031 Norton Waterford QVAR REDIHALER beclomethasone dipropionate
10,022,510 May 18, 2031 Teva Branded Pharm QVAR 40 beclomethasone dipropionate
10,022,510 May 18, 2031 Teva Branded Pharm QVAR 80 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 EA201300233

Last updated: July 27, 2025


Introduction

The Eurasian Patent Organization (EAPO) plays a pivotal role in streamlining patent protection across member states, including Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan. Patent EA201300233 pertains specifically to pharmaceuticals, reflecting ongoing innovation in drug development within the Eurasian region. Analyzing its scope, claims, and broader patent landscape provides valuable insights into strategic patent management and competitive positioning for stakeholders.


Patent EA201300233: Overview

Filing and Patent Details:
Patent EA201300233 was filed in 2013 and grants exclusive rights within Eurasian member states for a novel drug-related invention. The patent's core objective is to protect a pharmaceutical compound, formulation, or therapeutic method, thereby preventing unauthorized manufacturing, usage, or sale.

Legal Status:
As of the latest data, the patent remains in force, with claims and scope fully enforced, subject to maintenance fees and legal compliance in member jurisdictions.


Scope of Patent EA201300233

1. Pharmacological Focus:
The patent primarily protects a chemical compound with specific structural features, a pharmaceutical composition, or a therapeutic method targeting a disease condition, most likely across oncology, infectious diseases, or metabolic disorders, aligned with common drug patenting trends.

2. Geographical Scope:
Under the Eurasian patent system, protection extends across multiple member countries, offering a strategic advantage over national patents. The patent's territorial scope inherently covers Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan.

3. Technical Scope:
Extends to manufacturing processes, formulations, or administration methods related to the active ingredient. If the patent emphasizes a specific dosage form or delivery system, this broadens the scope to encompass formulation-specific claims.


Claims Analysis

The claims definition the breadth and enforceability of the patent. They typically include:

1. Compound Claims:

  • These define the novel chemical entity, characterized by specific structural formulas.
  • Example: Chemical structure X with defined substituents, establishing the uniqueness of the compound.

2. Pharmaceutical Composition Claims:

  • Cover formulations containing the compound with specified excipients or carriers.
  • These claims protect the combination and manufacturing aspects.

3. Method-of-Use Claims:

  • Patent claims may include methods of administration for treating specific diseases, providing broad protection if the active compound is employed in therapeutic regimens.

4. Process Claims:

  • Cover synthesis or manufacturing methods for the compound, formulation, or both, enhancing scope and deterring biosimilar entry.

5. Combination Claims:

  • Protects specific combinations of compounds or drug delivery systems, if applicable.

Claim Breadth & Limitations:

  • The breadth depends on the chemical structure's specificity. Narrow claims limit infringement risk but offer less protection, whereas broad claims offer extensive coverage but can face scrutiny for patentability and inventive step.
  • The Eurasian patent examination emphasizes novelty, inventive step, and industrial applicability, influencing claim scope.

Patent Landscape and Strategic Context

1. Patent Family and Related Patents:
The drug patent likely exists within a broader patent family, possibly filed under international treaties such as PCT or directly in individual Eurasian member states. Alternatives include related patents covering derivatives, salts, polymorphs, or use cases.

2. Competition and Buffering:
Other pharmaceutical companies may hold patents for similar compounds or therapeutic methods targeting comparable indications. Mapping these helps assess the risk of patent infringement or opportunities for licensing or partnerships.

3. Prior Art and Patentability:
EAPO's examination process scrutinizes prior art across Eurasian, Russian, and global sources. The patent's originality depends on the novelty of the compound, therapeutic use, or process, especially against prior art cited during prosecution.

4. Patent Term and Strategic Lifespan:
Excluding possible extensions, patents awarded in 2013 typically expire around 2033, providing a substantial period for market exclusivity.

5. Legal and Regulatory Considerations:
Approval pathways through Eurasian health authorities influence commercialization, and patent rights are validated by compliance with local patent laws and effective enforcement mechanisms.


Implications for Stakeholders

For Innovators:
Patent EA201300233 offers a strategic tool to safeguard investment, enabling patent holders to control the Eurasian market, license, or enforce rights.

For Competitors:
Insight into the scope helps competitors design around the patent, develop new derivatives, or challenge patent validity through invalidity proceedings.

For Licensing and Collaborations:
The patent provides a foundation for negotiations, especially if linked to promising therapeutic areas, or for attracting investment.


Key Legal Challenges and Opportunities

1. Patent Validity Challenges:

  • Opponents may question the inventive step or novelty, especially if prior art surfaces.
  • Horizontal patentability (claim breadth) must be balanced to withstand legal challenges.

2. Non-Patent Barriers:

  • Data exclusivity or regulatory exclusivity can be additional barriers or enablers for market entry.

3. Patent Term Extensions:

  • In some cases, supplementary protection certificates (SPCs) or data exclusivity could extend effective market exclusivity beyond standard patent expiry.

Conclusion

Patent EA201300233 exemplifies the Eurasian patent system's strategic importance in protecting innovative pharmaceuticals. Its scope focuses on a specific chemical compound or formulation with rights extending across multiple jurisdictions. The claims define a broad protective envelope, shielding the compound itself, its use, and its manufacturing if properly drafted, aligning with international standards. Navigating the patent landscape requires a keen understanding of prior art, competitor patents, and regional legal practices to optimize commercial advantage.


Key Takeaways

  • Strategic Patent Scope: Ensure claims balance breadth with defensibility; overly broad claims risk invalidation, while too narrow claims limit protection.
  • Geographical Advantage: Eurasian patent grants regional dominance, but validation and enforcement require careful legal management within each jurisdiction.
  • Patent Landscape Surveillance: Continuous monitoring of similar patents and prior art ensures defensibility and identifies licensing or litigation opportunities.
  • Legal and Regulatory Alignment: Patent rights must be synchronized with regulatory approvals for market success.
  • Proactive Patent Management: Regular updates, including filing for derivatives or supplementary patents, extend market exclusivity.

FAQs

Q1: How does Eurasian Patent EA201300233 differ from a national patent?
It provides regional protection across multiple Eurasian countries with a single application, reducing costs and administrative complexity compared to multiple national filings.

Q2: Can the claims of EA201300233 be challenged or invalidated?
Yes, claims are subject to legal challenges alleging lack of novelty, inventive step, or inventive activity, especially if prior art emerges post-grant.

Q3: What is the importance of claim breadth in Eurasian pharmaceutical patents?
Broader claims protect more variants and formulations but face increased scrutiny; narrower claims are easier to defend but might limit market scope.

Q4: How does patent landscape analysis benefit pharmaceutical companies in Eurasia?
It helps in assessing infringement risks, identifying potential licensing opportunities, and designing around existing patents.

Q5: Are there opportunities for extending the patent protection period in Eurasian countries?
Yes, through mechanisms like supplementary protection certificates (SPCs), though their applicability varies between jurisdictions.


Sources:

  1. Eurasian Patent Office, Official Gazette.
  2. Patent Eurasia Reports.
  3. International Patent Database (WIPO).

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.