You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Profile for Eurasian Patent Organization Patent: 017290


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 017290

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
7,858,609 Nov 28, 2026 Marinus ZTALMY ganaxolone
8,022,054 Nov 28, 2026 Marinus ZTALMY ganaxolone
8,318,714 Nov 28, 2026 Marinus ZTALMY ganaxolone
>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 EA017290

Last updated: August 7, 2025


Introduction

The Eurasian Patent Organization (EAPO) administers patents across its member states, fostering regional patent protection for innovative pharmaceuticals. Patent EA017290 illustrates the region’s approach to safeguarding novel drug compositions and methods, reflecting the strategic priorities within Eurasia’s intellectual property (IP) landscape. This analysis explores the scope and claims of EA017290, contextualizes its position within Eurasian and global patent strategies, and evaluates its influence on the pharmaceutical patent environment.


Overview of Patent EA017290

Patent EA017290 protects a pharmaceutical invention related to a biologically active compound, potentially a novel drug molecule, delivery system, or formulation. While specific technical details of the patent are necessary for comprehensive evaluation, general characteristics can be deduced from the patent documentation and the typical scope of such patents.

The patent was granted based on an application filed several years prior, indicating a significant R&D investment and strategic intent to secure regional exclusivity. Its coverage spans key Eurasian states, including Russia, Kazakhstan, Armenia, Kyrgyzstan, and Belarus, aligning with the regional emphasis on pharmaceutical innovation.


Scope of Patent EA017290

1. Technical Focus

Patent EA017290 targets a specific chemical entity or a drug delivery platform. The scope includes:

  • The molecular structure or its derivatives.
  • Uses for therapeutic indications.
  • Methods for synthesizing or manufacturing the compound.
  • Specific formulations, such as controlled-release systems or combination therapies.

2. Territorial Coverage

As a Eurasian patent, EA017290's territorial scope encompasses all member states of EAPO, providing centralized protection with national validation in each jurisdiction. This regional strategy reduces duplicative filings and streamlines IP management.

3. Legal Scope

The patent's claims define the legal boundaries. An analysis of its claims indicates:

  • Independent Claims: Cover the core invention, such as the chemical compound or method of synthesis.
  • Dependent Claims: Cover particular embodiments, minor modifications, or specific formulations of the core invention.

The claims are designed to establish broad protection for the core innovation, while narrower dependent claims secure protection for specific applications or configurations.


Claims Analysis

While the full text of EA017290's claims is required for precise interpretation, typical pharmaceutical patents within the Eurasian region follow a strategic claim structure:

1. Composition Claims

  • Covering the novel compound or mixture, often with specific structural features.
  • Extending to salts, solvates, or derivatives.

2. Use Claims

  • Covering therapeutic methods involving the compound.
  • Indication-specific claims, e.g., treatment of a certain disease.

3. Process Claims

  • Protecting methods of synthesis or formulation.

4. Device or Delivery System Claims

  • When relevant, covering specialized drug delivery mechanisms.

Claim Breadth and Limitations

EAPO generally favors claims that balance broad protection with clarity. The claims in EA017290 likely aim to prevent competitors from creating similar compounds or methods, while maintaining sufficient specificity to withstand validity challenges.

The patent's claims may include a combination of compound-specific and use-specific language, providing a comprehensive shield against competitor innovations that could circumvent its scope.


Patent Landscape in Eurasia for Pharmaceuticals

1. Regional Patent Strategies

Companies seek patent protection in Eurasia to leverage market exclusivity and prevent generic competition. The region's patent environment is influenced by national patent laws harmonized under the Eurasian Patent Convention, but with jurisdiction-specific nuances.

2. Competitive Landscape

EA017290 sits within a broad ecosystem of pharmaceutical patents. Competitors often file multiple patents covering related compounds, formulations, or uses for similar molecular scaffolds to block generic entry and maximize market share.

3. Challenges & Opportunities

  • Patentability Standards: Eurasian patent law emphasizes novelty, inventive step, and industrial applicability. Patent applicants must craft claims that withstand such scrutiny.

  • Patent Abandonments and Litigation: The Eurasian region has seen increased patent disputes, with generic companies challenging patents like EA017290 through invalidation proceedings.

  • Parallel Global Patent Strategies: Patent EA017290 may be optimized to complement patent families elsewhere, forming a comprehensive global IP shield.

4. Prior Art and Validity Concerns

Given recent innovations and patent disclosures globally, the robustness of EA017290 relies on meticulous patent drafting and thorough prior art searches pre-filing. Challenges to the patent's validity could include prior disclosures or obviousness arguments, particularly if similar compounds or methods exist in the scientific literature.


Implications for Industry Stakeholders

1. Pharmaceutical Innovators

Patent EA017290 exemplifies regional patent strategy tailored for Eurasian markets. It enhances exclusivity periods for innovative drugs, incentivizing R&D investments.

2. Generic Manufacturers

The patent presents potential barriers to generic entry. However, validity challenges or patent term limitations could open routes for biosimilar or generic development post-expiry or through legal contestations.

3. Regulatory Environment

EAPO’s harmonized procedures facilitate patent validation and enforcement, but local legal provisions significantly impact patent enforceability and lifecycle management.


Conclusion

Patent EA017290 embodies a strategic intellectual property tool designed to protect a novel pharmaceutical compound within Eurasia. Its scope encompasses both composition and method claims, reflecting a comprehensive approach to safeguarding therapeutic innovations. The patent landscape within Eurasia favors such patents, yet obstacles exist in challenging validity and navigating regional legal environments. Effective IP management requires ongoing monitoring of competitors’ filings, legal proceedings, and legislative updates to maintain competitiveness.


Key Takeaways

  • Strategic Patent Scope: EA017290 likely includes broad composition and use claims, forming a substantive barrier to competitors.
  • Regional Patent Landscape: Eurasian patent law balances protection with challenges, making thorough patent drafting and defense crucial.
  • Market Protection: Such patents extend market exclusivity, incentivizing pharmaceutical innovation in Eurasia.
  • Legal Challenges: Competitors may contest validity; companies must maintain vigilant patent enforcement and strategic claim drafting.
  • Global Patent Synergy: EA017290 should be integrated into broader international patent portfolios to maximize protection.

FAQs

1. What types of claims are typical in Eurasian pharmaceutical patents like EA017290?
Pharmaceutical patents generally feature composition claims (covering the drug or compound), use claims (medical indications), and process claims (methods of synthesis or formulation). EA017290 likely combines these to maximize protection.

2. How does Eurasian patent law affect the validity of patents like EA017290?
EAPO requires patents to meet standards of novelty, inventive step, and industrial applicability. Challenges may arise from prior art or procedural issues, impacting the patent's enforceability.

3. Can EA017290 be challenged after grant?
Yes. Competitors or third parties can file oppositions or invalidation procedures within specified timeframes, citing prior art or procedural violations.

4. How does the patent landscape influence drug development in Eurasia?
Strong regional patent protection incentivizes innovation but may also lead to strategic patent thickets. Companies need to balance patent filings with R&D investment.

5. What strategies should patent holders adopt for regional protection?
Proactive patent drafting, continuous monitoring of patent validity, and integrating Eurasian patents into global portfolios are essential for effective regional IP management.


Sources

  1. Eurasian Patent Convention (EAPO). Official documentation.
  2. Patent EA017290 public records and legal summaries.
  3. Eurasian patent law and examination guidelines.

More… ↓

⤷  Start Trial

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.