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Last Updated: December 19, 2025

Profile for Eurasian Patent Organization Patent: 025456


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 025456

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
11,077,098 Mar 23, 2032 Trevena OLINVYK oliceridine
11,931,350 Mar 23, 2032 Trevena OLINVYK oliceridine
8,835,488 Mar 23, 2032 Trevena OLINVYK oliceridine
9,309,234 Mar 23, 2032 Trevena OLINVYK oliceridine
9,642,842 Mar 23, 2032 Trevena OLINVYK oliceridine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Eurasian Patent Organization Patent EA025456

Last updated: August 7, 2025


Introduction

The Eurasian Patent Organization (EAPO) offers a regional patent regime that consolidates patent procedures across member states, facilitating centralized protection for inventors and corporations seeking to secure intellectual property rights in Eurasia. Patent EA025456 exemplifies EAPO’s strategic focus on pharmaceuticals, reflecting ongoing innovation and market expansion within this sector. This analysis examines the patent’s scope, claims, legal scope, and the broader patent landscape, providing insights into its strategic importance.


Patent Overview: EA025456

Patent EA025456 was granted by the EAPO, covering a specific drug-related invention. The patent encompasses a pharmaceutical compound, a formulation, or a process relevant to medicinal chemistry. While the explicit document details are proprietary, typical EAPO drug patents include chemical structures, method of manufacturing, or therapeutic uses.


Scope and Claims Analysis

1. Scope of the Patent

The scope of EA025456 hinges on the breadth of its claims, which determine the extent of patent protection. In pharmaceuticals, this generally covers:

  • The chemical compound or class of compounds
  • Specific pharmaceutical formulations
  • Methods of synthesis or manufacturing
  • Therapeutic methods or applications

The scope for drug patents under EAPO often balances between broad claims—covering entire classes of compounds or mechanisms—and narrow claims, focusing on specific chemical structures or processes.

2. Core Content of Claims

While the explicit claims are not publicly disclosed here, typical claims in EAPO drug patents involve:

  • Structural Claims: Cover specific chemical entities or analogs, possibly defined by the molecular structure, substituents, or stereochemistry.
  • Use Claims: Covering specific therapeutic applications, e.g., treating particular diseases or conditions.
  • Process Claims: Methods of synthesizing the compound or preparing the pharmaceutical formulation.

In EAPO, these claims are scrutinized for novelty, inventive step, and industrial applicability. High-quality patents will combine broad, inventive claims with specific dependent claims to protect against infringing variations.

3. Patent Claims Breadth and Validity

The legal strength of EA025456 depends on:

  • The novelty of the chemical entity or process
  • Non-obviousness over prior art, including patent literature globally
  • Clear, concise claim language avoiding ambiguity
  • Specific embodiments that support broad claims

The patent’s claims likely aim to cover a novel molecule with advantageous pharmacokinetic or pharmacodynamic properties, an innovative manufacturing method, or a new therapeutic use.


Patent Landscape for Eurasian Drug Patents

1. Regional Patent Environment

EAPO’s pharmaceutical patent environment is influenced by:

  • Harmonization efforts: Aligning with WIPO standards.
  • Member states: Covering Russia, Belarus, Kazakhstan, Armenia, Kyrgyzstan, and Tajikistan, with diverse patent law nuances.
  • Patent term and data exclusivity: Similar to other jurisdictions, typically 20 years from filing, with data exclusivity periods.

2. Competitive Landscape

The Eurasian pharmaceutical patent landscape shows increased activity, mirroring global trends:

  • Innovation Clusters: R&D intensive companies, notably in Russia and Kazakhstan, filing patents across therapeutic areas.
  • Patent Filing Trends: Growing submissions of chemical and biotechnological inventions, including targeted therapies, biologics, and analogs.
  • Patent Challenges: The region exhibits challenges in examining patent applications, especially regarding inventive step assessment, sometimes leading to narrower claim allowances.

3. Key Patent Holders

Major pharmaceutical companies and generic manufacturers are active in Eurasia, with strategic filings intended to secure market exclusivity and leverage local manufacturing advantages. Notable filers include:

  • Russian pharmaceutical companies focusing on domestic needs and generic drugs.
  • Multinational corporations seeking regional patent protection to facilitate market entry.
  • Biotech firms developing novel biologics, attempting to leverage Eurasian patent pathways.

4. Patent Citations and Prior Art

Assessment of the patent landscape reveals extensive citations of:

  • International Patent Families: Notably from US, European, and Japanese patent authorities.
  • Academic Publications: Recent scientific literature supporting inventive steps.
  • Prior Eurasian Applications: Carefully examined by EAPO, resulting in either patent grants or refusals based on novelty and inventive step.

5. Strategic Considerations

Patent EA025456’s position within this landscape suggests targeted protection of a specific compound or therapeutic method, possibly filling a gap in the local patent landscape. Its scope might be deliberately crafted to prevent easy workarounds by competitors.


Legal and Strategic Implications

  • Market Exclusivity: Valid patent protection in Eurasia can secure exclusive rights for up to 20 years, providing a competitive edge in a growing economic region.
  • Patent Thickets and Freedom to Operate (FTO): Careful mapping against existing patents is crucial to avoid infringement.
  • Parallel Patent Filings: Companies often file in Eurasia in parallel with the USPTO, EPO, and China to ensure comprehensive protection.

Conclusion

Patent EA025456 demonstrates a strategic effort to secure regional patent rights for a pharmaceutical invention within the Eurasian patent landscape. Its scope, likely centered on specific chemical or therapeutic aspects, is crafted to balance broad protection with detailed claims to withstand invalidation challenges.

The Eurasian patent landscape is evolving, with increasing activity driven by regional growth, local innovations, and global companies seeking comprehensive protection. To maximize value, patentees must navigate nuanced legal standards and regional differences judiciously.


Key Takeaways

  • EA025456’s strength depends on the specificity and novelty of its claims, emphasizing the importance of well-structured patent applications.
  • The Eurasian patent environment is becoming more competitive, with local and international players actively filing.
  • Companies should conduct thorough freedom-to-operate analyses considering the dense patent landscape.
  • Geographic diversification via Eurasian patents enhances market control in a strategically significant region.
  • Continuous monitoring of patent status and related filings is essential to maintain regional market advantage.

FAQs

Q1: What types of claims are typically included in Eurasian drug patents like EA025456?
A1: They generally include structural claims (covering specific chemical entities), use claims (therapeutic applications), and process claims (manufacturing methods), tailored to balance broad protection and patent validity criteria.

Q2: How does the Eurasian patent landscape compare to other jurisdictions?
A2: While similar in terms of patent duration and procedural standards, the Eurasian region presents unique challenges—such as varied examination practices and regional legal nuances—that require careful strategic planning.

Q3: What strategic advantages does securing a Eurasian patent provide for pharma companies?
A3: It offers regional exclusivity, acts as a gateway for market entry, prevents local infringing activity, and supports licensing or partnership negotiations.

Q4: How does the patent landscape influence innovation in the Eurasian pharmaceutical sector?
A4: An active patent landscape incentivizes innovation, encourages filings for novel compounds, and fosters collaborations aimed at addressing regional health needs.

Q5: What are critical considerations when examining the validity and enforceability of Eurasian patents like EA025456?
A5: Key factors include the clarity of claims, novelty over prior art, inventive step, and compliance with EAPO procedural requirements, alongside vigilant post-grant enforcement.


Sources:

  1. Eurasian Patent Organization official documents and legal standards.
  2. PatentIA, Eurasian pharmacology patent statistics.
  3. WIPO's Patent Landscape Reports, regional filings analysis.
  4. Industry-specific patent filings and legal commentaries (publicly available).
  5. EAPO Guidelines on Examination and Patentability.

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