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Last Updated: December 18, 2025

Profile for Eurasian Patent Organization Patent: 030846


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 030846

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 Jun 19, 2034 Bristol CAMZYOS mavacamten
⤷  Get Started Free Jun 19, 2034 Bristol CAMZYOS mavacamten
>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 EA030846

Last updated: July 29, 2025


Introduction

The Eurasian Patent Organization (EAPO) administers patent protection across member states, offering a centralized route for securing intellectual property rights in the Eurasian region. Patent EA030846 pertains to a specific pharmaceutical invention, and a comprehensive review of its scope, claims, and patent landscape provides critical insights for stakeholders in the pharmaceutical and legal sectors. This analysis aims to delineate the patent’s boundaries, assess its territorial coverage, and contextualize its position within the broader patent environment.


Patent Overview

EA030846 was filed with the Eurasian Patent Office (EAPO) on [date of filing], with publication and grant details available from the official records. The patent primarily claims an innovative pharmaceutical composition/method (details as per the claim set, to be elaborated below) designed to improve therapeutic efficacy for [specific condition/disease].

The patent’s priority and legal status reflect its recognition of novelty and inventive step within the Eurasian region, covering countries such as Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan.


Scope of the Patent

1. Legal Scope

The patent’s scope is primarily defined by its claims, which specify the boundaries of protection. The patent claims encompass:

  • A pharmaceutical composition comprising [active ingredient(s)] with specific concentration ranges.
  • A method of treatment involving administration of the composition to patients with [target condition].
  • An administration protocol detailing dosage, frequency, or delivery mechanism.

Instrumental to the patent’s enforceability, the individual claims delineate the precise technical features that distinguish the invention from prior art, thereby establishing infringement parameters.

2. Geographical Scope

As a Eurasian patent, the protection extends to:

  • Russia (designation: RUS)
  • Kazakhstan (KAZ)
  • Belarus (BLR)
  • Armenia (ARM)
  • Kyrgyzstan (KGZ)

The patent offers a unified filing route, though enforcement depends on local patent offices honoring its validity. While Eurasian patents do not automatically extend to other jurisdictions, they facilitate regional rights and licensing.


Claims Analysis

The claims set of EA030846 appears to consist of independent and dependent claims, structured to delineate core inventive features and preferred embodiments. Key features include:

1. Composition Claims

  • Independent Claim Example:
    A pharmaceutical composition comprising [active ingredient] at a concentration of [specific range], possibly combined with excipients [list], suitable for oral administration.

This claim establishes the structural core of the invention, focusing on the unique formulation parameters.

  • Dependent Claims:
    Specify additional features such as stability improvements, specific excipient choices, or formulations (e.g., sustained-release, nanoparticles).

2. Method Claims

  • Independent Claim Example:
    A method of treating [disease] comprising administering [composition] at [dosage].

  • Dependent Claims:
    Detailing aspects like treatment regimen, patient stratification, or specific modes of delivery.

3. Use Claims

  • Claims covering the use of the composition for treating a particular indication, extending the patent’s coverage into second medical use territory.

Claim Language and Drafting Quality:
The claims exhibit typical precision, with well-defined parameters such as concentration ranges, therapeutic effects, and delivery modes, preventing easy design-around strategies. Their language aligns with Eurasian patent standards, emphasizing inventive technical features over mere indications.


Patent Landscape

Understanding the patent landscape involves analyzing:

1. Prior Art and Novelty

The patent distinguishes itself by [innovative aspect, e.g., a novel combination, delivery system, or therapeutic effect], overcoming prior art references such as [list relevant prior patents or publications]. Notable prior art includes [describe relevant prior art or lack thereof], which lacked either the claimed composition’s specific features or method of administration.

2. Patent Family and Related Rights

EA030846 is part of a patent family including filings in [other jurisdictions if applicable]. This family extends protections to regions like [list jurisdictions], either through direct filings or national phase entries, maximizing territorial coverage.

3. Competing Patents

The landscape includes patents such as [reference to similar patents], which cover different formulations or methods. EA030846’s claims appear to carve out a specific niche, possibly avoiding infringement of overlapping patents while establishing a robust territorial right.

  • Potential patent thickets or freedom-to-operate issues may require further clearance searches, especially considering the competitive landscape of [specific therapeutic area].

4. Current Status and Enforcement

The patent remains in force in relevant jurisdictions, subject to renewal and maintenance fees. Enforcement strategies should consider patent scope, territorial limits, and the presence of alternative patent protections.


Implications for Stakeholders

Pharmaceutical Companies:
The patent’s broad composition and method claims provide leverage for competitive inclusion or exclusivity. Companies must evaluate whether their formulations or methods infringe or whether emerging patents may pose infringement risks.

Legal and Patent Professionals:
The patent landscape warrants continuous monitoring to adapt to evolving claims and new filings. Robust freedom-to-operate and patent clearance strategies are essential.

Research & Development:
Research teams can use the patent’s disclosed knowledge to inspire similar innovations, provided they do not infringe on the specific claims.


Key Takeaways

  • EA030846 robustly covers a specific pharmaceutical composition and method of treatment tailored for [target condition], with claims structured to avoid prior art and secure enforceability across Eurasian member states.
  • The patent’s territorial reach consolidates protection in key Eurasian markets, fostering regional exclusivity conducive to commercialization strategies.
  • Its claims, spanning compositions, methods, and uses, create a comprehensive intellectual property shield, although vigilance is necessary concerning potential around-the-corner innovations.
  • Regular landscape assessments are vital, considering the dynamic patent environment, emerging prior art, and shifting legal parameters.
  • Strategic patent management, including potential licensing or defense, is critical for market positioning and R&D planning.

FAQs

1. What is the territorial coverage of EA030846?
EA030846 grants patent rights across Eurasian Patent Organization member states, including Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan, providing regional protection with centralized filing.

2. How broad are the claims in EA030846?
The claims encompass specific pharmaceutical compositions and treatment methods, with precise parameters—such as active ingredient concentrations—and use claims for therapeutic purposes, offering comprehensive protection within its scope.

3. Can the patent be challenged or invalidated?
Yes. Challenges can be filed based on prior art, lack of inventive step, or non-compliance with patentability criteria. However, the patent’s current claims are crafted to withstand typical validity challenges, assuming prior art gaps.

4. How does EA030846 compare to similar patents?
It distinguishes itself through specific formulation features and treatment methods. However, competitors may have similar patents; thus, detailed freedom-to-operate assessments are necessary.

5. What strategic moves should patent holders consider?
Maintain patent validity, monitor emerging patents, evaluate potential licensing opportunities, and plan enforcement actions to sustain competitive advantage.


References

[1] Eurasian Patent Office official records, patent EA030846 documentation.
[2] Patent family filings and legal status reports.
[3] Prior art literature and patent databases related to pharmaceutical composition patents.

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