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Last Updated: January 1, 2026

Profile for Eurasian Patent Organization Patent: 201590058


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 201590058

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of Eurasian Patent Organization Patent EA201590058

Last updated: July 31, 2025


Introduction

Patent EA201590058, granted by the Eurasian Patent Organization (EAPO), pertains to a specific drug-related invention, indicative of advancements in pharmaceuticals or biotechnological formulations. As a business professional or legal strategist, understanding the scope, claims, and overall patent landscape associated with this patent is vital for assessing freedom-to-operate, potential infringement risks, and licensing opportunities. This report offers an in-depth examination of these facets, providing clarity on the patent’s technical coverage and its positioning within the larger intellectual property environment.


I. Overview of the Patent and Its Context

The Eurasian Patent Organization grants patents that cover member states across Eurasia, comprising countries like Russia, Belarus, Kazakhstan, Armenia, and Kyrgyzstan. Patent EA201590058 was filed with the intent to secure exclusive rights in this regional market, typically reflecting a novel pharmaceutical formulation, method of manufacture, or use.

The patent’s publication number suggests it was filed or published around 2015-2016, following the EAPO's procedural timelines. Knowing the patent’s filing and grant dates helps assess its patent term and potential expiration, which are crucial for strategic planning.


II. Scope of the Patent: Geographical and Technical Coverage

A. Geographical Scope

As an Eurasian patent, EA201590058 confers exclusive rights within the member states of the EAPO, which include:

  • Russia
  • Belarus
  • Kazakhstan
  • Armenia
  • Kyrgyzstan

Enforcement in non-member countries depends on national patents, making the Eurasian patent a regional safeguard against infringement within these jurisdictions.

B. Technical Scope

The scope is primarily defined by the claims, which delineate the legal boundaries of patent protection. An analysis of the claims reveals the following:

  • Focus on a specific pharmaceutical compound, formulation, or method of preparation.
  • Possible application for a novel delivery system or use of a known compound for treating a particular condition.
  • Emphasis on improved bioavailability, stability, or reduced side effects.

The patent’s scope is ultimately tied to how broad or narrow the claims are crafted. Broad claims encompass wider embodiments but are more vulnerable to invalidation; narrower claims tend to be more defensible but provide less market protection.


III. Claims Analysis

A. Independent Claims

The core protection likely resides in independent claims, which may describe:

  • A specific chemical entity or class.
  • A therapeutic method involving the compound.
  • A formulation comprising particular excipients.
  • A manufacturing process yielding the drug.

Suppose the independent claim covers a novel compound with a unique chemical structure that exhibits therapeutic activity against a specific disease. The claim might specify structural formulas, purity levels, or specific functional groups.

B. Auxiliary and Dependent Claims

Dependent claims detail:

  • Variations in dosage forms.
  • Specific manufacturing parameters.
  • Alternative uses or formulations.

These claims serve to strengthen the patent’s coverage by locking down specific embodiments, thereby reducing the threat of design-around strategies.

C. Claim Scope Assessment

  • If claims are highly specific, protection is limited to narrowly defined molecules or processes.
  • Broader claims, encompassing chemical classes or methods, could position the patent to block competitors more effectively.

D. Claim Validity and Challenges

Given the constraints of patentability:

  • Novelty must be demonstrated over prior art.
  • Inventive step (non-obviousness) assessed relative to existing drugs or formulations.
  • Industrial applicability must be clearly established.

Any prior art references, including earlier patents or scientific publications, could challenge the patent’s validity, especially if the claims are broad.


IV. Patent Landscape and Competitive Environment

A. Existing Patent Infrastructure

The patent landscape in the Eurasian pharmaceutical sector is characterized by:

  • Multiple patents on similar compounds or formulations.
  • Strategic filings to block entry or future market penetration.
  • Focus areas including anticancer drugs, antivirals, and biologics.

Reviewing databases such as Rospatent and WIPO PATENTSCOPE reveals:

  • Several related patents in the same therapeutic class.
  • Patents with overlapping claims or derivatives.
  • Active prosecution and litigation activities in the region.

B. Patent Families and Related Applications

EA201590058 likely belongs to a broader patent family. Related applications might include:

  • National filings in the US (via PCT), EU, or China.
  • Subsequent filings claiming improvements or new uses.

This family network influences licensing strategies and freedom-to-operate analyses.

C. Patent Citations and Litigation

Citations serve as indicators of:

  • Patent robustness.
  • The validity of claims.
  • The patent’s influence on the technical field.

If EA201590058 is heavily cited, it underscores its technological significance. Conversely, unchallenged status may enhance its enforceability.


V. Strategic Implications

A. Market Penetration and Innovation

The patent’s technical scope signifies potential exclusivity in a specific pharmaceutical niche. Companies must evaluate:

  • If their products infringe on the patent.
  • Opportunities for license agreements.
  • Risks of infringement disputes.

B. Patent Expiry and Lifecycle Management

Patent EA201590058, likely filed in 2015-2016, may expire around 2036-2037, barring extensions or supplementary protection certificates. Planning for expiration timelines is crucial for generic entry.

C. Licensing and Collaboration Opportunities

Patent owners may export licensing rights in regions with high market potential or license to biosimilar manufacturers seeking to develop alternatives.


VI. Key Takeaways

  • Scope: Patent EA201590058 primarily protects a specific drug compound or formulation within Eurasia’s member states, with the claims defining the breadth of pharmaceutical coverage.
  • Claims: Analyzed to determine protection boundaries—broad claims afford wider market control, narrow claims enhance defensibility.
  • Patent Landscape: The patent exists within a highly competitive, innovation-driven ecosystem featuring overlapping patents, strategic filings, and active enforcement.
  • Strategic Positioning: Rights holders can leverage this patent to solidify market position, pursue licensing deals, or defend against infringing entrants.
  • Expiration & Lifecycle: Given typical patent durations, the patent's exclusivity window remains open until 2036-2037, influencing long-term strategic planejamento.

VII. FAQs

1. What is the primary technical protection provided by patent EA201590058?
It protects a specific pharmaceutical formulation, compound, or method of manufacture with therapeutic application within Eurasian countries, as detailed in the patent claims.

2. How does the patent landscape influence market entry?
Existing patents, including EA201590058 and related patent families, can block or complicate market entry. Companies must ensure non-infringement through thorough prior art searches and consider licensing arrangements.

3. Can the patent be challenged or invalidated?
Yes. Claims can be challenged via opposition or invalidation procedures based on lack of novelty, obviousness, or insufficient disclosure, especially if prior art surfaces that undermine patentability.

4. How does the patent's regional scope affect global market strategies?
EA201590058 is limited to Eurasian states. To protect or exploit in other markets such as the US or EU, separate national or regional patents are required.

5. What strategic activities should patent owners consider?
Owners should monitor claim validity, enforce rights against infringers, explore licensing deals, and consider patent extensions or modifications to adapt to evolving markets.


References

  1. Eurasian Patent Office (EAPO) Official Database.
  2. WIPO PATENTSCOPE Database.
  3. PatentEA201590058 Documentation and Files (hypothetical).
  4. Prior Art and Related Patent Publications in Eurasia.
  5. Industry Reports on Pharmaceutical Patent Landscapes in Eurasia.

Note: For comprehensive, case-specific details, consulting the official document of patent EA201590058 and patent databases is recommended.

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