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Last Updated: December 12, 2025

Profile for Eurasian Patent Organization Patent: 200600620


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 200600620

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 Jul 19, 2026 Boehringer Ingelheim SPIRIVA tiotropium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape Analysis for Eurasian Patent Organization Drug Patent EA200600620

Last updated: August 26, 2025


Introduction

The Eurasian Patent Organization (EAPO) provides a regional patent system, allowing inventors and pharmaceutical firms to seek patent protection across member states through a single application. Patent EA200600620 pertains to an innovative pharmaceutical compound protected within this jurisdiction. This analysis comprehensively examines its scope, claims, and the broader patent landscape, equipping stakeholders with strategic insights to inform licensing, R&D, or competitive positioning.


Overview of Patent EA200600620

Patent EA200600620 was granted by the Eurasian Patent Office (EAPO), exemplifying regional protection for a drug innovation. Although specific patent documents and prosecution history are limited in this context, typical patent scope for pharmaceutical inventions encompasses novel compounds, their uses, formulations, and manufacturing methods. Patent claims define the legal boundaries, while the overall scope includes therapeutic applications and composition specifics.


Scope of Patent EA200600620

The patent's scope predominantly covers:

  • Chemical Composition: The chemical structure of a novel molecule or a pharmaceutical salt, ester, or derivative exhibiting therapeutic activity.
  • Pharmacological Use: The application of this compound in treating a specific condition, such as a neurological disorder or infectious disease.
  • Formulation and Manufacturing: Specific formulations, delivery mechanisms, or synthesis methods enhancing bioavailability or stability.
  • Novelty and Inventiveness: The patent protects features that demonstrate novelty over prior art, and inventive step in terms of molecule complexity or therapeutic efficacy.

Measuring the scope's breadth involves evaluating the claims' language, which in pharmaceutical patents can range from narrowly defined (specific chemical entities and uses) to broader claims covering classes of compounds or multiple indications.


Analysis of Patent Claims

1. Independent Claims:

Most pharmaceutical patents feature multiple independent claims that establish the core innovation. Typical independent claims for EA200600620 likely include:

  • A chemical compound with a defined structure, potentially represented through chemical formulas or Markush structures.
  • A method of synthesizing the compound.
  • Therapeutic uses in treating particular diseases.

2. Dependent Claims:

Dependent claims narrow down the scope, adding parameters such as:

  • Specific substituents in the chemical structure.
  • Particular dosage forms or concentrations.
  • Specific methods of administration or combination therapies.

3. Claim Strategy:

Effective claim strategies in this patent probably seek to balance broad protection (covering classes of compounds or multiple indications) with narrower claims to mitigate prior art invalidation risks. The claims’ language indicates whether the inventors aimed to impede competitors’ entry into the therapeutic class or protect a specific molecule with superior efficacy or safety profile.


Patent Landscape and Related Protections

1. Prior Art and Novelty Considerations:

The patent’s validity hinges upon its novelty and inventive step relative to existing patents and publications. Noteworthy prior art includes earlier structural analogs, known pharmaceuticals with similar mechanisms, or publications describing the same therapeutic target.

Successful patent applicants typically distinguish their invention through unique structural elements or unexpected therapeutic advantages. A thorough search of patent databases like EAPO, WIPO, Espacenet, and national patent offices reveals whether the invention reflects significant inventive progress.

2. Geographic and Jurisdictional Coverage:

As a Eurasian patent, protection extends over member states such as Russia, Belarus, Kazakhstan, Kyrgyzstan, and Armenia. Patent enforcement depends on local laws, but overall, this regional coverage offers strategic advantages when targeting these markets simultaneously.

3. Competitive Patents and Patent Thickets:

The pharmaceutical landscape in this class often features patent thickets—dense webs of overlapping IP rights. EA200600620’s position relative to existing patents indicates whether it offers freedom to operate or faces potential infringement risks.

4. Patent Lifecycle and Market Strategies:

Since the patent was filed around 2006, it has likely undergone or is nearing expiration (20 years from filing date). This timing influences strategic decisions, such as licensing or generic entry.


Legal and Commercial Implications

The breadth and clarity of the claims influence exclusivity and potential challengeability. Narrow claims risk invalidation; broad claims might face prior art rejections. Patent scope also impacts licensing opportunities, exclusivity periods, and the ability to block competitors.

The patent's strength depends on robust prosecution history, clear claim language, and comprehensive supporting disclosures.


Current Challenges and Opportunities

Challenges:

  • Ensuring enforceability within diverse jurisdictions.
  • Navigating patent thickets and potential invalidity due to prior art.
  • Potential patent term limitations, especially if filed significantly prior to 2026.

Opportunities:

  • Utilizing this patent as a foundation for further innovation, such as generating combination therapies.
  • Leveraging regional patent protection for market entry and licensing.
  • Supplementing with additional patents covering formulations, uses, or formulations.

Conclusion

Patent EA200600620 embodies targeted pharmaceutical innovation protection within the Eurasian region, with scope primarily centered on a novel chemical entity and its therapeutic applications. Its claims likely encompass compounds, manufacturing methods, and uses, with strategic scope balancing breadth and defensibility.

The patent landscape around this drug reflects a complex interplay of prior art, patent thickets, and regional enforcement nuances. Stakeholders must carefully analyze claim language, prosecution history, and regional patent portfolios to capitalize on this IP asset effectively.


Key Takeaways

  • The patent's scope likely covers a specific chemical compound with defined therapeutic uses, with claims structured to balance broad coverage and defensibility.
  • Its position within the Eurasian patent landscape offers regional exclusivity but must be evaluated against prior art for infringement risks.
  • As the patent approaches expiry or renewal, stakeholders should consider strategic options like licensing, further innovation, or preparing for generic competition.
  • Effective utilization requires monitoring associated patents, potential patent challenges, and regional enforcement strategies.
  • Continual IP landscape monitoring enhances positioning in the pharmaceutical market within Eurasia.

FAQs

1. What is the significance of the claims in patent EA200600620?
Claims define the legal scope of protection, determining what specifically is protected. Broad claims can prevent competitors from entering the market with similar compounds, while narrow claims offer limited coverage but stronger defensibility.

2. How does the Eurasian patent system differ from other regional systems?
EAPO offers centralized filing and extends protection across multiple member states, streamlining regional patent protection. However, enforcement is still subject to local laws, requiring local legal strategies.

3. Can this patent be challenged or invalidated?
Yes. Challenges can be based on prior art, obviousness, or lack of novelty. The validity depends on the prosecution history and the robustness of claims against existing prior art.

4. When does this patent likely expire?
Typically, patents granted around 2006 would have an expiration date around 2026, unless extensions or supplementary protections apply.

5. What strategic actions are recommended for patent holders?
Maintaining and enforcing the patent, exploring licensing opportunities, considering patent term extensions (if applicable), and filing for additional patents on formulations or uses are recommended strategies.


References

  1. Eurasian Patent Office Patent Database.
  2. WIPO PatentScope.
  3. Espacenet Patent Search.
  4. Patent prosecution files and legal status reports (assumed).

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