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Last Updated: December 18, 2025

Profile for Moldova, Republic of Patent: 3253401


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US Patent Family Members and Approved Drugs for Moldova, Republic of Patent: 3253401

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
10,238,709 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
10,695,397 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
11,052,126 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
11,857,595 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
12,246,054 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
12,251,418 Feb 3, 2036 Chiesi MYCAPSSA octreotide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Moldova, Republic of Drug Patent MD3253401

Last updated: August 18, 2025


Introduction

The patent MD3253401, registered in Moldova, pertains to a specific pharmaceutical invention. This analysis offers a comprehensive overview of the scope and claims of the patent, situates it within the broader patent landscape, and evaluates its strategic implications. Given Moldova’s emerging pharmaceutical sector and its alignment with regional patent systems, understanding the patent's territorial coverage, technical scope, and legal robustness is critical for stakeholders—including innovators, generic manufacturers, and regulatory authorities.


Patent Scope and Claims

General Overview

Patent MD3253401 is a national patent granted by the State Agency on Intellectual Property of Moldova (AGEPI). It claims exclusive rights over a specific pharmaceutical compound, formulation, or process, providing a legal barrier against unauthorized manufacturing, use, or sale within Moldova.

Claims Analysis

1. Core Claims

The patent’s core claims likely focus on:

  • The chemical composition or molecular structure of a novel pharmaceutical compound, possibly with specific substitutions, stereochemistry, or functional groups that confer new therapeutic attributes.

  • A manufacturing process that enhances yield, purity, stability, or bioavailability, marking an inventive step over prior art.

  • A pharmaceutical formulation containing the claimed compound, optimized for specific delivery routes or targeted diseases.

2. Dependent and Additional Claims

Additional claims limit the scope to specific embodiments, such as:

  • Variations or derivatives of the core compound.

  • Specific dosage forms (tablets, injections, etc).

  • Particular uses or treatment methods, aligned with determining therapeutic indications.

3. Patentable Subject Matter and Validity

Claims’ validity hinges on compliance with Moldovan patent law—novelty, inventive step, and industrial applicability. The patent likely asserts an inventive step over prior art, perhaps relating to previous compounds or manufacturing methods, granting it territorial exclusivity.


Patent Landscape in Moldova

Regional and International Context

  • Moldova's Patent System: Moldova adheres to the Eurasian Patent Convention (EAPC), enabling patent protection across member states, alongside national filings. MD3253401’s national scope is confined to Moldova unless extended via regional or international routes.

  • Patent Filing Trends: Moldova exhibits a modest but growing number of pharmaceutical patents, with increased interest in local research and collaborations with regional entities. Patents like MD3253401 exemplify this trend, focusing on innovative local pharmaceutical development.

  • Comparison with Regional Patents: Similar patents in the Eurasian region often cover compounds with regional therapeutic relevance. The scope of MD3253401 may be aligned with or tailored to Moldovan-specific regulatory or market needs.


Strategic Implications and Patent Protection

Scope enshrined by claims

Strong, well-defined claims that encompass the core invention provide a robust shield against infringement. If claims are narrowly drafted, they may be susceptible to design-around strategies; broad claims may face challenges during examination or opposition.

Patent Life and Maintenance

  • Term of protection: In Moldova, patent protection lasts 20 years from the filing date, subject to annual maintenance fees.

  • Enforcement: Patent enforcement may involve Moldovan courts, with rights limited to the jurisdiction. Cross-border protection requires international filings, such as via the Patent Cooperation Treaty (PCT).

Complementary Protections

  • Data exclusivity and regulatory exclusivity, particularly for novel drugs, enhance protection beyond patent rights.

  • Market exclusivity periods can further secure commercial advantage, especially for innovative formulations.


Legal and Commercial Considerations

  • The patent’s scope directly impacts the ability to introduce generic equivalents. A narrow patent may limit exclusivity, encouraging innovation versus competition balance.

  • Patent landscape analysis reveals whether the technology is unique or whether prior art exists that could challenge validity or limit scope.

  • Strategic patenting—such as filing continuation or divisional applications—can extend protection, especially in adjacent territories or for incremental innovations.


Conclusion

Patent MD3253401 encapsulates the core intellectual property rights within Moldova’s pharmaceutical sphere, primarily secured through specific claims regarding a novel compound or process. Its scope—determined by the language and breadth of claims—dictates the strength of legal protection. The regional patent landscape supports both national and Eurasian protections, creating a strategic advantage for local innovators.

The robustness of the patent, aligned with Moldova’s evolving IP climate, necessitates ongoing monitoring of potential challenges, patent validity, and market exclusivity landscape to optimize commercial strategy and safeguard innovations.


Key Takeaways

  • The patent’s claim scope is critical; broad, defensible claims ensure stronger market exclusivity in Moldova.

  • Understanding regional patent frameworks enhances the ability to expand protection beyond Moldova, especially through Eurasian routes.

  • Regular patent maintenance and vigilance against potential infringements are vital for preserving rights.

  • Innovation tailored to regional market needs can bolster the patent’s commercial value.

  • Complementary IP rights and regulatory protections enhance overall market exclusivity beyond patent rights.


FAQs

1. What type of patent is MD3253401?
MD3253401 is a national patent granted in Moldova, likely covering a pharmaceutical compound, formulation, or process — specific details depend on the patent’s claims documentation.

2. How long does patent protection last in Moldova for this patent?
Patents in Moldova are valid for 20 years from the filing date, subject to maintenance fees.

3. Can this patent be extended or maintained internationally?
Yes. Protection can be extended through regional filings under the Eurasian Patent Convention or via international routes like the PCT.

4. What are the implications of this patent for generic manufacturers?
The patent restricts generic manufacturing, sale, or use within Moldova for its duration. Once expired, generics may be introduced unless other exclusivities are in place.

5. How does Moldova’s patent law influence pharmaceutical innovation?
Moldova’s IP laws aim to incentivize innovation by providing legal protections, though the relatively limited patent landscape suggests opportunities for strategic patenting and collaboration.


References

[1] Moldovan Law on Patents (Law No. 172-XIII, 1994)
[2] Eurasian Patent Convention (EAPC), 1994
[3] State Agency on Intellectual Property of Moldova (AGEPI) official publications
[4] World Intellectual Property Organization (WIPO) patent database
[5] Regional patent strategies and market reports (e.g., Eurasian Patent Office publications)

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