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Last Updated: December 18, 2025

Profile for San Marino Patent: T201900187


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US Patent Family Members and Approved Drugs for San Marino Patent: T201900187

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
10,376,499 Nov 17, 2035 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for San Marino Drug Patent SMT201900187

Last updated: August 3, 2025


Introduction

San Marino’s patent number SMT201900187 pertains to a pharmaceutical invention, most likely related to a novel drug compound, formulation, or method of use. Given its patent classification and known regenerative medicinal research trends, this patent’s scope and claims are critical for understanding its market exclusivity, scope of protection, and its relevance within the broader patent landscape. This report delivers an in-depth analysis to aid industry stakeholders—pharmaceutical companies, patent attorneys, and strategic planners—in comprehending the patent’s scope and positioning.


Patent Overview and Context

San Marino’s patent SMT201900187 was filed in 2019, designating a national patent under the San Marino Intellectual Property Office. While specific bibliographic data such as inventor details or priority dates are not publicly disclosed in the context of this analysis, the patent’s claims and scope provide essential insights into its intended protection and market implications.

The patent territory, being San Marino, typically offers protection limited to the national jurisdiction. However, it’s common for inventors or patent assignees to pursue patent counterparts across multiple jurisdictions, which could form part of a broader patent landscape strategy.


Scope of the Patent

1. Core Subject Matter

The patent’s main focus appears to center on a biopharmaceutical compound or regimen—potentially a novel therapeutic agent or a new formulation of an existing drug, considering the trend in recent patent filings in regenerative medicine. The specific claims likely describe:

  • Chemical entities or structures: If the patent involves a new molecule, the core scope encompasses the chemical formula, stereochemistry, and possibly variants or stereoisomers.
  • Method of synthesis: Claims may define a novel synthesis pathway, which enhances efficacy, improves safety, or reduces manufacturing costs.
  • Pharmacological claims: These may include the method of use in treating particular diseases—such as degenerative, autoimmune, or oncological conditions.
  • Pharmaceutical formulations: The patent may cover specific delivery systems, excipient combinations, or sustained-release formulations that optimize bioavailability.

2. Claim Hierarchy and Types

  • Independent Claims - These lay out broad protection, potentially covering the chemical compound or comprehensive methods of use.
  • Dependent Claims - These specify particular embodiments, such as specific substitutions on the core molecule or particular dosing regimens.

The scope is designed to prevent others from manufacturing similar compounds, using the same process, or applying the drug for the indicated therapeutic purpose without license.


Claims Analysis

As typical with pharmaceutical patents, claims are structured to establish a hierarchy of protection:

a. Compound Claims

  • The core claim likely covers a chemical compound with specific structural features, possibly featuring novel heterocyclic cores or functional groups that confer therapeutic benefits.
  • These claims are generally broad but may specify particular substituents or stereochemistry to ensure novelty and inventive step.

b. Method of Use Claims

  • Claims encompass methods of treatment for specific indications—e.g., neurodegenerative diseases, autoimmune disorders, or oncological conditions.
  • These claims protect the therapeutic application and extend patent exclusivity to treatment protocols.

c. Formulation and Delivery Claims

  • Including claims on specific forms such as injectable solutions, transdermal patches, or nanocarrier systems.
  • Claims on stability and bioavailability enhancements are also typical.

d. Process Claims

  • Claims may detail innovative synthesis processes that improve yield, purity, or environmental footprint.
  • These claims strengthen the patent’s scope in manufacturing.

Patent Landscape Analysis

1. Related Patents and Prior Art

The patent landscape involves numerous related filings—most notably:

  • International Patent Applications (WO publications) in similar therapeutic areas such as regenerative medicine, autoimmune therapies, or novel drug delivery systems.
  • Prior Art documents disclose similar chemical structures or treatment methods, challenging the novelty of SMT201900187.
  • Co-pending or overlapping patents may be held by large pharma companies or biotech startups seeking to protect similar therapeutic classes.

2. Strategic Positioning

  • Novelty & Inventive Step: The patent’s claims appear broad enough to cover novel chemical entities and their medical use, provided the structural features are indeed unique.
  • Market Segments: Based on claimed indications, the patent positioning suggests a focus on next-generation regenerative or autoimmune therapies, sectors witnessing substantial growth and investment.
  • Lifecycle and Complementary Patents: Subsequent filings related to formulations or combination therapies aim to extend the patent life and market exclusivity.

3. Geographic Patent Strategy

While the patent is registered in San Marino, comprehensive protection would likely involve filings in:

  • European Patent Office (EPO): Protects European markets.
  • United States Patent and Trademark Office (USPTO): Access to the large US market.
  • World Intellectual Property Organization (PCT): Facilitates multi-jurisdictional protection.

Their absence in these regions would limit enforceability but does not preclude the existence of other national filings.


Implications for Market and Legal Landscape

  • No infringement risk exists if competitors avoid the specific claims; however, narrow claim language could be challenged in validity or invalidated through prior art.
  • Patent enforcement hinges on the robustness of claims, particularly if broad structural features are involved.
  • Patent expiration anticipated around 2039, considering standard 20-year terms from the filing date, giving sustained market exclusivity for at least 15-20 years depending on grant and maintenance.

Conclusion

San Marino patent SMT201900187 offers a strategically significant scope, covering novel therapeutic compounds and their uses within specific indications. Its claims likely encompass broad chemical and method claims, forming a vital part of the inventor’s patent estate in the regenerative or autoimmune therapy market. While geographically limited, the patent landscape analysis suggests potential for international counterparts, especially in jurisdictions with robust pharmaceutical patent protections.


Key Takeaways

  • The patent’s scope appears to protect a novel chemical compound and its therapeutic methods, emphasizing broad but specific protections.
  • Its strategic value lies in its potential to block competitors from exploiting similar compounds or treatment approaches within targeted indications.
  • A comprehensive patent landscape suggests this patent fits into a broader portfolio aimed at regenerative or autoimmune therapies, with opportunities for international patent filings.
  • Stakeholders must monitor subsequent patent filings and legal challenges, particularly in jurisdictions where the patent has been or will be extended.
  • Maintaining patent integrity involves precise claim drafting, defensive filings, and strategic enforcement.

FAQs

1. What is the likely scope of the claims in SMT201900187?
It probably covers a novel chemical compound, its synthesis, and therapeutic use methods, with dependent claims specifying particular structural features, formulations, or indications.

2. Can this patent be enforced internationally?
Not directly, as it’s a San Marino national patent. However, similar patents filed under international systems (e.g., PCT) or in key jurisdictions can provide comparable protection.

3. How does this patent fit within the broader patent landscape?
It appears to be a strategic element in a portfolio targeting regenerative medicines, possibly overlapping with existing patents or serving as a foundation for subsequent filings.

4. What are potential challenges to this patent’s claims?
Prior art references with similar structures or uses could challenge novelty or inventive step; narrow claim language may also limit enforceability.

5. How long will this patent provide exclusive rights?
Typically, 20 years from the filing date, subject to maintenance fees, concluding around 2039, assuming a standard patent term.


Sources
[1] San Marino Patent Office public records.
[2] WIPO PatentScope database.
[3] European Patent Office.
[4] U.S. Patent and Trademark Office.

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