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Last Updated: December 28, 2025

Profile for San Marino Patent: T202200461


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US Patent Family Members and Approved Drugs for San Marino Patent: T202200461

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
11,534,433 Jun 10, 2039 Scynexis BREXAFEMME ibrexafungerp citrate
>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 SMT202200461

Last updated: August 4, 2025


Introduction

San Marino patent SMT202200461 represents a noteworthy development within the pharmaceutical patent landscape. As an intellectual property asset, it warrants detailed scrutiny to understand its scope, claims, and strategic positioning within the global patent architecture. This analysis provides an in-depth review aimed at business professionals, R&D leaders, and patent strategists seeking to assess the patent’s strength, potential impact, and landscape implications.


Patent Overview

San Marino patent SMT202200461 was granted in 2022, with an application filing likely prior to that, reflecting recent innovative developments. While specific bibliographic details, such as assignee and inventor information, are necessary for comprehensive understanding, this analysis articulates the typical considerations for a patent of this nature—presumed to relate to a novel pharmaceutical compound or formulation.


Scope of the Patent

1. Geographical Coverage

San Marino patent SMT202200461 provides inventors and applicants protection within the microstate of San Marino and, through international patent treaties such as the Patent Cooperation Treaty (PCT) and European Patent Convention (EPC), potentially extends to broader jurisdictions, including the EU, and possibly other key markets dependent on national validation or extension.

2. Technical Field

The patent appears to cover a specific pharmaceutical invention—likely a new molecular entity (NME), a novel formulation, or a unique method of synthesis. As is standard, the scope encompasses:

  • The chemical composition, including the molecular structure, substituents, and stereochemistry;
  • Specific formulations or delivery mechanisms;
  • Methods of manufacturing or synthesizing the compound;
  • Use claims for treating or diagnosing particular medical conditions.

The scope’s breadth hinges on the breadth of claims—whether they are narrow (specific compounds or methods) or broad (covering classes of compounds or multiple formulations).


Claims Analysis

1. Claim Structure

Patent claims in pharmaceutical inventions typically follow hierarchical structures comprising:

  • Independent Claims: Define the core invention broadly, e.g., a chemical compound, its pharmaceutically acceptable salts, or a method of treatment.
  • Dependent Claims: Narrow the scope to specific embodiments, such as particular substitutions, dosage forms, or methods of administration.

2. Likely Claim Types

  • Compound Claims: Covering the novel chemical entity, including its stereochemistry and functional groups.

  • Use Claims: Covering the use of the compound for specific therapeutic applications, such as treating a disease.

  • Formulation Claims: Covering specific pharmaceutical compositions, including excipients and delivery systems.

  • Process Claims: Detailing synthesis or manufacturing methods, establishing manufacturing exclusivity.

3. Claim Breadth and Validity

The strength of the claims depends on how narrowly or broadly they are drafted. Broad claims afford extensive protection but are more vulnerable to challenges based on novelty or inventive step. Narrow claims are often easier to defend but offer limited protection.

Given recent trends in patent drafting, SMT202200461 likely emphasizes a combination of core compound claims with specific embodiments to balance validity and scope.

4. Potential Patentability Challenges

  • Novelty: The claims must distinguish over prior art. Given the rapid development of pharmaceutical compounds, prior art searches, including patent and non-patent literature, reveal whether the core compound or application is genuinely innovative.

  • Inventive Step: Demonstrating that the invention involves an inventive step over existing compounds or methods, perhaps through improved efficacy, safety, or manufacturing advantages.

  • Utility: The claims probably specify therapeutic indications, supporting the patent's utility.


Patent Landscape Considerations

1. Patent Family and Related Applications

SMT202200461 is potentially part of a broader patent family, including filings in major jurisdictions such as the European Patent Office (EPO), the United States Patent and Trademark Office (USPTO), China, Japan, and other markets. Family members amplify coverage and market exclusivity.

2. Competitor and Prior Art Analysis

  • A thorough landscape review indicates whether similar compounds or methods are patent-protected elsewhere.

  • Prior art includes scientific literature and existing patents that disclose structurally similar molecules, therapeutic uses, or manufacturing techniques.

3. Patent Citations

The patent’s citations, both citing and cited references, reveal its position in the innovation landscape and potential for patent infringement or freedom-to-operate assessments.

4. Composition of the Patent Landscape

  • The landscape comprises a dense cluster of pharmaceutical patents related to, for example, kinase inhibitors, monoclonal antibodies, or other classes, depending on the invention.

  • Overlapping claims from competing patents can influence licensing, litigation risk, or freedom-to-operate considerations.


Strategic Implications

1. Market Exclusivity

The patent potentially grants market exclusivity for the claimed compound or use for a typical term of up to 20 years from the earliest priority date, subject to maintenance fees.

2. Innovation and Differentiation

  • If the patent covers a structurally or functionally unique compound with demonstrated improved efficacy or reduced side-effects, it positions the holder competitively.

  • Narrow claims may limit the scope but facilitate easier approval or licensing.

3. Patent Challenges and Legal Risks

  • The patent might face challenges based on prior art, especially if similar compounds or methods have been disclosed.

  • Patent expiry or risk of infringement claims require ongoing vigilance.

4. Licensing and Collaborations

  • The patent’s positioning influences strategic partnerships, licensing opportunities, and R&D collaborations.

  • A broad scope enhances valuation, while narrower claims may guide licensing strategies for specific markets or indications.


Conclusion

San Marino patent SMT202200461 exemplifies a strategic asset in the pharmaceutical patent landscape, with a scope likely encompassing specific chemical entities or their uses. Its strength depends on precise claim drafting, thorough prior art clearance, and effective landscape positioning. For stakeholders, understanding its scope and claims is critical for assessing market opportunities, licensing potential, and infringement risks.


Key Takeaways

  • The scope of SMT202200461 mainly hinges on how broadly its claims are drafted, balancing protection with validity.

  • The patent landscape analysis underscores the importance of examining related patents and prior art to evaluate infringement risk and freedom-to-operate.

  • The patent’s strategic value depends on its geographic coverage, claim breadth, and exclusivity period remaining.

  • Effective patent management, including monitoring enforcement and potential challenges, is vital for maximizing commercial benefits.

  • Integrating patent insights with ongoing R&D and market analysis fosters an informed approach to portfolio development.


FAQs

Q1: What factors determine the strength of the claims in patent SMT202200461?
A: The claims' strength hinges on their novelty, inventive step, and clarity. Specifically, how distinctly the patent distinguishes the compound or method from prior art, and how broad or narrow the claims are drafted.

Q2: How does the patent landscape influence the development of similar drugs?
A: The landscape highlights existing protections, potential licensing opportunities, and infringement risks. It guides R&D to focus on non-infringing, innovative modifications and helps avoid costly litigation.

Q3: Can the protection of SMT202200461 be extended beyond San Marino?
A: Yes, through patent filings in other jurisdictions via regional or national applications, and by leveraging international treaties such as the PCT to facilitate multi-market protection.

Q4: What are common challenges faced by patents like SMT202200461?
A: Challenges include prior art invalidity, claim non-infringement, patent infringement disputes, and maintaining patent validity through timely fee payments.

Q5: What is the significance of the claims related to therapeutic use in this patent?
A: Use claims extend patent protection to specific medical indications, providing market exclusivity for particular treatments, which is commercially valuable in pharmaceutical licensing and marketing.


References

  1. [1] European Patent Office (EPO) Patent Documentation.
  2. [2] World Intellectual Property Organization (WIPO) Patent Landscape Reports.
  3. [3] Patent application SMT202200461, official publication.
  4. [4] Relevant scientific literature and prior art disclosures.

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