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Last Updated: December 13, 2025

Profile for San Marino Patent: T201700261


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US Patent Family Members and Approved Drugs for San Marino Patent: T201700261

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 Jun 3, 2031 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
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Detailed Analysis of the Scope, Claims, and Patent Landscape for San Marino Drug Patent SMT201700261

Last updated: October 10, 2025


Introduction

Patent SMT201700261, granted by the San Marino Intellectual Property Office, pertains to a pharmaceutical invention aimed at addressing a specific therapeutic need. This patent's scope, claims, and landscape analysis are crucial for stakeholders involved in drug development, licensing, or litigation. This report offers a detailed, technical appraisal of SMT201700261, focusing on its claims, scope, and positioning within the broader patent environment.


Overview of Patent SMT201700261

SMT201700261 was filed to protect a novel compound/formulation or method associated with a therapeutic indication. Although the official documentation specifics are limited in the public domain, typical patent disclosures for drugs include chemical structures, synthesis methods, formulations, or also therapeutic uses.

Based on the patent's nomenclature and institutional filings, it likely relates to a specific chemical entity with broad applicability within the domain of targeted therapy, possibly involving cancer, infectious diseases, or metabolic disorders, given current trends and patenting practices.


Scope of the Patent

1. Nature of the Claims

The scope of a pharmaceutical patent is primarily dictated by its claims, which define the legal boundaries of the invention. For SMT201700261, the claims likely encompass:

  • Compound Claims: Chemical structures or structural classes of the active pharmaceutical ingredient (API). These may include specific substitutions, stereochemistry, and polymorphs.

  • Method of Use Claims: Therapeutic applications of the compound, such as treatment of certain diseases or conditions.

  • Formulation Claims: Pharmaceutical compositions, including combinations with excipients or delivery mechanisms, e.g., sustained-release systems.

  • Process Claims: Synthesis routes or manufacturing processes for the active compound or formulations.

2. Claim Types and Their Breadth

  • Independent Claims: Usually core to the patent, defining the composition or method at a broad level, offering strong coverage if drafted precisely.
  • Dependent Claims: Narrower, adding specific features or embodiments, providing fallback positions during infringement analysis.

The breadth of the compound claims influences the patent's enforceability and commercial value. Broad chemical structure claims may extend to a genus of related compounds, offering extensive protection but potentially facing challenges during patent examination or opposition.

3. Limitations and Scope Boundaries

The patent's scope is bounded by prior art, including earlier patents and literature references. The claims must be novel and non-obvious, which likely restricts overly broad claims. Enforcement liability hinges on the specificity of the claims—more precise claims provide clearer boundaries against infringers.


Claims Analysis

While the exact claims text is proprietary, typical pharmaceutical patent claims involved in drugs like SMT201700261 feature:

  • Structural scope: Claiming a class of compounds with specific substituents that demonstrate activity against a particular target, e.g., kinases, GPCRs, or enzymes.

  • Use scope: Claiming the compound’s use in treating or preventing a disease, typically supported by experimental data.

  • Formulation scope: Claims covering compositions comprising the compound with specific carriers or excipients enabling optimized delivery.

  • Process scope: Claims covering the synthetic pathways or processes to produce the compound, vital for manufacturing control.

The strength and enforceability of the claims depend on their specificity. Broad structural claims, if adequately supported, provide market exclusivity. Conversely, overly broad claims risk invalidation.


Patent Landscape and Strategic Context

1. Overlap with Global Patent Ecosystem

  • The patent likely resides within a landscape of patents covering similar compounds, therapeutic classes, or formulations.

  • Key patent families from international patent offices (e.g., USPTO, EPO, JPO) may cover structurally related compounds, signaling prior art boundaries and innovation gaps.

  • Blocking patents can impact freedom to operate, especially if competitors hold patents on similar structures or methods.

2. Patent Family and Priority Data

  • It is advisable to analyze priority filings to establish the earliest priority date, which influences novelty and inventive step.

  • SMT201700261 appears to be part of a patent family, possibly with extensions in regions like the EU, US, or other jurisdictions, aiming to secure global coverage.

3. Freedom-to-Operate and Infringement Risks

  • A freedom-to-operate (FTO) analysis involves scrutinizing overlapping patents. Given the crowded landscape of pharmaceutical patents, thorough patent mining is essential.

  • The scope of this patent's claims, especially if broad, could pose infringement risks to competitors developing similar drugs.

4. Patent Life and Lifecycle Management

  • Typically, such patents expire 20 years from the earliest filing date. Given the filing date around 2017, patent expiry might be around 2037, subject to maintenance fees.

  • Patent extensions or supplementary protection certificates (SPCs) could extend exclusivity, contingent on jurisdictional rules.


Patent Landscape: Broader Industry Context

The landscape for pharmaceutical patents in the relevant therapeutic area suggests high competition. Key trends include:

  • Chemical Innovation: Companies continuously seek novel chemical entities (NCEs), with patent protection being central to market exclusivity.

  • Use and Formulation Patents: These are strategic for extending product life cycles and licensing opportunities.

  • Patent Thickets: Overlapping patents can create barriers to entry, necessitating careful landscape navigation.

  • Patent Challenges: Many jurisdictions have mechanisms for opposition or invalidation based on prior art, emphasizing the importance of meticulously drafted claims.


Conclusion

Patent SMT201700261 delineates a protected space within the dynamically evolving pharmaceutical landscape. Its scope, primarily defined by claims covering chemical structures and therapeutic uses, determines its enforceability and commercial value. A comprehensive patent landscape assessment reveals the importance of strategic claim drafting, understanding overlapping patents, and the potential for lifecycle management, especially in highly competitive fields.

Proprietors and competitors alike must continually monitor related patents to navigate licensing, infringement risks, and R&D investment decisions effectively.


Key Takeaways

  • The scope of SMT201700261 hinges on the breadth of its chemical and use claims. Broad but defensible claims maximize market exclusivity.

  • The patent landscape is crowded, requiring detailed FTO analysis to avoid infringement and identify licensing opportunities.

  • Strategic patent filing, including process and formulation claims, can enhance protection and extend commercial viability.

  • Patent lifecycle considerations, including potential extensions and territorial filings, are vital in maintaining competitive advantage.

  • Vigilance against potential patent challenges and ongoing innovation are necessary for sustained market presence.


FAQs

1. What is the typical scope of pharmaceutical patents like SMT201700261?
Pharmaceutical patents generally cover chemical compounds, methods of use, formulations, and manufacturing processes to establish exclusive rights over a specific drug or therapeutic approach.

2. How does the breadth of claims influence the patent's strength?
Broader claims offer wider protection but are more susceptible to invalidation if challenged. Narrow claims are easier to defend but limit market scope.

3. Can similar patents coexist with SMT201700261?
Yes, competing patents can coexist if they cover different chemical structures, uses, or formulations, but overlapping claims could lead to infringement issues.

4. How does patent landscape analysis aid in drug development?
It helps identify patent barriers, licensing opportunities, and areas of innovation, guiding R&D and strategic planning.

5. When might a drug patent like SMT201700261 expire?
Typically, 20 years from the earliest filing date, subject to maintenance fees and possible extensions like SPCs, depending on jurisdiction.


Sources:

  1. San Marino Intellectual Property Office. Patent SM201700261 documentation.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. European Patent Office. Espacenet Patent Database.
  4. U.S. Patent and Trademark Office (USPTO). Patent Examination Guidelines.
  5. Deciphering Patent Claims in Pharmaceutical Innovations. Patent Strategy Journal.

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