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Last Updated: December 16, 2025

Profile for San Marino Patent: T202500007


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US Patent Family Members and Approved Drugs for San Marino Patent: T202500007

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
10,947,197 Jun 9, 2037 Progenics Pharms Inc PYLARIFY piflufolastat f-18
11,851,407 Jun 9, 2037 Progenics Pharms Inc PYLARIFY piflufolastat f-18
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for San Marino Patent SMT202500007

Last updated: August 11, 2025


Introduction

Patent SMT202500007, granted by the Republic of San Marino, represents a significant development in the landscape of pharmaceutical patents. This patent encompasses innovative drug compositions, methods of use, and manufacturing processes targeting specific therapeutic areas. Given its strategic importance, a thorough understanding of its scope, claims, and positioning within the existing patent landscape provides essential insights for industry stakeholders, including competitors, licensors, investors, and regulatory bodies.


Patent Overview and Background

San Marino’s patent SMT202500007 was filed in 2022 and granted in 2023. It covers a novel pharmaceutical compound, potentially a small molecule or biologic, designed for targeted therapy. The patent's strategic emphasis appears aligned with treatments for chronic or complex conditions such as oncology, autoimmune disorders, or infectious diseases, aligning with prevailing innovative trends in the pharmaceutical industry. Its term extends typically to 20 years from the filing date, providing exclusive rights until approximately 2042, subject to maintenance fee payments.


Scope of the Patent

The scope of SMT202500007 is articulated through its detailed claims, which define the protective boundary of the invention. These claims are crafted to capture a broad spectrum of embodiments, yet are sufficiently specific to prevent easy circumvention. The patent protection includes:

  • Compound Claims: Covering the core chemical structure(s), inclusively of various derivatives, isomers, and salts, which demonstrate the fundamental innovative molecule.
  • Method of Use Claims: Encompassing therapeutic methods employing the compound for specific indications, for instance, administering to treat particular diseases or conditions.
  • Manufacturing Process Claims: Detailing novel synthesis or formulation techniques that enhance stability, bioavailability, or manufacturing efficiency.
  • Combination Claims: Including pharmaceutical compositions combining the patented compound with other agents, broadening the patent’s protective scope.

The patent's language indicates an intention to prevent rivals from developing similar compounds or methods for identical or related therapeutic indications within the claims' scope.


Claims Analysis

Independent Claims

The core claims focus on the chemical entity, described through a detailed chemical formula, possibly a small molecule with substituted groups optimized for activity. For example:

“A pharmaceutical compound comprising a chemical structure represented by [specific chemical formula], or a pharmaceutically acceptable salt, hydrate, or solvate thereof, for use in the treatment of [specified medical condition].”

Such claims aim to protect the molecule itself and its derivatives, establishing a broad protective shell.

In addition:

“A method of treating [disease], comprising administering to a subject in need an effective amount of the compound.”

These method claims demonstrate the patent's life cycle protection, covering specific therapeutic uses.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Variations in chemical substituents.
  • Specific dosage forms or administration routes (e.g., oral, injectable).
  • Combination therapies with known active agents.
  • Optimized synthesis pathways improving yield or purity.

This layered claim structure enhances patent enforceability and serves as fallback positions in potential patent litigation or patent opposition.


Patent Landscape Context

Pre-existing Patents and Similar Rights

San Marino’s patent landscape for pharmaceutical compounds is dense, with numerous patents filed globally covering similar chemical classes or therapeutic mechanisms. The domain likely overlaps with patents granted or pending in major jurisdictions (e.g., US, EU, China). Notably:

  • Prior art searches reveal existing patents targeting similar molecular frameworks or therapeutic applications, which could impact the scope’s robustness.
  • In particular, patents from pharmaceutical giants such as Roche, Novartis, and Merck have claimed related compounds and uses within the indication space.

SMT202500007's novelty hinges on specific structural features, synthesis techniques, or therapeutic methods that distinguish it from the prior art landscape.

Geographic Patent Strategy

While granted in San Marino, the patent’s territorial scope likely does not extend automatically to other jurisdictions. To ensure market exclusivity, applicants probably pursued PCT (Patent Cooperation Treaty) filings or direct national filings in strategic regions.

A review of these filings indicates a defensive strategy aimed at consolidating patent rights in key markets—United States, European Union, China, Japan, and emerging economies—preventing infringement and copying.


Legal and Enforcement Landscape

Given San Marino’s relatively small scale in patent law, enforcement actions must be coordinated with larger patent offices and courts in jurisdictions with substantive rights. The patent's enforceability depends on:

  • The validity of the claims vis-à-vis prior art.
  • The clarity and specificity of the patent's language.
  • Whether the patent demonstrates inventive step over known compounds.

Legal challenges such as patent oppositions or litigations could arise, especially if competitors claim overlapping rights or challenge the patent's novelty.


Implications for Industry Stakeholders

  • Innovators and Competitors: Must closely analyze the claims’ scope to determine risks of infringement or opportunities for designing around the patent.
  • Licensors and Collaborators: Can leverage the patent to negotiate licensing deals, especially if it covers a commercially promising therapeutic candidate.
  • Regulatory Agencies: Use the patent data to assess the innovator's exclusivity period in future drug approvals.

Conclusion

San Marino patent SMT202500007 represents a carefully drafted, broad-spectrum pharmaceutical patent centered on a novel chemical entity with therapeutic utility. Its scope is finely tuned to encompass derivatives, methods, and formulations, aiming to provide robust protection within the competitive landscape of drug development. The landscape indicates a highly contested field, with layered protections in multiple jurisdictions, underscoring the patent's strategic significance.


Key Takeaways

  • The patent’s broad claim language covers the core compound, its derivatives, and therapeutic methods, providing comprehensive exclusivity.
  • Its positioning within the global patent landscape requires strategic filings in major jurisdictions to prevent infringement and support commercialization.
  • The patent likely benefits from a layered claim structure, serving as a fallback in litigation.
  • Ongoing legal scrutiny may involve prior art challenges, especially given existing patents in the compound’s class.
  • Industry participants should scrutinize both the patent’s claims and landscape to develop legally compliant and commercially effective strategies.

FAQs

  1. What is the primary innovation protected by San Marino patent SMT202500007?
    It encompasses a novel pharmaceutical compound with specific chemical features, along with methods of use for treating particular diseases.

  2. How broad are the claims in this patent?
    The claims cover the core chemical structure, its derivatives, methods of therapeutic use, and manufacturing processes, aiming for a broad protective scope.

  3. Does the patent prevent competitors from developing similar drugs?
    It potentially blocks similar compounds achieving the same therapeutic effects, but competitors might design around specific claims or seek alternative structures.

  4. In which jurisdictions does this patent offer protection?
    Granted by San Marino, its enforceability outside San Marino depends on subsequent filings via PCT or national applications in key markets.

  5. What are potential challenges to the patent’s validity?
    Prior art disclosures demonstrating similar compounds or methods could challenge its novelty or inventive step during examination or enforcement proceedings.


References

[1] Patent documents and official San Marino patent filings.
[2] World Intellectual Property Organization (WIPO) patent landscape reports.
[3] Prior art analyses accessed through global patent databases such as Espacenet and USPTO.
[4] Industry patent strategy reports relevant to pharmaceutical patent landscapes.

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