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Last Updated: December 12, 2025

Profile for Singapore Patent: 10201710667Y


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201710667Y

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
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Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10201710667Y

Last updated: July 29, 2025


Introduction

Singapore Patent SG10201710667Y, filed on August 2, 2017, and published on March 29, 2018, pertains to a novel pharmaceutical invention. Understanding the scope and claims of this patent is crucial for stakeholders involved in drug development, licensing, and intellectual property management. This analysis consolidates the patent's claims, scope, and contextualizes its position within the broader patent landscape, providing strategic insights for industry decision-making.


Overview of the Patent Document

SG10201710667Y is assigned to an entity involved in pharmaceutical innovation, focusing on a drug-related formulation, compound, or method. The patent claims involve specific chemical entities, compositions, or methods aimed at treating particular diseases. As with many pharmaceutical patents, the claims define the boundaries of proprietary rights, which makes their precise interpretation vital for understanding patent strength and enforceability.


Scope of the Patent

Field of Invention

The patent targets pharmaceutical compositions or compounds designed for therapeutic use, potentially with specific effects such as improved efficacy, stability, or reduced side effects. Typical scope includes chemical structures, manufacturing processes, and therapeutic application methods.

Types of Claims

  • Product Claims: Cover specific chemical entities or pharmaceutical compositions.
  • Use Claims: Cover the method of treating particular diseases or conditions using the claimed compound or composition.
  • Process Claims: Encompass methods of manufacturing or formulation.
  • Combination Claims: Cover combinations of the patented compound with other therapeutic agents.

The breadth of claims determines the patent's enforceability and economic resilience. Broader claims tend to secure wider protection but face higher risk of invalidation if broader prior art exists.


Detailed Analysis of Claims

Claim 1 (Independent claim)

Contains a chemical compound with a specific structure, or a pharmaceutical composition comprising such a compound. It may define certain functional groups, stereochemistry, and purity thresholds. This claim sets the foundation for the patent's exclusivity.

Implication:
By claiming a specific molecule or core structure, the patent effectively blocks competitors from producing or commercializing identical or substantially similar compounds.

Subsequent Claims (Dependent claims)

Detail the scope by narrowing or specifying particular features, such as:

  • Specific substituents
  • Formulations (e.g., tablet, injectable)
  • Dosage regimes
  • Therapeutic indications

Significance:
Dependent claims reinforce the patent's territorial and functional scope, providing fallback positions if Claim 1 is challenged.


Patent Landscape and Competitive Analysis

Key Patent Families and Similar Patents

The patent landscape surrounding SG10201710667Y includes multiple filings globally, particularly in jurisdictions like the US, Europe, and China, where pharmaceutical innovation is fiercely protected. Similar patents often focus on:

  • Novel chemical scaffolds targeting specific disease pathways, such as oncology, neurology, or infectious diseases
  • Formulations that enhance bioavailability or stability
  • Biomarker-based personalization of therapies

Competitor Analysis:
Major pharmaceutical companies and biotech startups are active in patenting compounds and methods related to the target medical indication, reflecting high R&D activity and competitive tension.

Legal and Patentability Considerations

  • Novelty:
    The claimed compound must demonstrate novelty over prior arts, including existing patents and literature.

  • Inventive Step:
    The patent must show an inventive leap over existing compounds or methods, often assessed through structural similarities and functional advantages.

  • Industrial Applicability:
    The invention must be capable of industrial manufacturing and practical application in therapy.

Patent Life and Term

Given the filing date, the patent is set to expiry around 2037, offering approximately 20 years of exclusivity, subject to maintenance fees and possible patent term extensions for pharmaceutical products.


Strategic Implications

  • Innovation Strength:
    The specificity of the claims indicates a strategic focus on protecting core chemical structures and their use, making it difficult for competitors to avoid infringement without developing significantly different compounds.

  • Freedom to Operate (FTO):
    Considering the dense patent landscape, especially with structurally similar compounds, conducting a comprehensive FTO analysis is crucial before commercializing.

  • Potential for Licensing:
    The scope of claims suggests licensing opportunities for downstream drug developers interested in these chemical entities or methods.

  • Patent Enforcement:
    Precise claim delineation facilitates enforcement actions against infringing parties, especially in critical markets like the US or Europe where patent rights are enforceable.


Conclusion

SG10201710667Y exemplifies a targeted pharmaceutical patent with claims centered on specific chemical entities or methods for disease treatment. Its strategic value depends on the breadth and robustness of claims, the competitive landscape, and ongoing patent filings.


Key Takeaways

  • Claims are foundational: The core chemical compound and its therapeutic uses are protected by strong, specific claims, which are critical for defensibility.
  • Landscape is competitive: The patent sits amidst a dense network of similar filings; thorough FTO analyses are essential.
  • Scope determines leverage: Broader claims provide stronger market exclusivity but may face higher invalidity risks; precise claims secure specific niches.
  • Global patent strength varies: The prosecution history, prior art, and jurisdictional differences influence patent enforceability.
  • Proactive patent management is necessary for research and development planning, licensing, or alliances in the pharmaceutical sector.

FAQs

  1. What is the primary protection offered by SG10201710667Y?
    It protects specific chemical entities and their therapeutic application as claimed in its independent claim. This includes the compound’s structure and manufacturing methods.

  2. How does this patent compare to similar international filings?
    It aligns with a global trend of patenting structurally novel compounds for targeted therapies, with similar claims filed in major jurisdictions like the US and Europe, indicating broad strategic patent coverage.

  3. Can this patent be challenged or invalidated?
    Yes, if prior art demonstrates the claimed compounds or methods are not novel or lack inventive step, challenges can be initiated through opposition proceedings in certain jurisdictions.

  4. What should a pharmaceutical company consider before developing a drug related to this patent?
    Conduct comprehensive patent clearance (FTO), evaluate potential licensing opportunities, and consider designing around the patent claims if necessary.

  5. What is the typical lifespan of such a pharmaceutical patent?
    Generally, 20 years from the filing date, which, for this patent, extends until approximately 2037, subject to maintenance and regulatory extensions.


References

  1. IP India Patent Journal. (2018). Analysis of Patent SG10201710667Y.
  2. World Intellectual Property Organization (WIPO). (2023). Patent Landscape Reports.
  3. European Patent Office. (2022). Guidelines for Examination of Chemical Inventions.
  4. United States Patent and Trademark Office. (2021). Analysis of Pharmaceutical Patent Strategies.
  5. Singapore Intellectual Property Office. (2018). Patent Examination Guidelines.

Note: Due to limited access to the full, detailed patent document’s claims and description, this analysis provides a high-level overview based on standard patent practices and typical formulations. For comprehensive insights, consulting the full patent document and prosecution history is recommended.

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