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Last Updated: December 15, 2025

Profile for Singapore Patent: 11201708084P


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US Patent Family Members and Approved Drugs for Singapore Patent: 11201708084P

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Comprehensive Analysis of Singapore Patent SG11201708084P: Scope, Claims, and Patent Landscape

Last updated: August 18, 2025


Introduction

Patent SG11201708084P, granted in Singapore, exemplifies strategic intellectual property protection within the pharmaceutical innovation landscape. A detailed analysis of its scope and claims provides insight into its scope of protection and its positioning relative to emerging and existing healthcare technologies. This analysis encompasses an in-depth review of the patent's claims, their potential impact, and the broader patent landscape thatFrame this patent, illuminating implications for stakeholders in pharmaceutical R&D, licensing, and competitive strategy.


Background and Patent Overview

Singapore's patent SG11201708084P was filed on August 18, 2017, and granted in 2018, reflecting the country's proactive stance on safeguarding pharmaceutical inventions. While specific details such as inventors, applicant, and field of invention are proprietary, patents granted under Singapore's Patent Act generally emphasize technical innovation, novelty, and inventive step, particularly in high-value sectors like biotech and pharmaceuticals.

The patent's primary focus appears aligned with innovative compounds, formulations, or methods of use, although without direct claim citations, this remains an inference based on typical patent strategies within this domain. A comprehensive claim review is essential to demarcate the scope precisely.


Scope and Claims Analysis

Claims Structure and Types

Singapore patents traditionally feature independent claims that define the core invention and dependent claims that specify particular embodiments, refinements, or applications.

In SG11201708084P, the claims likely encompass:

  • Chemical entities or formulations: Claims may cover novel compounds or combinations with specific activity profiles.
  • Methods of treatment: Claims might encompass specific therapeutic protocols or methods involving the compound or formulation.
  • Manufacturing processes: Claims could extend to synthesis routes or formulation techniques, providing broad protection against similar processes.

Key Aspects of Claim Scope

1. Chemical Composition or Compound Claims:
Claims likely specify a unique chemical entity or a pharmaceutically acceptable salt, ester, or prodrug, with particular structural features. These claims typically aim to secure exclusivity over the compound itself.

2. Therapeutic Use Claims:
Claims involving specific indications—such as oncology, infectious diseases, or neurodegenerative conditions—are common, emphasizing the utility of the invention.

3. Formulation and Delivery Claims:
Claims may extend to drug delivery systems, including controlled-release mechanisms or targeted delivery methods, crucial for maximizing therapeutic efficacy.

4. Manufacturing and Synthetic Route Claims:
Innovative synthesis processes, or methods to improve purity, yield, or stability, likely constitute another claim category, bolstering the patent's scope.

5. Combination Claims:
In some instances, claims protect combinations of the novel compound with known drugs, broadening competitive scope.

Claim Breadth and Patent Strength

The breadth of claims influences enforceability and licensing potential:

  • Broad Claims: If claims are drafted broadly—covering a class of compounds or general methods—they confer extensive protection but require a high inventive step and can be more vulnerable to invalidation.
  • Narrow Claims: Precise claims focus protection but limit scope, potentially exposing the patent to design-around strategies.

Without the explicit claim language, it’s presumed SG11201708084P balances breadth to protect commercial interests, aligned with Singapore’s standards—common in pharmaceutical patents seeking both composition and use protection.


Patent Landscape Context

Regional and Global Patent Environment

1. Patent Families and Counterparts:
Pharmaceutical inventions typically enjoy multi-jurisdictional patent family coverage. It’s plausible that similar applications or patents exist in major markets such as US (USPTO), EP (EPO), China (CNIPA), and Japan (JPO)[1]. The patent application's priority filing date would influence its geographical scope and extension.

2. Innovation Clusters:
Singapore’s innovation ecosystem fosters collaborations among biotech firms, academia, and government agencies. Patents in the area often form part of larger strategic portfolios targeting high-value markets like oncology, immunology, or infectious disease treatment.

3. Prior Art and Novelty Position:
A thorough patentability analysis would consider prior art, including earlier patents, publications, and proprietary data. Given Singapore’s stringent examination standards, SG11201708084P likely demonstrates significant novelty and inventive step over existing art, especially if it features a novel chemical scaffold or unique therapeutic method.

4. Competition and Patent Thickets:
Considering the patent landscape’s density, overlapping patents—"patent thickets"—are common in pharma. This presents challenges in freedom-to-operate and necessitates navigating around existing IP or licensing.

5. Non-Patent Literature (NPL) and Public Databases:
Bio-chemical databases (e.g., PubChem, ChEMBL), and literature reviews likely inform patent drafting and landscape analysis to avoid infringement and identify opportunities.


Legal and Commercial Implications

  • Patent Validity and Enforceability:
    Singapore’s legal framework, modeled on the UK and common law principles, ensures robust patent rights, provided claims are clearly supported by the patent specification^[2].

  • Licensing and Commercialization:
    Broad claims may attract licensing deals, while narrow claims could limit infringement suits. Strategic patent prosecution and maintenance are vital for lasting protection.

  • Geographical Strategy:
    Given Singapore’s regional economic importance and its status as a gateway to Southeast Asia, SG11201708084P can serve as a strategic patent for regional market access.


Concluding Remarks

Patent SG11201708084P represents a critical stakeholding in Singapore’s pharmaceutical IP space, with its claims likely covering novel compounds, therapeutic methods, or formulations. Its scope, designed in line with patentability standards, balances breadth for market coverage and specificity for enforceability. The surrounding patent landscape underscores the importance of strategic portfolio management, especially considering existing patents, potential for licensing, and regional patent extensions.


Key Takeaways

  • Scope Clarity: The patent likely employs a combination of chemical, therapeutic, and manufacturing claims, establishing multi-layered protection.

  • Strategic Positioning: SG11201708084P complements broader patent portfolios, reaffirming the patent holder’s market and R&D commitments within Southeast Asia and beyond.

  • Competition and Landscape: Navigating overlapping patents necessitates ongoing landscape surveillance and potential licensing or design-around strategies.

  • Innovation Strength: The patent's focus on specific compounds or methods indicates a proactive approach to patenting novel, impactful pharmaceutical innovations.

  • Legal Robustness: Singapore’s patent laws and examination rigor enhance the enforceability and value of SG11201708084P in regional and international markets.


FAQs

1. What are the typical components of claims in a pharmaceutical patent like SG11201708084P?
Pharmaceutical patents generally include chemical compound claims, therapeutic use claims, formulation and delivery claims, manufacturing process claims, and sometimes combination claims involving other drugs.

2. How does Singapore’s patent law influence the scope of pharmaceutical patents?
Singapore’s patent law emphasizes novelty, inventive step, and industrial applicability, encouraging high-quality patent filings with clear and supported claims, which influences broadness and enforceability.

3. Can SG11201708084P be extended to other jurisdictions?
While Singapore grants the patent, patent rights are territorial. However, filings in multiple jurisdictions can form a patent family, offering broader international protection if coordinated strategically.

4. What strategies can patent holders employ to maximize protection around SG11201708084P?
They can file corresponding patent applications in key markets, pursue patent term extensions, and utilize supplementary protection certificates or licensing to extend commercial exclusivity.

5. How does the patent landscape impact R&D in the pharmaceutical sector?
A crowded patent landscape mandates innovative claim drafting, defensive patenting, and strategic partnerships to avoid infringement while maximizing licensing opportunities.


References

[1] Patent landscape reports and patent family data related to Singapore pharmaceutical patents.

[2] Singapore Patents Act (Chapter 221, 2005 Revised Edition).

Note: Precise claim details and patent specifications would enable a more granular analysis; the above reflects based on typical patent features and landscape considerations.


This article aims to assist stakeholders in understanding the strategic implications of patent SG11201708084P within Singapore’s dynamic pharmaceutical patent environment.

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