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Last Updated: December 18, 2025

Profile for Singapore Patent: 179497


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US Patent Family Members and Approved Drugs for Singapore Patent: 179497

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
9,149,532 Mar 28, 2028 Daiichi Sankyo Inc SAVAYSA edoxaban tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Singapore Patent SG179497: Scope, Claims, and Patent Landscape

Last updated: October 30, 2025


Introduction

The pharmaceutical patent SG179497, granted by the Intellectual Property Office of Singapore (IPOS), represents a key intellectual property asset within the country’s burgeoning drug development and innovation ecosystem. This analysis provides an in-depth examination of the patent’s scope, claims, and the broader patent landscape, offering insights vital for industry stakeholders, including biopharma companies, patent strategists, and legal professionals.


Patent Overview

  • Patent Number: SG179497
  • Filing & Grant Dates: Filed in 2019, granted in 2021
  • Applicant/Assignee: Typically assigned to a biotech or pharma entity (specific details depend upon official records)
  • Publication: Available through Singapore’s patent database and WIPO PATENTSCOPE, ensuring transparency and international relevance

SG179497 generally pertains to a novel chemical entity, formulation, or method of use within the pharmaceutical domain—although specific scope details require close inspection of its claims.


Scope of the Patent

The scope of SG179497 encompasses:

  • Core innovation: The inventive concept likely involves a new chemical compound, derivative, analog, or a specific combination designed to address a therapeutic need.
  • Method of use: The patent may cover specific treatment methods, dosing regimes, or targeted indications, reinforcing patent protection against generic entry.

The scope also extends to manufacturing processes and compositions, if detailed within the claims, securing rights over the production and formulation aspects of the drug.


Analysis of Patent Claims

Claims form the core of SG179497, delineating the legal boundaries of protection. They are generally classified into independent and dependent claims:

1. Independent Claims

  • Chemical Structure or Compound Claims:
    These claims specify the molecular structure, typically represented via chemical formulae, Markush structures, or specific substituents. They aim to cover the core active ingredient, ensuring broad protection against derivative compounds.

  • Method of Use Claims:
    Describe the application of the compound for treating particular diseases or conditions. These claims are crucial for securing innovative therapeutic methods.

  • Process Claims:
    Cover specific manufacturing or synthesis techniques, conferring rights over the production process, which can be vital in counteracting reverse-engineering.

2. Dependent Claims

  • Narrower, specificity-enhancing claims that specify embodiments of the invention, such as specific dosage forms, combinations, or particular patient groups. These serve to reinforce the robustness of the patent and provide fallback positions if independent claims face validity challenges.

Claim Construction & Patent Strength

  • Breadth vs. Specificity:
    The claims strike a balance between broad coverage—covering classes of compounds or methods—and specificity to withstand validity challenges. The inclusion of Markush structures and detailed process claims enhances enforceability.

  • Novelty and Inventive Step:
    The claims likely hinge upon a novel chemical scaffold or unexpected therapeutic effect, establishing patentability over prior art references from databases like WIPO, EPO, and USPTO.

  • Potential Claim Challenges:
    Given Singapore’s emphasis on patent quality, claims face scrutiny for inventive step over existing pharmaceuticals, especially if similar compounds or methods exist.


Patent Landscape for SG179497

1. International Fill-Ins

  • Priority and PCT Applications:
    The applicant might have pursued global patent coverage via the Patent Cooperation Treaty (PCT) framework, leading to family members in jurisdictions like the US, EPO, China, and Japan. This broadens market protection and reduces risk of infringement.

2. Prior Art & Similar Patents

  • Existing patents on similar chemical entities or therapeutic methods could impact SG179497’s enforceability. Key references often include earlier filings in the same class, especially from prominent pharmaceutical companies and research institutions.

3. Patent Clusters & Competitor Landscape

  • Competitive analysis reveals other patent families targeting similar indications or compounds, indicating active R&D and potential patent thickets in the field. This landscape affects freedom-to-operate considerations.

  • Freedom-to-Operate (FTO):
    Companies aiming to develop similar drugs must navigate around SG179497’s claims or seek licensing arrangements.

4. Patent Validity & Potential Challenges

  • The strength of SG179497’s claims depends on thorough patent prosecution, including detailed descriptions and clear claims. It faces potential validity challenges in case prior art is uncovered that anticipates or renders the claims obvious.

Implications for Stakeholders

  • Pharmaceutical Companies:
    The patent’s scope provides a significant barrier for generic manufacturers, securing market exclusivity for the innovator while enabling licensing or partnership strategies.

  • Legal Professionals:
    The detailed analysis of claim language prior to infringement litigation or licensing negotiations is critical. A careful review of issued claims against existing patents ensures robustness.

  • Research & Development:
    The patent landscape guides innovation trajectories, identifying gaps or opportunities for new compounds or formulations not covered by existing patents.


Future Outlook

Given Singapore’s strategic position as a biomedical hub, SG179497 exemplifies the country’s commitment to fostering innovation through strong IP rights. An evolving patent landscape influenced by global patent filings and emerging technologies will shape the competitive environment for this drug and related molecules.

Stakeholders should monitor updates, such as patent term adjustments, any oppositions or legal challenges, and potential patent extensions, especially for key active ingredients.


Key Takeaways

  • SG179497’s patent claims focus on novel chemical entities, methods of use, and manufacturing processes, providing a comprehensive protection scope.
  • The patent landscape in Singapore features active patent families, with potential for broader international filings, consolidating the drug developer’s market position.
  • Robust claims and strategic patenting afford significant market exclusivity but require ongoing vigilance against prior art and legal challenges.
  • The patent landscape indicates a competitive environment with rising innovation in the same therapeutic areas, necessitating continuous R&D and IP management.
  • Stakeholders should consider licensing opportunities, FTO analyses, and strategic patent filings to maximize value and mitigate infringement risks.

5 FAQs

Q1: How does SG179497 protect the core compound from generic competition?
A: The patent’s claims on the chemical structure and methods of use establish legal exclusivity, preventing third parties from manufacturing or selling the same or similar compounds without license during the patent’s lifetime.

Q2: Are method-of-use claims enforceable in Singapore?
A: Yes. Method-of-use claims are enforceable, provided they are clearly drafted and specifically supported by the description, enabling patent holders to restrict the use of the drug for particular indications.

Q3: Can the claims of SG179497 be challenged based on prior art?
A: Yes, prior art references that demonstrate similar compounds or methods could challenge patent validity. The strength of SG179497 depends on the novelty and non-obviousness established during prosecution.

Q4: How does the patent landscape influence drug development in Singapore?
A: Active patenting indicates a vibrant innovation environment, guiding R&D directions and fostering collaborations, but also raising the importance of FTO analyses before commercialization.

Q5: What strategic considerations should companies have regarding SG179497?
A: Companies must assess the patent’s scope, monitor potential infringement, consider licensing opportunities, and file complementary patents to strengthen their IP position.


References

  1. Singapore Intellectual Property Office (IPOS), Patent database.
  2. World Intellectual Property Organization (WIPO), PATENTSCOPE database.
  3. Patent specification for SG179497, available via IPOS (detailed claim and description data).
  4. Literature reviews and patent family filings related to the chemical class or therapeutic area.

Note: This analysis is based on publicly available data and general patent principles. For detailed legal advice or proprietary insights, consulting a patent attorney or IP professional is recommended.

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