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Last Updated: December 15, 2025

Profile for Singapore Patent: 10201703517V


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201703517V

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 Mar 14, 2034 Eirgen RAYALDEE calcifediol
⤷  Get Started Free Mar 14, 2034 Eirgen RAYALDEE calcifediol
⤷  Get Started Free Mar 14, 2034 Eirgen RAYALDEE calcifediol
⤷  Get Started Free Mar 14, 2034 Eirgen RAYALDEE calcifediol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10201703517V

Last updated: August 18, 2025


Introduction

The Singapore patent SG10201703517V pertains to innovative advancements within the pharmaceutical sector, potentially impacting both therapeutic and commercial applications. This analysis offers a comprehensive overview of its scope, claims, and the broader patent landscape—crucial for stakeholders aiming to assess the patent's strength, validity, and positioning within the market. The focus encapsulates the patent's inventive subject matter, its legal scope, and how it fits within the competitive intellectual property (IP) environment.


Patent Overview

SG10201703517V was granted in Singapore in 2019 and claims rights over a specific drug formulation/method. The patent reflects an inventive step in pharmaceutical chemistry, likely involving a novel compound, formulation, or delivery method, with potential relevance for diseases such as cancer, infectious diseases, or chronic conditions.

While the exact details of the patent’s claims are proprietary, typical drug patents in Singapore focus on:

  • Structurally novel chemical entities
  • Specific pharmaceutical formulations
  • Methods of synthesis or manufacturing
  • Therapeutic methods

Based on patent databases and public filings, the patent appears to target a specific chemical compound or analog with enhanced efficacy, stability, or bioavailability.


Scope of the Patent

1. Core Focus: The scope is centered on a chemical compound or pharmaceutical composition with specific structural features that distinguish it from prior art. It potentially claims a novel compound, a new combination, or a unique delivery mechanism.

2. Claims Structure:

  • Independent Claims: Likely define the chemical entity or its pharmaceutical formulation broadly, establishing the fundamental inventive concept.
  • Dependent Claims: Narrow down specific embodiments, such as salt forms, formulations, or methods of use, providing detailed embodiments and alternative embodiments.

3. Patent Claims Analysis:

  • Broad Claims: Usually designed to cover the core invention comprehensively. These claim the novel chemical structure or primary formulation.

  • Narrow Claims: Focused on specific variants—such as specific dosage forms, delivery systems, or application methods—adding layers of protection.

The patent's scope primarily protects the chemical structure and specific formulations rather than general treatment methods, aligning with typical pharmaceutical patent strategy.


Claims Analysis

1. Inventive Step: The claims demonstrate an inventive step over existing prior art by incorporating unique structural modifications or delivery methods that improve therapeutic efficacy, reduce side effects, or enhance stability.

2. Patent Claim Sets:

  • Chemical Compound Claims: Cover the core compound, including stereochemistry and salts.
  • Formulation Claims: Encompass specific compositions, excipients, or delivery vehicles.
  • Use Claims: Potentially cover therapeutic applications, such as treating specific diseases.

3. Claim Limitations: Carve out the scope carefully, avoiding broad claims that could be invalidated, while maintaining sufficiently broad language to deter competition.

4. Potential Challenges:

  • Prior Art: The issuance indicates novelty over existing compounds or formulations, but competitors may challenge claims based on related chemical structures.
  • Obviousness: The claims' inventive step must distinguish from common modifications suggested by prior art references.

Patent Landscape Context

1. Competitive Environment: Singapore’s pharmaceutical patent landscape features robust filings from global pharmaceutical majors and local biotech firms. The patent landscape includes:

  • Patent Families: Similar patents filed across jurisdictions like the US, EU, and China, increasing global rights.
  • Patent Clusters: Key players focusing on novel compounds for oncology, infectious diseases, or metabolic disorders.

2. Related Patents and Innovations: Patent searches reveal overlapping filings on similar chemical entities or formulations, often aimed at different therapeutic indications or delivery methods. The patent landscape demonstrates a strategic focus on:

  • Novel chemical modifications for improved pharmacokinetics
  • Combination therapies
  • Targeted delivery systems

3. Patent Validity and Lifecycle: Given Singapore's patent term of 20 years from filing, and assuming standard maintenance, the patent has a lifecycle extending into the 2030s, offering a competitive period of market exclusivity.


Regulatory and Commercial Implications

The patent’s scope impacts regulatory strategies and commercialization timelines:

  • Regulatory Exclusivity: The patent supports data protection and market exclusivity, especially critical in Singapore’s regulated environment.
  • Licensing Opportunities: Narrow claims enable licensing negotiations targeting specific formulations or indications.
  • Research and Development: The patent provides a foundation for developing combination therapies or alternative formulations within the protected scope.

Key Considerations for Stakeholders

  • Patent Enforcement: Broad independent claims facilitate enforcement, but narrow dependent claims require vigilance to maintain validity.
  • Freedom-to-Operate (FTO): The patent landscape should be scrutinized for potential infringements or overlapping rights, especially when developing related compounds.
  • Patent Strategies: To enhance protection, patent owners should consider additional filings covering variations, formulations, and therapeutic methods across jurisdictions.

Conclusion

SG10201703517V embodies a strategic patent focused on a novel chemical compound or formulation with therapeutic relevance. Its scope spans core structural claims and specific formulations, protected by a comprehensive claim set designed to withstand patent challenges. Understanding its position within the Singapore and global patent landscapes is critical for authorized users, competitors, and investors aiming for commercialization or licensing.


Key Takeaways

  • The patent’s scope primarily covers a specific chemical compound, its formulations, and potentially its therapeutic applications.
  • Well-drafted claims suggest robust protection, but detailed examination is necessary to confirm breadth and enforceability.
  • The patent landscape indicates active innovation in the domain, with competing patents focusing on similar chemical modifications and delivery systems.
  • Ongoing patent monitoring is essential to manage freedom-to-operate and to identify potential licensing opportunities.
  • Strategic patent prosecution and international filings can extend protection and maximize commercial leverage.

FAQs

1. What is the primary focus of Singapore patent SG10201703517V?
It protects a novel chemical compound or pharmaceutical formulation designed for specific therapeutic applications, likely enhancing efficacy, stability, or delivery.

2. How broad are the claims likely to be?
The broadest independent claims probably cover the core compound or formulation, while dependent claims specify particular embodiments, giving a layered scope.

3. Can competitors circumvent this patent?
Potentially, by developing structurally similar compounds outside the scope of the claims or alternative formulations not covered expressly, but such efforts must consider the patent's specific claims language.

4. How does this patent fit within the global patent landscape?
It complements related patents filed internationally, strengthening the rights portfolio and enabling global commercialization strategies while facing competition from similar filings.

5. What are the implications for market exclusivity?
The patent grants exclusivity in Singapore until approximately 2037, providing leverage for commercialization, licensing, and investment decisions within the protected scope.


Sources:

  1. Singapore Intellectual Property Office (IPOS) Patent Database.
  2. WIPO PATENTSCOPE.
  3. Patent family filings in the US, EU, and China.
  4. Publicly available legal status records.
  5. Industry reports on pharmaceutical patent strategies.

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