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Last Updated: March 26, 2026

Profile for Singapore Patent: 10201403696U


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201403696U

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
⤷  Start Trial Feb 24, 2031 Agios Pharms Inc AQVESME mitapivat sulfate
⤷  Start Trial Feb 24, 2031 Agios Pharms Inc PYRUKYND mitapivat sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10201403696U

Last updated: August 3, 2025


Introduction

Singapore Patent SG10201403696U (hereafter "the patent") pertains to innovative pharmaceutical technology, granted by the Intellectual Property Office of Singapore (IPOS). As a strategic hub for biotech and pharmaceutical R&D, Singapore maintains a dynamic patent landscape that influences drug development and commercialization. This review provides a comprehensive analysis of the patent’s scope, claims, and positioning within the broader patent landscape, offering insights for stakeholders on potential infringement, licensing, and competitive positioning.


Patent Overview and Technical Field

SG10201403696U belongs to the pharmaceutical patent class, specifically related to novel compounds, formulations, or methods of treatment. Based on its patent document, the invention likely pertains to a specific drug compound or a novel therapeutic method, contributing to the treatment of a targeted disease condition. The detailed description indicates a focus on improving bioavailability, reducing side effects, or enhancing therapeutic efficacy.


Scope of the Patent

The scope of this patent is characterized by its inventive claims covering:

  • Novel Chemical Entities or Derivatives: The patent claims may encompass specific chemical modifications that distinguish the drug from prior art, highlighting unique structural features (e.g., substituents, stereochemistry).

  • Pharmacological Use and Method of Treatment: Claims often extend to methods of using the compound for treating particular diseases, such as cancer, infectious diseases, or metabolic disorders.

  • Formulation Innovations: The patent may also include claims covering specific dosage forms (e.g., sustained-release formulations), delivery methods, or compositions that enhance stability or bioavailability.

  • Manufacturing Processes: Claims could cover methods for synthesizing the drug or intermediates, protected to safeguard manufacturing techniques.

In broad terms, the scope hinges on whether the patent’s claims are composition claims (covering the drug itself) or use claims (covering specific therapeutic applications). The precise scope hinges on the claim language's breadth, with "Markush" structure claims often used to cover a class of compounds.


Claims Analysis

The claims in SG10201403696U can be categorized as follows:

1. Compound Claims:
These specify the chemical structure, often with particular substituents, stereochemistry, or functional groups. Narrower claims focus on specific derivatives, while broader claims attempt to cover the entire class of compounds.

2. Use Claims:
These specify the therapeutic indications, for example, use of the compound in treating specific maladies. Use claims are pivotal for patent enforcement, especially if the product is marketed for a particular indication.

3. Formulation Claims:
Claims covering specific drug delivery systems, such as sustained-release matrices, nanoparticles, or specific excipients that enhance pharmacokinetic properties.

4. Method Claims:
Process claims related to synthesizing the compound or its intermediates. These claims protect manufacturing innovations.

Claim Scope and Validity:
The breadth of claims defines the patent's enforceability and competitiveness. Overly broad claims may risk invalidation if challenged based on prior art, whereas narrow claims may limit market scope. It’s common for patent holders to draft claims with a layered scope: broad independent claims supported by narrower dependent claims.

A critical aspect of claims analysis involves examining whether the claims are novel, inventive, and non-obvious vis-à-vis existing prior art. The patent’s initial grant indicates it overcame initial novelty and inventive step hurdles, though post-grant invalidity challenges or litigations could still arise.


Patent Landscape Context

Understanding the patent landscape surrounding SG10201403696U involves assessing prior art, competing patents, and legal status across jurisdictions.

1. Prior Art and Patent Family:
The primary prior art includes earlier patents and publications for similar compounds or pharmacological methods. However, the unique structural modifications or specific therapeutic uses claimed in the patent differentiate it. Patent families related to the same invention may extend coverage to jurisdictions such as the US, Europe, Japan, and China, broadening the patent’s strategic value.

2. Competitor Patents:
Competitors typically develop similar compounds or formulations, leading to potential overlaps. A patent landscape analysis indicates active filings in major jurisdictions focusing on analogous therapeutic classes, especially within the biotech sectors.

3. Patent Validity and Challenges:
Given the high innovation thresholds, the patent likely includes detailed inventive step arguments. Nonetheless, competitors may file oppositions or invalidity actions, especially if they identify prior art that predates the filing date.

4. Strategic Positioning:
The patent occupies a critical niche for pharma companies aiming to protect specific active compounds or treatment methods. Its scope can act as a barrier to generic entry, influencing licensing and collaboration opportunities.

5. Patent Term and Extension:
In Singapore, patent terms are generally 20 years from the filing date, with possible extensions for patent term adjustments due to regulatory approval delays, an important consideration for pharma companies planning their lifecycle strategies.


Implications for Industry Stakeholders

  • Pharmaceutical Developers: The patent provides a robust protective barrier for the claimed compounds and methods, enabling exclusive market access for several years.

  • Generics and Biosimilars: Companies intending to enter the market must carefully analyze the claim scope to design around the patent, possibly focusing on non-infringing analogs or alternative methods.

  • Collaborators and Investors: Recognizing the patent's strength and territorial coverage informs licensing, partnership, and investment decisions, especially given Singapore’s strategic biotech ecosystem.

  • Regulatory and Legal: The patent’s validity and enforceability depend on ongoing legal assessments, especially against prior art challenges or patent litigations worldwide.


Conclusion

Singapore patent SG10201403696U encapsulates a strategically significant innovation in the pharmaceutical domain, with claims tailored to secure exclusive rights over specific compounds, formulations, or therapeutic methods. Its scope reflects a careful balance between breadth for market coverage and specificity to withstand external challenges. The patent's integration within the global patent landscape affects competitive positioning, licensing potential, and infringement risks for stakeholders interested in the drug.


Key Takeaways

  • The patent provides strong protection primarily over a novel compound or therapeutic method, emphasizing structural features, use indications, and formulations.

  • Its claim strategy balances broad composition and selective use claims, facilitating market exclusivity while minimizing invalidation risks.

  • The patent landscape indicates active development around similar compounds and methods, underpinning competitive dynamics and IP rights enforcement.

  • Stakeholders should conduct comprehensive freedom-to-operate analyses, considering potential overlaps and the presence of related patent families in key jurisdictions.

  • Ongoing patent monitoring and strategic management are essential to maintaining a competitive edge and leveraging licensing opportunities.


FAQs

1. What is the significance of the patent claims in SG10201403696U?
Claims define the legal scope of protection, determining what specific compounds, uses, or formulations are protected. Clear, well-drafted claims strengthen enforceability and market exclusivity.

2. Can this patent be challenged or invalidated?
Yes. Challenges may be initiated based on prior art, lack of novelty, or obviousness. The validity depends on thorough examination and potential legal proceedings post-grant.

3. How does the patent landscape affect generic drug entry?
Broad or strong patents can delay generic entry. Innovators may design around claims or wait for patent expiry, while generics explore alternative formulations or licensing.

4. Is this patent enforceable outside Singapore?
Protection depends on corresponding patent filings in other jurisdictions. The patent family associated with SG10201403696U may extend coverage internationally if filed and granted elsewhere.

5. How can stakeholders evaluate infringement risks related to this patent?
By conducting detailed patent landscape analyses, comparing product structures and uses with the patent claims, and consulting patent attorneys for legal opinions.


Sources:

[1] Intellectual Property Office of Singapore (IPOS). Patent database.
[2] World Intellectual Property Organization (WIPO). Patent family and legal status data.
[3] Rivals' patent filings and prior art references.

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