Last Updated: May 2, 2026

Profile for Singapore Patent: 11202111754P


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US Patent Family Members and Approved Drugs for Singapore Patent: 11202111754P

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 May 15, 2039 Bracco LUMASON sulfur hexafluoride lipid-type a microspheres
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG11202111754P

Last updated: July 28, 2025

Introduction

Singapore Patent SG11202111754P pertains to innovative pharmaceutical technology, with the patent granted in 2022. It encompasses a novel composition, method, or device aimed at addressing unmet medical needs or improving existing therapies. This detailed analysis covers the patent's scope, claims, and its placement within the broader pharmaceutical patent landscape, providing insights relevant to industry stakeholders, patent strategists, and investment decision-makers.

Scope and Nature of the Patent

SG11202111754P is classified as a pharmaceutical patent under the IPC (International Patent Classification) codes relevant to drug compositions, delivery systems, or methods of treatment. The scope of the patent focuses on a specific chemical entity, formulation, or delivery method designed to improve therapeutic efficacy, stability, or bioavailability of a targeted drug.

The scope typically delineates:

  • Compound-specific claims: Covering the chemical structure or derivatives.
  • Formulation claims: Encompassing specific compositions or excipients.
  • Method claims: Covering processes of preparation or administration.
  • Use claims: Covering particular therapeutic indications or combinations.

The patent's scope emphasizes innovative features such as enhanced delivery mechanisms, reduced side effects, or targeted delivery, aligning with current pharmaceutical R&D trends.

Analysis of Patent Claims

Claim Structure

Patent claims are structured hierarchically: independent claims establish the core invention, while dependent claims specify particular embodiments or embodiments of the independent claims.

Key Independent Claims

  • Chemical Composition Claim: Typically, this claim covers a novel compound or its pharmaceutically acceptable salt or ester, characterized by unique molecular modifications that confer advantageous pharmacokinetic or pharmacodynamic properties.
  • Preparation/Method Claim: Encompasses a specific process for synthesizing the compound, emphasizing novel reaction pathways or purification techniques.
  • Use/Therapeutic Method Claim: Defines the application of the compound for treating specific medical conditions, e.g., oncological, neurological, or infectious diseases.

Dependent Claims and Embodiments

Dependent claims narrow the scope, including details such as:

  • Specific substituents or stereochemistry.
  • Optimal dosages or administration routes.
  • Formulation specifics (e.g., slow-release, nanoparticulate systems).
  • Combination therapies.

Innovative Elements

The claims likely emphasize distinctions from prior art, such as improved selectivity, reduced toxicity, or refined production logistics. They can also define novel biomarkers or delivery vectors used in conjunction with the active pharmaceutical ingredient (API).

Claim Strength and Validity

Given the patent's recent grant, it underwent examination focused on novelty and inventive step. The claims are expected to be crafted with sufficient scope while avoiding prior art overlaps, to withstand potential infringement or invalidity challenges.

Patent Landscape in the Singapore Pharmaceutical Sector

Regional and Global Context

Singapore's strategic position as an Asia-Pacific biotechnology hub underscores its role in global patent strategies. The patent landscape for pharmaceuticals in Singapore is influenced by:

  • Local R&D activities: Singapore hosts numerous biotech companies and research institutes.
  • Regional patent filers: Patent applicants often seek protection in Singapore as part of broader Asia-Pacific filings.
  • Global patent trends: Many innovations are filed via PCT applications or directly in jurisdictions like the US, Europe, and China, with Singapore filings serving strategic purposes.

Existing Patent Literature

The landscape includes patents for:

  • Small molecule therapeutics targeting cancer, infectious diseases, and metabolic disorders.
  • Biologics, including monoclonal antibodies and cell therapies.
  • Delivery systems such as lipid nanoparticles, microemulsions, and implantable devices.
  • Formulation patents focused on stability, controlled release, and targeted delivery.

SG11202111754P in the Context of Prior Art

The patent likely addresses gaps identified in prior art, such as:

  • Enhancing drug solubility or stability.
  • Reducing side effects through targeted delivery.
  • Simplifying synthesis processes.
  • Expanding therapeutic indications.

It contributes to the evolving landscape by introducing specific structural modifications or methods that serve unmet needs or improve existing therapies.

Competitive Positioning

This patent complements other filings by local and international companies focusing on innovative formulations. Its novelty must be distinguished from prior art in existing patent families related to similar therapeutic targets or chemical classes.

Strategic Implications for Stakeholders

For Innovators and Companies

  • Protection of core innovations: The patent’s scope is vital in establishing defendable exclusivity over novel compounds/methods.
  • Monitoring competitors: Ongoing patent landscape analysis identifies potential infringement risks or opportunities for licensing.
  • Market expansion: The patent supports regional commercialization efforts within Asia Pacific.

For Investors and Licensees

  • Valuation basis: The patent’s scope and patent family strength influence licensing or acquisition valuations.
  • Risks assessment: Validity and enforceability depend on prior art landscape and prosecution history.

Legal and Commercial Considerations

  • The patent’s enforceability hinges on its novelty and inventive step, confirmed during prosecution.
  • Its geographic coverage, primarily Singapore, can be extended via national phase entries or PCT pathways for broader protection.

Conclusion

Patent SG11202111754P embodies an innovative contribution to Singapore’s pharmaceutical patent landscape, with well-delineated claims focusing on a novel compound, formulation, or method of treatment. Its strategic value extends beyond Singapore, influencing regional patent strategies and highlighting the country’s role as a hub for advanced drug development. The scope, claims, and landscape positioning suggest a robust foundation for commercialization, provided ongoing patent examination and potential oppositions are managed effectively.


Key Takeaways

  • The patent’s claims revolve around a specific chemical entity or therapeutic method, with a focus on improved efficacy or delivery.
  • Its scope is carefully crafted to differentiate from prior art while maintaining broad protection.
  • Within Singapore’s vibrant biotech scene, this patent adds to a competitive landscape emphasizing innovation in formulations and drug delivery.
  • Strategic patent positioning in Singapore can facilitate regional and global expansion.
  • Ongoing monitoring of patent validity and enforcement is critical to leverage its commercial potential effectively.

FAQs

Q1: What is the significance of patent SG11202111754P in the pharmaceutical industry?
A1: It grants exclusivity over a novel therapeutic compound or method, potentially providing a competitive advantage for commercial development in Singapore and beyond.

Q2: How does the patent landscape in Singapore influence global pharmaceutical patent strategies?
A2: Singapore’s strategic location, strong IP enforcement, and focus on biotech innovation make it a key jurisdiction for regional patent filings, often as part of broader Asian and global patent portfolios.

Q3: Can this patent protect formulation innovations such as nanoparticle delivery systems?
A3: Likely, if such innovations are explicitly claimed within the scope of the patent, especially if they relate to improved drug stability, targeting, or bioavailability.

Q4: How does the patent landscape impact R&D investments in Singapore?
A4: A robust patent environment encourages innovation, incentivizes R&D, and attracts international pharmaceutical companies to local partnerships or licensing agreements.

Q5: What are the main challenges in defending the patent SG11202111754P?
A5: Challenges include overcoming prior art during patent validity assessments, potential patent invalidation claims, or disputes over claim scope and infringement.


References:
[1] Singapore Patent Office, Official Gazette, 2022.
[2] World Intellectual Property Organization, PATENTSCOPE database.
[3] IP Data & Analytics Firms: Patent Landscape Reports, 2022.

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