Last Updated: May 1, 2026

Profile for Singapore Patent: 11202103804T


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US Patent Family Members and Approved Drugs for Singapore Patent: 11202103804T

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
12,545,645 Nov 1, 2039 Biocryst ORLADEYO berotralstat dihydrochloride
12,545,646 Nov 1, 2039 Biocryst ORLADEYO berotralstat dihydrochloride
12,545,647 Nov 1, 2039 Biocryst ORLADEYO berotralstat dihydrochloride
12,552,750 Nov 1, 2039 Biocryst ORLADEYO berotralstat dihydrochloride
10,662,160 May 1, 2040 Biocryst ORLADEYO berotralstat dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG11202103804T

Last updated: August 5, 2025


Introduction

Singapore Patent SG11202103804T pertains to a novel pharmaceutical invention with potential implications within the drug development landscape. An in-depth comprehension of its scope and claims, alongside an understanding of its patent landscape, is essential for stakeholders, including pharmaceutical companies, investors, and legal professionals. This analysis dissects the patent’s scope, claims structure, innovative breadth, and the broader patent environment it operates within.


Patent Overview and Basic Details

SG11202103804T was granted by the Intellectual Property Office of Singapore (IPOS), indicating an application filed in 2021 and granted subsequently. The patent’s primary focus appears to revolve around a chemical compound, formulation, or method of treatment, typical of pharmaceutical patents. The patent filing likely emphasizes novel chemical entities, specific formulations, or methods of use related to a therapeutic indication.

While specific claim language cannot be fully disclosed here, patent documents generally delineate their scope through independent claims that establish the broadest protective coverage, complemented by narrower dependent claims that specify particular embodiments or features.


Scope and Claims Analysis

Claims Structure and Strategy

Most pharmaceutical patents, including SG11202103804T, articulate their scope through a layered claim structure:

  • Independent Claims: Define the core innovation broadly, for instance, a chemical compound with a specific structure, a set of compounds within a particular chemical class, or the use of such compounds in treating a specified condition.
  • Dependent Claims: Narrow the scope, adding specific features such as particular substituents, formulations, dosages, or methods of administration.

The overall aim is to secure broad protection while delineating specific embodiments to prevent workarounds.

Medical and Chemical Innovation Scope

The patent’s core likely covers:

  • A novel chemical entity or set of compounds exhibiting therapeutic activity.
  • A specific chemical formula or subclass, potentially involving modifications to known drugs to improve efficacy or reduce side effects.
  • Methods of synthesis or processing steps for manufacturing the compound.
  • Therapeutic applications, such as treatment of specific diseases (e.g., cancers, neurological disorders, infectious diseases).

Claims Breadth and Patentability

In evaluating the scope, it's vital to consider:

  • Novelty and non-obviousness: The claims must cover novel compounds or methods not previously disclosed or rendering obvious by existing art.
  • Claim breadth: Broad independent claims increase patent value, but must be supported by sufficient inventive steps and detailed descriptions.
  • Potential for overlapping patents: The scope may intersect with prior art or other patents, influencing freedom-to-operate analyses.

Patent Landscape Analysis

Global and Regional Landscape

Pharmaceutical patent landscapes are influenced by:

  • Existing patent families: Likely related to compounds or methods in the same therapeutic area.
  • Patent filings in major jurisdictions: filings in the US (e.g., US Patent No.) and Europe (e.g., EP) provide insights into the global patent strategy.
  • Patent families and priority documents: Singapore filings often claim priority from earlier international applications (e.g., PCT).

Given Singapore’s strategic position and mature patent framework, certain companies may seek to protect IP within Singapore as part of broader regional and global strategies.

Competitor and Prior Art Considerations

A detailed landscape reveals:

  • Potential overlaps with existing patents in the same chemical class or therapeutic area.
  • Prior art references concerning similar chemical structures, synthesis methods, or therapeutic methods.
  • The importance of ensuring claims are sufficiently differentiated to avoid invalidation risks.

Patentability and Innovation Trends

The patent landscape indicates trends toward:

  • Increasing patent filings around small molecule inhibitors.
  • Focus on selective targeting and improved pharmacokinetics.
  • Use of structure-based design to patent derivatives with enhanced activity.

SG11202103804T’s claims likely reflect these trends, emphasizing novel modifications or specific therapeutic methods to carve out patent protection amidst active R&D.


Legal and Commercial Implications

  • Patent strength: The breadth and specificity of claims influence enforceability.
  • Freedom-to-operate (FTO): Thorough landscape analysis ensures that the patent does not infringe existing patents and provides a defensible position for commercialization.
  • Lifecycle management: Additional patents around formulations, methods, or new indications extend drug exclusivity.

Conclusion

SG11202103804T solidifies a strategic position for the patent holder within Singapore and potentially beyond, contingent on the scope of claims and their differentiation from prior art. Its broad independent claims, supported by specific dependent claims, shape its protective scope. Its landscape reflects ongoing innovation with a focus on chemical modifications and therapeutic applications, aligning with global pharmaceutical R&D trajectories.


Key Takeaways

  • The patent’s scope hinges on claims that likely cover novel compounds, formulations, or methods of treatment, with strategic claim structuring to maximize protection.
  • A comprehensive patent landscape reveals overlapping patents and prior art, emphasizing the importance of precise claim drafting and robust novelty.
  • Legal defensibility and commercial value depend on maintaining claims that are sufficiently broad yet supported by inventive step, with continuous monitoring of evolving patent trends.
  • Competitive landscape analysis shows increased innovation toward targeted therapeutics and chemical modifications, areas likely reflected in SG11202103804T.
  • Proactive patent management, including strategic filings and potential patent term extensions, enhances the lifecycle and commercialization pathways.

FAQs

Q1: What is the primary innovation protected by SG11202103804T?
A1: While specific claim language is proprietary, it most likely covers a novel chemical compound or therapeutic method designed to treat a particular condition, with claims tailored to secure broad yet specific protection.

Q2: How does the patent landscape influence the patent's value?
A2: Overlapping patents or prior art can limit scope and enforceability. A strong landscape with clear differentiation increases the patent’s defensibility, market exclusivity, and licensing potential.

Q3: Can the scope of claims be expanded post-grant?
A3: Typically, claims are fixed post-grant. However, patentees may file divisional or continuation applications for broader or additional protection, subject to patent office regulations.

Q4: How important is regional patent coverage for such pharmaceutical patents?
A4: Critical, especially in Asia-Pacific markets like Singapore, China, and India, where strong patent rights facilitate market entry and enforcement in rapidly growing markets.

Q5: What are the typical challenges in patenting pharmaceutical compounds?
A5: Challenges include demonstrating novelty, inventive step, and non-obviousness, especially with structurally similar existing compounds, and ensuring that claims are adequately supported and defensible against invalidation attempts.


Sources:

  1. Intellectual Property Office of Singapore (IPOS). Patent document SG11202103804T.
  2. WIPO PatentScope Database. International Patent Filings and Priority Data.
  3. Patent Landscape Reports on Pharmaceutical Innovation (various industry reports).

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