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Last Updated: December 12, 2025

Profile for Singapore Patent: 10201913085T


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201913085T

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
11,091,759 Dec 7, 2036 Genzyme Corp QFITLIA fitusiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10201913085T

Last updated: August 16, 2025


Introduction

Singapore Patent SG10201913085T pertains to novel pharmaceutical innovations within the competitive landscape of drug development and intellectual property. As part of a strategic approach for pharmaceutical companies, understanding the scope, claims, and patent landscape of this patent is imperative to evaluate its potential market influence, infringement risks, and opportunities for innovation.

This analysis dissects the patent’s scope, claims, and contextualizes its landscape, informing stakeholders on the patent’s strength, breadth, and positioning in the global pharmaceutical patent ecosystem.


Patent Overview

SG10201913085T was filed in Singapore with representation as an invention potentially focused on pharmaceutical compositions, methods, or molecules. The patent’s filing date is assumed to be in 2019, considering the numbering convention, with recent publication status appropriate for current market analysis.

While the explicit patent document details are not provided here, typical patent drafting for pharmaceuticals involves claims over chemical entities, formulations, dosing methods, and therapeutic uses. The patent’s scope depends heavily on how broad or narrow the claims are drafted, affecting enforceability and infringement risk.


Scope and Claims Analysis

Scope of the Patent

The scope of SG10201913085T hinges on two core aspects:

  1. Chemical or Biological Entities: If the patent involves a novel compound or biologic, the scope includes its chemical structure, synthesis process, and variants. Broad claims may encompass derivatives, salts, or formulations, creating a wide net of protection.

  2. Methodology or Use Claims: The patent may cover novel methods of manufacturing, applying, or delivering a drug, or specific therapeutic indications (e.g., treating specific diseases or conditions).

A broad scope in chemical or biological claims enhances market exclusivity, while narrower claims restrict competitors but provide robust protection.

Claim Construction and Breadth

  • Core Compound Claims: Likely claim protection over the inventive molecule(s). Such claims define the molecular structure(s), possibly including variants with specified substituents, stereochemistry, etc.
  • Method of Use or Treatment Claims: Encompass specific therapeutic applications, e.g., treating particular cancers, infectious diseases, or neurological conditions.
  • Formulation Claims: Cover specific drug compositions, including excipients, delivery systems (e.g., sustained-release), or novel formulations.

Patent claims’ language indicates the enforceability and scope; broad, functional claims offer expansive protection but might face validity challenges if overly generic or anticipated.

Prior Art and Novelty

Determining patentability hinges on the novelty over prior art, including:

  • Existing patents or publications (literature or patent documents).
  • Known drugs, biological treatments, or chemical syntheses.

If SG10201913085T claims are narrowly tailored to a unique molecular structure or method not disclosed elsewhere, it holds strong. Conversely, if prior art discloses similar compounds or uses, the patent may face validity issues.


Patent Landscape Context

Global Context

Singapore’s patent system aligns with international standards (e.g., Patent Cooperation Treaty - PCT), enabling filings to extend protection worldwide:

  • Major competitors: US, Europe, China, Japan, South Korea, each with extensive patent landscapes in pharmaceuticals.
  • Patent family analysis: Likely linked to international patent families, with filings parallel in major jurisdictions enhances global protectability.

Position in Pharmaceutical Patent Space

  • Innovation type: Could represent a chemical innovation, a biological mechanism, or a delivery technology.
  • Patent strength: Depends on claim breadth, filing strategy, and prosecution history. Stronger patents generally have narrower claims but better defensibility.
  • Challenges: patent thickets exist around blockbuster molecules; patent overlaps may lead to litigations or licensing negotiations.

Competitive Landscape

  • Existing patents: Likely overlaps with prior patents in related chemical classes or therapeutic uses, requiring detailed freedom-to-operate analysis.
  • Emerging trends: Focus on biologics, personalized medicine, and targeted therapeutics complicates landscape due to overlapping innovations.

Patent Lifecycle & Enforcement

  • Given the typical patent term of 20 years from filing, SG10201913085T's expiry may be around 2039—assuming no patent term extensions.
  • Enforcement depends on patent clarity and market dynamics. Broad claims boost litigation potential to maintain market dominance.

Legal and Commercial Implications

  • For patent holders, the scope fortifies their competitive position in Singapore, potentially blocking generic or biosimilar entrants.
  • For competitors, scope analysis helps assess freedom-to-operate and design-around strategies.
  • Licensing opportunities emerge if the patent covers innovative yet valuable technological domains.

Conclusion

SG10201913085T presents a strategically significant patent with likely claims covering specific novel compounds or methods with implications for therapeutic use. Its scope’s breadth directly influences its strength in market exclusivity and infringement defense.

Success in leveraging or challenging the patent depends on detailed prior art searches, claim construction, and ongoing vertical and horizontal patent landscape mapping within the sector.


Key Takeaways

  • Scope determination hinges on whether claims encompass broad chemical structures or narrow, specific molecules/methods.
  • Patent strength benefits from balanced broad claims and solid novelty over prior art.
  • Landscape positioning requires continuous monitoring of existing patents, especially in biologics and targeted therapies.
  • Global protection alignment via international patent applications enhances commercial value.
  • Strategic considerations involve licensing, freedom-to-operate, and infringement risk assessments.

FAQs

Q1: How does claim breadth influence the enforceability of SG10201913085T?
A: Broader claims offer wider protection but risk invalidation if overly generic or anticipated by prior art; narrower claims may be more defensible but limit scope.

Q2: Can this patent be challenged for validity?
A: Yes, through prior art invalidation procedures, especially if prior disclosures or similar molecules exist.

Q3: How does the patent landscape affect drug commercialization strategies?
A: It guides licensing, collaboration, or design-around strategies, ensuring freedom to operate and market exclusivity.

Q4: What is the significance of patent family analysis related to SG10201913085T?
A: It assesses international protection scope, enabling global market access and legal enforcement.

Q5: What are the risks of patent infringement in the Singapore pharmaceutical market?
A: Risks include legal disputes, injunctions, and royalties; careful patent landscaping mitigates such risks before market entry.


References

  1. Patent document SG10201913085T (Official publication).
  2. World Intellectual Property Organization (WIPO) patent landscape reports.
  3. Singapore Patent Act and Regulations.
  4. Relevant filings and patent classifications.
  5. Industry reports on pharmaceutical patent strategies.

Note: Due to the absence of the full patent text and claims, specific claim language and precise scope are inferred based on typical pharmaceutical patent standards. For detailed legal opinion or infringement analysis, consult the full patent document and conduct comprehensive prior art searches.

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