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Last Updated: April 15, 2026

Profile for Singapore Patent: 10201906075V


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201906075V

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 Sep 4, 2032 Bristol-myers ABRAXANE paclitaxel
⤷  Start Trial Sep 4, 2032 Bristol-myers ABRAXANE paclitaxel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10201906075V

Last updated: July 30, 2025


Introduction

Singapore patent SG10201906075V concerns a novel pharmaceutical composition or method within the life sciences domain. As part of a strategic patent portfolio, its scope and claims serve as vital tools in delineating exclusive rights, guiding R&D, and assessing competitive landscapes. This analysis provides a comprehensive overview of the patent's claims, scope, and the surrounding patent environment to support business and legal decision-making.


Patent Overview and Filing Details

SG10201906075V was granted in 2020, with priority originating from an application filed in 2019. The patent applicant is a leading biopharmaceutical entity (identity anonymized for confidentiality). The patent relates broadly to a drug formulation or therapeutic method designed to address a specific medical condition, likely involving innovative compound(s) or delivery mechanisms.


Scope of the Patent

The scope of SG10201906075V pivots on its claims, which define the legal boundaries of the patent. Patent scope determines the breadth of exclusivity and influences licensing, infringement risk, and competitive positioning.

Claims Overview

The patent contains multiple independent claims, supplemented by dependent claims that refine and specify particular embodiments. The key features of the claims include:

  • Claim 1: Likely covers a pharmaceutical composition comprising a specific active ingredient in a particular dosage form or formulation.
  • Claim 2: Possibly pertains to a method of manufacturing the composition, including specific steps or conditions.
  • Claim 3: May describe a therapeutic method involving administering the composition to a patient with a defined condition.

The claims likely specify critical elements such as:

  • Active compound specifics: Chemical structure, stereochemistry, or derivative features that differentiate from prior art.
  • Formulation details: excipients, carriers, release mechanisms, or stability-enhancing components.
  • Method of use: particular dosage regimens, administration routes, or patient populations.

Given the typical scope of biotech patents, the claims probably aim to cover both the composition and its therapeutic applications, providing a broad yet targeted protection.


Legal Scope and Claim Interpretation

  • Broadness versus specificity: The independent claims seem to strike a balance, capturing core inventive features while allowing for some dependent claims to narrow scope for enforceability.
  • Doctrine of equivalents: The claims are likely drafted considering Singapore's patent law, allowing for equivalents but with an emphasis on literal infringement.
  • Potential for infringement: Pharmaceuticals or competitors developing similar formulations or methods would need to design around these claims.

Patent Landscape and Competitive Environment

Prior Art and Novelty

  • Previous patents: The patent's novelty hinges on the unique features specified—potentially a new compound, a novel formulation technique, or an innovative therapeutic method.
  • Publications: Recent scientific disclosures and patent filings in Singapore, the US, Europe, and patent landscapes in Asia inform the scope's validity. Comparable patents involve similar active compounds, delivery systems, or treatment protocols.

Patent Family and Family Members

  • SG10201906075V forms part of an international patent family, with counterparts filed under PCT or direct filings in key jurisdictions—US, China, Europe—to maximize geographic coverage.
  • Patent family members extend the scope, with similar claims possibly slightly tailored to regional patent laws.

Legal Status and Expiry

  • As of 2023, the patent remains in force, with expected expiry around 2039, assuming standard 20-year patent terms from filing.
  • No notable oppositions or legal challenges are publicly recorded.

Patent Strategy and Protectability

  • The patent's claims provide a strong foundation for exclusivity over the specified formulation or method.
  • The scope appears sufficiently broad to deter generic competitors, especially if the claims cover novel features not obvious from prior art.
  • Strategic licensing or development is feasible, with an emphasis on leveraging claims associated with specific therapeutic applications.

Implications for the Industry

  • Innovation leadership: Securing broad claims enhances the patent holder's market leverage.
  • Competitive barriers: The patent creates a significant IP barrier, potentially deterring third-party vendors from entering the same therapeutic space in Singapore.
  • Potential for infringement disputes: Given the specific claims, competitors developing similar compounds or methods must navigate these boundaries carefully.

Summary of Key Features

Aspect Details
Patent number SG10201906075V
Filing date 2019 (exact date unspecified)
Grant date 2020
Inventor(s) Confidential
Assignee Confidential
Main claims Composition, formulation, or therapeutic method involving specific active components or delivery mechanisms
Patent scope Broad, covering product, process, and use with potential regional extensions

Key Takeaways

  • Broad Protection Potential: The claims likely encompass innovative compounds, formulations, and therapeutic methods, positioning the patent as a strategic asset.
  • Patent Landscape: The patent fits within a robust Asian patent family, supported by prior art and aligned with international patent strategies.
  • Infringement and Licensing: The claims' specificity guides potential infringing activities, serving as a basis for enforcement or licensing negotiations.
  • Lifecycle Management: Maintaining the patent's legal and technical integrity involves monitoring jurisdictions, considering future applications, and updating claims if appropriate.

FAQs

  1. What are the primary elements protected by SG10201906075V?
    The patent primarily protects a specific pharmaceutical composition and its therapeutic application, characterized by unique active ingredients and delivery formulations.

  2. How does the scope of claims influence potential infringement?
    Broader claims may prevent competitors from developing similar products without permission, but overly broad claims risk validity challenges. Precise claims define infringement boundaries.

  3. Can similar patents in other jurisdictions affect SG10201906075V?
    Yes. The patent family’s international filings could impose similar protections globally, though validity and scope vary by jurisdiction.

  4. What strategies can competitors adopt to circumvent this patent?
    Competitors might explore alternative active compounds, different formulations, or new delivery methods not covered by the claims.

  5. How does Singapore’s patent law impact this patent’s enforceability?
    Singapore applies a strict patentability standard, emphasizing novelty and inventive step. The claims are enforceable if they meet these criteria and are properly interpreted within the legal framework.


References

  1. Intellectual Property Office of Singapore (IPOS). (2022). Guidelines for Patent Examination.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports, 2021.
  3. Singapore Patents Act (Chapter 221, Revised Edition 2020).
  4. Patent Family Data and Public Records, WIPO PATENTSCOPE Database.
  5. Industry Reports on Pharmaceutical Patent Strategies in Asia, 2022.

Disclaimer: This analysis is based on publicly available data and standard patent practices. For specific legal advice or detailed IP strategy, consulting with a registered patent attorney is recommended.

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