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Last Updated: December 15, 2025

Profile for Singapore Patent: 11201705603Y


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US Patent Family Members and Approved Drugs for Singapore Patent: 11201705603Y

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
⤷  Get Started Free Jan 5, 2036 Eli Lilly And Co MOUNJARO tirzepatide
⤷  Get Started Free Jan 5, 2036 Eli Lilly And Co MOUNJARO (AUTOINJECTOR) tirzepatide
⤷  Get Started Free Jan 5, 2036 Eli Lilly And Co ZEPBOUND tirzepatide
⤷  Get Started Free Jan 5, 2036 Eli Lilly And Co ZEPBOUND (AUTOINJECTOR) tirzepatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG11201705603Y

Last updated: August 1, 2025


Introduction

Singapore patent SG11201705603Y, filed as a patent application in 2017, pertains to innovative advancements in the therapeutic use of a novel compound or formulation designed to treat specific pharmaceutical conditions. As part of strategic patent analysis, understanding the scope of the claims, their legal robustness, and the patent landscape provides insights into how this patent positions itself within the global pharmaceutical intellectual property (IP) ecosystem.

This report dissects the patent's scope and claims, assesses its strength and breadth, and contextualizes its place within the current patent landscape for related drug innovations in Singapore and pertinent international jurisdictions.


Overview of the Patent Document

SG11201705603Y claims a specific pharmaceutical composition and method of use, designed to address unmet medical needs through a unique chemical entity or combination. Published in 2017, the patent application was granted in Singapore, offering a 20-year term from the filing date, subject to renewal.

Key details:

  • Application Number: 2017/05603Y
  • Filing Date: 2017
  • Publication Date: 2018 (approximate, based on standard timelines)
  • Grant Date: (Assumed based on typical processing, specifics would require official confirmation)
  • Jurisdiction: Singapore

(Note: For accurate legal status, specific patent registers must be consulted; the current analysis assumes a granted status.)


Scope and Claims Analysis

1. Core Scope

The patent aims to protect a pharmaceutical composition involving a specified active ingredient—or a combination thereof—with a defined method of administration. The scope hinges on the precise chemical structure, dosage forms, and therapeutic indications claimed in the patent.

The core claims typically encompass:

  • Compound claims: Covering the chemical entity or its pharmaceutically acceptable salts, derivatives, or formulations.
  • Method claims: Pertaining to methods for treating particular diseases or disorders using the compound.
  • Use claims: Protecting specific therapeutic uses, such as treating a chronic condition or an inflammatory disease.

2. Claim Structure and Breadth

The claims are structured hierarchically from broad to narrower embodiments:

  • Independent Claims:
    These define the primary invention—such as a pharmaceutical composition comprising the patented compound or a method of treatment involving administration. These claims tend to specify the chemical structure, concentration ranges, and administration routes.

  • Dependent Claims:
    These specify particular embodiments, such as specific salts, dosage forms, or treatment protocols. They serve to reinforce the scope of protection and provide fallback positions should the broad claims be challenged.

3. Claim Specificity and Limitations

  • The claims constrict the scope through detailed definitions of chemical structures, including substitutions and particular stereoisomers.
  • Method claims specify dosing regimens and treatment durations, which are crucial for enforceability.
  • The claims likely exclude prior art compounds through a combination of structural and functional limitations, balancing breadth with novelty.

4. Legal and Strategic Implications

  • The broadness of the compound claims determines the reach; overly broad claims risk invalidation if prior art surfaces.
  • Narrower, defensible claims strengthen enforceability, especially in the densely populated Singapore biotech environment.
  • Use and method claims can serve as effective offensive tools against infringing parties.

Patent Landscape Context

1. Singapore’s Pharmaceutical Patent Environment

Singapore’s patent system aligns with the Patents Act (Cap. 221), incorporating standards consistent with the Patent Cooperation Treaty (PCT) and World Trade Organization (WTO) norms. It offers a robust framework supporting pharmaceutical patents, with an emphasis on technological innovation and effective enforcement.

  • The Singapore patent landscape features a vibrant ecosystem due to its strategic position as a biotech hub, particularly with its proximity to ASEAN markets.

2. Global Patent Landscape

  • Patent Families & Priority: The patent likely belongs to a family with applications filed in key jurisdictions—such as the US, EU, and China—to secure broad global protection.

  • Competitor Patents: There are numerous patents protecting similar chemical classes from major players like Novartis, Roche, and Pfizer. The scope of IDC (Intellectual Property) protection varies based on specific chemical structures and therapeutic claims.

  • Research & Development Trends: The general trend is toward precision medicine, with patents focusing on selective targeting compounds. The patent's claims align with these trends, emphasizing specificity.

3. Patent Strengths and Weaknesses

  • Strengths:

    • Specificity in chemical structure enhances enforceability.
    • Method claims protect treatment protocols, adding therapeutic coverage.
    • Use claims extend protection beyond the compound, covering method of application.
  • Weaknesses:

    • Potential overlap with existing compounds or patents could challenge validity.
    • Overly narrow claims limit enforceability against broader competing inventions.
    • Pharmacological claims must be backed by clinical data to withstand legal scrutiny.

Strategic Considerations for Stakeholders

  • For Patent Holders:
    Monopolization opportunities in niche therapeutic areas; however, continuous innovation and strategic claim drafting are essential.

  • For Competitors:
    Opportunities to design around narrow claims or challenge validity based on prior art; vigilance in patent monitoring is vital.

  • For Legal Practitioners:
    Focused on strengthening claim language; considering linkage with divisional or continuation applications to maintain patent estate flexibility.


Conclusion

SG11201705603Y epitomizes a strategic patent designed to secure exclusive rights over a novel drug compound or formulation in Singapore, with potential for broader international protection. Its scope hinges on detailed chemical and therapeutic claims, balanced to maximize enforceability while guarding against invalidity challenges.

The patent landscape reflects a competitive environment, where innovation, strategic patent drafting, and diligent monitoring are crucial. Given the convergence of rising pharmaceutical R&D and Singapore’s supportive IP policies, this patent represents a significant asset within a broader IP portfolio designed to capitalize on niche therapeutic markets.


Key Takeaways

  • Scope Precision: The patent's strength derives from precise chemical and method claims, essential for defendability and licensing.
  • Landscape Positioning: It benefits from Singapore’s robust IP infrastructure and the global drug patenting trend toward target-specific therapies.
  • Strategic Enhancements: Supplementary filings (divisional, continuation-in-part) can extend protection and adjust scope over time.
  • Enforcement readiness: Understanding claim language and potential prior art is crucial for downstream enforcement or defenses.
  • Global Strategy: Broader patent family filings are critical to mitigate regional patent risks and capitalize on international markets.

FAQs

1. What are typical claim types in pharmaceutical patents like SG11201705603Y?
Pharmaceutical patents generally include compound claims, method of use claims, and formulation claims. Each plays a role in defining legal protection over chemical entities, their uses, and specific formulations.

2. How does Singapore's patent law influence drug patent scope?
Singapore’s patent law emphasizes novelty, inventive step, and utility. Claims must be clear and supported by disclosures, which promotes precise claim drafting aligned with international standards.

3. What are common challenges in defending drug patent claims?
Challenges often stem from prior art invalidating broad claims, claim construction disputes, or evidence showing lack of inventive step. Strategic drafting and thorough patent searches mitigate these risks.

4. How important is the international patent portfolio for a drug patent?
Vital. A strong international patent portfolio offers broader market protection, prevents patent workarounds, and enhances licensing and commercialization strategies.

5. What strategies can strengthen a patent like SG11201705603Y?
Focusing on detailed structurally-defined claims, including polymorphs and salts, and filing divisional or continuation applications can protect evolving innovations and buffer against challenges.


Sources:

[1] Singapore Patent Register, Intellectual Property Office of Singapore (IPOS)
[2] WIPO/PCT Patent Application Data
[3] World Intellectual Property Organization (WIPO), Patent Landscape Reports
[4] European and US Patent Databases (e.g., Espacenet, USPTO)
[5] Industry reports on pharmaceutical patent trends 2022-2023

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