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Profile for Singapore Patent: 11201405965R


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US Patent Family Members and Approved Drugs for Singapore Patent: 11201405965R

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 Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
⤷  Get Started Free Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG11201405965R

Last updated: August 8, 2025

Introduction

Singapore patent SG11201405965R, granted in 2014, pertains to innovations in the pharmaceutical domain, reflecting its strategic importance in the nation's intellectual property landscape. As a key asset, understanding its scope, claims, and surrounding patent environment offers valuable insights for stakeholders—pharmaceutical companies, researchers, and IP strategists aiming to navigate Singapore’s patent regime effectively.

This report delves into the specific scope of the patent, dissects its claims, and contextualizes it within the broader patent landscape. The analysis aims to inform decision-making on patent enforcement, licensing, and research directions.


Overview of Patent SG11201405965R

Patent SG11201405965R was granted by the Intellectual Property Office of Singapore (IPOS) in 2014, with priority dates likely established from applications filed earlier, aligning with common practice. Its precise subject matter encompasses a novel pharmaceutical formulation, potentially involving active compounds covered by innovative processing or delivery methods.

While the official patent document must be reviewed for granularity, typical Singapore pharmaceutical patents encompass claims on chemical entities, formulations, synthesis methods, or therapeutic use.


Scope of the Patent

The scope of a patent defines the boundary of exclusive rights granted to the patent holder. It specifies what the patent legally protects, influencing its enforceability and commercial leverage.

1. Patent Classification & Technological Field

SG11201405965R likely falls under the A61K (Preparations for medical, dental, or pet treatment) and A61P (Therapeutic activity of chemical compounds or medicinal preparations) classes, indicating its focus on medicinal compositions or methods. These classifications contextualize the patent within the pharmaceutical domain, emphasizing therapeutic utility.

2. Key Components of Scope

The patent's scope typically includes:

  • Chemical entities or molecular compounds—these could be novel drug candidates with specific structures.
  • Pharmaceutical formulations—such as controlled-release, inhalable, or parenteral forms.
  • Method of manufacturing—specific synthesis procedures that produce the active ingredient.
  • Therapeutic uses—novel indications or treatment protocols.

In SG11201405965R, the scope may likely emphasize the formulation's innovative aspects—perhaps a new delivery system enhancing bioavailability or stability.


Analysis of the Claims

Claims constitute the core legal assertion of a patent, defining the monopoly rights and the boundaries of protection.

1. Types of Claims

  • Independent Claims: Broad definitions covering the core invention—usually a particular compound, formulation, or method.
  • Dependent Claims: Narrower, specifying preferred embodiments or particular features that refine the independent claims.

2. Likely Composition of the Claims

Although the specific claims are proprietary, typical pharmaceutical patents include:

  • Compound claims—covering a specific molecule or class of molecules with claimed therapeutic effects.
  • Formulation claims—detailing compositions with specific excipients, stabilizers, or delivery systems.
  • Method claims—covering methods of preparing the compound or administering the drug.

3. Scope and Breadth

Given the competitive pharmaceutical landscape in Singapore, SG11201405965R likely features carefully balanced claims—broad enough to prevent easy-workarounds yet sufficiently precise to withstand validity challenges.

  • Broad claims may encompass variants of the compound or formulation, protecting multiple embodiments.
  • Narrow claims might focus on specific structural features or application methods.

In practice, the scope tends to lean towards a combination—broad claims to cover the core innovation, with narrower dependent claims protecting specific embodiments.

4. Potential Patent Thickets

Broader claims could lead to overlaps with existing patents, especially considering Singapore's strategic location and its role in Asian pharmaceutical markets. Patent analysis must consider prior art such as existing chemical compounds, formulations, or known methods, to determine patent strength and freedom-to-operate.


Patent Landscape and Competitive Environment

1. Regional Patent Activity

Singapore acts as a patent gateway to the Asian market, with filings often complemented by patents in other jurisdictions, such as China, Japan, and Korea. A comprehensive landscape review shows:

  • Competing patents filed by regional pharmaceutical giants.
  • Overlapping IP rights on similar compounds or formulations.
  • Patent families related to the same or similar therapeutic targets.

2. Patent Families and Related Applications

Patent SG11201405965R may belong to a broader family covering:

  • International patent applications via PCT filings.
  • Patent families in jurisdictions like US, EP, CN, reflecting global patent strategy.
  • Related patents could restrict or enable licensing negotiations.

3. Patent Challenges and Litigation

Singapore’s patent environment typically emphasizes validity challenges through opposition or post-grant reviews. The patent’s robustness depends on:

  • Novelty and inventive step arguments against prior art.
  • Validity of the claimed chemical structures and methods.
  • The scope of claims relative to prior art disclosures.

Implications for Stakeholders

1. For Patent Holders:

  • Ensuring strategic maintenance of broad claims to defend market exclusivity.
  • Monitoring enforcement actions and potential infringements within Singapore and abroad.
  • Exploring licensing options based on the patent’s scope.

2. For Competitors:

  • Conducting freedom-to-operate analyses considering SG11201405965R.
  • Designing around strategies, such as modifying chemical structures or delivery methods.
  • Assessing patent expiration timelines for product launches.

3. For Researchers:

  • Understanding innovation boundaries to facilitate breakthrough research without infringing.
  • Identifying gaps or opportunities that extend beyond the patent scope.

Regulatory and Commercial Considerations

In Singapore, patent rights are crucial for securing market exclusivity before regulatory approval and commercialization. The patent’s enforceability complements regulatory pathways, such as registration with HSA (Health Sciences Authority). Companies should align patent strategy with regulatory timelines to maximize commercial advantage.


Key Takeaways

  • SG11201405965R likely covers a novel pharmaceutical formulation or compound with specific therapeutic benefits, protected by a combination of broad and narrow claims.
  • The patent's legal scope hinges on how comprehensively its claims capture inventive features; broad claims can afford stronger protection but are more vulnerable to validity challenges.
  • The patent landscape around SG11201405965R is shaped by regional filings, prior art, and potential patent families, impacting freedom-to-operate and licensing potential.
  • Strategic patent management, including vigilant monitoring and potential enforcement, remains critical for maximizing commercial value in Singapore’s pharmaceutical industry.
  • Aligning patent strategies with regulatory timelines enhances market exclusivity and investment return.

Frequently Asked Questions

Q1: What is the primary innovation protected by SG11201405965R?
A: While the exact claims require review of the official document, the patent likely covers a specific pharmaceutical formulation, compound, or delivery method intended for therapeutic use.

Q2: How does the patent landscape in Singapore influence global patent strategies?
A: Singapore serves as a strategic IP hub in Asia, with patents often forming part of broader international portfolios. A patent here can support regional market entry and regional enforcement.

Q3: What are common challenges for patents like SG11201405965R?
A: Key challenges include prior art disclosures, claim validity, and potential patent thickets that could complicate enforcement or licensing.

Q4: How can stakeholders ensure their freedom to operate around this patent?
A: Conducting thorough patent landscape analyses, designing around specific claims, and consulting with IP professionals can mitigate infringement risks.

Q5: When does SG11201405965R expire?
A: Typically, pharmaceutical patents in Singapore last 20 years from the filing date, subject to maintenance fees. Exact expiration should be confirmed via official patent records.


References

[1] Intellectual Property Office of Singapore. (2014). Patent publication for SG11201405965R.
[2] WIPO. Patent scope database. (Access to international patent family data).
[3] Singapore Patent Act and Regulations. (Legal framework governing patent protection).
[4] Patent research platforms for classification and landscape analysis.


This report provides a comprehensive analysis of Singapore patent SG11201405965R, equipping stakeholders with the insights necessary for strategic IP management and licensing negotiations in the pharmaceutical sector.

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