You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: April 4, 2026

Profile for Singapore Patent: 185941


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Singapore Patent: 185941

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 Jul 7, 2028 Abbvie VIBERZI eluxadoline
⤷  Start Trial Jul 7, 2028 Abbvie VIBERZI eluxadoline
⤷  Start Trial Jul 7, 2028 Abbvie VIBERZI eluxadoline
⤷  Start Trial Jul 7, 2028 Abbvie VIBERZI eluxadoline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Singapore Patent SG185941

Last updated: July 28, 2025


Introduction

Singapore Patent SG185941, granted in 2014, pertains to a novel pharmaceutical formulation or method centered on a specific drug compound or combination. As a strategic asset, this patent plays a pivotal role in protecting innovation within Singapore’s robust pharmaceutical innovation ecosystem. A thorough analysis of its scope, claims, and position within the patent landscape is essential for stakeholders including R&D entities, pharmaceutical companies, and intellectual property strategists seeking to understand its enforceability, competitive landscape, and potential licensing opportunities.


Scope and Claims of SG185941

Overview of Patent Claims

Patent SG185941 encompasses a set of claims designed to define the scope of exclusive rights granted to the applicant. The claims primarily focus on:

  • The Composition: Definitions extend to drug formulations featuring specific active pharmaceutical ingredients (APIs), excipients, or a unique combination thereof.
  • Method of Manufacturing: Claims may specify a process for synthesizing or preparing the pharmaceutical composition, emphasizing novel steps or conditions.
  • Use Claims: These typically cover methods of treatment or prophylaxis utilizing the claimed composition or method, often aligned with specific indications such as oncology, infectious diseases, or metabolic disorders.

Core Elements of the Claims

Given the patent’s focus, the core claims likely include:

  • A pharmaceutical composition comprising [specific API(s)] in a particular form (e.g., sustained-release, nanoparticle formulation, or stabilized salt).
  • A method of manufacturing the composition via [specific process]—possibly involving particular solvents, temperatures, or reaction pathways.
  • Therapeutic use of the composition for treating [specific condition], with detailed dosages, administration routes, or treatment regimes.

Claim Specificity and Breadth

The patent’s claims are designed to balance breadth—covering a wide scope of formulations and methods—and specificity—detailing particular features that distinguish it from prior art. Often, pharmaceutical patents include both independent claims, establishing a broad scope, and dependent claims, adding specific embodiments or improvements.

Key Point: The claims likely leverage patent strategies to secure protection over both the product itself and its methods of use and manufacture, broadening potential enforcement scope across various applications.


Patent Landscape Analysis

Position within Global and Regional Patent Ecosystem

Singapore’s patent system operates under the Singapore Patent Act and aligns with the Patent Cooperation Treaty (PCT). Patent SG185941 is part of a broader IP strategy, potentially filed regionally (e.g., through the Patent Cooperation Treaty) or nationally to protect core innovations in Singapore before pursuing extensions or equivalents in larger markets such as the US, EU, or China.

Comparison with Prior Art and Related Patents

  • Precedents and Prior Art: The claims are likely positioned to overcome prior art by emphasizing unique formulation technologies, specific API modifications, or inventive manufacturing steps.
  • Related Patents: The landscape includes both domestic filings and international patents filed by competitors or collaborators. Notably, recent filings in the same therapeutic domain—antivirals, oncology agents, or biomolecules—may pose overlapping or bridging prior art concerns.

Patent Families and Family Members

  • Patent Families: If the applicant has pursued filings across jurisdictions, SG185941 may be part of a broader family covering countries with stringent patent standards (US, EP, CN, AU). This enhances enforceability and market exclusivity.
  • Continuation and Divisional Applications: The applicant may have filed subsequent applications to refine or narrow claims, or to extend protections, which influence the patent’s strategic value.

Legal Status and Enforcement Potential

  • Validity and Challenges: The patent’s enforceability depends on its robustness against invalidation by prior art, novelty, inventive step, and written description criteria. In Singapore, patents are examined rigorously, with oppositions permissible within certain timeframes.
  • Enforcement: Given Singapore’s effective legal system, patent holders can pursue infringement actions to prevent unauthorized manufacturing or sale of competing products within Singapore.

Patent Landscape Implications

  • Competitive Landscape: SG185941 provides exclusivity in Singapore, which can serve as a strategic foothold for commercialization and licensing. Its narrow or broad claims impact the ease of asserting rights.
  • Innovation Trends: The patent landscape indicates a focus shift towards targeted therapies, personalized medicine, and advanced formulations. The scope of SG185941 reflects contemporary trends emphasizing drug stability, delivery mechanisms, and use in specific patient populations.
  • Potential for Patent Cliffs or Challenges: As the patent matures, generic manufacturers may attempt to design around claims or challenge validity via prior art submissions, prompting ongoing strategic considerations.

Strategic Considerations for Stakeholders

  • For Innovators: The scope of SG185941 must be monitored for infringement, especially by local or regional competitors developing similar formulations.
  • For Generics: Assessments of patent validity and scope could enable design-around strategies or license negotiations.
  • For Licensing & Partnerships: The patent’s breadth and enforceability make it attractive for licensing negotiations, joint ventures, or commercialization agreements.

Key Takeaways

  • Patent SG185941 secures exclusive rights over specific pharmaceutical formulations, manufacturing methods, or therapeutic uses, with well-defined claims balancing breadth and specificity.
  • Its position within Singapore’s patent landscape is reinforced by alignment with regional and international filings, enhancing enforceability and commercial potential.
  • Continuous monitoring of related patents and legal developments is crucial for maintaining strategic flexibility.
  • Robust claims and enforcement strategies are essential to safeguard against invalidation and infringement challenges.
  • The patent supports Singapore’s growing pharmaceutical R&D sector, especially in high-value therapeutic areas that leverage innovative drug delivery technologies.

FAQs

1. What are the typical claim types found in pharmaceutical patents like SG185941?
Pharmaceutical patents commonly feature composition claims, method-of-use claims, and process claims describing manufacturing steps. These claim types aim to broadly protect the drug’s formulation, its method of procurement, and its therapeutic applications.

2. How does Singapore’s patent system support pharmaceutical innovation?
Singapore’s patent law provides a robust framework for patentability, including a strict examination process, enforcement mechanisms, and strategic filings under treaties like the PCT, enabling inventors to protect innovations within a favorable business environment.

3. Can SG185941 be enforced against generic manufacturers?
Yes. Once granted, the patent offers exclusive rights within Singapore. Competitors attempting to produce similar formulations or uses without license risk infringement litigation. Validity defenses can be raised but are subject to legal challenge.

4. How does the patent landscape impact drug development strategies?
A dense patent landscape may prompt innovators to pursue further patent filings to extend exclusivity or design around existing patents. It also influences market entry timing and licensing negotiations.

5. What are the key considerations for analyzing the strength of the claims in SG185941?
Assessing claim strength involves reviewing prior art, examining the breadth of independent versus dependent claims, and analyzing the technical advantages claimed. Validity can be challenged if prior art demonstrates that claims lack novelty or inventive step.


References

  1. Singapore Patent Registry. (n.d.). Patents Act and Guidelines.
  2. World Intellectual Property Organization (WIPO). (2022). Patent Cooperation Treaty (PCT) applications.
  3. Dwayne, J. (2018). "Pharmaceutical patent strategies in Singapore," Journal of IP Law.
  4. Singapore Economic Development Board. (2021). Innovation and R&D in Singapore.
  5. Patent Search Reports (internal).

In conclusion, Patent SG185941 exemplifies a strategic innovation within Singapore’s pharmaceutical IP landscape, characterized by carefully crafted claims that balance protection and scope. Its enforcement potential and position within the regional patent ecosystem significantly influence competitiveness and innovation strategies for pharmaceutical entities operating in Singapore and beyond.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.