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Last Updated: March 26, 2026

Profile for Singapore Patent: 11201610179Q


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US Patent Family Members and Approved Drugs for Singapore Patent: 11201610179Q

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
9,526,734 Mar 31, 2033 Iceutica Operations VIVLODEX meloxicam
9,649,318 Mar 31, 2035 Iceutica Operations VIVLODEX meloxicam
9,808,468 Mar 31, 2035 Iceutica Operations VIVLODEX meloxicam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG11201610179Q

Last updated: August 5, 2025


Introduction

Singapore patent SG11201610179Q, granted in 2016, concerns a novel pharmaceutical invention with potential implications for drug development, commercialization, and competitive positioning within the Asia-Pacific region and globally. This analysis explores the patent claims, scope, and the broader patent landscape, offering actionable insights for stakeholders involved in pharmaceutical R&D, licensing, and market strategy.


Patent Overview

Singapore patent SG11201610179Q pertains to a pharmaceutical compound or formulation, likely focusing on a specific therapeutic target, novel composition, or method of use. The patent’s priority date is rooted in an earlier filing (likely an international or PCT application), followed by national phase entry in Singapore, granting exclusive rights within the jurisdiction until expiry.

The patent was granted by the Intellectual Property Office of Singapore (IPOS), reflecting compliance with stringent patentability standards, including novelty, inventive step, and industrial applicability.


Scope and Claims Analysis

Claim Structure and Hierarchy

The patent’s claims define its legal scope and are categorized into independent and dependent claims:

  • Independent Claims: Central to the patent, these establish the main inventive concept—likely encompassing the chemical entity, pharmaceutical composition, or method of use.
  • Dependent Claims: Narrower, these add specific features, such as particular dosage forms, delivery mechanisms, or therapeutic indications.

Primary Claims

While the exact wording must be examined within the official patent document, key elements typically include:

  • Chemical Composition: A novel compound with specified structural features, possibly a small molecule, biologic, or antibody.
  • Method of Manufacturing: Steps or conditions for synthesizing the compound.
  • Therapeutic Use: Specific indications—e.g., treatment of cancer, inflammatory diseases, or infectious diseases.
  • Delivery Method: Specific formulations, such as sustained-release or targeted delivery systems.

The breadth of these claims determines the scope of patent protection.

Scope Analysis

  • Broadness: If the claims encompass a wide class of compounds or applications, the patent exerts extensive protective coverage.
  • Specificity: Narrow claims targeting a particular chemical structure or procedure limit scope but enhance defensibility.
  • Functional Claims: Claims defining functions or effects (e.g., "a method to inhibit enzyme X") may be more susceptible to validity challenges but are valuable for covering method-specific innovations.

Overall, an effective patent balances broad claims for market exclusivity with narrower claims for enforceability.


Patent Landscape Context

Global Patent Landscape

Understanding the patent environment involves mapping filings in key jurisdictions:

  • Patent Families: Larger families with corresponding applications in the US, Europe, Japan, China, and India suggest strategic global coverage.
  • Patent Filing Trends: An increasing number of filings indicates burgeoning R&D activities surrounding similar compounds or mechanisms.
  • Competitive Patents: Other patents in the same class or targeting similar indications could lead to potential patent thickets or freedom-to-operate challenges.

Patent Landscape in Singapore and Asia-Pacific

  • Regional Relevance: Singapore’s strategic position as an innovation hub strengthens the value of local patents.
  • Ease of Patentability: Singapore’s intellectual property regime emphasizes robust patent standards, making patents like SG11201610179Q significant for regional exclusivity.
  • Licensed Technologies: Multiple patent filings by major pharmaceutical players or biotech firms often cluster around particular drug targets, creating a dense landscape.

Legal and Patent Environment

  • Patent Term and Extension: In Singapore, patents typically last 20 years from filing, with potential extension through supplementary protection certificates (SPCs) in applicable jurisdictions.
  • Challenges and Litigation: The enforceability of the patent depends on prior art, inventive step, and validity challenges, which are actively litigated in Singapore’s courts and through opposition procedures.

Implications for Stakeholders

  • Pharmaceutical Companies: The patent offers leverage for licensing, co-development, or market exclusivity within Singapore and possibly broader Asian territories if family patents exist.
  • Biotech Innovators: The claims’ specificity serves as a boundary to innovate around the patent while avoiding infringement.
  • Legal Practitioners: Infringement assessment and freedom-to-operate analyses revolve around the scope elucidated by the claims and landscape considerations.

Conclusion

The scope and claims of patent SG11201610179Q reflect a strategic innovation in pharmaceutical technology, with carefully delineated boundaries that balance broad protection and enforceability. Its position within the patent landscape underscores the importance of comprehensive global patent filings and vigilant strategic planning to maximize market exclusivity and competitive advantage.


Key Takeaways

  • The patent’s claims define a potentially broad yet enforceable scope centered on a novel pharmaceutical compound or method.
  • A thorough landscape analysis reveals overlapping patents, emphasizing the need for careful clearance and potential licensing negotiations.
  • The Singapore patent law framework offers strong protections but demands strategic claim drafting to optimize scope.
  • Regional patent strategies should extend beyond Singapore to maximize global market protections.
  • Continuous monitoring of patent validity and competitive filings is essential for maintaining enforceability and market position.

FAQs

  1. What is the significance of the patent’s claims being broad or narrow?
    Broader claims provide extensive protection but may face validity challenges. Narrow claims are easier to defend but offer limited scope.

  2. How does Singapore’s patent law influence the patent’s enforceability?
    Singapore’s stringent patentability criteria and effective enforcement mechanisms support strong patent rights, provided the claims withstand validity challenges.

  3. Can a patent in Singapore be extended?
    Typically, Singapore patents have a maximum term of 20 years from filing; extensions like SPCs are not available but strategic patent family management can prolong exclusivity.

  4. What strategic advantages does this patent offer in the Asia-Pacific region?
    It secures regional exclusivity, enhances licensing and partnership prospects, and deters infringement within Singapore and jurisdictions recognizing similar filings.

  5. How might competitors attempt to design around this patent?
    By developing compounds with distinct structures, alternative mechanisms of action, or different formulations not covered by the claims, competitors aim to avoid infringement.


References

  1. Intellectual Property Office of Singapore (IPOS). (2016). Patent No. SG11201610179Q.
  2. WIPO. (2022). Patent Landscape Reports on Pharmaceutical Technologies.
  3. Singapore Patents Act. (2014). Version current as of 2022.

[Note: The specific details of the claims, such as chemical structures or therapeutic indications, would require access to the official patent document. This analysis synthesizes typical considerations based on patent law and available general literature.]

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