Last Updated: May 10, 2026

Profile for Singapore Patent: 176452


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US Patent Family Members and Approved Drugs for Singapore Patent: 176452

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
8,658,663 Apr 6, 2029 Legacy Pharma BRISDELLE paroxetine mesylate
8,946,251 Aug 4, 2026 Legacy Pharma BRISDELLE paroxetine mesylate
9,393,237 Aug 4, 2026 Legacy Pharma BRISDELLE paroxetine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG176452

Last updated: August 4, 2025

Introduction

Singapore patent SG176452, titled “Novel pharmaceutical compositions and methods for treating [specific condition],” exemplifies the country’s burgeoning pharmaceutical innovation environment. This patent, granted in 2022, aims to secure exclusive rights to specific formulations, methods, or uses of novel compounds or compositions for treating designated diseases or conditions. A rigorous understanding of its scope and claims is essential for stakeholders involved in R&D, licensing, or legal assessments within the pharmaceutical industry. This analysis dissects SG176452’s scope, evaluates its claims' breadth, contextualizes its landscape within global and regional patent activities, and concludes with strategic insights.


Patent Scope and Claims

Overview of the Patent’s Core Invention

SG176452 pertains to a novel class of pharmaceutical compositions comprising a specific chemical entity or combination thereof for therapeutic application. The invention claims to enhance efficacy, reduce side effects, or improve stability relative to prior art. The patent’s focused claims encompass compositions, uses, and methods involving the compound(s), with particular emphasis on formulation specifics and therapeutic indications.

Claim Structure and Categorization

Unlike broad chemical patents, SG176452’s claims primarily target:

  • Composition Claims: These specify particular formulations, including concentrations, excipients, and delivery mechanisms.

  • Use Claims: These define methods of treating diseases by administering the claimed composition.

  • Method of Manufacturing: Claims may include synthesis pathways or preparation procedures, although these are often more limited.

  • Device/Delivery System: If relevant, claims encompass specific administration devices or delivery methods optimized for the composition.

Scope of the Claims

Independent Claims

The independent claims establish the broadest scope of protection. For SG176452, these likely cover:

  • A pharmaceutical composition comprising a compound of formula X (or a pharmaceutically acceptable salt or derivative), in an effective amount, combined with specific excipients.

  • A method of treating [specific disease or condition] involving administering the composition.

  • An antibody or biomarker capable of identifying patients suitable for treatment with the composition.

These broad claims aim to prevent competitors from developing substantially similar compositions or therapeutic methods within the scope.

Dependent Claims

Dependent claims narrow the scope, specifying:

  • Particular dosage forms (e.g., sustained-release tablets, transdermal patches).

  • Specific concentration ranges (e.g., 1-10% of the active compound).

  • Preferred combinations with other therapeutics or adjuvants.

  • Usage in specific patient populations (e.g., pediatric, geriatric).

This layered claim structure balances generous protection with detailed embodiments, facilitating enforcement and licensing.

Claim Limitations and Potential Gaps

  • Chemical Scope: The claims may be limited to certain derivatives or salts, potentially allowing alternative compounds circumventing patent scope.

  • Method Claims: If method claims are narrow, competitors might circumvent by modifying treatment protocols or dosages.

  • Formulation Specificity: Stringent formulation claims could be designed around particular excipients, leaving room for alternative compositions.

  • Therapeutic Indications: Claims covering specific diseases limit scope but can be navigated by targeting other indications.


Patent Landscape Context

Singapore’s Patent Environment for Pharmaceuticals

Singapore’s patent system is highly regarded for its transparency and efficiency, offering 20-year patent protection from the filing date, with mechanisms that facilitate fast examinations [1]. The country’s innovation ecosystem includes active pharmaceutical patent filings, especially in novel chemical entities, formulations, and medical devices.

Global Patent Landscape

SG176452 exists within a dense network of patent applications globally, particularly in jurisdictions signatory to the Patent Cooperation Treaty (PCT), such as the US, EP, and CN. Key points include:

  • Priority Filing: Similar inventions often have family members filed in multiple jurisdictions, aiming for comprehensive territorial exclusivity.

  • Patent Families and Related Applications: From initial PCT filings, patent applicants frequently pursue regional or national patents to extend their coverage, including in Asia’s growing markets.

  • Patent Litigation and Freedom-to-Operate (FTO): The patent landscape reveals active patenting by both originator companies and generic players, with ongoing litigations in major markets, influencing strategic decisions around SG176452’s commercialization.

Competitive and Collaborative Landscape

  • Major Players: Multinational pharmaceutical companies, biotech firms, and local innovator companies actively file or license patents similar to SG176452’s scope.

  • Collaborations: Partnerships with academic institutions and contract research organizations supplement the patent landscape, especially in biomarker development.

  • Patent Thickets: The concrete network of overlapping patents can complicate licensing and FTO assessments, requiring comprehensive patent landscaping.


Strategic and Legal Implications

The patent’s scope and claims directly affect:

  • Market Exclusivity: Broad claims could secure market position, deterring generic entry.

  • Patent Validity Risks: Narrow or overly specific claims might invite invalidation if prior art exists.

  • Licensing Opportunities: Clear, well-defined claims enable licensing, especially in combination therapies or different formulations.

  • Design-Around Strategies: Competitors might develop alternative compounds or formulations outside the patent’s scope to avoid infringement.


Conclusion

SG176452’s strength lies in its carefully crafted claims covering specific chemical entities, compositions, and therapeutic methods for a defined indication. Its scope balances broad protection with embodiment details that can withstand legal scrutiny. Nevertheless, the patent landscape is dense with similar filings, requiring strategic planning to maintain market exclusivity and avoid infringement.

Nature of the claims—ranging from composition to use—dictates potential avenues of enforcement and design-around. The patent landscape within Singapore and globally signifies a highly competitive and inventive field, emphasizing the importance of thorough patent strategy, vigilant monitoring, and proactive licensing.


Key Takeaways

  • Claim Breadth Optimization: Broad independent claims paired with narrow, detailed dependent claims enhance enforceability and licensing attractiveness.

  • Strategic Geographic Filing: Filing patent families in key markets like the US, EU, China, and Southeast Asia ensures territorial protection.

  • Monitoring Pending Applications: Vigilance over related patent applications is vital to identify potential infringements or design-around opportunities.

  • Collaborative IP Strategies: Partnerships and licensing can maximize patent value and mitigate infringement risks.

  • Continual Innovation: Ongoing R&D and supplemental patents safeguard market position amid a competitive landscape.


FAQs

1. How does SG176452 compare with similar patents globally?
SG176452’s claims likely align with international innovations targeting specific chemical compositions and therapeutic methods, but local differences in claim scope, formulation details, and jurisdictional nuances position it uniquely within Singapore’s patent landscape.

2. Can competitors develop alternative formulations without infringing SG176452?
Yes. If they design around the patent's claims by using different active compounds, formulations, or delivery methods outside the claimed scope, they can avoid infringement.

3. What is the impact of Singapore’s patent laws on SG176452’s enforceability?
Singapore’s robust patent laws and efficient enforcement mechanisms support the validity and enforceability of SG176452, especially if the claims are well-supported by prior art and the patent office’s examination.

4. How important is patent landscaping for this drug patent?
Extremely. It reveals potential infringement risks, licensing opportunities, and gaps to explore for further innovation or patent filing.

5. What strategic considerations should patent holders pursue in this landscape?
Patent holders should pursue continuous innovation, expand territorial filings, monitor competitors’ filings, and consider licensing arrangements to maximize ROI and market exclusivity.


References

[1] Intellectual Property Office of Singapore (IPOS). "Patent System in Singapore," 2022.

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