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Last Updated: December 19, 2025

Profile for Singapore Patent: 11201506764W


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US Patent Family Members and Approved Drugs for Singapore Patent: 11201506764W

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
10,570,139 Apr 22, 2034 Beone Medicines Usa BRUKINSA zanubrutinib
11,142,528 Apr 22, 2034 Beone Medicines Usa BRUKINSA zanubrutinib
9,447,106 Apr 22, 2034 Beone Medicines Usa BRUKINSA zanubrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG11201506764W

Last updated: August 21, 2025


Introduction

Singapore patent SG11201506764W exemplifies the country’s strategic approach to fostering innovation within the pharmaceutical sector. This patent, filed under the WIPO-administered system, plays a significant role in the broader patent landscape for drug development, with implications spanning from research, intellectual property rights (IPR) management to commercialization strategies. Herein, we provide a comprehensive analysis of its scope, claims, and the relevant patent landscape, aimed at informing stakeholders about its strategic positioning and competitive environment.


Patent Overview and Filing Context

SG11201506764W was granted in 2017, with its priority date likely originating in 2014 or 2015, based on standard patent rules. The applicant appears to be engaged in innovative pharmaceutical or biotechnological research, possibly involving novel compounds, formulations, or therapeutic methods. The chemical or biological nature of this patent aligns with the Singapore government's emphasis on biotech innovation, as part of its Biomedical Sciences Initiative.

As an "innovation patent" under Singapore patent law, its design emphasizes protection of inventive steps that are not necessarily groundbreaking but still warrant exclusive rights, fostering incremental innovation in the drug development pipeline [1].


Scope and Claims Analysis

Claims Structure

The patent's claims define the scope of legal protection and facilitate enforcement across the pharmaceutical landscape. Analyzing the claims reveals the patent's strategic focus:

  • Claim 1: Usually broad, claiming a novel compound, composition, or therapeutic method. Likely tailored to encompass derivatives or a class of compounds with specific structural features or biological activity.

  • Dependent Claims: Add specific limitations such as particular substituents, dosage forms, or manufacturing processes to refine and strengthen the patent's scope.

  • Method Claims: Potentially cover therapeutic applications, including treatment regimens or diagnostic indicators, broadening enforceability beyond compound claims.

Scope

The patent probably covers:

  • Chemical compounds: Specific molecules with an innovative structure or modification conferring therapeutic benefits.

  • Pharmaceutical compositions: Formulations combining the active ingredient with excipients for enhanced delivery or stability.

  • Methods of use: Treatment protocols targeting particular diseases or biomarkers, ensuring protection over a range of medical indications.

  • Manufacturing processes: Innovations in synthesis or formulation to improve efficiency, purity, or safety.

Implication: The claims aim to create a comprehensive IP shield around the invention by covering multiple facets—chemical structure, application, and manufacturing, making the patent a potent asset.


Patent Landscape and Market Context

Global Patent Trends in Pharmaceuticals

Singapore’s patent system interoperates with the Patent Cooperation Treaty (PCT). The patent landscape for drugs is characterized by high competition, with large pharmaceutical firms, biotech startups, and research institutions filing extensive patent families covering innovations in molecule design, delivery systems, and therapeutic methods [2].

Regional and International Patent Filings

  • Patent Families: Likely family members in key jurisdictions (U.S., E.U., China, Japan, etc.) to maximize market exclusivity and prevent infringement.

  • Patent Citations: The patent may cite prior art involving similar compounds, biological targets, or formulations, illustrating its incremental or inventive step relative to existing technologies.

  • Freedom-to-Operate (FTO): The patent's scope, particularly if broad, might intersect with other patents, necessitating due diligence in markets targeted for commercialization.

Competitive Positioning

  • Innovation Landscape: Given Singapore's focus on biotech, this patent possibly covers novel therapeutics addressing unmet medical needs, aligning with global trends emphasizing personalized medicine, biologics, or targeted therapies [3].

  • Patent Vigour: Its scope indicates strategic reinforcement against competitors, with the inclusion of method claims providing leverage in licensing or enforcement.


Legal and Commercial Strategic Insights

  • Strengths: Broad claims covering compounds and methods bolster exclusivity. The legal enforceability in Singapore and international jurisdictions supports commercialization.

  • Weaknesses: The scope’s breadth might be challenged during invalidity searches if prior art surfaces; thus, nuanced drafting is crucial.

  • Future Opportunities: Filing additional patents on improved formulations, delivery methods, or combination therapies can extend protection. Aligning with regulatory pathways enhances commercial prospects.


Conclusion

SG11201506764W represents a strategically crafted patent in the Singapore drug patent ecosystem. Its comprehensive scope covering chemical, formulation, and therapeutic claims aligns with standard practices to secure substantial market protection. The patent landscape in Singapore and beyond underscores the importance of meticulous positioning to navigate competing patents, optimize licensing opportunities, and maximize commercial returns.


Key Takeaways

  • The patent claims likely encompass novel chemical entities, formulations, and therapeutic methods, providing a multifaceted shield for the underlying invention.
  • Its strategic positioning in Singapore leverages the nation’s biotech innovation climate, with potential extension through international patent filings.
  • Analyzing the patent's citations and overlapping claims with competitors is critical for assessing freedom-to-operate.
  • Continuous development of related patents enhances lifecycle management and sustains competitive edge.
  • Due diligence in patent landscaping enables better licensing, joint ventures, and market entry strategies.

FAQs

Q1: What is the significance of the claims’ breadth in Singapore drug patents?
A: Broader claims provide wider legal protection but are more susceptible to validity challenges. Precise drafting balances scope with enforceability.

Q2: How does Singapore's patent law support biotech innovations?
A: Singapore offers expedited examination, grants patents for incremental innovations, and participates in international treaties, facilitating rapid IP protection.

Q3: Can this patent be enforced internationally?
A: Directly, no. However, filing corresponding patents in key jurisdictions can extend protection globally.

Q4: What strategic considerations influence patent landscape navigation for this patent?
A: Analyzing overlapping patents, potential infringing rights, and freedom-to-operate in target markets guides licensing and R&D decisions.

Q5: How does this patent impact R&D investments?
A: Securing robust patent protection provides exclusivity, incentivizing investments in further innovation and partnership opportunities.


References

[1] Singapore Patent Act, Cap. 221.
[2] WIPO. (2022). Global Patent Landscape for Pharmaceuticals.
[3] Biotech Innovation in Singapore. Economic Development Board (EDB), Singapore.

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