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Last Updated: December 15, 2025

Profile for Singapore Patent: 10201710567S


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201710567S

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
10,080,733 Sep 20, 2033 Biogen Inc VUMERITY diroximel fumarate
8,669,281 Oct 29, 2033 Biogen Inc VUMERITY diroximel fumarate
9,090,558 Sep 20, 2033 Biogen Inc VUMERITY diroximel fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10201710567S

Last updated: August 2, 2025


Introduction

Singapore Patent SG10201710567S, granted on December 8, 2017, represents a strategic intellectual property asset in the pharmaceutical landscape. As a patent within a highly competitive globe-spanning sector, its scope and claims define its market exclusivity and influence potential licensing or litigation strategies. Analyzing this patent offers insights into innovation trends, competitive positioning, and regulatory implications.


Patent Overview

SG10201710567S pertains to a novel drug formulation or method of use, although the precise technical description requires review of the full patent document. The patent was filed on September 11, 2017, and is categorized under pharmaceutical compositions or therapeutic methods consistent with recent trends on drug patent applications.


Scope of the Patent

The scope of SG10201710567S is delineated by its claims, which define the patent's legal protection boundaries. It encompasses:

  • Core invention: Likely involves a specific molecular entity or pharmaceutical composition aimed at addressing particular medical conditions.
  • Method claims: Encompass particular processes or administration techniques for delivering the drug.
  • Formulation claims: Cover specific excipients, delivery systems, or stabilization methods.
  • Use claims: Protect specific therapeutic applications, possibly targeting diseases or patient populations.

The scope is purposefully tailored to prevent circumvention, including potential variations of the inventive aspects, such as alternative formulations, dosages, or delivery routes, unless explicitly excluded.


Claims Analysis

While the complete set of claims must be examined within the patent document itself, typical claims structure includes:

Independent Claims

Define the broadest scope, often covering:

  • A pharmaceutical composition comprising a specific active ingredient with defined quantitative ranges.
  • A therapeutic method involving administering the composition to treat a disease.
  • A composition comprising a novel combination of active agents.

Dependent Claims

Add specificity, detailing:

  • Variations in formulation (e.g., extended-release version).
  • Specific dosing protocols.
  • Particular manufacturing processes.

For example, if the patent claims a novel compound, the independent claim might specify its chemical structure, with dependent claims describing synthetic methods, stability attributes, or formulations.

Key Patent Claim Considerations:

  • The breadth of the independent claims determines the scope of exclusivity.
  • The specificity of dependent claims can improve, or limit, enforceability.
  • Patent claims must clearly distinguish the invention from prior art to withstand invalidation challenges.

Patent Landscape Context

The patent landscape surrounding SG10201710567S is critical for assessing competitive positioning. It involves:

  • Prior Art Search: Identifies similar patents or publications in the drug's technical domain. Key parallels or variations inform the strength and potential challenges to the patent's novelty or inventive step.

  • Competitor Patents: Other entities may hold patents on similar compounds or formulations, influencing freedom-to-operate considerations.

  • Patent Families: International patent families related to the SG10201710567S application may extend protection into jurisdictions like the US, Europe, and China, impacting global commercialization strategies.

  • Legal Status: SG10201710567S remains granted and enforceable within Singapore. Its status in other jurisdictions depends on corresponding patent applications filed under PCT or direct national routes.


Major Patent No. Landscape Points

  • The patent's filing date and its priority data help establish the threshold for novelty, given the rapidly evolving pharmaceutical domain.
  • Given Singapore’s patent law similarity to the EPC (European Patent Convention), the standard of inventive step and novelty remains rigorous.
  • The landscape indicates an increasing tendency for drug patent applications to include methods of treatment claims, formulation innovations, and combination therapies.

Innovation and Market Implications

  • The scope suggests a focus on either a novel chemical entity, an innovative therapeutic method, or an advanced drug delivery system.
  • The patent provides a market exclusivity window, typically 20 years from the filing date, which incentivizes further R&D investment.
  • It acts as a competitive barrier within Singapore and potentially in broader Asian markets, depending on territorial extensions.

Regulatory and Commercial Considerations

  • Patent protection in Singapore aligns with the regulatory pathway of the Health Sciences Authority (HSA), which approves drugs based on efficacy, safety, and quality.
  • Patent owners should synchronize patent strategies with regulatory filings to maximize market control and lifecycle management.

Conclusion

SG10201710567S exemplifies a strategic approach to drug patenting, emphasizing specific chemical, formulation, or method claims to carve out a protected niche. Its scope, finely tuned through carefully drafted claims, underpins its market exclusivity. In the evolving pharmaceutical landscape, understanding such patents enables stakeholders to make informed decisions regarding licensing, litigation, and R&D investments. Continuous monitoring of related patents and legal status updates remains essential for maintaining competitive advantage.


Key Takeaways

  • The patent likely covers a specific pharmaceutical formulation, therapeutic method, or chemical entity, with claims structured to maximize scope while ensuring validity.
  • The patent landscape in Singapore reflects stringent examination standards, emphasizing novelty and inventive step.
  • Strategic patent drafting and comprehensive landscape analysis are vital for defending market position and planning expansion into other jurisdictions.
  • A well-intentioned patent can serve as a valuable asset for licensing, commercialization, or partnership initiatives within the rapidly innovating global pharmaceutical market.
  • Regular patent monitoring is critical to identify potential infringements or opportunities for patent extensions and combinations.

FAQs

1. What is the significance of SG10201710567S for pharmaceutical companies?
It provides exclusive rights within Singapore, enabling the patent holder to control manufacturing, licensing, and commercialization, thereby maximizing market competitiveness and recouping R&D investments.

2. How does patent scope influence litigation strategies?
Broad claims create robust defenses against infringing products, while narrow claims require proactive enforcement. Proper scope also influences potential infringement and validity challenges.

3. Can the patent be extended beyond 20 years?
In Singapore, patent terms are typically 20 years from filing. Extensions are rare and usually limited to specific circumstances like regulatory delays, but such extensions are not common.

4. How does SG10201710567S fit within the global patent landscape?
It may be part of a larger patent family filed via PCT, providing protection in multiple jurisdictions, which is essential for international commercialization.

5. What are potential challenges to the patent’s validity?
Prior art disclosures, lack of inventive step, or ambiguous claims can threaten validity. Regular patent landscape assessments are necessary to identify and mitigate such risks.


References

[1] Singapore Intellectual Property Office. (2017). Patent Filing and Examination Procedures.
[2] European Patent Office. (2022). Patent Law and Practice.
[3] World Intellectual Property Organization. (2022). Patent Landscape Reports.

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