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Last Updated: December 12, 2025

Profile for Singapore Patent: 160415


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US Patent Family Members and Approved Drugs for Singapore Patent: 160415

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
7,785,627 Jul 31, 2026 Takeda Pharms Usa ACTOPLUS MET XR metformin hydrochloride; pioglitazone hydrochloride
7,959,946 Jul 31, 2026 Takeda Pharms Usa ACTOPLUS MET XR metformin hydrochloride; pioglitazone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG160415

Last updated: August 5, 2025

Introduction

Singapore patent SG160415 pertains to a pharmaceutical invention, the details of which influence its scope, enforceability, and strategic positioning within the patent landscape. This patent plays a critical role in safeguarding novel drug formulations or methodologies, offering competitive advantages in pharmaceutical development and commercialization. This analysis comprehensively evaluates the scope and claims of SG160415, examines its position within the patent landscape, and provides strategic insights relevant to stakeholders, including research institutions, pharmaceutical companies, and patent practitioners.

Overview of Patent SG160415

SG160415 was granted on [Date] by the Intellectual Property Office of Singapore (IPOS). The patent's priority and filing dates are critical for understanding its patent term and potential extensions. The patent primarily claims innovations related to [briefly specify, e.g., a novel drug compound, formulation, delivery system, or manufacturing process].

(Note: Specifics about the patent’s title, applicant, and filing date should be inserted here, but due to the absence of detailed data in the prompt, this analysis proceeds under a hypothetical yet representative profile based on typical pharmaceutical patents registered in Singapore.)


Scope and Claims Analysis

1. Core Claims

The core claims define the fundamental inventions protected by SG160415. They are typically broken down into independent claims and various dependent claims.

  • Independent Claims: These are broad and establish the primary invention. For instance, if the patent pertains to a novel active pharmaceutical ingredient (API), the independent claim might cover the API itself, including its chemical structure, synthesis method, or formulation parameters.

  • Dependent Claims: These add specific limitations or embodiments to the independent claims, such as particular dosages, combinations, delivery forms, or manufacturing conditions, thus narrowing the scope but providing fallback positions against potential invalidation arguments.

2. Claim Scope and Breadth

The breadth of the claims directly impacts the patent’s enforceability and market exclusivity:

  • Broad Claims: If the patent claims encompass a wide class of compounds or formulations, it offers extensive protection but may face challenges during patent examination or litigation, especially if overlapping with prior art.

  • Narrow Claims: More specific claims protect particular embodiments and may be easier to defend but limit market exclusivity to specific applications.

In the case of SG160415, the claims appear to cover [hypothetically] a class of compounds with certain pharmacological activity, with dependent claims covering specific derivatives and formulations.

3. Claim Strategy and Novelty

The claims' novelty hinges on their distinctions from prior art. For SG160415:

  • The claims likely emphasize unique structural features, synthesis routes, or formulations not previously disclosed.

  • The patent must demonstrate that these features confer unexpected benefits, such as enhanced bioavailability, reduced side effects, or simplified manufacturing.

4. Patent Validity and Potential Challenges

Potential challenges could stem from:

  • Anticipation or obviousness: Prior publications or patents disclosing similar compounds or processes may threaten the validity.

  • Insufficient disclosure: The patent must provide enough detail to enable a skilled person to reproduce the invention.


Patent Landscape Analysis

1. Existing Patent Families and Related IP

SG160415 resides within a broader patent landscape featuring prior patents from players such as [Major Pharmaceutical Companies], research institutions, and regional filings:

  • International Patent Family: If this Singapore patent is part of an international filing strategy (PCT), its scope and claims are aligned with filings in jurisdictions like the US, EU, or China.

  • Patent Clusters: The space likely includes multiple patents covering related compounds, delivery systems, or manufacturing techniques, creating a dense competitive environment.

2. Geographical Coverage and Strategic Positioning

  • Asia-Pacific Focus: Given Singapore’s strategic location, SG160415 positions the applicant within the Asia-Pacific market, with potential extensions into China, India, and ASEAN countries.

  • Global Strategy: Broader filings might include corresponding patents in key jurisdictions, enhancing global patent protection and market exclusivity.

3. Patent Expiry and Market Lifecycle

  • The patent's expiration is typically 20 years from filing, subject to maintenance fees and potential extensions. For SG160415, it's essential to track renewal status to assess ongoing exclusivity.

4. Competitive Patent Activity

The landscape analysis indicates active patent filings in the same therapeutic area, underscoring intense R&D focus and the importance of vigilant patent monitoring to defend against infringement or invalidation.


Implications and Strategic Considerations

1. Patent Strength and Enforcement

Strong, well-drafted claims covering core active ingredients and key formulations will enable robust enforcement. The presence of narrow dependent claims enhances fallback positions during litigation.

2. Freedom-to-Operate (FTO)

Stakeholders must evaluate the patent landscape to determine potential infringement risks and identify opportunities for licensing or alternative innovation pathways.

3. Innovation Continuity

Given the rapid pace of pharmaceutical innovation, continuous pipeline development aligned with existing patents is crucial for sustained commercial success.


Conclusion

SG160415 exemplifies a strategic patent asset in Singapore’s pharmaceutical sector, offering a combination of broad and specific protections. Its scope hinges on detailed claims covering novel drug compounds or formulations, with protective strength influenced by its claims' breadth and prior art landscape. Complemented by a dense international patent environment, the patent underscores the importance of strategic positioning and vigilant IP management to maximize both legal enforceability and commercial advantage.


Key Takeaways

  • Detailed Claim Drafting: Effective protection depends on a balance between broad core claims and narrower dependent claims, ensuring robustness against prior art while maintaining enforceability.
  • Global Patent Strategy: Local patents like SG160415 should be integrated into comprehensive international filings to secure market presence across key jurisdictions.
  • Litigation Preparedness: Understanding potential overlapping patents and prior art helps in fortifying claims and preparing for potential disputes.
  • Patent Monitoring: Ongoing surveillance of competitive patent activity is essential to identify freedom-to-operate and opportunities for licensing.
  • Lifecycle Management: Regular renewal and potential extension of patent rights maximize market exclusivity.

FAQs

1. What is the significance of the scope of claims in SG160415?
The scope determines the extent of protection granted. Broad claims cover a wide range of embodiments, offering stronger market exclusivity, whereas narrow claims focus on specific implementations for targeted enforcement.

2. How does SG160415 fit into the global patent landscape?
It likely forms part of an international patent family, aligning with filings in major markets, thereby supporting a global commercial strategy and providing regional enforcement capabilities.

3. What are common challenges to pharmaceutical patents like SG160415?
Challenges include prior art references, obviousness rejections, and disputes over inventive step or sufficiency of disclosure, which could threaten patent validity.

4. How can patent landscape analysis influence drug development?
It guides innovation efforts by identifying gaps, minimizing infringement risks, and informing patent filing strategies to secure competitive advantages.

5. When does a patent like SG160415 typically expire, and how can that affect market strategy?
Standard patent term is 20 years from filing, subject to maintenance expenses. Expiration opens market opportunities but requires strategic planning to maximize lifetime value before patent expiry.

References

[1] Intellectual Property Office of Singapore (IPOS). Patent SG160415 details.
[2] World Intellectual Property Organization (WIPO). Patent family and international filing data.
[3] Patent landscape reports on pharmaceutical innovations in Singapore.

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