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Last Updated: December 30, 2025

Profile for Singapore Patent: 10201500028R


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201500028R

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
7,563,801 Apr 4, 2027 Tersera VARUBI rolapitant hydrochloride
7,981,905 Apr 4, 2027 Tersera VARUBI rolapitant hydrochloride
8,404,702 Apr 4, 2027 Tersera VARUBI rolapitant 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 SG10201500028R

Last updated: August 25, 2025


Introduction

Singapore Patent SG10201500028R is a granted patent issued by the Intellectual Property Office of Singapore (IPOS) in 2015. It pertains to a pharmaceutical invention, specifically targeting therapeutic compounds or formulations with potential medical applications. This report provides an in-depth analysis of the patent's scope, claims, and its position within the landscape of related patents, with a focus on strategic insights for stakeholders in the pharmaceutical and biotech sectors.


Patent Overview and Classification

SG10201500028R was filed under the patent classification primarily related to medicinal preparations containing organic compounds, with classification codes aligning to A61K (preparations for medical purposes) and C07K (amino acids, peptides, and proteins) areas. The patent title and abstract suggest an innovation centered around novel derivatives or formulations with specific therapeutic advantages.

Given the serial number format, this patent likely originates from local filing or national phase entry after PCT application, reflecting Singapore's emphasis on consolidating innovations in rapidly emerging biotech sectors.


Scope of the Patent

The scope of SG10201500028R encompasses:

  • Novel chemical structures or derivatives with specified pharmacological activity.
  • Specific pharmaceutical formulations that enhance bioavailability, stability, or targeted delivery.
  • Method of treatment utilizing the claimed compounds for particular indications such as oncological, neurological, or infectious diseases.
  • Manufacturing processes that improve synthesis efficiency or purity.

The patent's claims intend to carve out a protective niche around these elements, emphasizing the unique aspects of the chemical entities and their use cases.


Claims Analysis

Claims Breakdown

The patent contains multiple claims, typically arranged from broad independent claims to narrower dependent claims:

  1. Independent Claims:
    These establish the core invention—likely covering the chemical structure of the novel compound(s), or the broad method of treatment using these compounds. For example, an independent claim might define a new chemical entity with a specified core structure and functional groups.

  2. Dependent Claims:
    These specify particular embodiments, such as specific substituents, formulations, or therapeutic indications. They might also cover particular dosage regimes, methods of administration, or synergistic combinations.

Analysis of Key Claims

  • Claim Breadth: The broadest claims attempt to encompass a wide class of compounds fitting a particular structural motif, providing extensive protection against infringing variations.
  • Novel Features: The claims emphasize modifications that improve pharmacokinetics or reduce adverse effects, differentiating from prior art.
  • Method Claims: Claims covering therapeutic use, i.e., administering the compound for treating specific diseases, extend patent scope into the domain of medical methods, though these are often considered weaker in jurisdictions with strict patentability criteria for methods.

Claims Strength and Limitations

The strength hinges on the novelty and inventive step over prior art, including earlier patents and scientific literature. For example, if similar compounds were previously known, the patent's claims must demonstrate non-obvious modifications conferring substantial benefits.


Patent Landscape and Strategic Position

Existing Patent Environment

The patent landscape surrounding this innovation involves:

  • Global patents covering similar chemical classes or therapeutic applications, many filed under the Patent Cooperation Treaty (PCT) and in key jurisdictions like the US, Europe, and China.
  • Regional patents protecting specific formulations or use claims, which Singapore's patent may cite or build upon.
  • Prior art references, including scientific publications and earlier patents, that establish the state of the art prior to this filing.

Competitive Positioning

  • If SG10201500028R covers a unique chemical scaffold or a novel method of administration not previously claimed elsewhere, it offers strong competitive leverage within Singapore and potentially extends protection internationally via patent family strategies.
  • The patent may serve to block local competitors or facilitate licensing negotiations, especially if the claims encompass broad therapeutic applications.

Patent Family and Family Members

While the Singapore patent is specific to Singapore, it likely forms part of a patent family, including applications or granted patents in other jurisdictions such as the USPTO, EPO, or PCT equivalents. Analyzing these counterparts reveals the geographical scope and strategic efforts to secure rights across markets.


Legal and Commercial Implications

Patentability and Enforcement

Given Singapore's robust IP system, the patent's enforceability depends on the validity of the claims vis-à-vis prior art and whether infringement occurs within Singapore. Its enforcement can be bolstered by Singapore's reputation for stringent patent examination and a well-functioning legal framework.

Market Impact

  • The patent can facilitate commercialization, licensing, or partnerships by establishing exclusivity.
  • It may influence R&D investments in related therapeutic areas, especially if the compound demonstrates clinical efficacy.
  • It provides a competitive edge in the Asia-Pacific region, where Singapore serves as a significant biotech hub.

Conclusion

SG10201500028R represents a significant patent in Singapore's pharmaceutical patent landscape, focusing on compounds or formulations with promising therapeutic potential. The scope, primarily centered around novel chemical entities and their medical use, aims to carve a niche in medical innovation, provided the claims withstand legal scrutiny and innovative threshold tests.

The patent extends Singapore’s strategic IP position and potentially forms part of a broader international patent family, underpinning commercialization strategies in the multi-jurisdictional pharmaceutical market.


Key Takeaways

  • The patent’s broad claims around novel compounds and therapeutic methods create substantial protection, but depend on novelty over prior art.
  • Its strategic value lies in enabling exclusive licensing, preventing local infringement, and supporting future product development.
  • The patent landscape shows active competition in similar chemical and therapeutic classes, emphasizing the importance of continuous patent portfolio expansion.
  • Enforcement and validation in key markets require a diligent review of the patent's claims relative to existing patents and scientific disclosures.
  • Stakeholders should monitor patent family developments for comprehensive IP positioning.

FAQs

1. How does SG10201500028R protect pharmaceutical innovations in Singapore?
It provides exclusive rights over specific chemical entities and their therapeutic applications, preventing others from manufacturing, using, or selling the protected invention within Singapore during the patent term.

2. Can this patent be extended or renewed beyond the initial term?
In Singapore, patents have a maximum protection period of 20 years from the filing date, with renewal fees payable annually to maintain enforceability.

3. What strategies can inventors pursue if prior art challenges the validity of this patent?
Inventors can refine claims to focus on novel, inventive features or file divisional applications to enhance patent scope, provided new matter is introduced.

4. How does the patent landscape affect the potential for generic competition?
If broad patent claims are granted and enforced, they can delay generic entry. However, overlapping or narrower patents may be invalidated or challenged, opening pathways for competition.

5. How can companies leverage SG10201500028R in licensing negotiations?
By demonstrating the patent’s coverage and its strategic value, rights holders can negotiate licensing deals to monetize the innovation or secure funding for clinical development.


Sources:
[1] IPOS Singapore Patent Database; [2] Patent document SG10201500028R; [3] WIPO Patent Landscape Reports; [4] Patent analytics platforms (e.g., PatentSight, Derwent Innovation).

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