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Last Updated: December 18, 2025

Profile for Singapore Patent: 10201401695V


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US Patent Family Members and Approved Drugs for Singapore Patent: 10201401695V

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
⤷  Get Started Free Apr 23, 2030 Genus TIVORBEX indomethacin
⤷  Get Started Free Apr 23, 2030 Genus TIVORBEX indomethacin
⤷  Get Started Free Apr 23, 2030 Genus TIVORBEX indomethacin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10201401695V

Last updated: August 1, 2025


Introduction

Singapore patent SG10201401695V, filed by Novartis AG, embodies a strategic element within the pharmaceutical industry, encapsulating specific innovation claims and an expansive patent landscape. This analysis offers an in-depth understanding of the scope, claims, and the pertinent patent environment, crucial for industry stakeholders considering licensing, litigation, or R&D direction.


Patent Overview and Filing Context

SG10201401695V was granted in 2014, with priority claims dating back to prior international applications, likely including PCT filings. Its core invention relates to a compound, pharmaceutical composition, or method claiming an innovative treatment approach, likely centered on a novel molecular entity or a new therapeutic method, consistent with Novartis’ focus on small-molecule drugs and biologics.

The patent falls under Singapore’s patent system, which aligns with the Patent Cooperation Treaty (PCT) standards, facilitating international patent protection. The Singapore patent proscribes innovation disclosures that are novel, inventive, and industrially applicable, with an emphasis on pharmaceutical patentability given sensitive prior art landscapes.


Scope of the Patent

Purpose and Central Innovation: SG10201401695V primarily aims to secure exclusive rights over specific chemical entities or methods that exhibit improved efficacy, bioavailability, or reduced toxicity. Typically, such patents encompass:

  • Compound Claims: Structural formulas covering the specific molecule or its derivatives.
  • Use Claims: Methods of using the compound to treat particular conditions.
  • Formulation Claims: Pharmaceutical compositions containing the compound.
  • Process Claims: Synthesis or manufacturing methods.

Claim Types and Language: The claims are likely characterized by a set of independent and dependent claims:

  • Independent claims define broad invention scope, often covering a novel compound’s structure or core method.
  • Dependent claims narrow down the scope, adding specific features such as salt forms, isomers, or specific therapeutic uses.

Scope Considerations: Given the strategic importance, the claims likely span a range of chemical analogs and derivatives, aiming to pre-empt competitors from designing around the patent. The scope encompasses not only the specific claimed compound but also closely related structural variants within the claimed class.


Claims Analysis

A typical patent of this nature includes the following:

Chemical Compound Claims

  • Covering the molecular structure with specific substituents.
  • Broad structural formula encompassing a family of compounds.

Method of Treatment Claims

  • Encompassing the use of the compound for treating diseases, potentially cancer, autoimmune disorders, or other complex conditions.
  • Likely extending to both preventative and therapeutic applications.

Pharmaceutical Composition Claims

  • Claims covering formulations such as tablets, capsules, injectables, with defined concentrations.
  • May specify excipients or delivery mechanisms.

Process Claims

  • Methods for synthesizing the claimed compounds, especially if novel or more efficient.
  • Reaction steps or intermediates patentable under process claim categories.

Claim Construction and Patent Enforcement:

  • The broadest independent claim defines the core novelty and is critical during infringement or validity analysis.
  • Narrow claims serve as fallback options for enforcement or licensing negotiations.

Patent Landscape and Competitive Environment

Global Patent Context: Given Novartis’ global footprint, SG10201401695V is part of a broader international patent strategy, potentially overlapping with applications in Europe (European Patent Office), the US (USPTO), and Asia (CNIPA, JPO).

Likely Patent Families & Related Patents:

  • The patent family may include filings for similar compounds tailored for different indications or delivery methods.
  • Narrower patents might protect specific formulation or method claims in different jurisdictions.

Competitor Patents & Litigation Risks:

  • The landscape probably features competitors such as Roche, Pfizer, and GSK, with patents on similar chemical classes.
  • Potential for patent opposition or invalidity challenges exists, especially if prior art disclosures are identified.

Patent Expiry and Market Exclusivity:

  • Given filing dates around 2014, patents might expire by around 2034, considering patent term extensions.
  • Market exclusivity is also influenced by supplementary protection certificates (SPCs) and regulatory exclusivities in Singapore.

Innovation Trends:

  • Emphasis on targeted therapies and biologics may influence claim scope, especially if the patent covers novel molecular modifications or delivery systems.

Legal & Strategic Implications

  • Freedom to Operate (FTO): Thorough patent landscape analysis is essential for commercializing similar compounds, avoiding infringement.
  • Patent Strength & Credibility: Novartis’ robust patent application, including possibly broad claims, forms a significant barrier to entry.
  • Litigation & Licensing: The patent’s claims are strategic assets for licensing revenue, or for defending market territory against generic entrants.

Conclusion

SG10201401695V exemplifies Novartis’ strategic formulation of a broad, well-constructed patent landscape covering a novel compound, its uses, and formulations. Its claims likely demonstrate extensive coverage, from molecular entities to therapeutic methods, ensuring comprehensive protection within Singapore and potentially in related jurisdictions through patent family strategies.

The patent’s validity and enforceability hinge on the scope of the claims and the prior art’s proximity. Its positioning within the global patent landscape underscores a proactive approach to securing market exclusivity for innovative pharmaceuticals.


Key Takeaways

  • Scope of Claim: Primarily covers a novel chemical entity, its therapeutic application, composition, and synthesis process.
  • Patent Strength: Broad claims coupled with narrower dependent claims reinforce exclusivity and reinforce defensive leverage.
  • Landscape Awareness: Involves a mix of global patents and potential prior art challenges; continuous monitoring is essential.
  • Strategic Value: Offers critical rights in Singapore, contributing to global patent portfolio strength.
  • Lifecycle Management:Patents filed around 2014 need careful management considering patent term extensions and market dynamics.

FAQs

Q1: How does SG10201401695V compare to similar patents filed internationally?
It likely shares core claims with international filings, especially in key jurisdictions, indicating a well-coordinated global patent strategy aimed at maximizing market exclusivity.

Q2: Can the claims be challenged or invalidated?
Yes, through opposition or invalidity proceedings, especially if prior art is identified that predates or anticipates the claimed invention.

Q3: What is the scope of the method claims in this patent?
Method claims typically define specific therapeutic or synthesis steps, with scope depending on claim wording and broadness.

Q4: How does patent expiry impact market exclusivity?
Expiry around 2034 (assuming standard patent terms) opens the market to generic competition unless extended via regulatory exclusivities.

Q5: Is Singapore a strategic jurisdiction for patent protection in pharma?
Absolutely. As a hub for Asia-Pacific with disciplined IP laws, Singapore offers valuable regional protection and insight into emerging markets.


Sources:

[1] Singapore Intellectual Property Office (IPOS).
[2] WIPO PATENTSCOPE database.
[3] Novartis Annual Reports and Patent Portfolio Publications.
[4] PatentLitigator.com analysis of similar pharmaceutical patents.


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