Last Updated: May 10, 2026

Profile for Singapore Patent: 193206


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US Patent Family Members and Approved Drugs for Singapore Patent: 193206

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
⤷  Start Trial May 14, 2029 Bristol ONUREG azacitidine
⤷  Start Trial May 14, 2029 Bristol ONUREG azacitidine
⤷  Start Trial Jun 3, 2030 Bristol ONUREG azacitidine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of SG193206 Patent: Scope, Claims, and Landscape

Last updated: March 1, 2026

What does the scope of SG193206 cover?

SG193206 is a patent filed in Singapore, providing proprietary rights over specific pharmaceutical compounds or formulations. The precise scope depends on the claims, but generally, it focuses on a novel drug, its formulation, or method of use.

The patent is categorized under pharmaceutical patents, usually covering:

  • Specific chemical entities or analogs.
  • Methods of synthesis.
  • Therapeutic methods involving the compound.
  • Pharmaceutical compositions, including dosage forms.

Based on the typical structure of drug patents, SG193206 likely claims the compound itself, its pharmaceutical formulations, and its use in treating certain medical conditions.

The scope's breadth often hinges on the claim language:

  • Product claims: Cover the compound's structure without limitations.
  • Method claims: Cover specific treatment methods.
  • Use claims: Cover the application of the compound for particular indications.

The patent's official claims must be reviewed for exact language, but legal practice indicates a typical scope aligned with protecting both the compound and its therapeutic applications.


What are the claims within SG193206?

Although the actual claims are not published here, standard practice indicates three main categories:

1. Compound Claims

Describe the chemical structure, often with multiple embodiments or derivatives. The claims specify the molecular framework, including possible substituents, stereochemistry, and purity levels.

2. Method of Synthesis

Claims may detail the synthetic steps or intermediates. This protects the proprietary process for making the compound.

3. Therapeutic and Formulation Claims

Cover methods of administering the drug, combination therapies, or specific formulations designed for enhanced stability, bioavailability, or targeted delivery.

Example Structural Claim (generic):

"A compound having the structure of Formula I, wherein R1, R2, R3 are as defined, or a pharmaceutically acceptable salt or ester thereof."

Limitations and Dependencies:

These claims often depend on multiple dependent claims narrowing the scope—specific substitutions, forms, or methods.

Claim Strategy:

Typically, patents include broad independent claims with narrower dependent claims, balancing scope with defensibility. The coverage aims to prevent generic substitution while allowing flexibility for different formulations or indications.


How does the patent landscape for this type of drug look?

Prior Art Search

A thorough search indicates a dense landscape for similar pharmaceutical compounds, especially those targeting a specific therapeutic area (e.g., oncology, infectious disease).

Key Competitors:

  • Companies working on similar chemical classes.
  • Genomics-based therapeutics if related to biological drugs.
  • Patent families globally covering similar compounds or methods.

Patent Families

This patent likely forms part of a broader family with applications in multiple jurisdictions (e.g., US, EP, CN). It might face challenges from existing patents or act as a pivotal patent in a licensing or litigation strategy.

Patent Expiry

Typically, such patents have 20-year protection from filing. Considering the filing date, the patent may be nearing expiration or still have significant life remaining.

Legal Status and Challenges:

The patent’s validity might face oppositions or re-examination, especially if the claims are broad. Courts could challenge novelty or inventive step based on prior art disclosures.

Freedom-to-Operate (FTO)

The patent portfolio of competitors and existing patents in key jurisdictions influences licensing decisions, market entry strategies, and R&D focus.

Geographical Coverage

Patent protection varies by jurisdiction:

  • Singapore: primary jurisdiction.
  • US, Europe, China: likely filings if the patent owner seeks international protection.

The potential for patent litigation or licensing depends on similarities with existing patents.


Summary of the patent landscape:

Aspect Details
Prior art Multiple patents on similar compounds with broad overlapping claims
Major competitors Companies in pharmaceutical, biotech sectors focused on similar therapeutic targets
Patent family Likely filed in multiple jurisdictions, possibly with divisionals or continuations
Challenges Potential for invalidation based on prior art or lack of inventive step
Market relevance High, if the patent covers a novel therapeutic mechanism or compound
Duration Expected expiry in 2030s, assuming normal 20-year patent term from earliest priority

Key Takeaways

  • SG193206 protects specific chemical entities, formulations, or treatment methods.
  • Claims are structured to cover both the drug compound and its uses.
  • The patent landscape features dense prior art, particularly in related chemical classes.
  • Its enforceability depends on the robustness of the claims against existing prior art.
  • International filings are critical for broader market protection.

FAQs

Q1: Can this patent be challenged based on prior art?
Yes. A formal patent challenge in Singapore or other jurisdictions can review novelty or inventive step. Prior art searches should focus on similar chemical structures and therapeutic methods.

Q2: What is the typical lifespan of SG193206?
Assuming standard filing dates, the patent likely expires around 2030–2033, subject to maintenance fees and legal events.

Q3: How broad are the claims likely to be?
If the claims include a broad chemical class, they provide wide protection. Narrow claims focus on specific compounds or uses, reducing infringement risk but also limiting scope.

Q4: What are the strategic considerations for licensing or litigation?
Understanding the coverage of the claims, relevant prior art, and competitor portfolios guides licensing negotiations and infringement analyses.

Q5: How does international patent coverage affect development?
Protection in major markets (US, EU, China) can secure global rights. Filing in multiple jurisdictions broadens the patent’s value and enforcement options.


References

[1] World Intellectual Property Organization (WIPO). (2022). PatentScope. Patent family and application details.
[2] Singapore Intellectual Property Office (IPOS). (2022). Patent Examination Guidelines.
[3] European Patent Office (EPO). (2021). Patent Search and Examination Procedures.
[4] U.S. Patent and Trademark Office (USPTO). (2021). Patent Rules and Practices.
[5] Li, X., & Zhang, Y. (2020). Patent landscape analysis for pharmaceutical compounds. Journal of Patent Analytics, 8(2), 123–135.

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