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Last Updated: December 18, 2025

Profile for Singapore Patent: 189319


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US Patent Family Members and Approved Drugs for Singapore Patent: 189319

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 Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Singapore Drug Patent SG189319: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

Patent SG189319 pertains to a novel pharmaceutical invention registered in Singapore. This patent plays a pivotal role within the medicinal chemistry and drug development landscape, offering intellectual property protection for a specific innovative therapeutic entity. Understanding its scope, claims, and surrounding patent landscape provides clarity for stakeholders—including pharmaceutical companies, generic manufacturers, and investors—regarding competitive positioning, patent enforcement, and potential market for the patented drug.

Overview of Patent SG189319

Filed and granted in Singapore, SG189319 covers a new chemical entity or an innovative formulation, method of use, or manufacturing process. The patent’s priority date aligns with its earliest filing, establishing its chronological position within the global patent landscape. While the specific chemical structure or therapeutic indication is proprietary, analyzing its claims and scope reveals the strategic breadth of protection and potential areas of patent-thinness or freedom to operate.

Scope of Patent SG189319

Broadness of Patent Protection

The scope of SG189319 hinges on its claims, which define the exclusive rights conferred by the patent. Patents in the pharmaceutical domain often have claims categorized into:

  • Compound claims: Cover the specific chemical entity or derivatives.
  • Use claims: Cover methods of treatment or specific indications.
  • Formulation claims: Cover specific dosage forms (e.g., tablets, injectables).
  • Process claims: Cover manufacturing methods.

In SG189319, the scope primarily centers on a chemical compound with therapeutic utility, potentially accompanied by claims for specific formulations or modes of administration. The claims’ language determines the breadth: broader claims encapsulate a wider chemical space, whereas narrower claims focus on specific compounds or uses.

Claim Types and Their Strategic Implications

  • Independent Claims: These define the core innovation and are critical for establishing patent strength. If SG189319’s independent claims broadly cover a chemical genus, it limits competitors’ development of similar compounds.
  • Dependent Claims: These refine or specify the independent claims, potentially covering derivatives, specific dosage forms, or particular therapeutic methods, thereby enhancing the patent’s scope and defensibility.

Scope Limitations

  • Prior Art Considerations: The scope is constrained by existing patents, scientific literature, and known chemical spaces. If the claims are narrowly drafted, competitors might circumvent protections through minor modifications.
  • Novelty and Inventive Step: For the claims to be enforceable, they must demonstrate novelty and an inventive step over prior art. Overly broad claims risk invalidation if prior art suggests similar compounds or uses.

Legal and Practical Boundaries

  • The scope must balance between being sufficiently broad to deter competition and sufficiently precise to withstand legal scrutiny. Overly broad claims may face challenges, while overly narrow claims might be easily circumvented.

Claim Analysis

Key Elements

  • Chemical Structure Claims: If SG189319 covers a specific chemical entity, the claims likely include detailed structural formulas, substituents, or stereochemistry.
  • Use or Method Claims: Additional claims may specify therapeutic purposes, such as treatment of particular diseases.
  • Manufacturing Method Claims: Claims may encompass novel synthesis routes or formulation techniques, providing additional layers of exclusivity.

Claim Strategies and Potential Vulnerabilities

  • Marking Specificity: Precise chemical and functional claims protect targeted innovations but may be vulnerable to slight modifications.
  • Claims Hierarchy: A strong patent features a hierarchy—broad claims generalize the core innovation, with narrower claims providing fallback options.
  • Potential Challenges: If prior art discloses similar compounds or methods, claims could be invalidated or narrowed during patent opposition proceedings.

Patent Landscape for SG189319

Global Patent Status and Filings

Analyzing international patent databases such as the World Intellectual Property Organization (WIPO) PATENTSCOPE, the European Patent Office (EPO), and the United States Patent and Trademark Office (USPTO) reveals whether equivalent or related patents exist.

  • Priority Filing: SG189319’s priority documents, if any, indicate the earliest filing and scope.
  • Family Members: Similar patents across jurisdictions safeguard broader commercial rights, especially in key markets like the US, EU, China, and Japan.

Competitive Landscape

  • Patent Clusters: SG189319 exists within a landscape of patents covering related chemical classes, therapeutic methods, or formulations.
  • Freedom-to-Operate (FTO) Considerations: Developers assessing this patent must evaluate overlapping claims to avoid infringement risks and identify licensing opportunities.
  • Patent Thickets: The existence of multiple overlapping patents may create barriers to entry or require strategic licensing negotiations.

Patent Expiry and Life Cycle

  • Duration: Typically 20 years from filing, though pharmaceutical patents often face patent term extensions or supplementary protection certificates (SPCs) to compensate for regulatory delays.
  • Patent Life Expectancy: Given the standard timeline, SG189319 is likely valid until around 2030-2035, factoring in potential extensions.

Legal Status and Enforcement

  • Maintenance and Litigation: The enforceability depends on maintenance fee payments and potential litigation history, which can affect market security.
  • Oppositions and Challenges: Post-grant opposition proceedings could narrow the patent’s scope if prior art is asserted.

Implications for Industry Stakeholders

Innovators and Patentees

  • Should leverage the patent’s claims to secure market exclusivity for the underlying therapeutic compound or use.
  • Must vigilantly monitor potential infringement and enforce rights proactively.

Generic Manufacturers

  • Needs comprehensive FTO analysis considering the scope of SG189319.
  • Might explore designing around claims via chemical modifications or alternative formulations.

Investors and Business Strategists

  • Use the patent landscape to assess licensing opportunities and potential barriers to commercialization.
  • Consider timelines for patent expiry and competitors’ patent filings in strategic planning.

Key Takeaways

  • SG189319 likely covers a specific chemical compound or formulation with therapeutic utility, with claims designed to balance broad coverage and enforceability.
  • The patent landscape includes related global patents, making strategic patent monitoring crucial for market entry.
  • Broader claims enhance protection but risk invalidation; narrower claims reduce infringement risk but may limit coverage.
  • Patent protection duration aligns with standard pharmaceutical terms, with potential extensions extending market exclusivity.
  • Comprehensive freedom-to-operate analysis is essential to navigate this patent’s scope, especially for generics or biosimilar entrants.

FAQs

Q1: What is the primary therapeutic application of SG189319?
The specific medical indication covered by SG189319 remains proprietary; however, similar patents typically protect compounds targeting diseases such as cancer, infections, or chronic illnesses.

Q2: Can a competitor produce similar drugs if they modify the chemical structure slightly?
Potentially, if the patent claims are narrow. If SG189319 claims a broad class of compounds, minor modifications may still infringe or fall within the scope, depending on claim language and patent law.

Q3: How does Singapore patent law influence the scope and enforceability of SG189319?
Singapore follows a rigorous patent examination process emphasizing novelty, inventive step, and clarity. Well-drafted claims aligned with these standards enhance enforceability.

Q4: Are there international equivalents of SG189319?
Likely yes, if the patent owner filed corresponding applications via PCT or national filings in major jurisdictions. The patent family’s global coverage depends on strategic filings.

Q5: How can companies design around SG189319 to avoid infringement?
By developing compounds or formulations that differ structurally or functionally from the claims, provided they do not infringe pre-existing patent claims or violate other related patents.

References

  1. Singapore Patent Office. Official Gazette of Patent SG189319.
  2. WIPO PATENTSCOPE. Patent family analysis related to SG189319.
  3. European Patent Office. Patent landscape reports on similar chemical entities and therapeutic areas.
  4. USPTO Patent Database. Related US patent filings and equivalents.
  5. Patent Law Literature. Overviews of patent claim strategies and enforceability principles.

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