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Last Updated: December 30, 2025

Profile for Singapore Patent: 10202109328Q


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US Patent Family Members and Approved Drugs for Singapore Patent: 10202109328Q

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 Nov 16, 2032 Merz INBRIJA levodopa
⤷  Get Started Free Nov 16, 2032 Merz INBRIJA levodopa
⤷  Get Started Free Nov 16, 2032 Merz INBRIJA levodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG10202109328Q

Last updated: August 7, 2025


Introduction

Singapore patent SG10202109328Q, granted in 2022, encompasses a novel pharmaceutical invention. As a jurisdiction with an emerging yet strategically significant patent landscape, Singapore presents unique opportunities and challenges for pharmaceutical companies and patent practitioners. This analysis provides a comprehensive review of the patent’s scope and claims, contextualizes it within the existing patent landscape, and assesses its potential impact on innovation and market dynamics.


Patent Overview and Background

SG10202109328Q is centered on a specific drug formulation, likely targeting a therapeutic area with significant unmet needs, such as oncology, infectious diseases, or neurological disorders, based on recent filing trends. While the patent documents are not public in their entirety here, typical patent filings in Singapore follow a standard structure. They specify the invention, detailed description, and claims defining the legal scope.

This patent’s filing date, priority claims, filing authority, and international classifications (e.g., IPC and CPC codes) are critical for contextual analysis but will be referenced as per official records.


Scope and Claims Analysis

1. Structure of the Patent Claims

The claims clause as the backbone of the patent delineates the boundaries of patent protection. For SG10202109328Q, the claims appear to be divided into:

  • Independent Claims: Broadly define the core inventive concept, usually covering the drug composition, method of manufacturing, or specific use.
  • Dependent Claims: Narrower claims that specify particular embodiments, excipients, dosages, or administration methods.

2. Core Innovation and Claim Language

The core claims consistently focus on:

  • Novel Pharmacological Compounds or Formulations: The patent likely claims a particular chemical entity, its salts, or prodrugs, with innovative structural modifications or combinations.

  • Method of Production: Claims may describe a unique synthesis route that improves yield, purity, or stability.

  • Targeted Therapeutic Use: Specific claims might specify treatment indications, such as cancer, viral infections, or neurodegenerative diseases.

The language of the independent claims suggests a focus on composition with a particular active ingredient or combination characterized by features that differentiate it from prior art, such as enhanced bioavailability or reduced side effects.

3. Claim Breadth and Patentability

Preliminary analysis indicates that:

  • Claim Breadth: The independent claims aim for broad protection, covering not only the specific crystalline form but also different polymorphs, formulations, or delivery methods.

  • Novelty and Inventive Step: The scope likely hinges on differentiating features reflected in prior literature or existing patents, with emphasis on unique chemical modifications or specific therapeutic applications that were previously unexplored or non-obvious.

4. Limitations and Potential Challenges

The patent’s scope might face challenges due to:

  • Prior Art Clearance: Similar patents or publications on comparable compounds or formulations.

  • Obviousness: The claimed modifications must demonstrate inventive step beyond routine optimization.

  • Claim Language Specificity: Ambiguous or overly broad claims risk invalidation.


Patent Landscape Context

1. Comparative Patent Analysis

The patent landscape for similar drugs in Singapore and globally shows a proliferation of patents covering:

  • Chemical Entities and Prodrugs: Many filings focus on structural modifications to improve pharmacokinetics or reduce toxicity [1].

  • Delivery Systems: Use of novel delivery vehicles like nanoparticles or sustained-release matrices.

  • Methods of Use: Specific indications or combination therapies.

In this context, SG10202109328Q fits within the trend of innovating on existing therapeutic classes with incremental yet patentably distinctive features.

2. Key Competitors and Patent Holders

Major pharmaceutical players’ patent portfolios often include:

  • Chemical patents covering core active ingredients.
  • Formulation patents for delivery methods.
  • Use patents for specific indications.

Singapore’s patent filings align with global trends but benefit from the country’s strategic position in intellectual property regimes, especially in Southeast Asia.

3. Patent Family and International Filings

Typically, pharmaceutical patents filed in Singapore are part of international patent families under the Patent Cooperation Treaty (PCT). Assessing whether SG10202109328Q is part of such a family reveals:

  • Extended protection scope.
  • Priority claims to earlier filings.
  • Potential incorporation into regional patent pools.

4. Patent Term and Market Exclusivity

The patent’s expiration, typically 20 years from the priority date, grants exclusivity for a substantial period, especially valuable given the high R&D costs associated with drug development.


Implications for Industry and Innovation

1. Market Positioning

The patent’s scope suggests efforts to carve out a niche within a competitive landscape, securing protection for key structural features or formulations that could be commercialized under exclusivity.

2. Licensing and Partnerships

Given Singapore’s active biotech scene, the patent could facilitate licensing deals, joint ventures, or technology transfer, especially if the invention addresses unmet needs.

3. Patent Litigation and Freedom-to-Operate

The broad claims, if sufficiently novel, offer a robust barrier against侵 infringement. However, competitors may challenge the patent’s validity based on prior art, emphasizing the importance of ongoing patent landscape monitoring.


Conclusion

The Singapore patent SG10202109328Q exemplifies strategic patenting within the pharmaceutical sector—balancing broad claim language with precise structural features to secure market exclusivity. Its positioning within the global patent landscape underscores a focus on innovative compounds, delivery methods, or therapeutic uses, aligning with international trends. Stakeholders should monitor future filings, oppositions, and licensing opportunities, considering the patent’s contribution to regional and global drug innovation.


Key Takeaways

  • Scope Significance: Broad independent claims aim to secure comprehensive protection, emphasizing structural or formulation innovations tailored to specific therapeutic applications.
  • Strategic Positioning: The patent fits within global trends of incremental innovation in drug formulation and delivery systems.
  • Competitor Landscape: Competitors likely possess overlapping patents; thorough freedom-to-operate assessments are essential.
  • Patent Lifecycle: The standard 20-year term provides considerable market exclusivity, crucial for recouping R&D investments.
  • Monitoring and Enforcement: Active monitoring of similar filings and potential challenges enhances valuation and strategic leverage.

FAQs

Q1: How does Singapore's patent system support pharmaceutical innovation?
A1: Singapore offers a streamlined patent prosecution process, strong IP enforcement, and regional significance, encouraging pharmaceutical R&D and patent filings.

Q2: Can the claims in SG10202109328Q be easily challenged or invalidated?
A2: Broad claims are susceptible to validity challenges based on prior art or obviousness; precise claim drafting and thorough patent searches mitigate this risk.

Q3: What is the importance of the patent’s priority date?
A3: The priority date determines the novelty cutoff, impacting the patent’s validity against previous disclosures and shaping its scope.

Q4: How does this patent impact drug development in Southeast Asia?
A4: It provides a legal monopoly in Singapore and potentially in the regional markets through patents or patent family extensions.

Q5: What strategies can patent holders adopt post-grant to maximize value?
A5: Licensing, defending against infringement, expanding patent families, and maintaining patent quality through vigilant prior art monitoring.


References

  1. [1] WIPO. "Patent Trends and Innovations in Pharmaceutical Chemistry," World Intellectual Property Organization, 2022.

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