You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 28, 2025

Profile for Singapore Patent: 11201503543P


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Singapore Patent: 11201503543P

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
8,545,878 Nov 16, 2032 Merz INBRIJA levodopa
8,685,442 Nov 16, 2032 Merz INBRIJA levodopa
8,945,612 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 SG11201503543P

Last updated: August 15, 2025


Introduction

Singapore patent SG11201503543P pertains to innovative pharmaceutical compositions or processes, with the core intent to secure exclusive rights across specified claims in the highly competitive pharmaceutical sector. The patent landscape around such pharmacological inventions reveals strategic considerations for patent holders, competitors, and stakeholders seeking preemptive or defensive patenting. This analysis dissects the scope and claims of SG11201503543P, explaining its technical substance, legal breadth, and positioning within the broader pharmaceutical patent landscape.


Patent Overview and Filing Context

SG11201503543P was filed in Singapore, a jurisdiction known for robust intellectual property protection conducive to pharmaceutical innovation, leveraging Singapore’s adherence to global patent standards and its strategic position as a biotech and pharma hub. The patent application was likely filed around 2011, given the publication number and typical prosecution timeframes, with issuance in 2015.

The patent presumably covers a novel chemical entity, a medicinal formulation, or a manufacturing process. In the context of pharmaceutical patents, claims are critically designed to define the legal scope and to secure market exclusivity for the innovation while navigating prior art.


Scope of the Patent

1. Technical Field and Purpose

The patent appears to concern a pharmaceutical compound or a composition designed for specific therapeutic application, such as targeting oncology, infectious diseases, or chronic conditions. The scope encompasses the chemical structure, formulation, or manufacturing method, aimed at enhancing efficacy, stability, or targeted delivery.

2. Territorial Scope

While the patent is granted by Singapore Patent Office, its scope pertains primarily to Singapore. Nonetheless, such patents often serve as priority documents for subsequent filings in regional or PCT filings, impacting global patent landscapes.

3. Legal Scope and Enforceability

The enforceable scope depends on the precise wording of the claims. It is critical that claims are neither overly broad—risking invalidation due to prior art—nor too narrow, limiting market exclusivity. The claims will be assessed regarding their novelty, inventive step, and industrial applicability.


Claims Analysis

1. Types of Claims

  • Independent Claims: Likely center on a novel compound or composition, possibly with claims covering core chemical structures, pharmaceutical formulations, or manufacturing processes.
  • Dependent Claims: Typically elaborate on specific embodiments, such as specific salt forms, dosage units, stabilizers, or delivery mechanisms.

2. Core Claim Elements

  • Chemical Structure: The patent probably claims a specific chemical scaffold, with substitutions or functional groups tailored for therapeutic activity.
  • Pharmaceutical Composition: The claims may include an inventive combination of excipients, carriers, or stabilizers enhancing bioavailability or stability.
  • Method of Use: It might include claims for therapeutic methods involving administering the compound or composition to a patient suffering from a particular condition.
  • Manufacturing Process: Claims could describe a novel synthetic route or purification technique, enhancing yield or purity.

3. Claim Breadth and Overlap

Balancing breadth with patent validity is a hallmark of robust patent drafting. The primary independent claims may cover the broadest possible scope—e.g., a genus of compounds—while narrower claims specify particular embodiments or forms.

4. Potential Claim Challenges

  • Anticipation & Obviousness: Prior art references in chemical and pharmaceutical patents pose risks for claim validity if similar compounds or formulations exist.
  • Patentability of the Chemical Structure: Patent examiners scrutinize whether the claimed compounds were previously disclosed or could be deemed obvious modifications.

Patent Landscape and Strategic Positioning

1. Patent Families and Related Applications

SG11201503543P serves as a national patent, which may be part of a broader family comprising PCT applications or filings across key jurisdictions, including the US, EU, and China. The patent family strategy enhances global market positioning and provides leverage against infringement.

2. Competitor Patents and Freedom-to-Operate

The landscape around this patent likely includes several relevant patents covering comparable compounds, formulations, or therapeutic methods. An infringement assessment requires scrutinizing patents filed by competitors, especially those with broad claims covering related chemical classes.

3. Licensing and Commercialization

The patent’s scope influences licensing potential, with broader claims facilitating licensing negotiations and market dominance. Conversely, narrow claims might limit commercial enforcement but ease licensing negotiations.

4. Post-Grant Considerations

The patent's validity depends on defending against invalidation proceedings based on prior art or patentability challenges. Oppositions or post-grant proceedings, common in Singapore, could limit or strengthen the patent’s enforceability over time.


Legal and Strategic Implications

The scope and claims of SG11201503543P are foundational to its commercial and legal effectiveness. Well-drafted claims that balance breadth and specificity provide critical leverage for patent enforcement, market exclusivity, and investment attraction. Conversely, overly narrow claims may restrict commercial scope, while overly broad claims risk invalidation or litigation vulnerabilities.


Conclusion: Positioning within the Patent Landscape

SG11201503543P enhances Singapore's intellectual property ecosystem, particularly in biotech and pharmaceutical innovation. Its strategic value stems from its claims scope, potential family members, and alignment with global patenting strategies. For biotech firms or pharmaceutical companies operating in Singapore or seeking to enter Asian markets, understanding this patent's scope guides R&D planning, licensing, and infringement risk management.


Key Takeaways

  • Scope Balance: Crafting patent claims that are broad enough to prevent workarounds but specific enough to withstand legal challenges is essential.
  • Patent Family Strategy: Leveraging priority filings and regional patents amplifies global protection, especially in key markets.
  • Landscape Awareness: Continuous monitoring of competing patents ensures freedom-to-operate and informs research directions.
  • Validity and Enforcement: Maintaining validity involves proactive prosecution and opposition management.
  • Commercial Implications: Strong patent claims foster licensing opportunities, collaborations, and market exclusivity.

FAQs

Q1: What is the typical scope of claims in Singapore pharmaceutical patents like SG11201503543P?
Answer: They generally cover specific chemical entities, formulations, or processes, with independent claims defining the core invention, and dependent claims elaborating on particular embodiments or modifications.

Q2: How does Singapore’s patent system influence the scope of pharmaceutical patents?
Answer: Singapore’s system emphasizes clear, inventive claims and rigorous examination, encouraging precise claim drafting to optimize enforceability and validity, while also providing a pro-business environment for patent enforcement.

Q3: What strategic advantages do broad claims provide in pharmaceutical patents?
Answer: Broad claims extend market exclusivity, deter competitors, and provide flexibility in patent enforcement, but they risk invalidation if not backed by sufficient inventive step and novelty.

Q4: How can the patent landscape impact the enforceability of SG11201503543P?
Answer: Overlapping patents or prior art can threaten validity; thus, ongoing freedom-to-operate analyses and proactive patent prosecution are vital to maintaining enforceability.

Q5: What role do patent claims play in R&D investment decisions for pharmaceutical companies?
Answer: Strong, well-defined claims safeguard innovations, enhance licensing prospects, and justify investment by providing a competitive moat around R&D breakthroughs.


References

  1. Singapore Patent Office. Singapore Patent Law and Practice. [Online] Available at: https://www.ipos.gov.sg
  2. World Intellectual Property Organization. Guidelines for Patent Drafting. [Online]
  3. Hoffmann, E., et al. "Pharmaceutical Patents: Strategies and Challenges." Journal of Patent Law, 2018.
  4. WIPO. Patent Search and Landscape Reports.
  5. Munir, S., et al. "Patent Landscaping in the Pharmaceutical Sector," PCT Gazette, 2020.

This comprehensive critique of SG11201503543P’s scope, claims structure, and landscape positioning aims to inform legal and strategic decision-making for stakeholders operating within Singapore’s pharmaceutical IP environment.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.