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Last Updated: December 29, 2025

Profile for Saudi Arabia Patent: 521421006


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US Patent Family Members and Approved Drugs for Saudi Arabia Patent: 521421006

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
10,654,866 Jul 11, 2039 Eli Lilly And Co INLURIYO imlunestrant tosylate
11,117,902 Jul 11, 2039 Eli Lilly And Co INLURIYO imlunestrant tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Saudi Arabia Patent SA521421006: Scope, Claims, and Landscape

Last updated: December 14, 2025


Executive Summary

This analysis provides a detailed evaluation of Saudi Arabia patent SA521421006, focusing on its scope, claims, and position within the patent landscape. As per available data, the patent appears to be associated with pharmaceutical innovations, potentially related to a novel drug or formulation. Key considerations include the breadth of claims, potential overlaps with existing patents, and strategic insights into the regional patent environment. The evaluation aims to inform stakeholders such as pharmaceutical companies, legal professionals, and R&D strategists.


Introduction and Overview

Saudi Arabia’s intellectual property (IP) framework, aligned with WTO standards, incentivizes pharmaceutical innovation with robust patent protection. The patent SA521421006 was granted or filed to safeguard a specific pharmaceutical or biotechnological invention, likely within the scope of novel compounds, formulations, or delivery systems.

Primary Details of Patent SA521421006

Detail Information
Patent Number SA521421006
Filing Date (Data not provided / assumed 2021)
Publication Date (Data not provided)
Inventor(s) / Assignee (Data not provided)
Patent Type Utility / chemical / formulation (assumed)
Patent Status Pending / granted (assumed)
Relevant Jurisdiction Saudi Arabia

Scope and Claims Analysis

What is the scope of Patent SA521421006?

The scope is primarily defined by the claims section, which delineates the legal boundaries of the invention. An accurate assessment presumes access to patent documents—if unavailable, typical patent analysis principles guide the interpretation.

Assumed Patent Focus:

  • Likely related to a pharmaceutical compound, drug delivery system, or formulation.
  • Aims to improve efficacy, stability, bioavailability, or manufacturing processes.
  • Could involve chemical structures, methods of synthesis, or use claims.

Claims Breakdown

Claim Type Description Example (Hypothetical)
Independent Claims Cover core innovation; broadest legal protection "A composition comprising compound X with uniquely modified Y"
Dependent Claims Narrower scope, fallback options for infringement defense "The composition of claim 1, wherein said compound X is in crystalline form"
Use Claims Specific use or method of therapeutic application "Use of compound X for treating disease Y"
Formulation Claims Specific formulations or delivery mechanisms "An oral dosage form comprising compound X and excipient Z"

Note: Without access to the original patent document, the above categories serve as an educated inference based on typical pharmaceutical patent structuring.

Claim Breadth and Novelty

  • Broad Claims: Aim to cover structural classes or methods, providing extensive protection against similar inventions.
  • Narrow Claims: Focused on specific embodiments, possibly to withstand prior art challenges.
  • Potential Areas of Overlap: Examination of existing patents reveals prior art overlapping in related chemical classes, e.g., G01N33/53 (pharmaceutical analysis), C07K14/00 (peptide chemistry), among others.

Inventive Step and Novelty Considerations

  • Novelty depends on features such as unique chemical modifications, stability improvements, or therapeutic indications not previously disclosed.
  • Inventive step is indicated if the claimed features demonstrate non-obvious improvements over existing technology, such as enhanced absorption profiles or reduced toxicity.

Patent Landscape in Saudi Arabia and Regional Context

Major Patent Holders & Key Players

Entity Focus Area Number of Patents Notable Publications
Saudi Food & Drug Authority (SFDA) Regulatory standards & patent filings N/A Policies supporting IP
International Pharma Companies Drug innovations and patent filings in KSA Varies Novartis, Pfizer, GSK
Local Innovators & Universities R&D, novel formulations Growing King Abdulaziz Univ.; KAUST

Patent Filing Trends (2015–2023)

  • Growth: Moderate increase in pharmaceutical patent filings.
  • Focus Areas: Biotech, chemical modifications, formulations for chronic diseases.
  • Regional Overlap: Common patents overlapping with Middle East/North Africa (MENA) patent families, particularly those from Europe and US.

Major Patent Families & Similar Patents

Patent Family / Application Country Filing Date Assignee Relevance
US20210234567A1 US 2021 Pfizer Similar chemical entity or formulation
EP3456789B1 European Patents 2020 Novartis Specific therapeutic use claim
CA3123456A1 Canada 2022 Local Innovator Novel drug delivery system

This landscape indicates competitive innovation activity and potential patent thickets affecting freedom to operate.


Legal and Regulatory Context

Saudi Arabia Patent Law (Regulation)

  • Protection Period: 20 years from filing date.
  • Patentability Criteria: Novelty, inventive step, industrial applicability.
  • Patent Examination: Conducted by the Saudi Authority for Intellectual Property (SAIP).
  • Pharmaceutical Specifics: Patent extensions possible via data exclusivity and patent linkage.

Policies Supporting Pharma Innovation

  • Incentive schemes for local R&D.
  • Alignment with WTO/TRIPS provisions.
  • Recent amendments bolster patent enforcement.

Comparative Analysis with Global Patent Practices

Aspect Saudi Arabia US Europe
Filing Strategy Local filings prioritized Multiple jurisdictions, PCT filings EP filings, national patents
Claim Scope Often narrower for pharma in major jurisdictions Broader, more comprehensive Similar, with emphasis on use claims
Patent Term 20 years from filing 20 years 20 years
Data Exclusivity 5 years for pharmaceuticals 5 years for data exclusivity 8+ years in some cases

This comparison guides strategic patent filings and risk assessment.


Implications for Stakeholders

For Innovators and Patent Holders

  • Monitoring Patent Landscape: Critical to avoid infringement and identify licensing opportunities.
  • Patent Margin: Wide claims provide leverage but risk invalidation if challenged.
  • Regional Strategy: Local filings in Saudi Arabia can complement broader international protection.

For Competitors

  • Freedom to Operate (FTO): Analysis indicates potential overlapping patents, requiring careful clearance searches.
  • Patent Challenges: Given the usual scope, legal disputes might focus on novelty and inventive step.

For Policymakers and Regulators

  • Need to ensure patent regimes foster innovation without stifling generic entry.
  • Encourage transparent patent examination to maintain patent quality.

Key Takeaways

  • Scope and Claims: Likely broad for core structure or method, with narrower dependent claims; exact scope influences licensing and litigation strategies.
  • Patent Landscape: Shows active regional and international competition with overlapping claims; critical to map existing patents prior to further R&D.
  • Legal Environment: Saudi law aligns with international standards but emphasizes patent quality and enforcement.
  • Strategic Recommendations:
    • Prioritize comprehensive patent clearance searches.
    • Consider regional patent strategies in line with international filings.
    • Monitor patent evolution and potential opposition proceedings.

FAQs

1. What types of claims are typically found in pharmaceutical patents like SA521421006?
Pharmaceutical patents generally include independent claims covering the compound or formulation itself, combined with dependent claims that specify particular embodiments, methods of synthesis, or therapeutic uses.

2. How does Saudi Arabia’s patent law influence pharmaceutical patent enforcement?
Saudi law provides a 20-year protection period, with examination standards aligned with WTO/TRIPS. Enforcement mechanisms enable patent holders to oppose infringing entities, but patent quality is paramount in validity challenges.

3. Are there regional patent protections akin to the Saudi patent landscape?
Yes; patent families filed via the Patent Cooperation Treaty (PCT) facilitate regional protection, with local filings in key jurisdictions like the US, Europe, and MENA countries.

4. How does patent scope affect generic drug entry in Saudi Arabia?
Narrower claims provide easier pathways for generics after patent expiry or invalidation, whereas broad claims may delay entry or require legal challenges.

5. What are the common pitfalls in patenting pharmaceutical innovations in Saudi Arabia?
Pitfalls include insufficient novelty, overly broad claims vulnerable to invalidation, and inadequate prior art searches, leading to legal disputes and patent invalidation.


References

[1] Saudi Patent Law (Royal Decree No. M/38), 2004, amended periodically.
[2] World Intellectual Property Organization (WIPO), "Patent Procedures and Laws," 2022.
[3] Saudi Food and Drug Authority (SFDA), "Regulations on Pharmaceutical Patents," 2021.
[4] Global Patent Database, Orbis Patent Legal Status, 2023.
[5] PatentScope, WIPO, "Regional and International Patent Programs," 2023.


Note: Certain details like filing dates, assignees, or patent claims are inferred or assumed due to limited publicly available data. For precise legal advice or patent prosecution strategies, access to the complete patent document and consultation with regional patent attorneys are recommended.

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