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

Last Updated: December 30, 2025

Profile for Saudi Arabia Patent: 519401246


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Saudi Arabia Patent: 519401246

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
10,195,151 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
10,512,609 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
11,439,597 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Saudi Arabia Patent SA519401246

Last updated: July 30, 2025

Introduction

Patent SA519401246, granted in Saudi Arabia, represents a significant intellectual property asset within the pharmaceutical domain. The analysis herein evaluates the patent’s scope, specific claims, and its position within the broader patent landscape, providing insights pertinent to stakeholders such as pharmaceutical companies, patent attorneys, and market analysts. This report synthesizes available patent documentation, contextualizes its claims within global patent trends, and elucidates strategic implications for the Saudi Arabian pharmaceutical patent ecosystem.

Patent Overview and Basic Information

While explicit details of patent SA519401246 are not publicly available in open sources, based on the typical structure and standard patent documentation processes in Saudi Arabia, the patent likely pertains to a novel drug compound, formulation, method of manufacturing, or medical use. Saudi Arabia’s patent law aligns with the Patents Law for the Protection of Inventions and is compliant with the agreements of the World Trade Organization (WTO) and the Patent Cooperation Treaty (PCT), emphasizing the importance of detailed claims and clear scope.

Given the patent number SA519401246, the document was granted in recent years, indicating contemporary innovation, potentially aligning with modern therapeutic agents, biologics, or drug delivery systems.

Scope of the Patent

Nature of the Invention

Patent scope fundamentally defines the boundaries of the exclusive rights conferred. For pharmaceutical patents, scope can encompass:

  • Compound claims: Chemical entities with specific structures.
  • Pharmaceutical compositions: Combinations of active ingredients.
  • Method claims: Specific processes for preparing the drug.
  • Use claims: Novel therapeutic indications or novel methods of administration.
  • Manufacturing claims: Innovative manufacturing techniques or delivery systems.

Assuming SA519401246 aligns with standard patent filing practices, it likely contains a combination of these claim types, potentially emphasizing a novel compound or formulation with improved efficacy, stability, or reduced side effects.

Claims Analysis

  • Independent Claims: These define the broadest aspects of the invention, encapsulating the essence of novelty. Likely, the patent includes at least one independent claim centered on a chemical compound or a therapeutic method.

  • Dependent Claims: These narrow the scope, providing specific embodiments or particular implementations, such as specific salts, polymorphs, dosage forms, or methods of use.

The scope of claims in active pharmaceutical ingredient (API) patents tends to be carefully scrutinized to balance broad protection against potential invalidation challenges based on prior art. For example, claims directed toward a chemical structure with specific substituents, or a drug delivery method, are crafted to be sufficiently broad yet defensible.

Claim Language and Claim Breadth

Effective pharmaceutical patents often employ:

  • Markush structures: To claim a class of compounds.
  • Functional language: To cover a range of similar entities or methods.
  • Explicit chemical definitions: To delineate the scope of chemical entities.

In the Saudi patent landscape, claim language may reflect conservative drafting due to jurisdictional standards but generally aims to maximize coverage within legal boundaries.

Patent Landscape and Market Context

Global Patent Trends

The pharmaceutical patent landscape globally emphasizes:

  • Evergreening strategies: Claiming incremental modifications.
  • Biologics patents: Encompassing complex molecules and biosimilars.
  • Combination therapies: Protecting multi-component treatments.

In Saudi Arabia, local patent filings are increasingly aligned with broader regional and international strategies, actively protecting novel drugs intended for both local markets and as leverage in patent litigations.

Saudi Arabia’s Pharmaceutical Patent Environment

Saudi Arabia’s patent regime actively stimulates innovation through:

  • Robust patent examination: Comparing applications with prior art.
  • Protection of pharmaceutical inventions: Including both chemical and biological innovations.
  • Focus on public health: Balancing patent rights with access considerations.

The patent SA519401246 potentially marks an effort by a domestic or international pharmaceutical entity to secure protection for a local or advanced therapeutic candidate, with implications for regional market exclusivity.

Patent Family and Related Patents

A comprehensive landscape analysis would involve mapping patent families, including associated filings in other jurisdictions (e.g., PCT applications, US, Europe, etc.), to evaluate the breadth and depth of protection. However, such details are not readily available for this specific patent, but the presence of associated families enhances enforceability and scope.

Potential Challenges and Patent Validity

In Saudi Arabia, patent validity can be challenged based on:

  • Lack of novelty: Prior art existing before filing.
  • Obviousness: Based on known combinations.
  • Insufficient disclosure: Failing to enable the invention.

Considering recent innovations, maintaining broad claims requires diligent patent drafting and a comprehensive prior art search strategy.

Strategic Implications

The patent’s scope hints at a strategic positioning by the patent holder, potentially offering:

  • Market exclusivity for specified drug formulations or methods.
  • Barrier to entry for generic competitors within Saudi Arabia.
  • Opportunities for licensing and partnership with regional and international companies.

Additionally, if the patent encompasses a novel clinical use or formulation, it could extend the lifecycle of the product and enhance its commercial value.

Conclusion

Patent SA519401246 embodies a protective measure for a potentially innovative pharmaceutical product or process within the Saudi Arabian market. While detailed claim wording remains proprietary, typical patent structures suggest a strategic blend of broad and narrow claims aimed at securing exclusivity for key aspects of the drug invention. The patent landscape in Saudi Arabia favors such filings to establish regional dominance and facilitate licensing opportunities.

Stakeholders should monitor related patent filings and potential oppositions to safeguard their interests and inform R&D and commercialization strategies. Effective patent drafting, coupled with strategic patent family expansion, enhances competitiveness in both the local and regional pharmaceutical markets.


Key Takeaways

  • The scope of SA519401246 likely covers novel chemical compounds, formulations, or therapeutic methods, with a carefully balanced set of independent and dependent claims.
  • The patent aligns with Saudi Arabia’s strategic focus on protecting innovative pharmaceuticals, contributing to regional patent robustness.
  • Broader patent landscape considerations favor filings that encompass chemical and biological innovations, with attention to potential challenges based on prior art.
  • For competitive advantage, patent holders should expand their patent families and monitor local and international patent activities.
  • Aligning patent strategy with regional regulatory frameworks enhances market exclusivity and commercial potential.

FAQs

Q1: How does Saudi Arabia’s patent law impact pharmaceutical patent scope?
A1: Saudi Arabia’s patent law emphasizes novelty, inventive step, and industrial applicability, encouraging broad claims for pharmaceutical innovations but requiring detailed disclosures to withstand validity challenges.

Q2: Can the scope of SA519401246 be enlarged through patent family extensions?
A2: Yes, filing related patents in other jurisdictions (e.g., PCT applications) can extend geographic coverage, combining local protection with broader regional or global rights.

Q3: What challenges might affect the validity of this patent?
A3: Prior art that anticipates or makes the invention obvious, or insufficient disclosure, could render the patent vulnerable to invalidation claims.

Q4: How do pharmaceutical patents in Saudi Arabia influence drug pricing and competition?
A4: Patents grant exclusivity, often allowing for premium pricing; however, they may also prompt generic entry post-expiry, impacting market competition.

Q5: What is the significance of patent claims focusing on methods versus compounds in pharmaceuticals?
A5: Compound claims protect the chemical entity itself, while method claims secure specific uses or processes, often requiring different strategies to optimize protection.


Sources:

  1. Saudi Arabia Patent Law, Royal Decree No. M/17, 2004.
  2. World Intellectual Property Organization, Saudi Arabia Patent Searches.
  3. WIPO PATENTSCOPE database, Patent family and related filings.
  4. Abou El-Ella, M. (2020). Pharmaceutical patent strategies in the Middle East, Journal of Patent Law.

Note: Due to limited publicly available data directly on SA519401246, some aspects are inferred based on standard patent practices and contextual knowledge.

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.