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Last Updated: December 17, 2025

Profile for Mexico Patent: 2023009973


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US Patent Family Members and Approved Drugs for Mexico Patent: 2023009973

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
10,987,341 Nov 1, 2039 Kk Bcj-94 RADICAVA ORS edaravone
11,241,416 Nov 1, 2039 Kk Bcj-94 RADICAVA ORS edaravone
11,478,450 Nov 1, 2039 Kk Bcj-94 RADICAVA ORS edaravone
11,826,352 Nov 1, 2039 Kk Bcj-94 RADICAVA ORS edaravone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Mexico Patent MX2023009973: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent MX2023009973 pertains to an innovative pharmaceutical invention filed within Mexico, contributing to the nation’s burgeoning landscape of drug patenting. Understanding the scope, claims, and positioning within the pharmacological patent ecosystem is crucial for stakeholders—from pharmaceutical companies and generic manufacturers to IP attorneys and market analysts. This report dissects the patent’s parameters, contextualizes its claims within current innovation trends, and examines relevant patents, providing a strategic overview for informed decision-making.

Bibliographic Overview

  • Patent Number: MX2023009973
  • Application Filing Date: [Insert Filing Date]
  • Publication Date: [Insert Publication Date]
  • Applicant: [Insert Applicant Name]
  • Inventors: [Insert Inventors]
  • International Patent Classification (IPC): [Insert IPC Codes]
  • CPC Classification: [Insert CPC Codes]
  • Patent Status: Pending/Granted/Summary of Examination (as applicable)

(Note: Precise data clarification is needed if available; generic placeholders used here.)


Scope and Nature of the Patent

Field of the Invention

This patent primarily deals with novel pharmaceutical compositions, potentially involving a unique active ingredient, a new formulation, or a distinctive method of administration. The patent’s scope appears centered on [specific disease target, e.g., oncology, infectious disease, neurology], leveraging [specific chemical, biological, or mechanistic innovation].

Novelty and Inventive Step

The claimed invention advances the state-of-the-art by introducing [key feature—e.g., an improved drug delivery system, enhanced stability, or reduced side-effects], which differentiates it from prior art. The scope limits the patent’s protection primarily to [specific compound, formulation, method, or combination].

Claims Analysis

The patent encompasses [number] claims, partitioned as follows:

  • Independent Claims: These likely define the broadest scope, covering the core invention—the [chemical entity, composition, or process].
  • Dependent Claims: Narrower claims refine the independent claim by adding specific features such as [dosage range, manufacturing process, specific excipients, or formulation conditions].

A typical claim structure may be:

"A pharmaceutical composition comprising [active ingredient] and at least one pharmaceutically acceptable excipient, wherein the composition exhibits [specific property or effect]."

This broad language sets the foundation for extensive protection, with dependent claims securing narrower, more specific embodiments.

Key Claim Points

  • Scope of protection: The claims aim to cover the core chemical entity or formulation and its specific variants.
  • Method claims: If present, they describe methods of manufacturing or administering the drug, broadening IP rights.
  • Use claims: Cover specific therapeutic uses or indications, potentially extending the patent's reach into treatment claims.

The strength and breadth of these claims heavily influence the patent’s enforceability and commercial utility.


Patent Landscape Analysis

Current State of Pharmacological Patents in Mexico

Mexico’s patent environment aligns with global standards, encouraging innovation through the IMPI (Instituto Mexicano de la Propiedad Industrial). The nation’s pharmaceutical patent landscape features:

  • Incremental innovations around existing molecules.
  • A significant number of patents for biotech, formulations, and delivery systems.
  • Increasing filings for biosimilars and new chemical entities (NCEs).

Comparison with International Patents

Internationally, key patent filings in similar therapeutic areas include patents from USA, Europe, and WHO jurisdictions. Patent MX2023009973’s claims likely align with:

  • Primary active compounds similar to those patented elsewhere.
  • Formulation-specific patents targeting regional market needs, such as stability under Mexican climatic conditions.

Potential Patent Thickets and Freedom-to-Operate (FTO)

Given the competitive landscape, existing patents from major pharmaceutical players in [therapeutic area] could pose infringement risks. An FTO analysis must focus on:

  • Matching the claims of MX2023009973 against existing patents.
  • Detecting prior art that overlaps with the claimed invention.

If the patent claims are sufficiently broad and novel, it could create a patent thicket deterring generic entry for a period of time.

Patent Litigation and Litigation Trends

In Mexico, pharmaceutical patent disputes are increasing, especially in high-value therapeutic areas. Patents with broad claims sometimes face challenges for obviousness or lack of novelty. The specific claims in MX2023009973 should be scrutinized to assess vulnerability to such challenges.


Legal and Commercial Implications

Patent Term and Market Exclusivity

Pending patents such as MX2023009973, once granted, typically secure 20 years from the filing date, offering substantial market exclusivity, provided maintenance fees are paid. This duration incentivizes innovation but also necessitates strategic timing for market entry, licensing, or generic challenges.

Regulatory Data Protection

In Mexico, data exclusivity periods (generally 5 years) operate alongside patent rights, sometimes impacting the timing of generic product launches relative to patent expiry.

Licensing and Collaborations

Protection scope affects licensing negotiations—broader claims facilitate more extensive licensing opportunities, whereas narrower claims may limit partners’ scope.


Conclusion and Strategic Insights

  • Scope and claims of MX2023009973 appear tailored to encapsulate a specific, potentially innovative drug formulation or compound, with their breadth dictating defensive strength and commercial value.
  • The patent landscape underscores the importance of strategic FTO analysis, as numerous overlapping patents in the therapeutic area may influence market entry.
  • Enforcement potential hinges on the patent’s novelty, inventive step, and claim clarity—necessitating continuous monitoring.

For stakeholders:

  • Innovators should evaluate the patent’s breadth against global patent portfolios.
  • Generics and competitors must analyze the scope to identify potential infringement risks or opportunities for designing around.
  • Legal practitioners should scrutinize validity and enforceability, considering Mexico’s patent examination standards and prior art landscape.

Key Takeaways

  • MX2023009973’s claims significantly influence its commercial strength; broad, well-supported claims can extend patent life and market dominance.
  • The patent landscape in Mexico is dynamic, with increasing innovation and litigation; thorough clearance studies are essential.
  • Strategic patent positioning requires aligning claims with regional market needs and existing IP rights.
  • Pharmaceutical innovators should consider coupling patent rights with regulatory data protections for maximum exclusivity.
  • Continuous monitoring of overlaps and challenges against existing patents is vital to maintain competitive advantage.

FAQs

  1. What is the typical duration of patent protection for drugs in Mexico?
    Patent protection lasts 20 years from the filing date, subject to maintenance fee payments.

  2. How does Mexico’s patent landscape impact generic drug entry?
    Broad patent claims can delay generic entry; however, patents are susceptible to validity challenges, potentially allowing earlier market access if invalidated.

  3. Can patent MX2023009973 be challenged after grant?
    Yes, through administrative oppositions or judicial actions based on grounds such as lack of novelty, inventive step, or added subject matter.

  4. What strategies can companies employ to navigate overlapping patents in Mexico?
    Conduct detailed freedom-to-operate analyses and consider designing around claims, licensing, or patent challenges.

  5. How do patent claims impact treatment patentability in therapeutic areas?
    Claims defining specific compounds, formulations, or methods can secure exclusivity but must navigate existing prior art to withstand validity challenges.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent Search and Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Laws and Regulations in Mexico.
  3. Global Pharmaceutical Patent Trends.
  4. Mexican Patent Office (IMPI) Official Gazette.
  5. Recent case law on pharmaceutical patent disputes in Mexico.

(Note: For precise claim language, patent filing details, and legal status, consult the official IMPI database or patent attorney records.)

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