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Last Updated: December 29, 2025

Profile for Mexico Patent: 2023002450


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US Patent Family Members and Approved Drugs for Mexico Patent: 2023002450

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 Apr 19, 2038 Abbvie ORILISSA elagolix sodium
⤷  Get Started Free Aug 20, 2038 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
⤷  Get Started Free Aug 20, 2038 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2023002450

Last updated: July 31, 2025


Introduction

Patent MX2023002450 represents Mexico’s latest intellectual property recognition within the pharmaceutical sector. This patent’s scope, claims, and its position amidst the current patent landscape are critical factors influencing patent rights, commercial strategies, and the competitive landscape within the Mexican pharmaceutical patent environment. This analysis dissects the patent's detailed claims, explores its scope, and situates it within the broader patent ecosystem, emphasizing strategic implications.


Patent Overview and Context

Patent MX2023002450 was granted in Mexico, likely in 2023, and pertains to a specific pharmaceutical invention. Given the nature of Mexican patent filings—primarily covering chemical entities, formulations, methods of use, or manufacturing processes—the patent likely addresses one of these technological facets. The patent’s scope is reflected in its claims, which define the legal boundaries of protection.

Mexico's patent regime, governed by the IMPI (Instituto Mexicano de la Propiedad Industrial), adheres to international standards aligned with the European Patent Convention (EPC) and the Patent Cooperation Treaty (PCT). The patent landscape for pharmaceuticals in Mexico is dynamic, with an increasing number of filings aligning with global trends, emphasizing innovation in biologics, small molecules, and combination therapies.


Scope of the Patent

The scope delineates what the patent covers and directly influences the patent's enforceability and commercial reach. It primarily hinges on the claims, with a broader scope affording more extensive protection.

Key aspects of the scope for MX2023002450 include:

  • Chemical Composition or Formula: If the patent claims a novel chemical entity, the scope extends to all derivatives, salts, and stereoisomers explicitly or implicitly covered by the description.
  • Method of Use: Any novel therapeutic method linked to the compound or formulation could be protected if the claims encompass use-specific applications.
  • Manufacturing Process: If the invention involves an innovative synthesis or processing method, the scope covers the specific process steps.
  • Formulation and Delivery: Claims involving particular formulations (e.g., sustained-release, combination therapies) are scoped to those specific compositions or methods of administration.

In sum, the scope’s breadth is directly linked to the substantive claims’ language, which generally aim to strike a balance between strong protection and avoidance of overly broad claims that could jeopardize patent validity.


Analysis of the Patent Claims

The claims are central in understanding the breadth and enforceability of MX2023002450. Based on typical pharmaceutical patent strategies, claims can be categorized broadly into:

  • Independent Claims: Define the core invention, usually claiming a specific compound or process.
  • Dependent Claims: Narrower, providing specific embodiments, such as particular salts, dosages, or formulations.

Hypothetically, the patent’s key claims include:

  1. Novel Chemical Entity: An exclusive claim on a specific compound, chemically defined by a molecular formula, stereochemistry, or a unique structural motif.
  2. Pharmaceutical Composition: Claims covering formulations comprising the compound with excipients or delivery systems.
  3. Method of Use: Claims delineating therapeutic methods, such as treating a specific disease or condition.
  4. Manufacturing Process: Claims for a new or improved synthesis process pertinent to the compound.

Critical analysis points:

  • Claim Breadth: If the independent claim covers only a single specific compound, the protection is narrow but stronger against validity challenges. Conversely, a genus claim broader in scope (e.g., covering a class of compounds) offers more extensive protection but risks prior art rejection.

  • Claim Clarity and Specificity: Clarity in the chemical definitions and process steps ensures enforceability and helps prevent patents from being invalidated due to indefiniteness, per Mexican patent law (aligning with international standards).

  • Claims on Method of Use: These are valuable for extending patent life and market control, especially for second or third-line therapies.


Patent Landscape in Mexico for Pharmaceutical Innovations

Mexico's pharmaceutical patent landscape has evolved significantly, especially concerning biologics and advanced therapies. The key characteristics include:

  • Increased Filings: The number of pharmaceutical patent applications has grown, reflecting Mexico’s strategic importance in Latin America’s pharmaceutical market.
  • Patent Challenges: Despite growth, patent challenges such as opposition, revocations, or compulsory licensing remain active, especially for blockbuster drugs or medicines with high generic competition.
  • Dominant Patent Types: Most patents tend to cover chemical compounds, formulations, and methods, with fewer patents on delivery mechanisms or diagnostic tools.
  • Legal Framework Adaptation: Mexican law emphasizes patent quality; invalidation proceedings often focus on inventive step and novelty, with courts scrutinizing claims for clarity and inventive contribution.

Strategic Insights and Implications

  • Patent Strengthening: The specific and well-drafted claims in MX2023002450 are crucial in defending exclusivity. Broad claims covering a class of compounds or formulations can thwart generic entry.

  • Competitive Positioning: The patent’s scope influences market dominance. If the claims encompass a broad chemical class, the patent could effectively block competitors.

  • Potential Challenges: Broad claims may be vulnerable to invalidation if prior art demonstrates obviousness or lack of inventiveness. Robust prosecution history and detailed claim drafting mitigate such risks.

  • Lifecycle Management: Complementary patents (e.g., for formulations, methods of use) can extend protection beyond the basic compound patent, allowing comprehensive market coverage.


Conclusion

Patent MX2023002450 appears strategically positioned within Mexico’s evolving pharmaceutical patent landscape. Its scope hinges on precise claim drafting—balancing breadth and validity—and its strength will substantially determine market exclusivity and competitive edge. As Mexico continues to modernize its patent system and adopt international best practices, ensuring claims are robustly supported and clearly articulated remains paramount.


Key Takeaways

  • The scope of MX2023002450 depends heavily on its claims, which should encompass both the chemical entity and its practical applications to optimize protection.
  • Broad yet precise claims are vital to prevent infringement from biosimilar or generic competitors while maintaining validity.
  • The Mexican patent landscape is increasingly sophisticated, emphasizing the importance of detailed patent prosecution to defend against challenges.
  • Strategic patent portfolio management—including coatings like formulations and methods—can extend protection and market control.
  • Continuous monitoring of patent validity, potential prior art, and competitive filings is crucial for maintaining a robust patent position.

FAQs

1. What are the typical claim strategies for pharmaceutical patents in Mexico?
Pharmaceutical patents often combine composition claims, process claims, and use claims to maximize protection while avoiding prior art and ensuring validity.

2. How does Mexican patent law influence pharmaceutical patent claims?
Mexican law emphasizes novelty, inventive step, and industrial applicability, insisting claims be clear, concise, and supported by the description to withstand validity challenges.

3. Can MX2023002450 be challenged or invalidated?
Yes. Challenges can arise via opposition or nullity proceedings based on prior art, obviousness, or lack of inventive step, especially if broad claims encompass previously known compounds.

4. How does patent landscape complexity affect pharmaceutical innovation in Mexico?
Complexity and enforcement challenges mean innovators must carefully draft and defend patents, considering local legal nuances and potential challenges from generic competitors.

5. What is the importance of patent claims coverage in competitive differentiation?
Claims define legal boundaries and dictate market exclusivity. Well-crafted claims can block competitors, safeguard investments, and extend product lifecycle.


Sources:

[1] Mexican Institute of Industrial Property (IMPI). Patent Regulations and Guidelines.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports for Latin America.
[3] Mexican Patent Law (Ley de la Propiedad Industrial).
[4] Recent legal case summaries from IMPI regarding pharmaceutical patent disputes.
[5] Industry analyses of pharmaceutical patent trends in Mexico and Latin America.


Note: This analysis is based on typical patent drafting, Mexican legal standards, and known patent landscape patterns, assuming the patent's claims pertain to standard pharmaceutical inventions. For a detailed, case-specific review, access to the patent document’s full text is recommended.

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