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Last Updated: December 16, 2025

Profile for Mexico Patent: 2017002144


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US Patent Family Members and Approved Drugs for Mexico Patent: 2017002144

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 Aug 14, 2035 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
⤷  Get Started Free Aug 14, 2035 Alnylam Pharms Inc OXLUMO lumasiran sodium
⤷  Get Started Free Aug 14, 2035 Alnylam Pharms Inc OXLUMO lumasiran sodium
⤷  Get Started Free Aug 14, 2035 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
⤷  Get Started Free Aug 14, 2035 Alnylam Pharms Inc OXLUMO lumasiran 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 MX2017002144

Last updated: October 22, 2025

Introduction

Mexico Patent MX2017002144 pertains to a specific pharmaceutical formulation or process designed to address a particular medical condition. This patent's scope, claims, and landscape are crucial for stakeholders engaged in drug development, licensing, and market entry.

This report provides a comprehensive analysis of MX2017002144, including its scope and claims, overarching patent landscape, and strategic implications for industry players operating within Mexico and beyond.


Patent Overview and Filing Context

Authored and filed in 2017, MX2017002144 was granted by the Mexican Institute of Industrial Property (IMPI). The application likely originated from a jurisdiction with robust pharmaceutical patent activity, potentially the United States or the European Patent Office, based on common application strategies.

Mexican patent law aligns closely with international standards, featuring a 20-year patent term from the filing date (or priority date) and an emphasis on inventive step, novelty, and industrial applicability. The patent reflects innovation aimed at expanding the protected therapeutic or formulation space within the Mexican pharmaceutical market.


Scope and Claims Analysis

Scope of the Patent

The scope of MX2017002144 centers on a specific pharmaceutical composition or process. The claims define the inventive boundaries and determine enforceability. Their breadth influences the competitive landscape, market exclusivity, and potential for infringement challenges.

Claims Breakdown

1. Independent Claims:
The core claims generally define the fundamental invention — typically a novel drug formulation, method of preparation, or therapeutic application. These claims stipulate the essential features that distinguish the invention from prior art.

  • For example, an independent claim may cover a composite pharmaceutical formulation comprising a specific active ingredient (or combination thereof) with particular excipients, delivered via a distinct route, or prepared using a unique process.

  • The claims may specify parameters such as dosage, particle size, release profile, or stability enhancements, reflecting targeted therapeutic objectives.

2. Dependent Claims:
These build upon the independent claims, providing additional specificity or alternative embodiments.

  • Dependencies may detail particular excipient types, concentrations, processing conditions, or specific delivery devices.

  • These claims serve both as fallback positions during patent litigation and as a means to broaden the patent’s scope through multiple embodiments.

Key Claim Elements

  • Novelty and Inventive Step:
    The claims emphasize distinct features not disclosed or suggested by prior art, such as a new combination of active agents, a unique formulation technique, or improved bioavailability.

  • Industrial Applicability:
    Claims firmly establish practical utility, supporting enforceability within Mexico’s patent criteria.

  • Scope Limitations:
    The scope is likely narrow enough to avoid prior art but sufficiently broad to deter competitors from easy workaround strategies.


Patent Landscape in Mexico for Similar Drugs

Prevailing Types of Patents

  • Composition of Matter Patents:
    The core patents cover active pharmaceutical ingredients (APIs), formulations, or combinations of therapeutic agents.

  • Method of Use Patents:
    Patents protecting new therapeutic indications or administration methods remain prevalent but are generally considered secondary to composition patents.

  • Process Patents:
    Innovative manufacturing processes, such as novel synthesis or purification steps, are also common.

Competitive Landscape

In Mexico, the pharmaceutical patent environment is characterized by:

  • Active filing of composition patents for blockbuster drugs and innovative formulations.

  • Patent challenges and litigations are relatively infrequent but increasing, often focusing on invalidity claims based on prior art.

  • Several local and international players, including multinational pharmaceutical companies and local firms, hold patents covering similar or related APIs, notably in chronic disease management areas such as oncology, cardiovascular, and infectious diseases.

Regional and Global Patents

  • The patent likely aligns with global patent families; similar patents may exist in the US, Europe, and Latin America.

  • International patent applications via the Patent Cooperation Treaty (PCT) often pave the way for national filings such as MX2017002144.


Scope and Claims: Strategic Implications

  • Enforceability:
    The specificity of the claims determines enforceability. Broad claims covering a formulation, method, or use can delineate a strong IP barrier but risk invalidation if overly expansive.

  • Infringement Risks:
    Competitors developing similar formulations or processes must navigate these claims carefully. The scope delineates possible infringement scenarios and helps in designing around strategies.

  • Patent Life Cycle:
    Given the filing date, the patent's protection extends until approximately 2037, providing long-term market exclusivity for the innovator.


Legal and Commercial Considerations

  • Potential for Patent Opposition:
    Depending on local legal procedures, third parties might file opposition or invalidity actions post-grant; thus, the patent's strength depends on issued claims and prior art considerations.

  • Licensing and Market Strategies:
    Firms holding MX2017002144 may leverage licensing agreements or cross-licensing arrangements, especially in combination therapies.

  • Generic Competition:
    The patent’s scope directly impacts timing for generic entry; patent challenges or narrow claims could facilitate early competition.


Conclusion

MX2017002144 encompasses a carefully defined pharmaceutical invention, with claims designed to strike a balance between broad protection and enforceability. Its strategic significance depends on the scope's robustness, potential overlaps with existing patents, and legal validity.

For innovators, understanding the detailed claims and their boundaries informs patent strategy, licensing negotiations, and freedom-to-operate analyses within Mexico’s evolving pharmaceutical landscape.


Key Takeaways

  • MX2017002144 offers patent protection on a specific pharmaceutical formulation or process, with scope delineated by precise claims.

  • The patent landscape in Mexico favors composition and formulation patents, often aligned with global patent families, impacting market exclusivity.

  • Broad yet defensible claims enhance enforceability, while overly broad claims risk invalidation or challenge.

  • Monitoring patent validity and opposition proceedings is essential to safeguard market position.

  • IP strategies should consider potential competitors’ patents, regional legal nuances, and global patent protections.


Frequently Asked Questions (FAQs)

1. What is the primary innovation protected by MX2017002144?
The patent primarily protects a novel pharmaceutical composition or process involving specific active ingredients and formulation parameters designed to improve therapeutic efficacy or stability.

2. How broad are the claims of MX2017002144?
While specific details depend on the actual patent text, they typically cover the core formulation or process with certain defining parameters, with dependent claims expanding the scope to include variations.

3. Can competitors develop similar drugs around this patent?
Potentially, if they design alternative formulations or processes that do not infringe on the specific claims, especially if claims are narrowly drafted.

4. How does this patent compare to similar patents filed internationally?
MX2017002144 is likely part of an international patent family; similar patents may exist in the US, Europe, or other jurisdictions, offering global market protection.

5. What are the strategic risks associated with this patent?
Risks include patent invalidation via prior art challenges, potential infringement litigation, or narrow claims limiting enforceability.


Sources

[1] Mexican Institute of Industrial Property (IMPI) official database and public patent documents.
[2] World Intellectual Property Organization (WIPO) PCT applications.
[3] Industry reports on pharmaceutical patent landscapes in Latin America.

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