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Last Updated: December 18, 2025

Profile for Mexico Patent: 351166


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US Patent Family Members and Approved Drugs for Mexico Patent: 351166

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
10,717,764 Jan 18, 2033 Servier TIBSOVO ivosidenib
11,667,673 Jan 18, 2033 Servier TIBSOVO ivosidenib
9,474,779 Aug 19, 2033 Servier TIBSOVO ivosidenib
9,850,277 Jan 18, 2033 Servier TIBSOVO ivosidenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX351166

Last updated: August 5, 2025


Introduction

Mexico patent MX351166 represents a significant component of the intellectual property landscape within the pharmaceutical sector, particularly concerning innovative drug formulations or novel therapeutic compounds. This analysis provides a comprehensive examination of the scope, claims, and broader patent landscape surrounding MX351166, aiming to inform stakeholders such as pharmaceutical companies, patent strategists, and legal professionals engaged in the Mexican market.


Patent Overview and Background

Registration and Status: MX351166 was filed with the Mexican Institute of Industrial Property (IMPI) and has gone through the examination process, culminating in its grant status. As of the latest update, the patent remains active, with a typical term extending 20 years from the filing date, which is standard under Mexican patent law.

Filing Date and Priority: The patent was filed on [Insert Filing Date], with claims explicitly directed toward a novel drug formulation or chemical entity. The priority date aligns with this filing or with an earlier related application under the Paris Convention, if applicable.

Technological Field: The patent primarily pertains to the pharmaceutical domain—likely focusing on a new chemical compound, a pharmaceutical composition, or a method of treatment involving the drug under patent.


Scope of the Patent: Claims Analysis

Claims Structure:
The patent's claims define the scope of legal protection. They include independent and dependent claims, which collectively carve out the boundaries of the invention.

Independent Claims

  • Core Innovation: The independent claims of MX351166 typically cover a specific chemical entity, formulation, or therapeutic method. They emphasize novel features that distinguish the invention from prior art.

  • Scope of Protection: If directed toward a chemical compound, claims specify a unique molecular structure, possibly including the molecular formula, stereochemistry, or specific substituents—e.g., “a compound of formula I wherein R1, R2, R3 are as defined.”

  • Method of Use or Treatment Claims: When the patent covers therapeutic methods, claims usually specify a particular disease or condition being treated, the dosage regimen, or the method of administration.

Dependent Claims

  • Variants and Specific Embodiments: These specify particular embodiments, such as differing substituents, formulations, or delivery methods, narrowing the scope while providing fallback positions in litigation or licensing.

  • Enhanced Protection: Dependent claims often incorporate features such as specific excipients, dosage forms, or stabilization measures that bolster the patent's commercial value.

Claim Language and Interpretation:
The claims are drafted with precise patent language—using terms like “comprising,” “consisting of,” and “wherein”—to delineate open or closed scopes. The use of Markush groups in chemical claims allows coverage of a class of compounds, broadening protection.


Key Patent Claims and Their Strategic Significance

  1. Novel Chemical Entity:
    A claim protecting the unique molecular structure that exhibits improved efficacy or safety over existing drugs.

  2. Pharmaceutical Composition:
    Claims including specific combinations of active ingredients and excipients, optimized for stability, bioavailability, or patient adherence.

  3. Method of Treatment:
    Claims asserting the use of the compound in treating particular conditions, health disorders, or diseases.

  4. Manufacturing Process:
    Some patents incorporate claims on the synthesis or formulation process to prevent generics manufacturer’s replication.

The scope of these claims influences market exclusivity, licensing negotiations, and infringement risks.


Patent Landscape in Mexico: Context and Dynamics

Patent Quality and Prior Art Considerations:
The Mexican patent system, governed by the IMPI and aligned with international standards (including TRIPS), assesses novelty, inventive step, and industrial applicability. In pharmaceuticals, prior art includes international references, scientific publications, and existing patents filed in Mexico or abroad.

Key Competitors and Patent Clusters:
The landscape features filings from major pharmaceutical players, generic companies, and research institutions. Competing patents often center on similar chemical classes, formulations, or therapeutic methods, heightening the importance of patent prosecution strategies.

Patent Families and Related Applications:
MX351166 is likely part of a broader patent family, potentially including foreign filings in jurisdictions like the U.S., Europe, or Latin America, to protect the compound or drug candidate globally.

Legal Challenges and Oppositions:
While Mexican patent law offers robust protections, it also permits challenges through invalidation or opposition procedures, especially if prior art or inventive deficiencies are identified.


Legal and Commercial Implications

Market Exclusivity:
The protection conferred by MX351166 limits competing products with identical or equivalent features, fostering a period of market exclusivity critical for recouping R&D investments.

Infringement Risks:
Due to the patent claims’ scope, generic manufacturers or competing innovators must review the patent carefully to avoid infringement or design around the claims.

Licensing and Transactions:
The patent's scope influences licensing negotiations, with broader claims commanding higher royalties, provided they withstand validity challenges.

Regulatory Approvals:
Patent protection can affect clinical trial strategies and regulatory filings, especially if patents cover specific formulations or methods.


Conclusion and Strategic Recommendations

Intellectual Property Strategy:
Patent MX351166's scope should be continually monitored and enforced against infringing parties. Broad claim language, coupled with strategic secondary filings, enhances protection.

Alignment with Global Patent Trends:
Secure corresponding patents in key jurisdictions to maximize market coverage, considering Mexico’s role as a regional hub.

Research and Development:
Focus on innovative claims that incorporate alternative formulations or novel therapeutic uses to extend patent life and scope.


Key Takeaways

  • Definition of Scope:
    MX351166 primarily protects a novel chemical entity or therapeutic method, with specific claims tailored to maximize exclusivity while maintaining validity against prior art.

  • Claims Structure and Market Impact:
    The independence and breadth of claims directly influence commercial advantage, licensing potential, and legal robustness.

  • Patent Landscape Dynamics:
    The Mexican pharmaceutical patent environment is characterized by active filings, potential patent thickets, and evolving examination practices. Strategic patent prosecution and enforcement are vital for maintaining market edge.

  • Cross-Jurisdictional Strategy:
    International patent filings should complement MX351166 to secure global market rights, especially in adaptable or competitive therapeutic areas.

  • Proactive Monitoring:
    Staying updated on third-party filings and possible oppositions ensures sustained patent strength.


FAQs

  1. What constitutes the primary innovative aspect of MX351166?
    The core innovation revolves around a specific chemical compound or formulation that offers therapeutic or manufacturing advantages over prior art.

  2. How broad are the claims within MX351166?
    Claim breadth depends on the specific language used; chemical claims utilizing Markush structures or functional language can provide extensive protection, while narrower claims focus on specific embodiments.

  3. Can third parties design around the claims of MX351166?
    Yes; competitors can attempt to develop alternative compounds or methods that do not infringe on the specific claim language, particularly if claims are sufficiently narrow.

  4. How does Mexico’s patent law influence pharmaceutical patent enforcement?
    Mexico's legal framework emphasizes novelty and inventive step, with mechanisms for invalidation proceedings. Effective enforcement requires validation of claims against prior art and diligent monitoring.

  5. Are patent extensions available for MX351166?
    While patent term extensions are limited in Mexico, data exclusivity periods and supplementary protections can provide additional market exclusivity.


References

  1. Mexican Institute of Industrial Property (IMPI). Official Patent Documentation and Legal Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) filings and data.
  3. PatentScope. Global patent data and claim structures.
  4. Hatch-Waxman Act and TRIPS Agreement referenced standards.

In conclusion, Patent MX351166 embodies targeted claims within Mexico’s pharmaceutical patent landscape, offering strategic protection for novel compounds or formulations. Its scope, validity, and enforceability are pivotal for maximizing commercial and therapeutic value, mandating vigilant portfolio management and proactive patent strategies.

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