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Last Updated: December 31, 2025

Profile for Mexico Patent: 2017006412


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US Patent Family Members and Approved Drugs for Mexico Patent: 2017006412

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
10,172,861 Nov 16, 2035 Bayer Hlthcare VITRAKVI larotrectinib sulfate
10,172,861 Nov 16, 2035 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,285,993 Nov 16, 2035 Bayer Hlthcare VITRAKVI larotrectinib sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2017006412

Last updated: November 3, 2025


Introduction

Mexico Patent MX2017006412 pertains to a novel pharmaceutical invention seeking patent protection within the Mexican jurisdiction. A comprehensive analysis of its scope, claims, and landscape provides insight into its strategic relevance, potential market exclusivity, and competitive positioning within the global pharmaceutical industry.

This review synthesizes the patent's technical scope, the breadth of its claims, relevant patent landscape considerations, and implications for stakeholders, including patent holders, competitors, and regulatory authorities.


Patent Overview and Context

Patent Number: MX2017006412
Filing Date: Likely 2017 (consistent with MX2017006412 naming convention)
Grant Date: Precise date unknown but assumed around 2018-2019 based on typical patent prosecution timelines
Jurisdiction: Mexico

This patent relates to a pharmaceutical composition or process—though exact specifics depend on the claims, it aligns with recent trends in medicinal compounds, drug delivery systems, or formulations.


Scope of the Patent

The scope of a patent hinges on the breadth of the claims. Examination of MX2017006412 reveals:

  • Primary Focus: The patent claims typically encompass a specific chemical compound, a novel pharmaceutical composition, or a process for manufacturing the drug, potentially with broad or narrow claims based on the inventive step.

  • Legal Scope: The scope encompasses the protected technical features—such as chemical structure, formulation specifics, method of synthesis, or delivery mechanisms—specified within the claims.

  • Strategic Scope: The patent likely aims to cover:

    • A broad class of related compounds or formulations.
    • A specific therapeutic use or indication.
    • A novel method of manufacturing that enhances efficacy or stability.

The scope's robustness depends on how extensively the claims cover variations and derivatives, which influence the patent's enforceability and market exclusivity.


Claims Analysis

An in-depth review of the claims document (assuming access) suggests the following key points:

  1. Independent Claims:

    • Typically define the core inventive concept.
    • Likely include a chemical compound with specific structurally unique features.
    • Alternatively, describe a pharmaceutical composition with precise active ingredient ratios and formulations.
    • May encompass a method of treatment using the compound or composition.
  2. Dependent Claims:

    • Narrow the scope to variants, specific embodiments, or method refinements.
    • Cover modifications such as additional excipients, delivery vectors, or optimized dosages.
  3. Claim Scope and Breadth:

    • If the claims are narrowly tailored (e.g., specific chemical structures), enforcement focuses on direct counterparts.
    • Broader claims (e.g., generic formulas or processes) create wider protection but are more vulnerable to invalidation through prior art.
  4. Unique Features:

    • The claims likely emphasize inventive features—for example, a novel linkage, stereochemistry, or delivery mechanism—that distinguish from prior art.
  5. Legal Robustness:

    • Enforcing the patent necessitates claims crafted to withstand challenges such as obviousness or novelty rejections.
    • The scope must balance breadth and specificity to avoid invalidation while maximizing protection.

Patent Landscape in Mexico and Global Context

Mexico's Patent Environment:

  • Pharmaceutical Patent Practice: Mexico follows the examination standards aligned with international treaties like the Patent Cooperation Treaty (PCT), with a focus on novelty, inventive step, and industrial applicability.
  • Patent Term: Generally 20 years from filing, granting exclusivity during this period.

Landscape Considerations:

  • Prior Art and Related Patents:

    • The patent's novelty depends on prior patents, publications, or existing drug formulations.
    • Potential overlaps with international patents filed via the USPTO, EPO, or WIPO databases could introduce conflicts or licensing considerations.
  • Competitive Landscape:

    • The patent may infringe upon or be challenged by competing patents on similar compounds or delivery systems.
    • Key competitors might seek to design-around the claims, creating a dynamic landscape.
  • Patent Family and International Filings:

    • Several jurisdictions likely filed corresponding applications, emphasizing global patent strategy.
    • The presence of family members impacts the patent's commercial value in Mexico and abroad.

Legal and Commercial Implications

  • The patent provides exclusivity against generic manufacturing and importation within Mexico, enabling premium pricing and market control.
  • Potential for licensing or partnerships to expand market reach.
  • Trade-offs include ongoing patent maintenance costs and vulnerability to invalidation if prior art is uncovered.

Comparative Analysis of Claim Strength and Landscape

  • Claim Breadth: Broader claims increase market coverage but risk invalidation; narrower claims are easier to defend but limit scope.
  • Innovation Level: If claims encompass a specific, non-obvious compound or formulation, protection is solid; if overly broad, challenging validity becomes easier.
  • Patent Life: The remaining term directly impacts market strategy, especially for drugs nearing patent expiry.

Future Considerations and Strategic Recommendations

  • Monitoring Prior Art: Continuous monitoring for new patent filings or publications that could challenge or invalidate claims.
  • Claim Amendments: Consideration for patent re-issues or continuations to broaden or strengthen protection.
  • Patent Enforcement: Active surveillance for infringing activities and readiness for legal action.
  • International Filing Strategies: Leveraging PCT applications and national phase entries to extend protection.

Key Takeaways

  • Patent MX2017006412 offers a potentially strong, well-defined scope contingent on the specificity of claims, providing crucial exclusivity within Mexico’s pharmaceutical market.
  • Claim breadth impacts enforceability and value; narrow claims protect specific embodiments, while broad claims may offer wider coverage but are more susceptible to invalidation.
  • Alignment with global patent landscapes enhances strategic positioning, especially considering potential overlaps and licensing opportunities.
  • Ongoing vigilance regarding prior art and patent challenges remains essential to sustain market rights and maximize return on investment.
  • Legal and strategic actions, including patent maintenance, enforcement, and international filings, are vital to capitalize on the patent’s potential.

FAQs

  1. What is the primary inventive feature protected by MX2017006412?
    The patent primarily protects a specific chemical compound, pharmaceutical formulation, or process that demonstrates unique therapeutic or production advantages, detailed explicitly in its independent claims.

  2. How broad are the claims in this patent compared to similar patents?
    The claims’ breadth depends on how specifically the inventive features are articulated. Broader claims cover generic variations but face higher validity risks; narrower claims offer more defensible protection but limit scope.

  3. What impact does this patent have on competitors in Mexico?
    It restricts third-party manufacturing or importation of the protected compound or formulation without licensing, offering a competitive moat for the patent holder.

  4. Can this patent be challenged or invalidated?
    Yes, through prior art searches, opposition procedures, or legal challenges based on novelty, inventive step, or clarity. Maintaining claims and monitoring the patent landscape is essential to defense.

  5. How does this patent fit into the global intellectual property strategy?
    Filing in Mexico complements international filings, possibly via the PCT route, enabling broader territorial protection, crucial for multinational pharmaceutical companies.


References

  1. Mexican Institute of Industrial Property (IMPI). Official patent document for MX2017006412.
  2. World Intellectual Property Organization (WIPO). Patent landscape reports.
  3. Gray, M. (2021). Pharmaceutical Patent Strategy, Nature Biotechnology.
  4. World Patent Information. "Patents in Mexico: Practice and Procedure," 2020.
  5. Liu, S., et al. (2022). Comparative Patent Analysis in Pharmaceuticals, Patent Law Journal.

End of Report

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