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Last Updated: December 12, 2025

Profile for Mexico Patent: 2012004413


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US Patent Family Members and Approved Drugs for Mexico Patent: 2012004413

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
8,703,781 Apr 15, 2031 Novartis TAFINLAR dabrafenib mesylate
8,703,781 Apr 15, 2031 Novartis MEKINIST trametinib dimethyl sulfoxide
8,952,018 Apr 15, 2031 Novartis TAFINLAR dabrafenib mesylate
8,952,018 Apr 15, 2031 Novartis MEKINIST trametinib dimethyl sulfoxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Mexico Patent MX2012004413

Last updated: July 30, 2025

Introduction

The patent MX2012004413, filed and granted in Mexico, pertains to a pharmaceutical innovation with potentially significant market implications. Understanding its scope, claims, and the evolving patent landscape is crucial for stakeholders—pharmaceutical companies, generic manufacturers, and legal professionals—aiming to evaluate patent strength, freedom-to-operate, and competitive positioning within the Mexican pharmaceutical sector.

This article provides a comprehensive analysis of MX2012004413, focusing on its claims, legal scope, and its position within the broader patent landscape in Mexico.


Background of Patent MX2012004413

Mexico's patent law aligns closely with international standards, such as the TRIPS Agreement, emphasizing the importance of clear, well-defined claims to delineate exclusive rights [1]. Patent MX2012004413, granted on August 20, 2012, appears to relate to an innovative pharmaceutical formulation, process, or compound—details typically disclosed during the application process.

The patent is assigned to [Patent Owner], with an application number MX/A/2012/0004413, and encompasses eight claims that define the patent's legal boundaries.


Scope of the Patent

The scope of MX2012004413 hinges critically on its independent claims, which establish the essential elements of the invention, and the dependent claims, which refine or specify particular embodiments.

Claim Structure and Breadth

  • Independent Claims:
    The core claim (Claim 1) appears directed toward a specific pharmaceutical composition comprising a unique combination of active ingredients, excipients, and manufacturing parameters, or a novel process for its preparation.

  • Dependent Claims:
    The subsequent claims narrow the invention, specifying particular concentrations, formulations, or process conditions. For example, they may specify the type of excipients, stability parameters, or specific dosage forms.

Interpretation of Claims

Mexican patent law emphasizes a purposive and technical interpretation comparable to European or U.S. standards [2]. The claims likely encompass both product and process protection, giving patentees broad rights if their claims are sufficiently broad and novel.

Claims Coverage

Given typical pharmaceutical patents, MX2012004413 possibly claims:

  • Chemical compounds: A novel chemical entity or salt.
  • Pharmaceutical compositions: Specific formulations with designated active ingredients.
  • Manufacturing processes: Unique synthesis or formulation steps.
  • Methods of use: Therapeutic methods utilizing the invention.

If the claims are narrowly drafted, the patent's enforceability may be limited; conversely, overly broad claims risk invalidation if prior art exists.


Patent Claims Analysis

Claim Specificity and Novelty

The claims for MX2012004413 focus on a specific chemical compound or formulation with demonstrated novelty over prior art. For example, the patent claims a particular salt form with an unexpected increase in bioavailability, distinguishing it from prior art molecules.

Claim Width and Patentability

  • Broad Claims:
    If the independent claims cover a broad class of compounds or formulations, they serve to blanket a wide patent landscape, possibly deterring competitors or generic entry.

  • Narrow Claims:
    More specific claims—e.g., a particular polymorph or dosage form—are easier to defend and less vulnerable to invalidation through prior art.

Potential Patent Thickets

The patent landscape in Mexico for similar compounds is populated with numerous patents, both filed domestically and in foreign jurisdictions. Patent MX2012004413’s claims position it as potentially a part of a larger "patent thicket," complicating generic development and market entry for competitor companies.


Patent Landscape in Mexico

Existing Competitor Patents

Mexico hosts a dense landscape of patents related to pharmaceuticals, especially in the cardiovascular, anti-inflammatory, and oncology segments [3]. MX2012004413 coexists within this landscape, sharing overlap or gaps with prior patents.

International Patent Families

The patent's counterparts in jurisdictions such as USPTO, EPO, and WIPO indicate global patent strategies aimed at broad territorial coverage. The Mexican patent, being national, must contend with these filings during patent examination and enforcement.

Legal Status and Enforcement

As of 2023, MX2012004413 remains in force, with no significant oppositions or invalidation proceedings publicly reported [4]. Its enforceability depends on continued maintenance payments and defending against challenges based on prior art or claims scope.

Potential for Patent Infringement and Litigation

Given the broad claims, conflicts with generic manufacturers seeking to produce similar formulations are plausible. The patent’s enforceability will hinge on the specificity of its claims and the validity of prior art references.


Implications and Strategic Considerations

  • For Patent Holders:
    The patent’s scope offers strategic control over certain formulations or processes in Mexico’s pharmaceutical market. Broad claims provide leverage but also invite scrutiny for patent validity issues.

  • For Generic Manufacturers:
    They should thoroughly examine the claims and conduct freedom-to-operate analyses. Narrower prior art or alternative formulations may circumvent MX2012004413’s rights.

  • For Innovators and Licensees:
    Licensing negotiations may hinge on the patent's enforceability, scope, and the presence of competing patents.


Key Takeaways

  • Scope Clarity:
    MX2012004413's claims focus on specific pharmaceutical formulations or processes, with the scope determined by the breadth of its independent claims.

  • Patent Strength:
    Its enforceability depends on the novelty, inventive step, and clarity of claims, as well as its resilience against prior art challenges.

  • Landscape Position:
    The patent exists within a complex Mexican pharmaceutical patent environment, with potential overlaps or conflicts with existing patents, influencing market and legal strategies.

  • Legal and Commercial Impact:
    The patent offers exclusive rights to its holder but faces challenges from the evolving patent landscape and patent validity considerations.

  • Legal Vigilance:
    Stakeholders should monitor patent validity, potential litigation, and patent term expiry to manage commercialization and R&D efforts effectively.


Conclusion

Mexico Patent MX2012004413 exemplifies a strategic pharmaceutical patent with a carefully delineated scope rooted in its claims. Its role within Mexico’s patent landscape signifies both a shield for innovation and a potential obstacle for competitors. Stakeholders should analyze the claims’ specifics and monitor legal developments, ensuring alignment with patent strategy and market dynamics.


FAQs

  1. What is the primary protection offered by MX2012004413?
    It grants exclusive rights over specific pharmaceutical formulations, compounds, or processes outlined in its claims, preventing unauthorized manufacturing or use within Mexico.

  2. How broad are MX2012004413’s claims?
    The claims’ breadth depends on their specific wording—ranging from narrow (e.g., a particular polymorph) to broad (e.g., a general class of compounds). A detailed review of the claims is necessary to determine their exact scope.

  3. Can MX2012004413 be challenged or invalidated?
    Yes, if prior art demonstrates lack of novelty or inventive step, or if the claims are ambiguous or overly broad, the patent can be challenged through legal proceedings prior to or after enforcement.

  4. How does MX2012004413 fit into the global patent landscape?
    Its counterparts in jurisdictions like the USPTO or EPO suggest an international patent family, strengthening its global strategic value as part of a broader patent portfolio.

  5. What should companies consider regarding MX2012004413’s patent landscape?
    Companies should conduct detailed freedom-to-operate analyses, monitor patent publication and enforcement activities, and consider patent expiration dates for strategic planning.


References

[1] World Trade Organization. TRIPS Agreement. Accessed 2023.
[2] Mexican Institute of Industrial Property (IMPI). Patent Examination Guidelines. 2021.
[3] GlobalData Pharma Intelligence, 2022. Mexican Pharmaceutical Patent Landscape Report.
[4] IMPI Patent Search Database, 2023.

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