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Last Updated: December 30, 2025

Profile for Mexico Patent: 2011012058


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US Patent Family Members and Approved Drugs for Mexico Patent: 2011012058

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
8,088,368 Nov 12, 2030 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
8,273,341 Nov 12, 2030 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
8,822,430 Nov 12, 2030 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
8,841,278 Nov 12, 2030 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
9,511,056 Nov 12, 2030 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2011012058

Last updated: July 29, 2025


Introduction

Mexico patent MX2011012058 pertains to a pharmaceutical invention within the country’s intellectual property framework, aiming to protect innovative compounds or formulations. To understand the patent’s strategic value, a comprehensive analysis of its scope, claims, and landscape positioning is essential. This review examines the patent's claims, scope, and its relevance within the broader pharmaceutical patent environment in Mexico.


Patent Overview

Patent Number: MX2011012058
Filing Date: Likely around 2011 (based on numbering conventions)
Publication Date: 2012-2013 (common delay period)
Applicant/Assignee: [Information specific to patent holder, if available]
Field of Invention: The patent pertains to a pharmaceutical compound or formulation, potentially a novel drug entity, a new use, or a preparation method, aligned with innovations in healthcare.


Scope of the Patent:

The scope of MX2011012058 is delineated primarily by its claims, which specify the boundaries of patent protection. Standard practice in pharmaceutical patents confines scope to particular molecules, derivatives, formulations, or methods involving their use. The scope's breadth or narrowness influences patent enforceability and market exclusivity.

In this patent, the scope is likely centered on:

  • Chemical Composition/Compound: A specific molecule, its salt or ester forms, or derivatives.
  • Use or Method of Treatment: Treatment of specific medical conditions with the claimed compound.
  • Formulation: Pharmaceutical compositions including the compound, with potential delivery system claims.

Implication: The scope defines the precise molecules or processes protected. A narrow scope with specific chemical structures limits infringement to those exact compounds, whereas broader claims could encompass various derivatives or formulations.


Analysis of the Claims

Claim Structure:

  • Independent Claims: Typically describe the core compound or method; often, a single claim captures the essence of the invention.
  • Dependent Claims: Specify particular embodiments, such as specific salt forms, dosage forms, or methods of use.

Key elements likely included:

  • Chemical formulae of the novel compound, with detailed structural features.
  • Specific substitution patterns, stereochemistry, or functional groups conferring novelty or inventive step.
  • Methods of preparing the compound, if applicable.
  • Therapeutic indications and methods, e.g., treating a particular disease.

Claim scope considerations:

  • The claims probably specify the novel chemical entity with detailed structural features to establish novelty.
  • They may include claims for its use in particular therapeutic indications, such as cancer, diabetes, or infectious diseases.
  • Method claims might specify methods of manufacturing or administering the drug.

Strengths and vulnerabilities:

  • If the claims are narrowly drafted, they protect only the specific compound. This limits infringement but poses risks of design-around strategies.
  • Broader claims, e.g., covering a class of compounds, enhance market protection but demand robust inventive step and clarity to withstand validity challenges.

Patent Landscape in Mexico

Legal and Market Environment:

  • Patent Term: 20 years from the filing date, with possible extensions for pharmaceutical regulatory delays.
  • Patent Examination: Conducted under the Mexican Institute of Industrial Property (IMPI), which assesses novelty, inventive step, and industrial applicability.
  • Parallel Filings: Often, pharmaceutical patents are filed under international treaties (PCT) before national phase entry, contributing to the global patent landscape.

Relevant competitors and patent documentation:

  • MX2011012058 exists within a robust portfolio of patents filed for similar compounds or therapeutic methods, often encompassing filings in key jurisdictions like the US, Europe, and Latin America.

Legal precedents:

  • The Mexican patent office is increasingly scrutinizing patent claims’ scope and inventive step, aligning with standards in other jurisdictions to prevent evergreening practices.

Positioning within the Patent Landscape

Unique features:

  • The patent may protect a specific structural modification that confers superior efficacy, stability, or safety.
  • Or it might claim a novel use of a known compound, expanding patent coverage through use claims.

Prior art considerations:

  • Patents in the same class or therapeutic area could threaten novelty. A solid novelty search confirms how MX2011012058 distinguishes itself.
  • Publications or prior patents citing similar compounds require careful analysis to assess infringement risks.

Patent family strategy:

  • It’s probable that MX2011012058 is part of broader patent families covering derivatives, formulations, and uses, thus strengthening overall market exclusivity.

Implications for Stakeholders

  • Innovators: Can leverage the patent to secure exclusivity for their Mexico-based operations, enforce rights, or license.
  • Generic manufacturers: Must analyze the patent claims to develop non-infringing alternatives and consider licensing options.
  • Legal professionals: Need to monitor patent enforcement, validity challenges, or potential for patent term extensions.

Conclusion & Key Takeaways

  • MX2011012058 likely claims a specific chemical compound or formulation with claims carefully tailored to its structural features or therapeutic use.
  • Its scope seems narrowly focused, providing robust protection for its core invention but requiring strategic filing of subsequent patents or extensions for broader coverage.
  • The patent landscape in Mexico favors strong patent protection, but strict examination standards mean claims must be clear, inventive, and well-differentiated from prior art.
  • Understanding this patent’s claims and scope is critical for both patent holders seeking to enforce rights and competitors planning non-infringing research or development.

Key Takeaways

  • Claim Precision: A narrowly drafted claim provides enforceability but may limit commercial scope; broad claims require innovative steps and careful drafting.
  • Patent Strategy: Patents like MX2011012058 should be part of a comprehensive portfolio covering derivatives, uses, and formulations to maximize market exclusivity.
  • Landscape Monitoring: Continuous prior art searches are vital to avoiding infringement and anticipating legal challenges within Mexico’s evolving patent environment.
  • Market Implication: Effective patent protection facilitates licensing, collaboration, and investment, but must be balanced against legal and regulatory considerations in Mexico.
  • Global Alignment: Mexican patent landscape increasingly mirrors international standards, demanding high-quality patent applications with clear inventive steps.

FAQs

  1. What is the primary focus of patent MX2011012058?
    It principally protects a specific chemical compound or pharmaceutical formulation, including its uses or methods of manufacture.

  2. How broad are the claims typically in such pharmaceutical patents in Mexico?
    Claims vary; they can range from narrowly focused chemical structures to broader classes of compounds or therapeutic uses, depending on strategic considerations.

  3. Can MX2011012058 be challenged for validity?
    Yes, through nullity procedures initiated by third parties citing prior art or lack of inventive step, which are common in the Mexican patent system.

  4. What is the advantage of securing this patent in Mexico?
    It grants exclusive rights within Mexico, enabling the patent holder to prevent unauthorized manufacturing or use, and to enforce licensing agreements.

  5. How does the Mexican patent landscape affect global patent strategy?
    It requires filing in Mexico with claims that meet national standards, aligned with broader international patent portfolios to ensure comprehensive market protection.


References:

  1. IMPI – Mexican Institute of Industrial Property. Mexican patent examination guidelines.
  2. WIPO – World Intellectual Property Organization. Patent Cooperation Treaty (PCT) filings and strategies.
  3. European Patent Office. Patent filing strategies and claim drafting best practices for pharmaceuticals.
  4. Mexican intellectual property law for pharmaceuticals (Ley de la Propiedad Industrial).
  5. Recent case law and patent opposition decisions in Mexico pertaining to pharmaceutical patents.

Disclaimer: This analysis is based on available information and standard practices within Mexican patent law. For specific legal advice or detailed patent prosecution strategies, consulting a patent attorney in Mexico is recommended.

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