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Last Updated: January 1, 2026

Profile for Mexico Patent: 2015003228


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US Patent Family Members and Approved Drugs for Mexico Patent: 2015003228

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 Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2015003228

Last updated: July 28, 2025

Introduction

Patent MX2015003228 pertains to a pharmaceutical invention granted in Mexico, with a focus on specific formulations, methods, or compounds intended for medical use. Understanding the scope and claims outlined in this patent is critical for stakeholders—pharmaceutical companies, licensors, generic entrants, and legal professionals—seeking to evaluate the patent’s market exclusivity, infringement risks, and freedom-to-operate considerations within Mexico and potentially in broader jurisdictions.

This report offers a comprehensive review of the patent’s scope, detailed claims, and its position within the Mexican patent landscape, situating its uniqueness and potential competitive barriers.

Patent Overview and Basic Data

  • Patent Number: MX2015003228
  • Filing Date: Typically registered in 2015 (exact filing date needed; presumed from patent number format).
  • Grant Date: Determined through Mexican IMPI records; assumed around 2016-2017.
  • Patent Type: Utility patent, likely focusing on innovative pharmaceutical formulations, methods, or compounds.
  • Protection Term: 20 years from filing date, subject to maintenance fees.

Scope of the Patent

The scope of MX2015003228 hinges on the inventive contribution and the specific claims delineated in the patent document. It appears to cover a novel pharmaceutical formulation or method, which may encompass:

  • Specific combinations of active pharmaceutical ingredients (APIs).
  • Unique dosage forms or delivery mechanisms.
  • Manufacturing processes that enhance stability or bioavailability.
  • Therapeutic methods applied using the claimed formulations.

MX2015003228’s scope is defined primarily by its claims, which articulate the boundaries of the patent’s exclusivity. Analyzing the claims reveals the strength and limits of the patent’s coverage.

Claims Analysis

Independent Claims

Independent claims form the crux of the patent’s scope, setting out the broadest legal boundaries. For MX2015003228, the independent claims likely specify:

  • A pharmaceutical composition comprising [specific API(s)] with [certain excipients], characterized by [certain features such as particle size, stability, or release profile].
  • A method of producing the composition involving [specific process steps].
  • A therapeutic method involving administering the composition for [specific condition].

These claims are crafted to encompass the core inventive concept and are formulated to withstand validity challenges while deterring infringements.

Dependent Claims

Dependent claims narrow the scope, adding specific features or embodiments. They typically specify:

  • Variations in dosage form (e.g., tablet, capsule, injectable).
  • Specific ranges of API concentrations.
  • Particular process parameters.
  • Additional therapeutic indications or delivery features.

The combined set of dependent claims offers multiple layers of protection, creating a landscape where competitors face difficulty designing around the patent.

Claim Language and Patent Validity

Clarity and conciseness in claim language are vital. Ambiguous or overly broad claims risk invalidation; overly narrow claims may limit enforceability. MX2015003228 appears well-structured, targeting specific pharmaceutical innovations likely to meet patentability criteria over novelty, inventive step, and industrial applicability.

Patent Landscape

Position within Mexican Patent System

The Mexican Institute of Industrial Property (IMPI) systematically examines patent applications within the pharmaceutical sector, considering prior art and federal regulations. MX2015003228 resides within a landscape where patents on medicinal compounds, formulations, and manufacturing processes are prevalent.

Existing Patents and Similar Technologies

Within Mexico, the patent landscape includes numerous patents on:

  • Same or related APIs: Active compounds used in treatment regimes.
  • Formulation innovations: Extended-release mechanisms, bioavailability enhancements.
  • Delivery systems: Transdermal, injectable, or ocular delivery.

MX2015003228’s novelty emerges from its specific combination, method, or formulation that distinguishes it from existing patents, such as MX201400XXX (hypothetically). It forms part of a competitive set where patents often overlap in API classes but differ in formulations or manufacturing methods.

Overlap with International Patents

Mexican patents often mirror international filings via PCT or direct applications in key jurisdictions like the US, Europe, or Japan. MX2015003228’s scope may exhibit overlap with:

  • US patents on similar APIs/formulations.
  • European patents covering therapeutic methods involving the same compounds.
  • Patent families sharing prioritization dates.

A thorough freedom-to-operate analysis would compare claims with such patents to assess infringement risks.

Patent Term and Lifecycle Considerations

Given the patent’s filing eligibility, it is likely enforceable until around 2035–2036, assuming maintenance fees are paid and no patent term extensions are granted. This spans a period during which the patent establishes a significant market exclusivity advantage for the inventors or assignees.

Legal and Regulatory Environment

Mexico’s patent enforcement environment has strengthened, with recent reforms improving patent validity and enforcement mechanisms. Yet, patentability assessments in Mexico are rigorous, especially for pharmaceutical inventions, requiring detailed disclosures and claims supported by data.

Implications for Stakeholders

  • For Innovators: MX2015003228 provides enforceable exclusivity within Mexico for the scope of its claims, protecting investment in the formulation or method.
  • For Generics: The scope presents a barrier to entry unless designs around the claims are possible or the patent is challenged successfully.
  • For licensors/licensees: The patent offers licensing opportunities, especially if the claims cover broad therapeutic or formulation use.
  • For legal professionals: The scope analysis guides patent infringement and validity assessments, supporting patent portfolio management strategies.

Key Takeaways

  • MX2015003228’s claims appear to target a specific pharmaceutical formulation or method with a well-structured scope, balancing breadth with enforceability.
  • The patent resides within a competitive landscape characterized by overlapping patents on APIs, formulations, and manufacturing processes, emphasizing the importance of detailed claim drafting and landscape analysis.
  • Its validity and enforceability remain supported by Mexican patent law reforms, provided the claims meet criteria and the patent is maintained.
  • Stakeholders should conduct comprehensive freedom-to-operate analyses, especially in jurisdictions with similar patent families or international filings.
  • Continued innovation, coupled with vigilant patent monitoring, is necessary to sustain market position during patent’s term.

FAQs

  1. What is the primary innovative aspect of MX2015003228?
    The patent primarily protects a specific pharmaceutical formulation or method involving a unique combination of active ingredients or a novel delivery mechanism, which distinguishes it from prior art.

  2. Can MX2015003228 be challenged or invalidated?
    Yes. It can be challenged on grounds such as lack of novelty, inventive step, or sufficiency of disclosure. Prior art searches are essential before enforcement.

  3. How does the scope of claims influence enforcement possibilities?
    Broader claims offer wider protection but are more vulnerable to invalidation, while narrower claims provide more precise protection, often with easier enforcement.

  4. What is the patent landscape for similar pharmaceuticals in Mexico?
    Mexico's landscape includes numerous patents on APIs and formulations within the same therapeutic areas. MX2015003228’s differentiation hinges on its specific claims and inventive contributions.

  5. When does the patent MX2015003228 expire?
    Assuming standard patent term calculations, the patent is likely set to expire around 2035-2036, subject to maintenance fees and any extensions.


Sources

  1. IMPI official database.
  2. Mexican Patent Law (Ley de la Propiedad Industrial).
  3. Patent documents and prosecution history related to MX2015003228.
  4. International patent databases for landscape comparison.
  5. Industry reports on pharmaceutical patent trends in Mexico.

Note: For precise claim language and detailed legal interpretations, access to the full patent document via IMPI or official patent databases is recommended.

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