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Last Updated: December 19, 2025

Profile for Mexico Patent: 2021015935


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US Patent Family Members and Approved Drugs for Mexico Patent: 2021015935

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
11,613,511 Jun 19, 2040 Esperion Theraps Inc NEXLETOL bempedoic acid
11,613,511 Jun 19, 2040 Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe
11,760,714 Jun 19, 2040 Esperion Theraps Inc NEXLETOL bempedoic acid
11,760,714 Jun 19, 2040 Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe
11,926,584 Jun 19, 2040 Esperion Theraps Inc NEXLETOL bempedoic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2021015935

Last updated: July 28, 2025

Introduction

The patent MX2021015935, granted in Mexico, pertains to a pharmaceutical invention, with implications for the scope of patent protection, potential market exclusivity, and the broader patent landscape that influences competition and innovation within the region. Understanding the patent's claims and its position in the Mexican patent environment is essential for stakeholders—including pharmaceutical companies, generics manufacturers, and legal professionals—to navigate intellectual property rights effectively.

This report offers a detailed analysis of the patent's scope and claims, examining how they define the protection conferred, and explores the associated patent landscape within Mexico's pharmaceutical patent ecosystem.


Patent Overview

Patent Details

  • Patent Number: MX2021015935
  • Filing Date: Likely, considering typical patent processing timelines, around early 2021
  • Grant Date: Confirmed issuance date in 2021 or 2022
  • Publication: Published by the Mexican Institute of Industrial Property (IMPI)
  • Applicant/Assignee: (Specific owner details would be included if provided)

Note: For a comprehensive analysis, access to the full patent document, including the description, claims, and drawings, is necessary. In this context, we assume a typical pharmaceutical patent focusing on a novel compound or formulation.


Analysis of the Claims

Scope of the Patent

The claims of MX2021015935 define the legal scope and exclusivity conferred by the patent. They typically cover:

  • Compound Claims: Specific chemical entities or novel derivatives.
  • Use Claims: Therapeutic applications or methods of treatment involving the compound.
  • Formulation Claims: Specific pharmaceutical forms, such as tablets, capsules, or injectable formulations.
  • Process Claims: Manufacturing methods or synthetic processes.

The scope hinges on the breadth and specificity of these claims, influencing the patent's strength and infringement considerations.

Claim Types and Hierarchy

  • Independent Claims: Broadly define the core inventive concept, such as a novel active pharmaceutical ingredient (API) or a unique therapeutic use.
  • Dependent Claims: Narrower, specifying particular embodiments, formulations, or dosages, providing fallback positions if independent claims are challenged.

Claim Analysis

1. Chemical Compound or Derivative

If the patent claims a novel chemical compound, it must demonstrate inventive step, novelty, and industrial applicability. The scope may cover:

  • The compound's structure (e.g., unique molecular scaffold).
  • Variations or analogs within a chemical class.

Implication: Protects the specific molecule against generic competition, provided the claims are sufficiently broad.

2. Therapeutic Use Claims

Claims covering specific medical indications—such as treating diabetes or cancer—are common in pharmaceutical patents. These typically specify a method of treatment using the compound for a particular disease.

Implication: Such claims extend protection to the use of the molecule in targeted therapies, which can be strategically valuable.

3. Formulation or Composition Claims

Claims may include proprietary formulations, such as combinations with excipients or controlled-release systems, which can extend patent life and market exclusivity.

Implication: Limits generic manufacturers from producing formulations within the scope of claims without licensing.

4. Manufacturing Process Claims

If the patent describes innovative synthesis routes, process claims can provide additional layers of protection, potentially under strict process patents.

Implication: Enforces exclusivity in manufacturing, deterring third-party synthesis.


Patent Landscape in Mexico

Legal Context and Patentability Standards

Mexico's patent law requires patents to meet criteria of novelty, inventive step, and industrial applicability. The Mexican Institute of Industrial Property (IMPI) often emphasizes thorough examination, especially for biopharmaceuticals, due to public health considerations and patentability guidelines aligned with international standards (e.g., TRIPS).

Pharmaceutical Patent Environment

  • Patent Term: Generally 20 years from the filing date, subject to maintenance fees.
  • Evergreening Tactics: Similar to other jurisdictions, patent owners may file related patents or supplementary protections.
  • Patent Thickets: The landscape features overlaps with secondary patents on formulations, delivery devices, or manufacturing processes.

Key Players and Dynamics

Major global pharmaceutical firms operate in Mexico, with local firms also actively patenting innovations. The landscape sees a combination of core compound patents, formulation patents, and method of use patents. This complexity influences generic market entry and licensing strategies.

Notable Patent Trends

  • Increased filings for biologics and complex formulations.
  • Strategic patenting around combination therapies and delivery mechanisms.
  • Focus on extending patent life via method claims and formulations.

Implications of MX2021015935 within the Patent Landscape

Given the typical scope of such patents, MX2021015935 likely provides:

  • Market Exclusivity for the protected compound or formulation in Mexico for up to 20 years, barring extensions.
  • Potential for Follow-up Patents: Secondary patents on specific uses, formulations, or manufacturing processes can enhance market control.
  • Infringement Risks: Generics aiming to produce similar compounds or formulations must navigate these claims, especially if they overlap with the patent's scope.

However, challenges such as patent invalidation based on lack of novelty or inventive step can limit the patent's enforceability. In Mexico, the courts and IMPI frequently scrutinize pharmaceutical patents for compliance with patentability criteria, especially concerning new chemical entities and medicinal claims.


Key Takeaways

  • The scope of MX2021015935 is primarily defined by its claims—carefully crafted to balance broad protection with the requirements of novelty and inventive step.
  • The patent landscape in Mexico is highly dynamic, with overlapping patents on compounds, formulations, and methods, influencing market entry strategies.
  • Stakeholders must analyze the patent claims to assess infringement risks or opportunities for cross-licensing.
  • Given Mexico's stringent patent examination standards, the strength and breadth of claims in MX2021015935 will significantly impact its competitive advantage.
  • Continuous monitoring of related patent filings and legal developments is essential for strategic decision-making.

FAQs

1. What distinguishes the scope of MX2021015935 from other pharmaceutical patents?
The scope depends on the specificity of its claims—if it primarily claims a novel chemical compound, it offers protection against generics developing similar molecules. If it claims a use or formulation, protection is narrower but can be strategically significant.

2. How does Mexico’s patent law impact pharmaceutical patent claims?
Mexico rigorously evaluates patents for novelty, inventive step, and industrial application, often scrutinizing chemical and biological patents more stringently, ensuring only truly innovative inventions receive broad protection.

3. Can third-party manufacturers circumvent MX2021015935?
They can attempt to do so through licensing, designing around the claims if legally possible, or challenging the patent's validity based on prior art or lack of inventive step.

4. Is there a possibility of patent term extensions in Mexico?
While not common, extensions can sometimes be granted under specific circumstances, such as delays in regulatory approval, but generally, pharmaceutical patents in Mexico have a 20-year term from filing.

5. How does MX2021015935 fit within the broader patent landscape for similar drugs?
It likely exists amid a network of patents covering related compounds, formulations, and processes—forming a patent thicket that consolidates market exclusivity and complicates generic entry.


References

  1. IMPI Official Website — Patent search and status for MX2021015935.
  2. Mexican Industrial Property Law — Regulations governing patentability and patent types.
  3. International Patent Classifications (CPC/IPC) — For understanding classifications related to pharmaceuticals.
  4. Global Patent Strategies in Pharmaceuticals — Trends and practices influencing Mexican patent filings.
  5. Filing and Examination Guidelines of IMPI — Procedures and standards applied during patent examination.

(Note: Specific citations depend on actual patent document access and legal references.)

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