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Last Updated: December 12, 2025

Profile for Mexico Patent: 2021003840


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US Patent Family Members and Approved Drugs for Mexico Patent: 2021003840

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 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
⤷  Get Started Free Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
⤷  Get Started Free Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2021003840

Last updated: August 10, 2025


Introduction

Patent MX2021003840, filed in Mexico, pertains to innovations within the pharmaceutical domain. A comprehensive understanding of this patent’s scope, claims, and its position within the current patent landscape is essential for stakeholders involved in drug development, licensing, and competitive intelligence. This report evaluates these aspects, emphasizing strategic implications, and navigates the broader patent environment in Mexico for pharmaceuticals.


Patent Overview and Bibliographic Details

  • Patent Number: MX2021003840
  • Application Filing Date: Likely in 2021 (assuming typical Mexican patent processing timelines)
  • Inventor/Applicants: Data specific to assignee or inventor(s) is unavailable in current context.
  • Publication Date: 2022 (approximate, based on processing timelines)
  • Assignee/Applicant: Unknown – a detailed search of the Mexican Institute of Industrial Property (IMPI) database is required for precise attribution.

Scope of the Patent

The scope of MX2021003840 is primarily defined by its claims, which delineate the legal boundaries of the patent rights. Based on typical pharmaceutical patent drafting and available disclosures:

  • The patent likely relates to a novel chemical entity, a pharmaceutical composition, or a method of use involving a specific drug candidate.
  • The scope possibly encompasses formulations, delivery mechanisms, or associated methods that enhance efficacy, stability, or bioavailability.
  • The patent could extend to derivatives, salts, polymorphs, or combinations predicated on the core active ingredient.

Note: Without the explicit claims text, this analysis presumes standard patent drafting practices in pharmaceutical innovations, which aim to cover a broad spectrum of embodiments around the primary invention.


Claims Analysis

The claims form the core of any patent and define the scope of exclusivity. Common types likely included in MX2021003840 are:

  1. Compound Claims: If the patent pertains to a chemical entity, the initial claim probably covers the structural formula of a novel compound, possibly including variants or isomers.
  2. Method Claims: Claims may encompass methods of preparing the compound, methods of treatment utilizing the compound, or specific dosing regimens.
  3. Formulation Claims: These might include specific pharmaceutical compositions, combinations, or delivery systems optimized for particular conditions.
  4. Use Claims: If the patent claims a new therapeutic application, it might specifically cover a novel indication or method of treatment.

Potential Claim Strategies and Limitations:

  • Broad Claims: The patent might attempt to claim wide-ranging chemical structures or methods, requiring detailed description to avoid invalidity based on prior art.
  • Narrow Claims: More specific claims help solidify enforceability but reduce scope.

In Mexican patent law, claim construction adheres to the doctrine of equivalents, allowing for broad interpretations if properly supported, but strict novelty and inventive step requirements restrict overly broad claims.


Patent Landscape in Mexico for Pharmaceutical Innovations

Regulatory and Patent Environment:

Mexico’s IP regime, governed by the IMPI and aligned with TRIPS standards, offers robust protection for pharmaceutical inventions. However, patenting drug compounds involves navigating specific hurdles:

  • Patentability Standards: Require novelty, inventive step, and industrial applicability, with an increased focus on inventive activity due to existing prior art.
  • Data Exclusivity: Typically 5 years for chemical entities, but patent protection provides longer-term exclusivity.
  • Compulsory Licensing & Challenges: Mexico’s laws permit compulsory licensing under certain circumstances, impacting patent enforcement strategies.

Key Patent Players and Activities:

  • Several multinational corporations and domestic entities conduct patent filings around pharmaceutical compounds, often targeting treatments for local diseases such as diabetes, obesity, or infectious diseases.
  • Mexico exhibits a rising patent application trend in pharma, reflecting ongoing innovation and strategic patenting efforts.
  • Local patenting practices emphasize early filings with broad claims, followed by narrow claims during prosecution.

Patent Landscape Specifics:

  • Recent patents in Mexican territory often cite prior art from the US, Europe, and Japan, signifying a global innovation footprint.
  • Patent filings include both chemical and biotechnological inventions, with supplementary filings focusing on formulations and methods.
  • Patent challenges in Mexico may involve invalidity actions based on prior art, particularly from foreign patent applications published before the Mexican filing date.

Implications for Stakeholders

For Innovators:

  • Securing broad claims in MX2021003840, especially around core chemical structures, can provide meaningful market exclusivity.
  • Regular monitoring of patent filings ensures awareness of potential infringement or freedom-to-operate issues.

For Generic Manufacturers:

  • The scope of MX2021003840 might prevent entering the Mexican market for specific indications, depending on the breadth of claims.
  • However, narrow claims or expiration dates could present market opportunities post-patent expiry.

For Legal and Patent Advisors:

  • Due diligence in Mexican patent filings is crucial for global patent management strategies, notably given differing examination standards across jurisdictions.
  • Potential patent oppositions or invalidity actions should consider prior art from globally influential patent offices.

Strategic Considerations

  • Patent Term and Lifecycle Management: Mexican patents generally have an term of 20 years from filing, though extensions or adjustments related to regulatory delays may apply.
  • Patent Cliffs and Lifecycle Extension: Supplementary protection certificates are not available in Mexico, making patent life cycle management critical.
  • Patent Enforcement Strategies: Active monitoring, licensing, or litigation should focus on the scope of claims, potential infringing products, and prior art.

Key Takeaways

  • MX2021003840 appears to encompass a targeted pharmaceutical invention, with claim scope likely centered on novel compounds or methods of treatment.
  • The patent landscape in Mexico favors broad, well-supported claims, with enforcement contingent on careful analysis of prior art and competitors’ filings.
  • Understanding Mexico’s patent regulations and filing trends is essential for maximizing patent strength and market positioning.
  • Maintaining strategic awareness of patent lifecycles, potential challenges, and regional patent policies enhances competitive advantage.
  • Companies should optimize claim drafting, monitor patent filings, and consider regional patent strategies for sustainable market exclusivity.

FAQs

1. How does Mexico’s patent law impact pharmaceutical patent enforcement?
Mexico’s law emphasizes novelty and inventive step similar to TRIPS standards, with mechanisms for patent invalidity and opposition. Enforcement involves civil proceedings, but access to patent litigation can be complicated by procedural delays.

2. Can MX2021003840 be extended beyond 20 years?
Generally, no. Mexican patents last 20 years from the filing date, though extensions like supplementary protection certificates are not available in Mexico.

3. What strategies should companies adopt regarding claim drafting in Mexico?
Firms should craft broad, robust chemical and method claims supported by detailed descriptions to reduce the risk of invalidity while ensuring enforceability.

4. How does prior art affect the patent landscape for pharmaceuticals in Mexico?
Prior art from global patent offices can limit patent scope or lead to invalidation. Continuous monitoring is necessary to identify potential non-obviousness issues.

5. What is the role of patent landscape analysis in drug development?
It helps identify innovation gaps, potential infringement risks, and opportunities for patentable improvements, guiding R&D and commercialization strategies.


References

  1. IMPI Patent Database: Official patent documents and prosecution history https://pct.impi.gob.mx/
  2. Mexican Industrial Property Law (LPI): Legal framework governing patents https://www.gob.mx/impi
  3. TRIPS Agreement: International standards for patentability and enforcement
  4. Pharmaceutical Patent Strategies: Considerations for Latin America—WIPO publications and industry reports
  5. Global Patent Landscape Reports: Pharmaceuticals—OECD and WIPO reports and analyses

This detailed patent landscape review aims to inform strategic decision-making for pharmaceutical innovators operating within Mexico’s regulatory and legal framework.

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