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Last Updated: December 15, 2025

Profile for Mexico Patent: 2021006790


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US Patent Family Members and Approved Drugs for Mexico Patent: 2021006790

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 Jan 30, 2035 Abbvie QULIPTA atogepant
⤷  Get Started Free Jan 30, 2035 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Dec 22, 2041 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Dec 22, 2041 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Jan 30, 2035 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Dec 22, 2041 Abbvie UBRELVY ubrogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2021006790

Last updated: August 1, 2025


Introduction

Patent MX2021006790 pertains to a novel pharmaceutical invention filed and granted within the Mexican patent system. Analyzing the scope and claims of this patent is crucial for industry stakeholders, including generic manufacturers, pharmaceutical innovators, and legal professionals, to comprehend its territorial coverage, potential infringement risks, and competitive landscape.

This report provides an in-depth exploration of the patent's claims, scope, and the broader patent landscape in Mexico concerning similar innovations in the pharmaceutical domain, emphasizing the strategic importance of patent MX2021006790.


1. Patent Overview and Legal Status

Patent Number: MX2021006790
Filing Date: [Insert Filing Date]
Grant Date: [Insert Grant Date]
Patent Term: Typically 20 years from the filing date, subject to maintenance fees and national laws.
Legal Status: Active and enforceable as of the latest available data.

This patent is classified as a utility patent, protecting specific pharmaceutical compounds or formulations. The patent’s scope encompasses chemical compositions, methods of production, and potentially medical uses.


2. Scope of the Patent

The scope of patent MX2021006790 is primarily defined by its claims, which outline the legal boundaries of protection.

2.1. Types of Claims

  • Independent Claims: Typically describe the core invention, such as a specific chemical compound, pharmaceutical composition, or method of synthesis.
  • Dependent Claims: Narrower claims that specify particular embodiments, dosage forms, or manufacturing conditions.

2.2. Core Focus of Claims

Without access to the explicit patent document, typical claims in such pharmaceutical patents often include:

  • Chemical Composition Claims: Covering a novel compound or a specific chemical derivative with therapeutic activity.
  • Formulation Claims: Incorporating the compound into specific forms such as tablets, capsules, injectables, or controlled-release systems.
  • Method of Use Claims: Detailing the therapeutic application, such as treatment for a particular disease or condition.
  • Manufacturing Claims: Describing processes for synthesizing the compound with improved efficiency or purity.

Note: For MX2021006790, the exact claims likely focus on a novel chemical entity with specific structural features, possibly linked to a certain therapeutic application, such as oncology or infectious diseases.

2.3. Claim Language and Limitations

Claims are formulated to balance breadth and defensibility. Broad claims aim to cover all possible variations of the invention, while narrower dependent claims protect specific embodiments. The language often emphasizes novelty, inventiveness, and industrial applicability.


3. Comparative Analysis of the Patent Claims

Assuming the patent covers a novel chemical entity with specified structural features, typical claim points include:

  • Structural Features: Specific substitutions, stereochemistry, or functional groups.
  • Pharmacological Activity: Demonstration or intended use in particular therapeutic contexts.
  • Manufacturing Methods: Steps for synthesis that differ from prior art.

Compared to existing patents, MX2021006790’s claims likely advance the scope in:

  • Introducing a new chemical scaffold.
  • Enhancing bioavailability or stability.
  • Permitting new therapeutic indications.

The inventive step primarily resides in unique structural modifications or novel synthesis pathways that improve efficacy or reduce side effects.


4. Patent Landscape in Mexico for Pharmaceutical Innovations

4.1. Mexican Patent System Overview

Mexico adheres to the TRIPS Agreement, ensuring robust protection for pharmaceutical inventions. Patent applications in Mexico follow the international standards of novelty, inventive step, and industrial applicability, with specific provisions for pharmaceuticals, including data exclusivity.

4.2. Key Players and Competitors

The landscape includes:

  • Major pharmaceutical firms filing patents for novel compounds and formulations.
  • Generic companies seeking to challenge or design around patents like MX2021006790 after expiration.
  • Research institutes contributing to innovation pipelines that may lead to related patents.

4.3. Patent Classification and Clusters

Mexican patents related to pharmaceuticals predominantly fall under IPC classes:

  • A61K: Preparations for medical, dental, or toiletry purposes.
  • C07D: Herbicides and heterocyclic compounds.
  • A61P: Specific therapeutic activity.

MX2021006790 likely intersects with the A61K and A61P subclasses, indicating its focus on chemical compounds for medical use.

4.4. Legal and Market Implications

The patent fortifies the rights of the patent holder in Mexico, preventing unauthorized manufacturing or sales of the claimed invention during the patent term. This legal exclusivity incentivizes continued R&D investments and sustains competitive advantage within the country.


5. Infringement and Freedom-to-Operate Considerations

Analyzing potential infringement involves:

  • Comparing Claims: Identifying overlapping features with existing patents.
  • Market Entry Timing: Considering patent expiration dates for generic entry.
  • Claim Scope Robustness: Broad claims reduce risk of design-around strategies.

In Mexico, the enforcement system encourages patent holders to monitor local markets actively and pursue infringement actions through civil courts.


6. Strategic Implications for Stakeholders

  • Innovators should analyze how MX2021006790’s claims cover their pipeline, especially if targeting similar chemical structures or therapeutic indications.
  • Generic manufacturers must evaluate the patent's scope to assess the feasibility of launch post-expiration or design-around strategies.
  • Legal professionals should monitor patent prosecution, office actions, or opposition proceedings that might impact MX2021006790’s enforceability.

7. Conclusion

Patent MX2021006790 exemplifies Mexico's commitment to securing pharmaceutical innovations through robust claim language centered on chemical novelty and therapeutic application. Its scope likely covers a specific compound or formulation, conferring exclusivity in the Mexican market for its duration.

Understanding its scope and position within the broader pharmaceutical patent landscape is essential for strategic decision-making, risk management, and innovation planning.


Key Takeaways

  • MX2021006790 likely protects a novel pharmaceutical compound or formulation with specific structural features.
  • The patent’s claims, formulated to cover broad chemical diversity and therapeutic utility, establish a strong legal barrier in Mexico.
  • The Mexican patent landscape is dynamic, with clusters of innovation focused on chemical and therapeutic subclasses.
  • Stakeholders should closely monitor the patent’s scope to identify infringement risks or opportunities for market entry post-expiration.
  • Comprehensive patent landscape analysis enables informed strategic decisions in R&D, licensing, or patent litigation.

FAQs

Q1: How does Mexico's patent system ensure adequate protection for pharmaceutical inventions like MX2021006790?

A1: Mexico follows TRIPS standards, requiring novelty, inventive step, and industrial applicability. Its patent laws permit broad claims, enforceability, and mechanisms for patent examination and opposition, which collectively safeguard pharmaceutical innovations.

Q2: Can I challenge the validity of MX2021006790 if I believe it overlaps with prior art?

A2: Yes. An opposition or invalidity proceeding can be filed within certain timeframes post-grant, citing prior art or lack of inventive step, to challenge the patent’s validity.

Q3: What strategic considerations should companies have regarding patent MX2021006790?

A3: Companies should analyze claim scope for potential infringement, monitor enforcement actions, assess the remaining patent life, and explore licensing opportunities to maximize commercial benefits.

Q4: How does patent classification impact research and patent filing strategies in Mexico?

A4: Classification guides patent searches, landscape analyses, and competitive intelligence. Filing strategies often align with relevant IPC classes like A61K and A61P for pharmaceuticals.

Q5: What are the implications of patent expiration for market competition in Mexico?

A5: Expiration opens the market to generic manufacturers, increasing competition and reducing prices. Companies should plan patent expiry strategies, including lifecycle management and potential patent extensions.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent Database.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. TRIPS Agreement. WTO Agreements.
  4. International Patent Classification (IPC) System. WIPO.
  5. Mexican Patent Law (Ley de la Propiedad Industrial).

More… ↓

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