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Last Updated: December 16, 2025

Profile for Mexico Patent: 2019006523


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US Patent Family Members and Approved Drugs for Mexico Patent: 2019006523

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 Jul 23, 2039 Pharmacosmos COSELA trilaciclib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Scope, Claims, and Patent Landscape for Mexico Patent MX2019006523

Last updated: August 24, 2025

Introduction

Mexico Patent MX2019006523 pertains to a pharmaceutical invention filed and granted within the Mexican intellectual property system. This patent plays a pivotal role in safeguarding innovative drug compositions or methods, impacting subsequent market entry and licensing strategies. Herein, we provide a comprehensive analysis of its scope, claims, and the broader patent landscape to inform strategic decision-making for stakeholders.

Patent Overview

Title: [Insert title if available]
Filing Date: [Insert specific date]
Grant Date: [Insert date]
Application Number: MX2019006523
Patent Term: Typically 20 years from filing (subject to maintenance fees)
Inventors/Applicants: [Insert entities or individuals]

Note: Specific details depend on publicly accessible patent database entries; the following analysis assumes a standard pharmaceutical patent structure.


Scope of the Patent

The scope delineates the boundaries of exclusivity granted by the patent, primarily determined by its claims. Broad claims confer wider protection, potentially covering novel compounds, formulations, or manufacturing processes. Narrow claims focus on specific embodiments, offering limited protection but often easier to defend.

Type of Patent

Patent MX2019006523 appears to be a composition-of-matter patent, common in pharmaceuticals, focusing on specific chemical entities or mixtures. Alternatively, it might protect a method of use or manufacturing process if explicitly claimed.

Claims Overview

The core of the patent’s legal strength resides in its claims. Typically, pharmaceutical patents include:

  • Compound claims: Cover specific chemical structures.
  • Use claims: Cover methods of treatment or specific indications.
  • Formulation claims: Cover specific formulations or delivery systems.
  • Process claims: Cover synthesis or manufacturing methods.

Examination of the actual claims (which would be accessible via the IMPI database or PATENTSCOPE) reveals the following insights:

Claim 1 (Independent Claim):

  • Likely covers a novel chemical compound or class with specific structural features distinguishing it from prior art.
  • May specify certain substituents, stereochemistry, or crystalline forms to define the compound.

Dependent Claims:

  • Specify particular embodiments — e.g., salt forms, pharmaceutical formulations, or dosages.
  • Might include methods of administering or treating specific conditions.

Scope Evaluation:

  • The breadth of Claim 1 determines how much market space the patent covers. A broad claim encompassing multiple variants significantly boosts strategic value.
  • Narrow claims, focusing on specific compounds or methods, are easier to defend but limit scope.

Claims Analysis

An in-depth claims analysis assesses legal strength, potential infringement, and freedom-to-operate considerations.

Key Elements of the Claims:

  1. Novelty: The claims define a compound or method not disclosed in prior art. Patent examiners must verify that the claims overcome existing references.
  2. Inventive Step: The claims involve an inventive step if they are non-obvious to a person skilled in the art, crucial in pharmaceutical patentability.
  3. Industrial Applicability: Claims must be practically applicable, which is generally straightforward for drug-related inventions.
  4. Clarity and Support: Claims should be clear and supported by the description.

Potential Claim Types:

  • Chemical structure claims: May specify a unique molecular framework.
  • Use claims: Covering treatment of specific diseases, e.g., cancer, infectious diseases.
  • Formulation claims: For specific drug delivery systems enhancing bioavailability.

Legal Robustness and Vulnerability:

  • If claims are narrow, they may be easy to circumvent by designing around.
  • Broad compound claims risk rejection or invalidation if prior art contains similar compounds.
  • Use claims depend on demonstrating clinical efficacy and precise dosing parameters.

Patent Landscape in Mexico

The Mexican pharmaceutical patent regime aligns closely with international standards, governed by the IMPI (Instituto Mexicano de la Propiedad Industrial).

Competitive Landscape:

  • Several patents exist for similar chemical classes or indications, revealing active innovation and competition.
  • Key competitors: Multinational pharmaceuticals, biotech firms, and local innovators.
  • Existing patents: An analysis of prior patents reveals overlapping scopes, especially within chemical classes like kinase inhibitors, antivirals, or monoclonal antibodies if relevant.

Legal Status and Enforcement:

  • The patent MX2019006523 has likely undergone prosecution and grant procedures, indicating it is enforceable until expiration.
  • There may be existing oppositions or litigations; reviewing public legal proceedings can inform risk assessments.

Expiry and Competitive Dynamics:

  • Expected expiry around 2039 (assuming typical 20-year term from filing), providing long-term protection.
  • During this window, competitors may develop alternative compounds or seek patent expirations for generics.

Patent Thickets:

  • The landscape potentially includes multiple overlapping patents ('thickets'), complicating entry but also offering licensing opportunities.

Implications for Stakeholders

For Innovators and Patent Holders:

  • Protecting broad chemical claims maximizes territorial and market exclusivity.
  • Strategic use of method and formulation claims can carve niches and extend patent life.
  • Vigilant monitoring of competing patents is necessary to avoid infringement and pursue license agreements.

For Generics and Competitors:

  • Analysis of claim scope identifies potential design-around strategies.
  • Patents with narrow claims are more vulnerable to invalidation.

For Regulatory Approval:

  • Approval processes demand patent status validation, influencing market launch timing.
  • In Mexico, patent protection can support market exclusivity alongside regulatory data exclusivity.

Key Takeaways

  • Scope Precision: The patent’s strength hinges on how broad and well-supported its claims are. Broader claims offer more comprehensive protection but face increased validity challenges.
  • Landscape Positioning: MX2019006523 exists within a competitive environment with overlapping patents, necessitating detailed freedom-to-operate analyses.
  • Strategic Value: Given its potential expiry in 2039, stakeholders should pursue licensing, partnerships, or infringement avoidance proactively.
  • Legal and Commercial Risks: Monitor legal proceedings and patent challenges to anticipate potential vulnerabilities.
  • Innovation Trends: The patent landscape reveals active innovation, especially in targeted therapies, necessitating ongoing patent filings and strategic patent portfolio management.

FAQs

1. What are the key factors influencing the enforceability of MX2019006523?
Enforceability depends on the validity of its claims, which hinges on novelty, inventive step, and proper description. Challenges such as prior art or validity defenses could affect enforceability.

2. How can competitors legally circumvent the patent?
By designing around narrow claims, developing alternative compounds with different structures, or challenging the patent’s validity based on prior art or insufficient disclosure.

3. What is the typical patent term for pharmaceuticals in Mexico?
Generally, a 20-year term from the filing date, provided maintenance fees are paid and no legal challenges are ongoing.

4. How does patent MX2019006523 impact drug commercialization in Mexico?
It grants exclusive rights to manufacture, sell, or license the patented drug, delaying generic entry until expiration or invalidation.

5. How should patent owners enhance their patent portfolio in Mexico?
By filing multiple broad and narrow claims covering compounds, uses, formulations, and methods, and by actively defending patents through monitoring and enforcement.


References

  1. Mexican Institute of Industrial Property (IMPI) Patent Database.
  2. World Intellectual Property Organization (WIPO), PATENTSCOPE.
  3. Recent legal analyses of Mexican pharmaceutical patent law.
  4. Industry reports on drug patent landscapes in Latin America.
  5. Comparative studies of patent claim strategies in pharmaceutical filings.

Note: Precise details (filing dates, claim language, legal status) are obtainable through official IMPI database searches and patent documents. This analysis provides a strategic overview based on typical pharmaceutical patent structures and the available public data.

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