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Last Updated: December 12, 2025

Profile for Mexico Patent: 2016013826


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US Patent Family Members and Approved Drugs for Mexico Patent: 2016013826

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 Apr 21, 2035 Aclaris ESKATA hydrogen peroxide
⤷  Get Started Free Apr 21, 2035 Aclaris ESKATA hydrogen peroxide
⤷  Get Started Free Apr 21, 2035 Aclaris ESKATA hydrogen peroxide
⤷  Get Started Free Jul 4, 2035 Aclaris ESKATA hydrogen peroxide
⤷  Get Started Free Apr 21, 2035 Aclaris ESKATA hydrogen peroxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 15, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2016013826


Introduction

Mexico Patent MX2016013826 pertains to a pharmaceutical invention registered within the Mexican patent system. This patent's strategic importance lies in its scope of protection, scope of claims, and positioning within the broader patent landscape for its respective therapeutic class. This analysis offers a comprehensive review to aid stakeholders in assessing patent strength, competitive positioning, and potential for licensing, manufacturing, or litigation.


Patent Overview and Background

Patent MX2016013826 was filed to secure exclusive rights over a novel drug compound, formulation, or therapeutic method. While the precise claims depend on the specific patent document, typical pharmaceutical patents encompass claims on active ingredients, methods of manufacturing, formulations, or treatment methods [1].

Understanding such patents requires dissecting their claims' scope, assessing prior art, and mapping their position in the global patent landscape.


Scope of the Patent

The scope of MX2016013826 can be characterized by examining its claims, which define the legal boundary of the patent monopoly.

1. Type of Claims:
The patent likely includes:

  • Compound Claims: Covering the active pharmaceutical ingredient (API), possibly with specific stereochemistry, polymorphs, or derivatives.
  • Formulation Claims: Covering specific compositions or delivery systems, such as extended-release formulations or combinations with other agents.
  • Method Claims: Covering methods of manufacturing or administering the drug, or therapeutic treatment regimes.

2. Breadth and Limitations:
If broad compound claims are granted, it may cover a wide class of molecules sharing common structural features, thereby creating a substantial patent barrier for generics or biosimilars. Conversely, narrow claims focus on a specific compound or formulation, which may be easier to challenge or design around.

3. Claim Type Analysis:

  • Independent Claims: Define the core innovation, providing the primary scope.
  • Dependent Claims: Add specific features, further narrowing the scope but strengthening patent enforceability.

4. Functional vs. Structural Claims:
Structural claims (chemical structure) tend to be more robust if well-supported. Functional claims (e.g., improved efficacy) can be more vulnerable unless supported by compelling data.


Claims Analysis

While the actual patent claims are proprietary, typical claims for a novel pharmaceutical patent may include:

  • A chemical compound comprising X group with specific stereochemistry.
  • A pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.
  • A method of treating indication using the compound.

The enforceability of these claims depends on:

  • Novelty: The claimed compound or formulation must not be disclosed or obvious from prior art.
  • Inventive Step: The invention must involve an inventive leap over existing molecules or methods.
  • Industrial Applicability: The invention must be capable of use in manufacturing or therapy, which is generally straightforward for pharmaceuticals.

Depending on claim drafting, broad compound claims covering a class of molecules may face challenges if similar compounds exist. Narrow claims tied to specific derivatives are easier to defend but offer limited protection.


Patent Landscape in Mexico

Mexico's pharmaceutical patent environment aligns with international standards, governed by the Mexican Industrial Property Law (LPI), which adheres to the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) [2].

1. Patent Term and Maintenance:
Patents are granted for 20 years from the filing date, assuming maintenance fees are paid timely. This provides a substantial window for market exclusivity.

2. Prior Art and Novelty Examination:
The Mexican Patent Office (IMPI) rigorously examines applications for novelty, inventive step, and industrial applicability.
Patents like MX2016013826 are examined against global patent databases, scientific publications, and existing medicinal compounds.

3. Patent Families and International Positioning:
Major pharmaceutical companies filing in Mexico often extend their patent families from US, European, and PCT applications, creating overlapping protection.

4. Challenges and Litigation:
Patent challenges in Mexico include legal invalidity or non-enforcement programs. Recent cases indicate a focus on patentability criteria and the scope of claims.


Comparative and Strategic Landscape

The Mexican patent landscape for pharmaceuticals shows increasing robustness, emphasizing patent quality and enforcement. Key considerations include:

  • Patent Term Extensions or Data Exclusivity: While Mexico does not offer supplementary data exclusivity like the US or EU, patents still provide significant exclusivity.
  • Patent Cliffs and Generics: Once patent MX2016013826 lapses, biosimilar or generic manufacturers may introduce competing products, especially if patent claims are narrow.
  • Patent Litigation Trends: Enforcement primarily occurs through civil litigation, with merit-based invalidation defenses common in challenging patents.

5. Global Context:
In comparison with international markets, Mexican patent claims tend to be aligned with global standards but may differ in claim scope due to local examination practices. For instance, broad claims may be more scrutinized or limited during prosecution.


Implications for Stakeholders

  • Pharmaceutical Innovators: Ensure that claims are drafted with maximal scope while maintaining validity, emphasizing inventive features.
  • Generic Manufacturers: Conduct detailed freedom-to-operate analyses, focusing on narrow claims and expiration dates.
  • Legal Strategists: Prepare for potential patent challenges based on prior art and claim interpretation within Mexico’s legal framework.

Conclusion

Patent MX2016013826 exemplifies a strategic patent that likely secures exclusive rights over a specific pharmaceutical compound, formulation, or method aligned with Mexico’s national patent laws. Its scope determined by its claims influences market exclusivity and legal protection strength.

The Mexican patent landscape remains a critical arena for pharmaceutical innovation, with rigorous examination processes ensuring quality patents. Stakeholders must continuously track patent prosecution, claim amendments, and potential litigation to optimize commercial and legal outcomes.


Key Takeaways

  • The strength of MX2016013826 hinges on the scope and breadth of its claims, emphasizing the importance of drafting both broad and specific claims.
  • Mexico’s patent landscape respects international standards but emphasizes local validity, requiring strategic patent prosecution and maintenance.
  • Considering Mexico’s market approach, any patent filing should account for potential patent challenges and the likelihood of generic competition after expiry.
  • Patent enforcement in Mexico is evolving, with a focus on clarifying claim scope and defending against invalidation.
  • Integrating patent landscape intelligence with global patent strategies enhances market positioning and innovation leverage.

FAQs

Q1: What strategies can strengthen the scope of pharmaceutical patents like MX2016013826 in Mexico?
A1: Draft comprehensive claims covering broad compound classes, formulations, and methods, supported by robust experimental data to establish novelty and inventive step, while ensuring claims are clear and supported.

Q2: How does Mexican patent law treat pharmaceutical invention claims compared to other jurisdictions?
A2: Mexico maintains standards similar to international norms, assessing novelty, inventive step, and industrial applicability; however, claim scope and prosecution strategies may differ, often favoring narrower claims for higher enforceability.

Q3: What are common challenges faced during patent examination of pharmaceutical patents in Mexico?
A3: Challenges include prior art disclosures, obviousness rejection, claim clarity issues, and ensuring specific inventive steps are demonstrated, notably amidst evolving legal standards.

Q4: How can companies assess the patent landscape for similar compounds in the Mexican market?
A4: Conduct prior art searches, analyze patent statuses and claims in IMPI, review international patent family filings, and monitor patent expiry dates to identify freedom-to-operate.

Q5: When does a pharmaceutical patent like MX2016013826 typically expire, and what factors influence its lifespan?
A5: Patents expire 20 years from the filing date, provided maintenance fees are paid on time. Factors such as patent extensions are not generally available in Mexico, but legal challenges can shorten effective exclusivity.


References

[1] World Intellectual Property Organization (WIPO), "Patent Drafting and Claims".
[2] Mexican Industrial Property Law (LPI).

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