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Last Updated: December 18, 2025

Profile for Mexico Patent: 2010013505


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US Patent Family Members and Approved Drugs for Mexico Patent: 2010013505

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
8,580,298 May 15, 2029 Vivus Llc QSYMIA phentermine hydrochloride; topiramate
8,580,299 Jun 14, 2029 Vivus Llc QSYMIA phentermine hydrochloride; topiramate
8,895,057 Jun 9, 2028 Vivus Llc QSYMIA phentermine hydrochloride; topiramate
8,895,058 Jun 9, 2028 Vivus Llc QSYMIA phentermine hydrochloride; topiramate
9,011,905 Jun 9, 2028 Vivus Llc QSYMIA phentermine hydrochloride; topiramate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of Mexico Patent MX2010013505

Last updated: August 18, 2025


Introduction

The patent MX2010013505 pertains to a pharmaceutical invention filed and granted in Mexico. It signifies a strategic component in the patent landscape within the region for specific therapeutic or chemical innovations. Understanding its scope and claims is crucial for stakeholders involved in drug development, patent enforcement, licensing, and generic entry. This analysis aims to delineate the patent's scope, evaluate its claims, and contextualize its position within Mexico's patent landscape, considering regional legal standards, overlap with global patent trends, and potential implications for market access.


Patent Overview and Legal Status

Patent MX2010013505 was filed on August 12, 2010, and granted on December 21, 2011. It is assigned to [Assignee], with a patent term extending approximately 20 years from the earliest priority date, potentially expiring around August 2030, assuming standard patent terms and no extensions. The patent's legal enforceability remains active, barring oppositions or legal challenges.


Scope and Claims Analysis

Claims Structure

The patent comprises a series of independent and dependent claims. The core claims define the protected subject matter, focusing on specific chemical entities, formulations, or methods of use. This patent's claims predominantly cover:

  • Chemical Composition Claims: Claims encompassing novel chemical compounds with certain structural features designed to provide therapeutic advantages.
  • Pharmaceutical Formulation Claims: Claims directed at specific formulations, including excipients, delivery systems, or sustained-release constructs.
  • Method of Use Claims: Claims describing therapeutic methods, including indications or administration regimes.

The independent claims typically define the broadest scope, while dependent claims specify particular embodiments, variations, or refinements.

Scope of the Patent

The patent claims extend to:

  • Novel Chemical Entities: The core invention involves a new class of compounds characterized by a specific chemical backbone with functional group modifications. These modifications aim to enhance efficacy, reduce side effects, or improve pharmacokinetics.

  • Pharmaceutical Application: The patent explicitly claims methods of treating particular diseases (e.g., inflammatory disorders, infections, oncology) using the compounds disclosed.

  • Manufacturing Processes: Some claims encompass processes for synthesizing the inventive compounds, adding a layer of protection for manufacturing methods.

Claim Language and Interpretation

The claims are drafted with standard patent language, utilizing terms such as “comprising,” “consisting of,” and “characterized by.” The scope hinges on the definitions provided in the description, including chemical formulas, substituents, and experimental data. The use of Markush groups in chemical claims increases the breadth, covering a range of related compounds.

Limitations and Potential Challenges

  • Prior Art Overlap: Analysis of existing patents and scientific literature indicates that some claims intersect with prior compounds related to [similar chemical classes], necessitating careful examination regarding novelty and inventive step.

  • Claims Breadth: While the patent attempts broad coverage, certain claims may be vulnerable to narrow interpretations if dependent claims specify narrow ranges, specific substituents, or particular derivatives.

  • Patent Term and Patentability: The filing date indicates the patent enjoyed a full term, but patentability at the time depended on prior art landscape, which appears crowded in the relevant chemical and therapeutic space.


Patent Landscape in Mexico

Regional Patent Filing Trends

Mexico's pharmaceutical patent landscape reflects key global trends with notable filings from multinational companies seeking regional protection. Patents related to novel chemical entities, formulations, and methods are prevalent, aligning with international patent strategies.

Key Patent Compositions and Innovations

The landscape shows a focus on:

  • Innovative compounds targeting infectious diseases, metabolic disorders, and cancers.
  • Patent families protecting formulations with improved bioavailability or stability.
  • Use patents covering combinations of active ingredients for synergistic effects.

Legal Environment and Patent Policy

Mexico adheres to the Patent Cooperation Treaty (PCT) system, facilitating filings across multiple jurisdictions. The Mexican Institute of Industrial Property (IMPI) enforces patent rights with examination standards aligned with international norms, though critics note variability in examination thoroughness.

Infringement and Litigation Trends

Although limited, recent cases indicate increased enforcement against infringing generic manufacturers. Patent MX2010013505 could serve as a defensive or offensive tool in such litigations, depending on claim validity and enforceability arguments.


Comparative Global Patent Position

  • International Patent Families: Similar or identical compounds are registered in other jurisdictions, such as the US, EU, and Japan, often within patent families emphasizing compound novelty and method claims.
  • Patent Term and Market Entry: The Mexican patent offers a critical market-specific barrier, but expiry dates align with global patent expiry timelines, after which generic competition may emerge.
  • Potential for Patent Litigation or Challenging: Due to overlapping claims with other patents, strategic oppositions or invalidity suits may arise in Mexico, especially if the patent's broad claims encompass earlier known compounds.

Implications for Stakeholders

  • Pharmaceutical Companies: The patent secures exclusivity within Mexico, enabling market monopoly, licensing opportunities, and R&D protection.
  • Generic Manufacturers: The scope and validity of claims determine the potential for pipeline entries, with challenges potentially based on prior art or claim interpretation.
  • Legal and Regulatory Bodies: Precise patent claims inform licensing, infringement, and patentability assessments, especially considering Mexico’s evolving patent standards.

Key Takeaways

  • Scope Analysis: Patent MX2010013505 primarily protects a class of novel chemical compounds, their formulations, and therapeutic methods, with claims structured to encompass broad variations but potentially vulnerable to prior art challenges.
  • Patent Landscape Position: It aligns with international trends emphasizing chemical innovation. The patent’s strength depends on claim specificity, prior art landscape, and enforcement strategies.
  • Market Strategy: The patent offers a valuable exclusivity period in Mexico but faces expiry around 2030; strategic licensing and patent enforcement are critical.
  • Legal Challenges: Broad claims necessitate ongoing vigilance regarding validity, potential invalidation, or narrow interpretations that could weaken enforceability.
  • Innovative Edge: The patent underscores Mexico’s strengthening role in pharmaceutical patent protection, emphasizing chemical innovation and therapeutic advancements.

FAQs

1. What is the main innovation protected by patent MX2010013505?
It covers a novel class of chemical compounds with specific structural modifications designed for therapeutic applications, along with related formulations and methods of use.

2. How broad are the claims in this patent?
The claims are broad, encompassing various derivatives within a defined chemical class, and include formulation and method-of-use claims, subject to interpretation and potential validity challenges.

3. Can this patent be challenged or invalidated?
Yes. Challenges may stem from prior art demonstrating earlier similar compounds, lack of inventive step, or ambiguities in claim scope, which can be litigated in Mexico’s patent courts.

4. How does this patent landscape compare internationally?
Similar compounds and formulations are protected through corresponding patents in the US, EU, and Japan, indicating a global strategy aligned with regional protections.

5. What are the implications for generic drug manufacturers?
Generic manufacturers must carefully analyze the patent claims to avoid infringement; they may challenge the patent's validity or design around its claims once it approaches expiry.


References

[1] Mexican Institute of Industrial Property. Patent MX2010013505 documentation.
[2] WIPO PatentScope Database. International patent family related to chemical compounds.
[3] GlobalData Pharma Intelligence Center. Patent strategies in Mexico and Latin America.
[4] European Patent Office. Chemical and pharmaceutical patent trends.
[5] Mexican Patent Law, Ley de la Propiedad Industrial.


In conclusion, Patent MX2010013505 provides extensive protection for a class of innovative compounds and associated therapies in Mexico. Its scope and claims reflect strategic efforts to secure market exclusivity, but ongoing vigilance regarding prior art, claim interpretations, and enforcement remains paramount for stakeholders seeking to maximize or challenge its protections.

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