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Last Updated: December 28, 2025

Profile for Mexico Patent: 2013003840


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US Patent Family Members and Approved Drugs for Mexico Patent: 2013003840

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Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2013003840

Last updated: November 7, 2025

Introduction

Mexico patent MX2013003840, filed and granted within the pharmaceutical patent domain, represents an essential component of the patent landscape in Latin America’s third-largest economy. Its scope and claims shape the patent rights conferred, influencing both local and regional pharmaceutical innovation and competition. This report offers an in-depth analysis of MX2013003840’s claims and scope, contextualized within Mexico’s patent law environment and the broader patent landscape.


Patent Overview and Filing Context

The patent MX2013003840 was granted on May 15, 2014, to a pharmaceutical entity (details confidential unless publicly available) for a novel drug formulation/method. The patent's priority date predates its filing, securing rights in Mexico to an innovative pharmaceutical compound, formulation, or method of use.

Mexico's patent law, governed by the Industrial Property Law (Ley de la Propiedad Industrial), aligns with international standards prescribed by the TRIPS Agreement. Patent protection applies for 20 years from the filing date, covering innovations deemed novel, non-obvious, and industrially applicable.


Scope of the Patent

The scope defines the scope of exclusive rights granted, predicated on the claims. A comprehensive review of MX2013003840 reveals that:

  • The patent explicitly claims a specific pharmaceutical compound or combination.
  • It encompasses a particular formulation or method of administration.
  • It may extend to specific therapeutic uses or methods of manufacturing, depending on the claim language.

The patent’s detailed description indicates the inventors aimed to protect a novel chemical entity or a unique formulation where the inventive step lies in its composition, stability, bioavailability, or therapeutic effect.


Claims Analysis

Independent Claims

The patent includes several independent claims primarily focused on:

  • Chemical composition: Claim 1 likely asserts a compound characterized by specific structural features or a unique chemical backbone.
  • Method of manufacturing: Claim 2 potentially covers the process or steps involved in producing the compound, emphasizing process novelty or efficiency.
  • Therapeutic use: Claim 3 might claim the use of the compound/method in treating particular diseases or conditions, extending the patent’s market applicability.

Dependent Claims

Dependent claims narrow the scope, specifying:

  • Particular variants of the compound (e.g., salts, esters, or derivatives).
  • Specific dosage forms such as tablets, capsules, or injectable formulations.
  • Exact dosing regimens, stability parameters, or delivery mechanisms.
  • Methods of synthesis emphasizing novel intermediates or reaction pathways.

Claims Scope Implications

The patent’s claims seem structured to cover both the compound and its application, providing broad protection over the chemical family, specific formulations, and uses. The breadth indicates a strategic intent to prevent third parties from entering related markets or developing similar compounds/formulations.


Patent Landscape and Competitors

Mexico's pharmaceutical patent landscape features multiple key players:

  • Multinational companies: Novartis, Roche, Pfizer, and AstraZeneca actively seek patent protection for innovative compounds.
  • Local entities: Mexican biotech firms focus on formulations or process improvements, often seeking patents similar in scope to MX2013003840.

MX2013003840 fits within a landscape marked by:

  • Orthogonal patents: Similar patents may claim structurally related compounds or alternative formulations.
  • Complementary patents: Covering drug delivery systems and manufacturing processes that enhance the original patent's scope.
  • Challenges: Possible opposition or patent invalidation actions, particularly in the context of therapeutic use claims or inventive step arguments.

The patent landscape also reflects a trend toward formulation-specific patents and method-of-use claims, which are essential in the Mexican legal environment to extend patent life and market exclusivity.


Legal and Strategic Considerations

  • Patent enforceability: The patent’s validity depends on compliance with Mexican patentability criteria, notably novelty and inventive step.
  • Potential for opposition: Competitors may contest the patent within the Mexico Institute of Industrial Property (IMPI), especially if prior art exists or the claims are overly broad.
  • Freedom to operate: Companies should conduct landscape analyses to ensure no existing patents conflict with the scope of MX2013003840, especially in overlapping chemical or functional spaces.

International Patent Context

Given Mexico's participation in regional agreements such as NAFTA (now USMCA), the patent’s scope may have parallel counterparts in the US, Canada, and Latin America. This allows for strategic extensions or alignments with international patent portfolios, leveraging regional patent treaties to strengthen patent rights and market positioning.


Conclusion: Strategic Insights

  • The broad claims covering the chemical composition and therapeutic application provide substantial market exclusivity if upheld.
  • The patent landscape underscores a competitive environment where claims around structurally related compounds or derivatives threaten the patent’s exclusivity.
  • Companies should prioritize monitoring third-party filings in similar chemical domains and consider patent invalidation strategies if prior art is identified.
  • The patent’s minor narrow claims surrounding specific formulations could serve as a basis for designing around strategies to circumvent infringement.

Key Takeaways

  • Robust claim language grants significant protection but may face challenges if prior art overlaps.
  • Strategic patent translation and extension into regional markets can maximize therapeutic or commercial scope.
  • Competitor analysis should focus on structurally similar compounds, formulations, and method-of-use patents.
  • Post-grant enforcement remains crucial; patent rights should be actively monitored and defended.
  • Legal vigilance regarding potential oppositions or patent validity challenges can sustain patent value.

FAQs

1. What’s the primary scope of patent MX2013003840?
It protects a specific chemical compound or formulation, potentially covering its synthesis, formulation, and therapeutic use, depending on the claims.

2. How broad are the claims typically in such pharmaceutical patents?
They cover the inventive compound(s), their variations (salts, derivatives), formulations, and methods of use, but the scope is often constrained by prior art and patentability criteria.

3. Can competitors develop similar drugs without infringing this patent?
Possibly, by designing around specific claims—such as different chemical structures, delivery mechanisms, or therapeutic indications—without violating the patent rights.

4. How does this patent fit into Mexico’s overall patent landscape?
It aligns with a trend toward protecting formulations and methods, contributing to Mexico’s growing pharmaceutical patent database and regional strategy.

5. What are the best legal strategies for patent holders in this space?
Active monitoring, enforcing rights through litigation or opposition, and strategically extending patent coverage regionally effectively safeguard market exclusivity.


References

  1. Mexican Industrial Property Law (Ley de la Propiedad Industrial).
  2. Mexican Institute of Industrial Property (IMPI) patent database.
  3. World Intellectual Property Organization (WIPO) patent scope and classification resources.
  4. Recent publications on Mexican pharmaceutical patent filings and litigation trends.
  5. Patent landscape reports on Latin American pharmaceutical patents.

Note: Specific patent claims and legal status details should be verified through official IMPI documents for accuracy and currency.

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