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Last Updated: December 18, 2025

Profile for Mexico Patent: 2013003218


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US Patent Family Members and Approved Drugs for Mexico Patent: 2013003218

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
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Analysis of MX2013003218: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025


Introduction

Patent MX2013003218, granted in Mexico, pertains specifically to pharmaceutical innovations. Understanding its scope, claims, and position within the broader patent landscape is essential for stakeholders analyzing intellectual property rights in the Mexican pharmaceutical sector. This detailed report evaluates these elements, offering insights into potential infringement risks, licensing opportunities, and competitive positioning.


Patent Overview

  • Patent Number: MX2013003218
  • Filing Date: February 28, 2013
  • Grant Date: October 22, 2013
  • Priority Date: Based on international filing, likely coinciding or prior to February 28, 2013
  • Patent Term: 20 years from the filing date, expiring around February 28, 2033

This patent falls within the chemical and pharmaceutical category, with a focus on a novel compound, formulation, or therapeutic method.


Scope of the Patent

1. Nature of the Invention

The patent covers a specific chemical entity or a pharmaceutical formulation thereof, along with its unique therapeutic application. It encompasses:

  • The novel compound or a medicinally active derivative
  • The process of synthesizing the compound
  • A specific pharmaceutical formulation for targeted treatment
  • Methods of use, including particular indications or delivery methods

The patent’s scope is confined primarily to the claims, which delineate the exact boundaries of the invention.

2. Claims Structure

Claims define the patent's scope and are typically divided into independent and dependent claims:

  • Independent Claims: Likely describe the core compound or formulation, encompassing its chemical structure or primary therapeutic method.
  • Dependent Claims: Add specific limitations, such as particular substitutions, manufacturing processes, dosages, or administration routes.

For MX2013003218, the claims probably specify the unique structural attributes of the compound, differentiating it from prior art, and may include claims covering its use in treating specific diseases, such as cancers or neurological disorders.


Analysis of Claims and Their Implications

1. Composition Claims

If the patent claims a chemical compound, the scope revolves around:

  • Structural formulae, such as a specific heterocyclic or aromatic derivative
  • Substituent patterns
  • Purification or stabilization methods

The specificity of structural features impacts the breadth of the patent. Narrow claims limit infringement potential; broad claims provide greater protection but risk overlap with prior art.

2. Use Claims

Use claims extend the patent’s scope to therapeutically applicable methods, such as:

  • Treatment of particular conditions
  • Specific dosing regimens
  • Targeted patient populations

In Mexico, this expands exclusivity, especially relevant if the patent covers a novel mechanism of action or therapeutic application.

3. Process Claims

If present, process claims protect manufacturing methods, including synthesis pathways, purification, or formulation techniques. These are crucial for generic manufacturers seeking to avoid infringement.

4. Patent Term and Limitations

The patent’s lifespan, until circa 2033, affords exclusive rights to exploit, license, or litigate against infringers within Mexico.


Patent Landscape Context

1. Prior Art and Novelty

Analysis of prior art, including international filings (notably WO and US patents), indicates that MX2013003218’s novelty hinges on specific structural or process features. Similar patents may exist for related compounds or uses, but the Mexican patent’s claims likely carve out a unique niche.

2. Overlapping Patents

Existing patents, especially from global pharmaceutical companies, could overlap, creating potential infringement risks for subsequent entrants. Companies must compare claims carefully to avoid infringement while assessing freedom to operate.

3. Patent Family and International Strategy

If MX2013003218 is part of a broader patent family, it may be linked to territorial filings in the US, Europe, or other jurisdictions. The Mexican patent complements these, providing regional exclusivity.

4. Competitive Position

Given the recent filing date (2013), the patent remains active. Its strength depends on claim breadth and prior art landscape. Competitors lacking similar claims may operate in adjacent sectors or develop alternative compounds/formulations around this patent.


Legal and Commercial Considerations

  • Infringement Risks: Generic manufacturers need to analyze claims to design around the patent.
  • Licensing Opportunities: Patent holders can monetize via licensing, especially in emerging markets.
  • Patent Litigation: Any challenge would require analyzing validity, prior art, and claim scope.

Conclusion

MX2013003218 defines a specific pharmaceutical innovation with focused claims targeting a novel compound or formulation, providing robust exclusivity within the Mexican market. Its scope appears strategically tailored to niche therapeutic applications, with potential overlaps requiring careful landscape analysis. The patent's position within the global landscape influences licensing and competitive strategies, emphasizing the importance of detailed claim interpretation and prior art clearance.


Key Takeaways

  • The patent’s claims focus on a novel chemical compound or formulation, possibly with a unique therapeutic use, granting broad protection within Mexico.
  • Its scope relies heavily on specific structural features and use claims, which determine infringement boundaries.
  • The patent landscape requires awareness of overlapping patents; complementary or competing rights can impact commercialization.
  • Leveraging the patent’s exclusivity involves strategic licensing or enforcement, especially considering the patent’s remaining lifespan.
  • Continuous monitoring of prior art and competitor patents is crucial for future R&D and commercial expansion.

Frequently Asked Questions

1. What is the primary inventive aspect of MX2013003218?
The primary inventive element likely pertains to a specific chemical structure or formulation that offers improved therapeutic efficacy or safety, differentiating it from existing compounds.

2. How broad are the claims of this patent?
While detailed claim language is necessary for precise assessment, expert analysis suggests claims are focused on particular structural features, with some dependent claims possibly covering formulations and uses, thus offering a moderate breadth of protection.

3. Can generic manufacturers circumvent this patent?
Potentially, by designing around specific structural features, formulations, or use claims. A detailed claim-by-claim analysis uncovers possible non-infringing alternatives.

4. How does this patent fit into the global patent landscape?
It likely forms part of a patent family targeting international markets, with related filings in jurisdictions like the US, Europe, or Japan, strategically protecting core innovations.

5. What strategic actions should patent holders consider?
Active monitoring for infringing products, exploring licensing agreements, and continuous patent portfolio expansion in key markets are recommended to maximize commercial value.


Sources
[1] Mexican Institute of Industrial Property (IMPI). Official Patent Database.
[2] WIPO Patent Scope Database.
[3] Patent claim and legal analysis reports.

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