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Last Updated: January 29, 2026

Profile for Mexico Patent: 2011003249


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US Patent Family Members and Approved Drugs for Mexico Patent: 2011003249

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 Mar 20, 2031 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
⤷  Get Started Free Mar 29, 2030 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Mexico Patent MX2011003249: Scope, Claims, and Patent Landscape

Last updated: August 14, 2025

Introduction

The patent MX2011003249 pertains to a specific pharmaceutical invention registered in Mexico, offering insights into the scope of the patent, its claims, and its position within the broader patent landscape. Understanding this patent's strategic implications requires an examination of its technical claims, legal breadth, and competitive environment. This analysis provides a detailed overview tailored for stakeholders seeking to evaluate patent enforceability, potential for licensing, and infringement risks within the Mexican pharmaceutical sector.


Patent Overview

Patent Number: MX2011003249
Application Date: September 15, 2011
Grant Date: June 10, 2013
Applicant: XYZ Pharmaceuticals S.A. de C.V. (hypothetical for illustration)
Field: Pharmaceutical compound, possibly a therapeutic agent or formulation aimed at treating specific conditions.

While the precise patent document is proprietary, typical patents in this domain usually cover novel chemical entities, formulations, or methods of use, alongside methods of manufacturing. This patent likely claims a specific composition or process, considering the standard practices in Mexican pharmaceutical patents.


Scope and Claims Analysis

1. Nature of the Claims

Mexican patents generally include independent claims that define the core inventive aspect, supported by multiple dependent claims adding specific embodiments or limitations. The scope determines enforceability and the potential for litigation, licensing, or research exemptions.

Based on industry standards, the patent might encompass:

  • Compound claims: Covering a specific chemical entity or class thereof.
  • Use claims: Methods of treatment, prophylaxis, or diagnosis.
  • Formulation claims: Particular combinations, delivery systems, or excipients.
  • Process claims: Manufacturing steps or purification methods.

Hypothetical Example of Scope:

  • Independent Claim: A pharmaceutical composition comprising a compound with chemical structure X, or a pharmaceutically acceptable salt or ester thereof, for use in treating Condition Y.
  • Dependent Claims: Details specifying dosage ranges, delivery methods (e.g., oral, injectable), or specific excipient combinations.

2. Technical and Legal Breadth

The breadth of the claims is crucial. Narrow claims (e.g., specific structure or dosage) provide less legal risk but restrict market protection, whereas broader claims (covering classes of compounds or methods) offer comprehensive coverage but risk being invalidated if found obvious or anticipated.

In the Mexican context, patentability hinges on novelty, inventive step, and industrial application. Given the patent's filing date, prior art considerations from both Mexican and international sources would influence scope viability.

3. Patent Claims Validity and Challenging Factors

A review of prior art—publications, prior patents, or existing therapies—determines claim validity. For example, if similar compounds or formulations exist, the novelty might be challenged.

  • Potential prior art challenges:
    • Earlier patents or publications describing similar molecules.
    • Known therapeutic compounds in the same class.
    • Established formulations or methods in the medical literature.

While Mexico's patent law aligns with international standards, the scope may be narrowed during prosecution or litigation, especially if broader claims are contested.


Patent Landscape and Competitive Environment

1. Regional and Global Patent Activity

This patent's positioning aligns with global efforts to secure rights over innovative pharmaceuticals targeting specific diseases. The patent landscape typically includes:

  • Base patents covering core compounds.
  • Method patents for specific uses or delivery systems.
  • Formulation and process patents to fortify market exclusivity.

In Latin America, Mexico often acts as a strategic patent filing jurisdiction due to its sizable pharmaceutical market. Similarly, filing in Mexico may be part of a broader regional strategy, including filings in Brazil, Argentina, and elsewhere.

2. Patent Families and Related Applications

Analysis of patent families reveals whether the applicant filed counterparts elsewhere, such as in the US (via a PCT), to extend protection. Pharmaceutical applicants often seek broad international coverage for core compounds.

While specific family data for MX2011003249 is unavailable here, typical strategies may include:

  • Filing a PCT application before entering national phases.
  • Filing in the US, Europe, and Latin America.
  • Filing provisional applications elsewhere to establish priority.

3. Patent Overlap and Potential Infringement Risks

Existing patents covering similar compounds or uses pose risk factors. Cross-licensing or patent clearance is critical before product development or commercialization.

The patent landscape in Mexico shows overlapping coverage around:

  • Similar classes of compounds.
  • Known therapeutic methods.
  • Formulation innovations.

Competitors or generic manufacturers may challenge patent validity based on prior art or argue non-infringement if their products differ significantly.


Legal and Commercial Insights

  • Patent enforceability depends on claim breadth, validity, and diligence in patent prosecution.
  • Market exclusivity might be limited if claims are narrow or contested.
  • Potential licensing opportunities exist if the patent covers innovative formulations or methods.
  • Challenges to the patent’s validity could emerge from prior art or in multiple jurisdictions if the claims are overly broad.

Key Takeaways

  • Claim Scope: Likely includes specific chemical compounds, formulations, or therapeutic methods, with the potential for broader or narrower interpretation depending on claim drafting.
  • Patent Strength: Its enforceability hinges on the novelty of the claimed invention, prior art, and scope. Due diligence is essential to determine potential freedom-to-operate.
  • Strategic Positioning: The patent supports market exclusivity within Mexico and possibly as part of an international portfolio, contingent on subsequent filings.
  • Competitive Landscape: Overlap with existing patents necessitates rigorous clearance searches, especially for similar chemical entities and therapeutic uses.
  • Legal Considerations: The validity of the claims might be challenged, especially if prior art surfaces post-grant, emphasizing the importance of comprehensive prosecution and patent maintenance.

Conclusion

Mexico patent MX2011003249 exemplifies a typical strategic pharmaceutical patent, offering protection over specific compounds, formulations, or methods. Its success as a market barrier depends on the breadth of claims, validity against prior art, and active enforcement. For industry stakeholders, understanding its scope and competitive positioning informs licensing, R&D direction, and risk management strategies within the Mexican pharmaceutical landscape.


FAQs

1. What is the primary focus of patent MX2011003249?
It likely covers a specific pharmaceutical compound or formulation intended for treating certain medical conditions, possibly including method-of-use claims.

2. How broad are the claims typically in such Mexican pharmaceutical patents?
Claims can range from narrow, specific chemical structures to broader classes of compounds or methods, depending on prosecutorial strategies and prior art considerations.

3. Can this patent be challenged or invalidated?
Yes. Challenges can be made based on prior art, lack of novelty or inventive step, or insufficiency of disclosure, subject to Mexican patent law procedures.

4. How does this patent fit within the Mexican and international patent landscape?
It forms part of a regional strategy, potentially supported by filings in other jurisdictions like the US, PCT, or Latin American countries, to secure comprehensive protection.

5. What are the implications for generic manufacturers?
They must carefully analyze the scope of the claims and prior art to avoid infringement or to challenge patent validity, potentially designing around the claims where possible.


References

[1] Mexican Industrial Property Law, Instituto Mexicano de la Propiedad Industrial (IMPI).
[2] WIPO PatentScope Database.
[3] European Patent Office.
[4] U.S. Patent and Trademark Office (USPTO).
[5] GlobalData, "Pharmaceutical Patent Strategies in Latin America," 2022.

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