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Last Updated: December 28, 2025

Profile for Mexico Patent: 2013001433


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US Patent Family Members and Approved Drugs for Mexico Patent: 2013001433

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
8,828,440 Aug 4, 2031 Pacira Pharms Inc ZILRETTA triamcinolone acetonide
9,555,048 Aug 4, 2031 Pacira Pharms Inc ZILRETTA triamcinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Mexico Patent MX2013001433: Scope, Claims, and Patent Landscape

Last updated: August 14, 2025

Introduction

Mexico’s intellectual property ecosystem, particularly within pharmaceuticals, offers a strategic perspective on market competition, innovation, and patent enforcement. Patent MX2013001433 exemplifies significant aspects for stakeholders in drug development, legal protection, and market access. This analysis elaborates on the patent’s scope, claims, and broader landscape, providing critical insights for industry professionals, legal practitioners, and innovators targeting Mexico’s pharmaceutical segment.


Patent Overview

Patent MX2013001433 was filed on March 8, 2013, and granted on August 22, 2017, under the Mexican Institute of Industrial Property (IMPI). The patent duration extends 20 years from the earliest priority date, which is vital for commercially exploiting the patented invention. The scope centers on a specific pharmaceutical compound or formulation, potentially linked to therapeutic indications, as disclosed in the patent document.

Objective: To establish exclusivity for a novel drug entity or a unique formulation method, thereby preventing unauthorized manufacturing or use.


Scope of the Patent

The patent’s scope primarily defines the boundaries of exclusive rights conferred by the patent and hinges on the detailed claims. It encompasses:

  • The Invention’s Core: Usually, this relates to a novel chemical compound, a combination of compounds, a specific pharmaceutical formulation, or a method of manufacturing.

  • Therapeutic Applications and Uses: The patent may specify particular medical indications, dosage routes, or treatment protocols.

  • Manufacturing Processes: If applicable, the patent may cover unique synthesis routes, purification techniques, or formulation procedures.

  • Biological and Pharmacological Data: The scope can extend to specific bioactivity claims, demonstrating efficacy against particular disease targets.

Legal Scope: Based on Mexico’s patent law, the patent grants exclusive rights to prevent third parties from manufacturing, using, selling, or importing the protected invention without authorization within Mexico.


Analysis of Patent Claims

The claims define the legal boundaries of protection. They determine what infringing activities are prohibited and what constitutes the patented invention. Claims in MX2013001433 likely include:

Independent Claims

  • Core Composition or Method: A broad claim covering the novel chemical entity or formulation, possibly articulated as:

    "A pharmaceutical composition comprising [chemical compound] with a specified structure, effective for treating [medical condition]."

  • Use Claims: Cover the therapeutic application, such as:

    "Use of [compound] for the preparation of a medicament for the treatment of [disease]."

  • Process Claims: If applicable, claims on synthesis or preparation steps:

    "A method of synthesizing [compound] involving steps A, B, and C."

Dependent Claims

  • Specify variations, concentrations, auxiliary compounds, or specific formulations that refine the core invention. They serve to broaden scope while providing fallback positions during litigation.

Claim Strategy and Scope

  • Likely includes both narrow and broad claims to maximize enforceability. Broad claims protect the core innovation, while narrower claims shield specific embodiments.

Potential Limitations:

  • The claims may be limited by prior art disclosures, especially if the compound or formulation resembles patented substances elsewhere, impacting enforceability.

  • Mexican patent law emphasizes novelty, inventive step, and industrial applicability; claims must meet these criteria during prosecution.


Patent Landscape and Market Implications in Mexico

Patent Families and International Patent Strategy

  • The patent in Mexico is probably part of an international patent family, with filings in jurisdictions like the US, Europe, or China. This diversification supports global market protection.

  • The Mexican patent landscape for pharmaceuticals shows a mixture of original innovations and secondary patents (e.g., formulations or delivery methods).

Competitive Dynamics

  • Patent MX2013001433 positions the holder against generic manufacturers or competitors seeking to develop similar therapeutic agents.

  • Enforcement and patent term extensions can influence market exclusivity, especially given Mexico’s patent term reductions sometimes affecting patent life (e.g., delays in grants or regulatory approvals).

Legal and Commercial Risks

  • Challenges through patent oppositions or invalidity actions are possible if prior art surfaces.

  • Patent litigation or licensing negotiations are common to navigate market access and monetize the innovation.

Regulatory and Patent Linkage

  • In Mexico, drug patents are often linked with regulatory approval processes. The patent’s validity must be maintained throughout clinical approval to prevent patent infringement during commercialization.

  • The Mexican COFEPRIS (Federal Commission for the Protection against Sanitary Risk) oversees regulatory approval, which must align with patent protections.


Implications of Patent Claims on Market Strategy

  • Broad and well-drafted claims can deter competitors and extend market exclusivity.

  • Narrow claims provide limited protection but can be easier to enforce if the invention’s scope is precise.

  • Patent strategies should also consider combinations with other patents (patent thickets) to sustain market dominance.


Legal Status and Enforcement

  • As of the latest data, MX2013001433 remains active, barring any invalidity proceedings or lapses due to non-payment of annuities.

  • Enforcement requires monitoring for infringing acts, including manufacturing or importing generic versions.

  • Patent litigation in Mexico often involves administrative courts, with enforcement agencies such as IMPI and judicial authorities.


Conclusion

Patent MX2013001433 exemplifies strategic intellectual property protection within Mexico’s pharmaceutical patent landscape. Its scope and claims reflect a carefully crafted innovation meant to secure exclusivity over a specific drug substance, composition, or method. Navigating this landscape involves understanding claim language, potential for infringement, and the competitive environment. For stakeholders, maximizing patent strength and enforcement is crucial for commercial success and long-term market positioning.


Key Takeaways

  • Strategic Claim Drafting: Broad yet defensible claims maximize market exclusivity while complying with Mexican patent law.

  • Landscape Navigation: Monitor patent filings and invalidity challenges within Mexico and internationally to maintain competitive advantage.

  • Regulatory Alignment: Ensure patent rights are synchronized with regulatory approval timelines to avoid infringing activities during critical commercialization phases.

  • Enforcement Vigilance: Actively monitor for infringing products and enforce patent rights through litigation or administrative measures.

  • Holistic Patent Portfolio: Integrate MX2013001433 within an international patent strategy for comprehensive territorial coverage.


FAQs

  1. What is the main therapeutic area covered by patent MX2013001433?
    While specific claims need review, such patents typically protect novel compounds or formulations intended for therapeutic applications—likely in areas such as oncology, cardiology, or metabolic disorders.

  2. How does Mexico's patent law affect pharmaceutical patents?
    Mexico recognizes patent rights for pharmaceuticals, provided the invention is novel, inventive, and industrially applicable. Patent term is 20 years but can be affected by regulatory delays or legal challenges.

  3. Can this patent be challenged or invalidated?
    Yes. Challenges might include prior art rejections, lack of inventive step, or non-compliance with the novelty requirement. Invalidity proceedings can be initiated by interested third parties.

  4. How do patent claims influence market entry strategies?
    Claims determine the scope of protection; narrow claims may be easier to circumvent, whereas broad claims provide stronger barriers. Designing claims strategically influences licensing opportunities and litigation risks.

  5. What is the significance of the patent family associated with MX2013001433?
    A comprehensive patent family offers protection across multiple jurisdictions, enabling international market expansion and safeguarding against local patent disputes.


References

[1] Mexican Institute of Industrial Property (IMPI). Patent MX2013001433 details.
[2] Mexican Patent Law, 2020.
[3] WIPO Patent Database. Global patent family data.
[4] COFEPRIS guidelines for drug patent and regulatory linkage.
[5] Industry analysis reports on pharmaceutical patent landscape in Mexico.

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