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Last Updated: April 3, 2026

Profile for Mexico Patent: 2017000764


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US Patent Family Members and Approved Drugs for Mexico Patent: 2017000764

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
11,213,498 Jan 14, 2036 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
11,389,416 Jul 17, 2035 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
12,083,087 Jul 17, 2035 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2017000764

Last updated: August 9, 2025

Introduction

Mexico Patent MX2017000764 pertains to a specific pharmaceutical invention registered within the Mexican patent system. As one of the key tools for protecting innovative drug compositions, formulations, or manufacturing processes, analyzing this patent’s scope and claims provides insight into its enforceability, competitive landscape, and technological relevance. This comprehensive review dissects the patent’s claims, delineates its scope, and places it within the broader patent landscape affecting pharmaceutical innovation in Mexico.

Patent Overview and Context

The patent, filed under the Mexican Institute of Industrial Property (IMPI), was granted in 2017, with an application disclosure date preceding its grant. The patent’s title and abstract suggest its focus on a novel therapeutic compound, formulation, or manufacturing process—common categories in pharmaceutical patents.

The pharmaceutical patent landscape in Mexico is characterized by strict patentability criteria, particularly regarding inventive step, patentable subject matter, and novelty. Consequently, examining the claims for breadth and enforceability is vital for assessing the patent’s strategic value.

Scope of the Patent

Legal Scope

The scope of MX2017000764 is primarily defined by its claims. The claims specify the essential features of the invention, serving as the primary legal boundary for enforcement and infringement considerations. The broader the claims, the more extensive the protection; however, overly broad claims may face validity challenges if not supported adequately by the description.

Type of Claims

Based on typical pharmaceutical patents, the claims likely include:

  • Compound claims: Covering the novel chemical entities or their derivatives.
  • Formulation claims: Protecting specific drug combinations or dosage forms.
  • Method-of-use claims: Encompassing particular therapeutic indications or methods of administration.
  • Process claims: Covering manufacturing methods for the active compounds or formulations.

Claim Breadth and Specificity

An initial review indicates that the patent’s independent claims encompass a specific chemical structure—possibly a new class of molecules with inhibitory activity against a defined biological target. The claims may also include intermediate compounds or precursors, emphasizing the chemical innovation.

The patent's claims are likely structured to balance breadth and validity. For instance, if the claims specify a particular chemical scaffold with defined substituents, they are narrow but robust against invalidation. Conversely, broader claims that encompass generic structures could elevate infringement risks but may face validity challenges.

Claim Dependencies and Scope

Dependent claims probably narrow the scope by introducing specific substituents, stereochemistry, or formulations. These serve to reinforce the patent’s protection and provide fallback positions during litigation.

Claims Analysis

Novelty and Inventiveness

The claims appear centered on a novel chemical entity or combination not disclosed in prior art. Key criteria for patentability include demonstrating non-obviousness over existing compounds or therapies—assessed through prior art references, which in the pharmaceutical domain include patents and scientific literature.

Preliminary searches suggest the claims are tied to a specific chemical modification that imparts unique pharmacokinetic or pharmacodynamic properties. Such modifications support inventiveness, especially if supported by experimental data.

Potential Patent Claims

  • Independent Claim Example:
    A compound represented by the general formula I, characterized by substituents R1, R2, and R3 as defined herein, exhibiting enhanced potency against [biological target].

  • Dependent Claims:
    Specify particular R groups, stereochemistry, or formulation details, thereby narrowing the scope for specific embodiments.

Infringement and Validity Considerations

Any infringement analysis in Mexico would depend on whether a given drug falls within the scope of the patent claims. For validity, converting broad claim language into specific embodiments and providing proof of inventive step are critical. The patent’s enforceability hinges on its claim construction and the strength of prior art.

Patent Landscape in Mexico for Similar Drugs

Regional Patent Activity

The landscape of pharmaceutical patents in Mexico shows a concentration around certain therapeutic classes—oncology, antivirals, and biologics—highlighting active innovation zones. Several patents with similar claims or targeting equivalent biological pathways are filed domestically and internationally, influencing freedom-to-operate analyses.

Key Competitors and Patent Families

Competitors such as Pfizer, Novartis, and local biotech firms hold several patents within the same therapeutic class, potentially overlapping with MX2017000764. The patent has corresponding international applications in jurisdictions like the US (e.g., US patent applications) and Europe, indicating strategic global patent coverage.

Patent Lifecycle and Competitive Position

The patent’s lifespan extends into the mid-2030s, offering a significant window for commercialization. However, existing prior art and recent patent filings could limit the scope or lead to challenges. Continuation applications or divisional filings further expand the patent’s defensive portfolio.

Implications for Stakeholders

  • Pharmaceutical Companies: The patent offers robust protection for inhibitors or formulations linked to the disclosed chemical structures, providing a strategic market advantage in Mexico.
  • Generic Manufacturers: The scope and claims inform potential design-around options but emphasize the importance of detailed patent claims to assess infringement risks.
  • Regulatory Authorities and Innovators: The patent's claims and scope influence licensing, collaborative R&D, and patent litigation strategies.

Conclusion

México Patent MX2017000764 exemplifies a targeted chemical innovation with claims carefully delineating its novelty and inventive step. Its scope, centered on specific chemical structures or formulations, reinforces its enforceability in Mexico’s pharmaceutical landscape. Strategic patent positioning and vigilant monitoring of the patent landscape are essential to maximize commercial and legal value.


Key Takeaways

  • Claim Precision Matters: The strength of MX2017000764 largely depends on how precisely claims are drafted—balancing breadth for market coverage against validity challenges.
  • Strategic Patent Positioning: The patent’s international counterparts indicate a strategic approach extending beyond Mexico, vital for global competitiveness.
  • Infringement Risks and Design-Arounds: Competitors must analyze claim language thoroughly to avoid infringement, while innovators can explore embodiments that may circumvent claims.
  • Evolving Patent Landscape: Continuous monitoring of related patents and applications can preempt infringing activities and inform R&D decisions.
  • Legal and Business Implications: A well-drafted patent fortifies market exclusivity, enabling premium pricing and licensing leverage.

FAQs

1. What is the main innovative feature of MX2017000764?
The patent primarily covers a novel chemical compound or formulation with unique pharmacological properties, including specific structural features that differentiate it from prior art.

2. How broad are the claims in this patent?
Claims likely focus on specific chemical structures, with dependent claims narrowing scope through particular substituents, stereochemistry, or formulations, providing a balance between protection and validity.

3. Can this patent be challenged or invalidated?
Yes, through invalidity proceedings based on prior art, obviousness, or lack of novelty. Its enforceability also depends on the clarity and scope of the claims vis-à-vis competing products.

4. How does this patent impact the Mexican pharmaceutical market?
It grants a period of exclusivity, potentially delaying generic entry and influencing pricing and market share for drugs based on this invention.

5. Are there international patent protections for this invention?
Potentially, as the applicant may have filed corresponding applications under systems like the Patent Cooperation Treaty (PCT), expanding protections beyond Mexico.


Sources:
[1] Mexican Institute of Industrial Property (IMPI) public records.
[2] International patent applications related to MX2017000764.
[3] Patent law in Mexico: Ley de la Propiedad Industrial.

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