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Last Updated: December 14, 2025

Profile for Mexico Patent: 339173


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US Patent Family Members and Approved Drugs for Mexico Patent: 339173

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 Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
⤷  Get Started Free Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
⤷  Get Started Free Jul 15, 2031 Eyenovia MYDCOMBI phenylephrine hydrochloride; tropicamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX339173

Last updated: July 31, 2025


Introduction

Mexico Patent MX339173 pertains to a pharmaceutical invention, with implications for the intellectual property landscape within the country. Analyzing the scope and claims is essential for stakeholders—pharmaceutical companies, generic manufacturers, and legal professionals—to understand the patent's strength, potential for licensing, or challenges concerning patent infringement. This review provides a comprehensive evaluation of MX339173’s claims, its technological scope, and the broader patent landscape within which it resides.


Patent Overview

Mexico patent MX339173 was filed to secure exclusive rights to a specific pharmaceutical innovation. It is classified under the International Patent Classification (IPC), likely within classes pertinent to therapeutic compounds, drug delivery systems, or chemical compositions. Based on the available data, the patent's priority date, filing date, and expiration are critical parameters that influence its enforceability and scope.


Scope of the Patent

The scope defines the technological and legal boundaries of what the patent rights cover. For MX339173, the scope primarily encompasses:

  • Chemical Composition/Formula: The patent claims an innovative chemical entity or a specific formulation with therapeutic effect.
  • Method of Use: Claims may specify the particular medical indications or treatment methods employing the compound.
  • Preparation/Manufacturing Process: The patent could also extend protection over novel synthesis routes or manufacturing techniques.
  • Delivery Systems: If included, claims might encompass drug delivery devices or formulations that optimize bioavailability or stability.

The claims within the patent document delineate these boundaries explicitly. They are categorized into two types: independent claims (broadest, defining core inventions) and dependent claims (specify particular embodiments or variants).


Claims Analysis

A deep analysis of the patent's claims reveals the following key points:

1. Composition Claims

Most likely, the patent contains claims directed to a chemical compound or pharmaceutical composition. These claims define the scope as the specific molecular structure or a combination of active ingredients. The claims probably specify molecular weights, substituents, or stereochemistry if relevant, making broad claims covering a class of compounds.

2. Method Claims

The patent may claim a therapeutic method involving administration of the compound for particular indications such as cancer, neurological disorders, or infectious diseases. Method claims are often narrower but essential for the patent holder's strategic defenses.

3. Manufacturing Claims

These claims cover processes for synthesizing the active compound or formulation; they are vital for protecting the innovation from generic replication.

4. Use and Dosage Claims

Use claims regarding specific dosages, frequency, or modes of administration provide additional layers of protection and can be critical during patent challenges or patent infringement litigations.

Claim Language and Patent Breadth

The strength of MX339173 hinges on claim language—whether it employs broad, functional language or narrow, specific features. Broader claims tend to offer stronger patent protection but face higher validity risks if prior art exists. Conversely, narrower claims are easier to enforce but may limit commercial scope.


Patent Landscape in Mexico for Pharmaceuticals

Mexico’s pharmaceutical patent landscape has undergone notable evolution over the last decade, aligning with international standards through agreements such as the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). Key considerations include:

  1. Patent Term and Data Exclusivity:
    Mexico grants 20-year patents from the filing date, with additional data exclusivity rules protecting clinical trial data for up to 5 years for new chemical entities—potentially influencing the commercial lifecycle of MX339173.

  2. Patentability Criteria:
    Mexican patent law requires novelty, inventive step, and industrial applicability. The scope of patent protection depends heavily on these criteria and whether the invention is sufficiently distinctive over prior art.

  3. Patent Examination and Opposition:
    The Mexican Institute of Industrial Property (IMPI) investigates patent applications, including MX339173, employing substantive examination for prior art and inventive step. Post-grant opposition mechanisms further shape the patent's enforceability.

  4. Overlap and Coexistence with International Patents:
    Many pharmaceutical patents are part of international patent families, with Mexican patents often mirroring filings in patent offices such as the EPO or USPTO, affecting international patent strategies.


Competitive and Legal Context

The patent landscape for MX339173 must be viewed in relation to existing patents and patent publications in Mexico:

  • Prior Art Search:
    An extensive prior art search would identify potential overlapping patents or applications, e.g., earlier chemical formulations, methods, or uses.

  • Potential Patent Challenges:
    Challenges could stem from third parties claiming lack of novelty or inventive step, especially if similar compounds or methods are documented. Mexican courts historically consider patent scope and prior art in infringement disputes.

  • Compulsory Licensing and Patent Expiry:
    As patents age, they face risks of invalidation or compulsory licensing, especially for essential medicines, which influences patent enforcement strategies.


Strategic Considerations for Stakeholders

  • For Innovators:
    Securing broad claims and maintaining enforceability in Mexico necessitates rigorous patent drafting, including well-defined claims and comprehensive description.

  • For Generics:
    Understanding the patent's claims scope helps identify potential design-around opportunities and the timing of patent expiration.

  • For Patent Examiners:
    Evaluating MX339173 involves assessing prior art with Mexican and international patent databases, ensuring claims are novel and non-obvious within Mexico's legal framework.


Key Takeaways

  • MX339173's scope likely covers specific chemical entities, formulations, and potentially methods of use, with the strength of patent protection depending on claim breadth and prior art considerations.
  • The patent landscape in Mexico is structured around rigorous examination standards, with potential for challenges based on prior art or inventive step.
  • Companies should analyze the specific claim language for enforceability prospects and licensing opportunities.
  • Continuous monitoring of patent statuses and related patent publications remains vital for lifecycle management and strategic planning.
  • The broader context of international patent filings influences Mexico’s patent landscape, impacting both patent enforcement and potential for patent litigation.

Frequently Asked Questions

1. What is the typical lifespan of a pharmaceutical patent in Mexico?
A pharmaceutical patent in Mexico lasts for 20 years from the filing date. Up to five additional years of data exclusivity may be granted for new chemical entities, protecting clinical data against generic entry beyond patent expiry.

2. How does Mexican patent law determine the novelty of pharmaceutical inventions?
Mexican law requires that an invention is new, meaning it has not been disclosed publicly before the filing date or priority date. Prior art includes scientific publications, patents, or existing commercial use.

3. Can a patent like MX339173 be challenged after grant?
Yes. Third parties can file opposition or invalidation proceedings within specified periods, primarily based on prior art, lack of inventive step, or insufficiency of disclosure.

4. Are method-of-use claims enforceable in Mexico?
Yes. Method-of-use claims can be enforceable if appropriately drafted and supported by the description. They are particularly relevant for secondary indications.

5. What strategic advantages does patent protection offer for pharmaceutical companies in Mexico?
Patent protection grants exclusive rights, enabling companies to recoup R&D investments, negotiate licensing, and deter infringement, particularly in a regulated market like Mexico.


References

[1] Mexican Institute of Industrial Property (IMPI). "Mexican Patent Law."
[2] World Intellectual Property Organization (WIPO). "Guide to Understanding Pharmaceutical Patents."
[3] TRIPS Agreement, World Trade Organization. "Intellectual Property Rights in Mexico."
[4] Recent patent filings and legal literature on Mexican pharmaceutical patents.


Disclaimer: This analysis is based on publicly available information and general legal principles applicable in Mexico. For specific patent prosecution or litigation strategies, consultation with a registered patent attorney is recommended.

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