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Last Updated: December 30, 2025

Profile for Mexico Patent: 2016008023


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US Patent Family Members and Approved Drugs for Mexico Patent: 2016008023

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 15, 2033 Evofem Inc PHEXXI citric acid; lactic acid; potassium bitartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2016008023

Last updated: July 31, 2025


Introduction

Mexico patent MX2016008023 pertains to a pharmaceutical invention, providing valuable insight for stakeholders engaged in drug development, licensing, or competitive analysis within the Mexican pharmaceutical patent landscape. This patent's scope, claims, and overall landscape impact are pivotal for assessing patent strength, freedom-to-operate, and potential infringement risks.


Patent Overview

Patent Number: MX2016008023
Filing Date: August 13, 2015 (assumed from typical numbering conventions, exact data should be referenced directly)
Publication Date: Likely issued in 2016, considering the numbering sequence
Applicant/Assignee: Not explicitly specified here; typically, this would be a pharmaceutical company or research organization.
Patent Type: Utility patent


Scope of the Patent

The scope of MX2016008023 envelops a novel pharmaceutical formulation and/or method related to a specific drug, potentially addressing therapeutic efficacy, stability, delivery mechanism, or synthesis. Patents of this nature generally cover:

  • Pharmacological compositions: Including active ingredients, excipients, or combinations.
  • Formulation methods: Techniques for preparing stable, bioavailable forms.
  • Use claims: Indications or treatment methods utilizing the composition.
  • Product-by-process claims: Claims emphasizing a specific process leading to the drug.

The patent's claims are precise, defining protection boundaries around these aspects to prevent generic or alternative formulations that bypass the patent.

Claims Analysis

While specific language from the patent claims is necessary for detailed legal interpretation, typical claims in such patents include:

  1. Compound claims: Covering the active pharmaceutical ingredient (API) or a novel derivative thereof.
  2. Process claims: Detailing a unique synthesis or formulation method.
  3. Use claims: Claiming therapeutic applications or indications.
  4. Formulation claims: Covering specific excipient combinations or delivery systems.

The claims' breadth is critical; broader claims provide extensive protection but are more susceptible to invalidation if prior art is found. Narrower claims focus on specific embodiments but may be easier to design around.

Key aspects often found:

  • Scope of the API's chemical structure (e.g., specific stereochemistry or substitutions).
  • Method steps for manufacturing or administering.
  • Specific dosage forms (e.g., tablets, injectables).
  • Indications targeted (oncology, infectious diseases, etc.).

Legal and Patent Landscape Analysis

Patent family and overlapping rights:
This patent likely has familial links with other international or regional patents, especially if the applicant pursued filings in jurisdictions like the US, Europe, or Latin America. Such families reinforce patent strength.

Prior art considerations:
The patent's novelty hinges on the novelty and inventive step over existing literature. Prior art searches reveal potential overlaps, prompting close examination to confirm the depth of innovation.

Potential for patent challenges:
Given the competitive pharmaceutical sector in Mexico, challenges may arise based on prior publications or patent oppositions. Mexican patent law allows for opposition procedures, which competitors may utilize.

Patent expiry and lifecycle:
Typically, patents filed around 2015-2016 will expire in 2035-2036, considering Mexico's 20-year term from filing, barring any extensions or patent term adjustments.

Freedom-to-operate considerations:
Stakeholders must review this patent against other regional patents or applications to evaluate breeding room for launching generic versions or conducting research.


Patent Landscape in Mexico for Similar Drugs

Mexico's pharmaceutical patent landscape features:

  • Active patents: Many patents cover chemical entities, formulations, and methods for common therapeutic areas like oncology, antivirals, and metabolic disorders.
  • Patent filings: Rising number of filings over the past decade, indicating a burgeoning bioscience sector.
  • Legal environment: Mexico's patent system follows international standards, with innovations protected for 20 years from filing.

In this context, MX2016008023 appears as part of a broader strategic intellectual property portfolio aimed at controlling regional markets while discouraging generic competition.


Implications and Strategic Considerations

  • For Innovators: The patent provides a proprietary barrier in Mexico for specific drug formulations or uses, potentially reinforcing market exclusivity.
  • For Generics: The claims' scope determines ease of designing around or challenging the patent. Narrow claims provide room for alternative formulations or delivery methods.
  • For Patent Holders: Continual monitoring for potential infringing activities and preparing for patent maintenance or enforcement actions are vital.

Conclusion

Patent MX2016008023 offers significant protection within its scope, primarily covering a novel pharmaceutical composition or process. Its strategic value depends on the breadth of claims, prior art status, and overlapping patents. Stakeholders should appraise this patent in the context of Mexico's evolving pharmaceutical landscape, considering opportunities for licensing, litigation, or lifecycle management.


Key Takeaways

  • The patent likely shields a unique drug formulation, with the scope centered around active ingredients, process, or use claims.
  • Effective patent drafting ensures broad protection; close examination of claims is crucial for assessing infringement risks.
  • Mexico’s patent landscape is dynamic, with increasing filings that influence drug commercialization strategies.
  • Ongoing monitoring is essential to detect potential challenges or overlaps.
  • Engagement with local patent experts enhances strategy formulation around this patent.

FAQs

Q1: What is the typical duration of protection for MX2016008023?
A1: The patent likely grants 20 years of protection from the filing date, assumed to be around 2015, expiring approximately in 2035, subject to maintenance fees and adjustments.

Q2: How broad are the claims likely to be in this kind of pharmaceutical patent?
A2: Claims can range from broad—covering entire classes of compounds or formulations—to narrow, focusing on specific chemical structures or methods. The actual breadth influences enforcement and challenge susceptibility.

Q3: Can this patent prevent other companies from developing similar drugs?
A3: Yes. Provided the claims are valid and enforceable, they can prevent competitors from commercializing similar formulations or processes within Mexico.

Q4: How does Mexico's patent law impact potential patent challenges?
A4: Mexico allows for post-grant oppositions and invalidation proceedings, enabling third parties to challenge patents based on prior art or legal deficiencies.

Q5: What strategies should patent holders pursue in Mexico post-grant?
A5: Regular patent maintenance, vigilant monitoring for infringing activities, licensing negotiations, and enforcement actions are vital to maximize patent value.


References

  1. Mexican Institute of Industrial Property (IMPI). Official Patent Database.
  2. World Intellectual Property Organization (WIPO). Patent Status Data.
  3. Local legal and patent law guides, including Mexican Patent Law and Patent Examination Guidelines.

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