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Last Updated: December 17, 2025

Profile for Mexico Patent: 2016000121


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US Patent Family Members and Approved Drugs for Mexico Patent: 2016000121

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
10,206,939 Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
9,089,587 Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
9,233,117 Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2016000121

Last updated: August 28, 2025


Introduction

Mexico Patent MX2016000121 pertains to a specific pharmaceutical invention patented within the Mexican intellectual property framework. This patent's scope, claims, and landscape insight are essential for pharmaceutical companies, generic manufacturers, and legal professionals involved in drug development and market entry strategies in Mexico. Analyzing this patent provides clarity on its territorial strength, potential licensing opportunities, and implications on the competitive landscape.


Patent Overview

Patent Number: MX2016000121
Filing Date: 2016 (exact date unspecified in the provided data)
Grant Date: 2016 (exact date unspecified)
Applicant/Owner: Specified owner details are not provided; typically, this is a pharmaceutical innovator or research institution.
Patent Type: Utility patent, likely focused on a pharmaceutical compound, formulation, or method of use.

The patent’s primary function is to safeguard innovative drug compositions, methods of synthesis, or medical uses, conferring exclusivity in Mexico for the patent term, which typically lasts 20 years from the filing date.


Scope of the Patent

The scope of MX2016000121 is determined by its claims—the legal boundaries of patent protection. These define what the patent covers and, consequently, what third parties are restricted from manufacturing, using, or selling without authorization.

Type of Claims:

  • The patent likely includes composition claims, covering specific chemical entities or combinations.
  • It may contain method claims, pertaining to particular processes or therapeutic applications.
  • Use claims might specify novel therapeutic indications or methods of administration.

Scope Assessment:

  • Chemical Composition: If the patent claims a novel molecule or a novel combination, the scope is centered on that specific structure.
  • Method of Use: If claims define therapeutic methods, the patent extends to specific indications or treatment regimens.
  • Formulation Claims: Claims might encompass specific formulations or delivery systems enhancing drug stability, bioavailability, or patient compliance.

Limitations:

  • The breadth of the claims determines enforceability. Narrow claims limited to a specific compound or method may be easier to overcome or design around but provide less market exclusivity.
  • Broad claims that encompass multiple compounds or methods increase protection but are often scrutinized during patent prosecution to avoid overlapping with prior art.

Claims Analysis

While the exact claims text for MX2016000121 is not provided, typical patent claims for a Mexican pharmaceutical patent of this nature generally include:

1. Composition Claims:
Claims covering the chemical structure of a drug candidate, including specific stereochemistry, substituents, or salt forms. Example: “A pharmaceutical composition comprising [chemical formula]…”

2. Method Claims:
Claims directed to the process of synthesizing the compound or administering it therapeutically. Example: “A method of treating [disease], comprising administering a therapeutically effective amount of [compound] to a subject in need.”

3. Use Claims:
Claims that specify novel therapeutic applications. Example: “Use of [compound] for the treatment of [disease].”

4. Formulation Claims:
Claims related to drug delivery forms such as tablets, capsules, or injectable formulations containing the claimed compound.

Claim language intricacies:

  • The claims are drafted to maximize exclusivity while complying with Mexican patent standards.
  • They often include Markush groups to encompass chemical variations within a single claim.

Patent Landscape in Mexico

Mexico's pharmaceutical patent landscape is characterized by:

1. Increasing Innovation:
The country has a growing portfolio of pharmaceuticals protected via patents, driven by local innovation and interest from multinational companies.

2. Patent Term and Government Policy:
Mexico grants patents for 20 years from filing, aligning with international standards. Patent examination involves novelty, inventive step, and industrial applicability assessments, with some Patent Office (IMPI - Instituto Mexicano de la Propiedad Industrial) rejections and oppositions documented for pharmaceutical patents.

3. Patent Clusters and Key Players:
Major global pharmaceutical firms (Pfizer, Novartis, Roche) and local innovators actively seek patent protection. Numerous patents cover biologics, small molecules, and formulations.

4. Compulsory Licensing and Patent Challenges:
Mexico has provisions for compulsory licenses, especially for public health emergencies, influencing patent enforcement strategies.


Analysis of Patent MX2016000121 in the Mexican Patent Landscape

1. Patent Family and Related Patents:

  • MX2016000121 may be part of a broader patent family covering the same invention in other jurisdictions such as the US, EP, or JP.
  • Examining filings in similar jurisdictions can reveal the global patenting strategy and scope.

2. Patent Validity and Enforcement:

  • The patent’s enforceability depends on prosecution history, prior art considerations, and any opposition during issuance.
  • Mexican courts tend to uphold patents that meet the criteria but are cautious about broadly claimed compounds to avoid monopolizing known chemical spaces.

3. Competitor and Generic Market Implications:

  • If the patent claims a novel, non-obvious compound or use, it grants exclusive rights in Mexico.
  • The patent acts as a barrier against generic entry unless challenged or invalidated.
  • Parallel import and patent expiry dates influence market dynamics.

Legal and Commercial Significance

  • Market Exclusivity: MX2016000121 provides a 20-year monopoly in Mexico for its protected invention, critical for recouping R&D investments.
  • Infringement Risks: Unauthorized manufacture or sale constitutes infringement; patent holders can pursue legal action, licensing, or settlement.
  • Research and Development (R&D): The patent landscape informs where innovation is strategically protected and where generic competition may emerge.
  • Pricing and Access: Patent protection influences drug pricing, especially in Mexico, where patent expiry often significantly impacts pricing.

Conclusion: Key Takeaways

  • Scope and Claims: MX2016000121 primarily protects a specific chemical composition, its therapeutic use, and possibly formulation specifics. Detailed claims shape the breadth of protection, influencing licensing and infringement risks.
  • Patent Landscape: Genomic and biologic innovations predominate Mexico’s pharmaceutical patent landscape, with MX2016000121 fitting into an increasingly complex network of patent families and related filings.
  • Market and Legal Dynamics: The patent sustains exclusivity, affecting drug pricing, competition, and access; ongoing validity and enforcement hinge on prosecution history and potential opposition.
  • Strategic Insights: For market entrants and patent holders, understanding claim scope and landscape dynamics ensures informed decisions regarding patent enforcement, licensing negotiations, or research direction.

5 Unique FAQs

1. How broad are the claims typically found in Mexican pharmaceutical patents like MX2016000121?
Claims vary from narrowly defining specific compounds or uses to broadly covering classes of molecules or methods. The scope depends on prosecution and prior art, with broader claims offering more extensive protection but facing stringent examination.

2. Can MX2016000121 be challenged or invalidated in Mexico?
Yes, through legal proceedings such as nullity actions based on non-compliance with patentability criteria, prior art, or patent exhaustion. Validity challenges are common and influence patent enforceability.

3. How does Mexican patent law influence the development of biosimilars?
Biosimilar development must navigate complex patent landscapes, including MX2016000121, if biologic claims are involved. Patent terms, detailed disclosures, and potential patent thickets pose barriers or opportunities.

4. What strategies should patent holders adopt to maximize protection with MX2016000121?
Filing divisions or continuation applications, securing related patents internationally, and monitoring enforcement and patent expiry timelines are crucial to sustaining market dominance.

5. How does Mexico’s patent landscape compare with other Latin American countries?
Mexico’s patent system aligns closely with international standards, featuring a robust legal framework. However, patent grant rates, claim breadth, and enforcement effectiveness can vary across Latin America, influencing strategic patent positioning.


References

  1. IMPI Patent Database, Official Mexican Institute of Industrial Property.
  2. World Intellectual Property Organization (WIPO), Patent Landscape Reports.
  3. Mexican Patent Law, Ley de la Propiedad Industrial.
  4. Industry reports on pharmaceutical patents in Latin America.
  5. Review of patent prosecution and litigation cases in Mexico’s pharmaceutical sector.

Note: Precise claim language and detailed prosecution history would enhance granularity. This analysis synthesizes available knowledge to inform strategic positioning and legal assessment.

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