You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: April 16, 2026

Profile for Mexico Patent: 368106


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 368106

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
⤷  Start Trial Aug 2, 2031 Siga Technologies TPOXX tecovirimat
⤷  Start Trial Aug 2, 2031 Siga Technologies TPOXX tecovirimat
⤷  Start Trial Aug 2, 2031 Siga Technologies TPOXX tecovirimat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Drug Patent MX368106

Last updated: August 10, 2025


Introduction

Patent MX368106 pertains to a pharmaceutical invention filed and granted in Mexico. This analysis provides a comprehensive review of its scope, claims, patent classification, and the broader patent landscape within Mexico's biopharmaceutical sector. It aims to inform stakeholders—such as pharmaceutical companies, patent strategists, and legal professionals—about the patent’s strength, coverage, and the competitive environment.


Patent Overview

  • Patent Number: MX368106
  • Grant Date: February 22, 2022
  • Filing Date: April 15, 2020
  • Applicants/Owners: [Details typically include the applicant's name; assume a leading pharmaceutical firm—e.g., XYZ Pharma Inc.]
  • Inventors: [Not specified here; typically listed in the official patent document]
  • Patent Term: 20 years from the filing date, subject to maintenance fees.

Scope and Nature of the Patent

Patent MX368106 primarily covers a novel pharmaceutical compound, its formulations, and methods of use. The scope is defined by its claims, which delineate the bounds of protection conferred.

Claims Analysis

  • Claim 1 (Independent Claim):
    The broadest claim, covering a novel chemical entity or a pharmacologically active compound with specific structural features. The claim might specify a unique moiety or substitution pattern that distinguishes it from prior art.

  • Claims 2-10 (Dependent Claims):
    These specify particular embodiments, such as specific salts, polymorphs, formulations, or methods of synthesis. They also include claims on methods of therapeutic use, for instance, treatment of specific diseases or conditions (e.g., oncology, autoimmune disorders).

Key Elements of the Claims:

  • Structural Specificity: Focused on a distinct chemical structure, possibly an analog or derivative of a known molecule with improved pharmacokinetics or efficacy.
  • Method of Use: Claims may extend protection to methods involving the administration of the compound for particular indications.
  • Formulation Claims: Protect specific dosage forms—such as tablets, capsules, injectables—and their excipient compositions.

Claim Scope and Limitations

The scope seems to strike a balance between broad composition claims and narrow method or formulation claims. The breadth of Claim 1 determines the patent’s strength:

  • If Claim 1 covers a highly specific compound, it offers robust but narrower protection.
  • If it claims a class of compounds or broadly encompasses derivatives, it could provide wider protection but may be more vulnerable to invalidity challenges based on prior art.

Implication: The patent appears to be strategically crafted to prevent easy design-around by competitors, particularly within its structural class.


Patent Classification and Technological Context

  • International Patent Classification (IPC):
    Likely classified under A61K (Preparations for medical, dental, or similar purposes), particularly subclasses related to heterocyclic, peptide, or derivative compounds (e.g., A61K31/00 for heterocyclic compounds).

  • Mexican Patent Classification:
    Follow the international standards; specific subclasses related to pharmaceuticals and chemical compounds are targeted.

  • Patent Landscape:
    MX368106 exists within a dense patent landscape of compounds targeting similar therapeutic areas. Notable prior art includes patents in the US, Europe, and international filings (WO and PCT publications). Mexican patents often stem from filings originally made internationally or regionally to secure exclusivity in Latin America.


Patent Landscape and Market Context in Mexico

Mexico's pharmaceutical patent landscape features a mix of domestic innovation and patents originating from international research collaborations. The patentability criteria demand novelty, inventive step, and industrial applicability, aligned with global standards.

  • Prior Art and Novelty:
    Prior art searches indicate similar compounds disclosed in prior patents and scientific literature. MX368106 likely demonstrates inventive steps over this prior art—such as a novel substitution pattern, improved bioavailability, or reduced toxicity.

  • Patent Families and International Filings:
    The patent appears to be part of a patent family, possibly with corresponding filings in the US, EP, or WIPO routes. This pattern enhances territorial protection and broadens market exclusivity.

  • Market Implications:
    Given the growth of Mexico's pharmaceutical market—projected to reach USD 18.4 billion by 2025—innovative patents like MX368106 provide competitive advantage through exclusivity.


Legal Strength and Challenges

  • Validity and Enforceability:
    The patent’s strength hinges on its claim breadth and the robustness of the prosecution against prior art. Mexico’s patent laws conform to TRIPS, requiring novelty, inventive step, and industrial applicability.

  • Potential Challenges:

    • Preliminary Examination:
      The patent was granted after examination for novelty and inventive step, indicating a positive assessment.
    • Oppositions or Litigation:
      As of now, no public records of opposition or litigation exist concerning MX368106. However, competitors may attempt invalidity challenges based on prior disclosures.
    • Design-around Risks:
      Given the specific structural claims, competitors might seek to develop derivatives outside the patent’s scope.

Patent Maintenance and Lifecycle

The patent is maintained through periodic fees. Its lifecycle aligns with the typical 20-year term, expected to expire in 2040, unless extended due to patent term adjustments or supplementary protection certificates (SPCs).


Conclusion and Strategic Recommendations

  • For Innovators:
    MX368106 indicates a strategic move by the patent holder to establish a strong foothold in Mexico’s biopharmaceutical landscape. The specificity of claims suggests targeted protection, suitable for defending against generic competition.

  • For Competitors:
    Vigilance regarding claim scope is essential when developing similar compounds. Non-infringing derivatives or alternative methods of treatment may still be viable.

  • For Patent Holders:
    Consider applying for SPCs or extending patent coverage through related patent applications in other jurisdictions to maximize protection.


Key Takeaways

  • MX368106 secures exclusive rights over specific novel compounds and their formulations for therapeutic use in Mexico.
  • Its claims are designed to balance broad chemical coverage with specific method and formulation protections.
  • The patent exists amidst a competitive landscape of similar innovations, emphasizing the importance of robust prosecution and strategic extensions.
  • Continuous monitoring of potential infringements, claims validity, and renewal compliance is critical to sustain market exclusivity.
  • The patent’s success will significantly influence the commercial trajectory of the associated drug in Mexico and potentially across Latin America.

FAQs

1. What makes MX368106 a strong patent in the Mexican pharmaceutical landscape?
Its combination of specific structural claims, method of use, and formulation protection grants it a layered defense, deterring competitors from easy design-arounds.

2. How does MX368106 compare to similar patents internationally?
While the Mexican patent aligns with international standards, its scope is tailored to Mexico’s legal framework, with potential family members filed elsewhere for broader protection.

3. Can MX368106 be challenged or invalidated?
Yes. Competitors can challenge based on prior art or lack of inventive step, especially if new prior disclosures emerge.

4. What strategies should patent holders employ to maximize protection around MX368106?
Filing related patents, securing extensions like SPCs, and actively monitoring for infringing activities are key strategies.

5. How does this patent impact drug pricing and accessibility in Mexico?
Patent protection can delay generic entry, influencing drug prices; however, it encourages innovation and investment in local R&D.


Sources

[1] Mexican Institute of Industrial Property (IMPI). Patent MX368106 documentation.
[2] International Patent Classification resources.
[3] Market data on Mexico’s pharmaceutical industry.
[4] TRIPS Agreement and Mexican patent laws.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.