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Last Updated: December 15, 2025

Profile for Mexico Patent: 390004


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US Patent Family Members and Approved Drugs for Mexico Patent: 390004

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
11,129,896 Sep 22, 2036 Organon Llc XACIATO clindamycin phosphate
12,303,563 Sep 22, 2036 Organon Llc XACIATO clindamycin phosphate
>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 MX390004

Last updated: August 9, 2025


Introduction

Patent MX390004 pertains to a pharmaceutical invention filed and granted in Mexico. Analyzing its scope, claims, and the broader patent landscape provides critical insights into its strength, enforceability, and positioning within the pharmaceutical intellectual property (IP) ecosystem. This assessment aims to guide industry stakeholders, from patent attorneys and pharmaceutical companies to investors, seeking informed decisions about the patent’s value, potential competitors, and market exclusivity.


Patent Overview and Basic Data

  • Patent Number: MX390004
  • Application Filing Date: [Insert date if available]
  • Grant Date: [Insert date if available]
  • Patent Term: Typically 20 years from the filing date, subject to maintenance and regional regulations.
  • Status: Granted, with enforceable rights, assuming no oppositions or challenges.
  • Ownership: [Insert assignee or inventor information, if available]
  • Relevant Jurisdiction: Mexico — a key market in Latin America with a complex IP landscape.

Note: Due to the specific nature of MX390004, detailed procedural data such as application number, priority date, and citations further contextualize the analysis.


Scope of the Patent

The scope of patent MX390004 likely encompasses a pharmaceutical compound or formulation, as indicated by typical claims in this class. The scope is determined primarily by the claims, which delineate the boundaries of the patent protection.

Given the common pattern in pharmaceutical patents, the scope may cover:

  • Novel chemical entities or derivatives with therapeutic activity.
  • Methods of use or treatment protocols utilizing the compound.
  • Manufacturing processes or formulations enhancing stability, bioavailability, or delivery.

Without access to the full text, typical elements potentially covered include:

  • The chemical structure of the active ingredient, possibly represented by a specific formula.
  • Specific polymorphs, salts, or esters that improve pharmacokinetics or stability.
  • Therapeutic indications, such as treatment of particular diseases (e.g., cancer, CNS disorders, infectious diseases).
  • Combination therapies involving the patented compound with other agents.

The scope’s breadth depends on how narrowly or broadly the claims are drafted. Narrow claims focus on specific compounds/formulations, whereas broader claims may cover classes of compounds or methods.


Claims Analysis

Claims are the core of the patent, framing the legal protection. They can be categorized as:

  • Independent Claims: Broadly define the core invention; typically chemical compounds, compositions, or methods.
  • Dependent Claims: Narrower, referencing independent claims, often covering particular embodiments or variants.

Typical claim structure in pharmaceutical patents:

  1. Compound Claim: Defines a specific chemical structure or its salts, esters, or polymorphs.
  2. Composition Claim: Covers formulations comprising the compound and excipients.
  3. Method Claim: Pertains to methods of treatment, use, or administration involving the compound.
  4. Process Claim: Describes manufacturing steps for the active ingredient or final formulation.

Potential Claim Language Examples (Speculative):

  • "A compound represented by the formula [structure], or a pharmaceutically acceptable salt thereof."
  • "A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier."
  • "A method of treating [disease], comprising administering an effective amount of the compound of claim 1."

Claim Strengths and Limitations:

  • Strengths: If claims are broad and well-supported by data, they can cover structurally similar compounds, offering extensive protection.
  • Limitations: Narrow claims may be easily designed around, reducing patent life or scope.

Current patent strategies often involve combining compound claims with method claims to strengthen enforceability.


Patent Landscape Analysis

Understanding the patent landscape involves examining:

  • Prior Art: Existing patents and publications that disclose similar compounds, formulations, or methods.
  • Related Patents: Other Mexican patents or international filings (e.g., PCT, US, EP) citing similar structures or indications.
  • Inventive Step and Novelty: Whether MX390004 introduces a genuinely inventive feature over existing documents.

Key considerations include:

  • Overlap with international patents:
    A patent family analysis shows whether MX390004 aligns with worldwide patent filings, indicating its novelty status.

  • Citations and references:
    Forward and backward citations reveal technological relationships, potential freedom-to-operate issues, or landscape breadth.

  • Patentability and infringement risk:
    The scope’s alignment with prior art impacts enforceability and potential litigation.

Sources such as WIPO’s PATENTSCOPE, INAPI (Mexican Institute of Industrial Property), and the European Patent Office provide relevant patent landscapes.

Recent trends in Mexican pharmaceutical patent landscape:
Mexico’s patent examination standards have become more aligned with international practices post-TRIPS, emphasizing novelty and inventive step. Patent filings for biotech and pharma are rising, with patent offices paying increasing attention to patent quality.


Legal and Commercial Implications

Market exclusivity:
MX390004 offers drug developers a period of market exclusivity to recover investment, typically through patent protection. The scope of claims directly influences potential revenue streams.

Patent challenges:
Competitors may challenge the patent’s validity through prior art, especially if claims are broad or if similar compounds exist. A strong, well-supported patent diminishes this risk.

Continued patenting strategy:
To extend protection, patentees often file related patents for new polymorphs, formulations, or uses, creating a patent family expanding coverage.


Conclusion

The patent MX390004 secures protection for a specific pharmaceutical invention in Mexico, with the scope defined by the claims—potentially covering novel compounds, formulations, and treatment methods. Its strength depends on the breadth of claims and the robustness against prior art. The Mexican patent landscape reflects a maturing environment emphasizing patent quality and relevance, especially for innovative therapeutics.


Key Takeaways

  • Claim drafting precision is crucial: Broad strategic claims maximize protection, but must be justifiable to withstand validity challenges.
  • Patent landscape awareness: Continuous monitoring of related patents ensures defensibility and identifies licensing opportunities.
  • Patentability relies on novelty and inventive step: Ongoing prior art searches are essential to validate the patent’s strength.
  • Regional strategies matter: To secure comprehensive protection, consider filing in multiple jurisdictions aligned with the Mexican patent’s scope.
  • Legal enforcement and market position: A well-maintained patent provides significant leverage against generic competition, bolstering market exclusivity.

FAQs

  1. What is the typical validity period of patent MX390004?
    Generally, pharmaceutical patents in Mexico are valid for up to 20 years from the filing date, subject to maintenance fees and regional regulations.

  2. Can MX390004 be challenged or invalidated?
    Yes. Oppositions or validity challenges can be filed based on prior art or procedural issues during prosecution.

  3. Does the scope of the claims determine the patent’s enforceability?
    Absolutely. Broader claims offer wider protection but must be fully supported by the disclosure to withstand legal scrutiny.

  4. How does the Mexican patent landscape influence pharmaceutical innovation?
    It incentivizes innovation through robust IP rights while requiring adherence to strict patentability standards to prevent evergreening or frivolous patents.

  5. Should companies consider filing similar patents internationally?
    Yes. For global market protection, filing in jurisdictions with significant markets and enforcing mechanisms is essential, especially for broad-spectrum compounds.


References

[1] Mexican Institute of Industrial Property (IMPI). Patent Database.
[2] World Intellectual Property Organization (WIPO). PATENTSCOPE.
[3] European Patent Office Search.
[4] International Patent Classifications relevant to pharmaceuticals.


Disclaimer: This analysis is based on available information and typical patent practices. For detailed legal advice, consulting a patent attorney with access to the full patent document and related technical disclosures is recommended.

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