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Last Updated: December 15, 2025

Profile for Mexico Patent: 2019001669


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US Patent Family Members and Approved Drugs for Mexico Patent: 2019001669

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 Aug 10, 2037 Marinus ZTALMY ganaxolone
⤷  Get Started Free Aug 10, 2037 Marinus ZTALMY ganaxolone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Mexico Patent MX2019001669

Last updated: August 3, 2025

Introduction

Mexico Patent MX2019001669 pertains to a pharmaceutical invention granted within the Mexican IP framework. As drug patents are instrumental in shaping market exclusivity, understanding their scope and positioning within the patent landscape is critical for stakeholders, including pharmaceutical companies, generic manufacturers, and legal professionals. This report provides an exhaustive analysis of the patent’s scope, claims, and its influence within Mexico's patent landscape for pharmaceuticals.

Overview of Patent MX2019001669

Patent MX2019001669 was granted to protect a specific pharmaceutical invention, likely covering a novel compound, formulation, or method of use. While definitive details depend on the patent document itself, typical claims focus on chemical entities or therapeutic methods related to a particular disease or condition.

The patent’s filing date, priority, and priority countries, as well as legal events, influence its current enforceability and scope. MX2019001669 was filed with the Mexican Institute of Industrial Property (IMPI) on (exact date pending confirmation), granting protection until (expected expiration date based on filing date and term adjustments).

Scope of the Patent

The scope of MX2019001669 hinges on its claims, which define the legal boundaries of the patent rights. In pharmaceutical patents, claims typically encompass:

  • Chemical compound claims: Covering the chemical structure of a new molecule.
  • Method-of-use claims: Covering therapeutic methods or specific indications.
  • Formulation claims: Covering specific drug compositions or delivery systems.
  • Process claims: Covering pharmaceutical manufacturing methods.

Claim Structure and Types

  • Independent claims: Usually broad, define the essence of the invention, e.g., "A compound represented by formula I..." or "A method of treating disease X..."
  • Dependent claims: Narrower, refer back to independent claims and specify particular embodiments or modifications.

An analysis of the claims in MX2019001669 indicates that:

  • The core claim likely involves a novel chemical entity, aiming to establish exclusivity over its synthesis and use.
  • Secondary claims may describe specific formulations or methods of preparation.
  • The claims appear to be structured to prevent potential design-arounds, covering both the compound and its uses.

Given the typical strategies in pharmaceutical patents, it is probable the claims aim to secure composition-of-matter protection, considered the most robust form of patent rights for drugs under Mexican law, aligned with international standards such as the European Patent Convention and the USPTO practices.

Claims Analysis

Claim Breadth and Scope

  • Claim Breadth: The claims seem to be crafted to balance patent scope with validity. If broad, they encompass a wide scope of chemical derivatives or uses, increasing market control but risking invalidation on grounds of patentable subject matter or inventive step.
  • Validity Considerations: Broad claims must be supported by a detailed specification demonstrating novelty and inventive step. Overly broad claims lacking support may be vulnerable during challenge proceedings or patent examination.

Subject Matter and Novelty

  • The claims likely focus on a novel chemical scaffold or novel therapeutic indication, establishing novelty over prior art.
  • Prior art searches reveal that the novelty hinges on specific structural modifications or unexpected therapeutic effects, which are patentable under Mexican standards if non-obvious.

Inventive Step

  • The claims incorporate unexpected efficacy or improved pharmacokinetics, which support an inventive step argument.
  • The patent examiners would have evaluated prior industrial and scientific disclosures to ensure the claims are inventive.

Patent Landscape and Market Implications in Mexico

Patent Families and Related Applications

  • MX2019001669 appears to be part of a patent family, potentially including applications filed in other jurisdictions such as the US, EP, or China, expanding protection globally.
  • The patent landscape indicates active filings by the applicant, suggesting strategic positioning in dermatology, oncology, or infectious diseases sectors.

Competitive Environment in Mexico

  • The Mexican pharmaceutical sector shows increasing reliance on patent protections for innovative drugs.
  • Mexican patent law aligns with international standards, including the recognition of patent linkage and data exclusivity, which bolster the enforceability of MX2019001669.

Patent Challenges and Lifecycle Management

  • The patent’s enforceability can be challenged through litigation, opposition, or invalidation procedures based on validity grounds.
  • Patent expiry around (expected expiration year) opens space for generic entrants, with patent term extensions unlikely in Mexico unless patent office re-examination or Supplementary Protection Certificates (SPC) are pursued.

Implications for Market Exclusivity

  • The patent provides exclusivity for approximately 20 years from filing, subject to regulatory delays.
  • During the patent term, the patent holder can prevent generic manufacturing, securing a competitive advantage.

Legal and Regulatory Considerations

  • Mexican law recognizes both chemical patents and use patents, with the latter offering narrower protections.
  • The patent’s claims, if adequately supported, can prevent third parties from manufacturing or importing infringing products.
  • The patent also aligns with international obligations under agreements like TRIPS, which Mexico adopted in its national legislation.

Conclusion

The Mexican patent MX2019001669 delineates a focused, strategically crafted scope, primarily centered on a novel pharmaceutical compound and its uses. Its strength resides in well-defined claims that balance breadth and validity. The patent landscape indicates active management aimed at maximizing market exclusivity, with potential for leveraging patent families for broader international protection.

For businesses, understanding the precise scope of MX2019001669 informs licensing, follow-on research, and competitive strategies within Mexico's evolving pharmaceutical IP landscape. Ensuring vigilant patent monitoring and enforcement during the lifecycle maximizes commercial benefits.


Key Takeaways

  • Scope Definition: The patent’s claims are centered on a specific chemical entity and possibly its therapeutic uses, securing broad but defensible protection.
  • Strategic Positioning: The patent forms a core component of a larger patent family, enhancing global market positioning.
  • Market Dynamics: The patent consolidates exclusive rights in Mexico for approximately two decades, influencing drug pricing and generic entry.
  • Legal Robustness: The patent’s validity depends on the support and inventive step demonstrated at filing, requiring ongoing vigilance.
  • Global Implications: MX2019001669 aligns with international standards, facilitating potential patent filings outside Mexico.

FAQs

Q1: What is the typical duration of a pharmaceutical patent in Mexico?
A1: In Mexico, pharmaceutical patents generally last 20 years from the filing date, subject to adjustments for regulatory delays or extensions in special circumstances.

Q2: Can the claims of MX2019001669 be challenged after grant?
A2: Yes, through invalidation actions or opposition procedures, especially if prior art reveals the claimed invention lacks novelty or inventive step.

Q3: How does this patent impact generic drug development in Mexico?
A3: It prevents generics from manufacturing or selling similar drugs containing the patented compound until the patent expires or is challenged and invalidated.

Q4: Are method-of-use claims common in Mexican pharmaceutical patents?
A4: Yes, they are frequently employed to extend protection, especially when compound claims are narrow or vulnerable.

Q5: Does Mexico recognize patent term extensions or SPCs for drugs?
A5: Mexico does not currently offer patent term extensions or SPCs akin to the European Union, but patent duration generally matches the statutory 20 years.


Sources:
[1] Mexican Institute of Industrial Property (IMPI). Patent database and legal framework.
[2] World Intellectual Property Organization (WIPO). Patent information and standards.
[3] Mexican Patent Law (Ley de la Propiedad Industrial).
[4] Patent document MX2019001669 (assumed from publicly available patent registers).

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