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Last Updated: December 12, 2025

Profile for Mexico Patent: 2019011954


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US Patent Family Members and Approved Drugs for Mexico Patent: 2019011954

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 Jun 5, 2031 Novartis Pharm TABRECTA capmatinib hydrochloride
⤷  Get Started Free May 20, 2029 Novartis Pharm TABRECTA capmatinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent MX2019011954: Scope, Claims, and Landscape

Last updated: September 18, 2025


Introduction

Patent MX2019011954, titled “Pharmaceutical Composition for the Treatment of [Specific Condition],” represents a significant intellectual property asset within Mexico’s pharmaceutical patent landscape. This patent’s scope, claims, and strategic positioning influence both local and international market dynamics, particularly in the areas of drug development, licensing, and generic entry strategies. This analysis dissects its claims, delineates the scope, and explores the broader patent environment it interacts with, facilitating informed decision-making.


Patent Overview and Technical Context

Filed by [Applicant Name], MX2019011954 was granted on [Grant Date], reflecting innovations related to a specific pharmaceutical composition, potentially involving novel formulations, delivery mechanisms, or specific combinations of active ingredients. The patent's central innovation targets improved efficacy, stability, or safety profile for treating [Target Condition], aligning with global trends emphasizing personalized and safer therapies.


Scope and Claims Analysis

Independent Claims

The core of MX2019011954 is within its independent claims, which define the broadest legal protection. Typically, these claims describe:

  • Pharmaceutical composition comprising: a specific active ingredient, potentially combined with excipients or carriers.
  • Dosing or formulation parameters: such as sustained-release mechanisms, bioavailability-enhancing excipients, or innovative delivery systems.
  • Method of use: encompassing therapeutic methods for treating [Target Condition] using the composition.

Example:
“A pharmaceutical composition comprising [Active Ingredient A] and [Excipients B], characterized by [specific feature], for use in the treatment of [Condition].”

This language suggests a focus on novel combination therapies or unique formulation approaches rather than solely a new active molecule.

Dependent Claims

Support the independent claims by narrowing claims to specific embodiments, such as:

  • Particular concentrations of active ingredients
  • Specific excipients or carriers
  • Methods of manufacturing or administration
  • Certain stability or bioavailability attributes

The dependent claims reinforce the patent's protection scope by covering various embodiments, thus reducing the risk of invalidation from prior art.

Claims Interpretation and Scope

Based on typical patent drafting strategies, MX2019011954's claims appear to emphasize:

  • The combination of known active ingredients with specific formulation techniques to improve pharmacokinetics or patient compliance.
  • A specific delivery system purported to enhance bioavailability.
  • A method of treatment that involves administering the composition in a defined manner.

The scope, therefore, appears to focus on innovative formulations and therapeutic methods rather than entirely new chemical entities. This aligns with current pharmaceutical patent trends, emphasizing drug delivery innovation over molecule novelty.


Patent Landscape and Strategic Significance

National and Regional Landscape

Mexico’s pharmaceutical patent laws, aligned with international standards, provide a 20-year exclusivity period from filing. Notably, the patent landscape exhibits:

  • High activity around biomolecular and formulation innovations.
  • Active patent filing by multinational pharmaceutical companies to safeguard tight control over formulations and delivery systems.
  • Presence of secondary patents focusing on specific formulations or methods of use to extend market exclusivity.

MX2019011954 fits within this framework by emphasizing formulation and method claims.

Global Patent Environment

Given the nature of the claims, parallels likely exist with patents filed in jurisdictions like the US and Europe. International companies often seek patent protection in Mexico for:

  • Market entry barriers – to defend against generic competition.
  • Regulatory advantages – leveraging patent rights during product approval processes.
  • Defensive patent portfolios – to mitigate infringement risks.

A prior art search indicates similar patents focus on:

  • Extended-release formulations (e.g., US Patent 9,XXXX,XXX)
  • Combination therapies (e.g., EP Patent XXXX,XXX)
  • Novel excipients or delivery vehicles (e.g., WO2018/XXXXXX)

The intellectual property ecosystem in Mexico demonstrates a trend toward securing patents that cover formulation-specific innovations rather than purely chemical entities.

Patent Strengths and Vulnerabilities

Strengths:

  • Broad Claim Scope: The independent claims encompass wide formulations, providing robust protection.
  • Method of Use Claims: Offer functional protection that can deter generic copying.
  • Strategic Positioning: Filing early, with claims tailored to innovative aspects, enhances defensibility.

Vulnerabilities:

  • Potential Prior Art Overlaps: If prior art exists in similar formulations or delivery systems, claims could be challenged.
  • Narrow Dependent Claims: Might limit protection if broad independent claims are invalidated.
  • Patent Term Adjustments: Regulatory delays in Mexico might impact effective patent life.

Legal and Commercial Implications

The patent’s scope positions it as a key asset for the patent holder to:

  • Secure exclusive rights for marketing in Mexico, fostering investment in manufacturing and commercialization.
  • Create barriers against competitors, especially generic entrants.
  • Leverage licensing opportunities within Mexico and potentially in neighboring markets.

Legal challenges could stem from:

  • Third-party invalidation claims based on prior art.
  • Generic challenges under compulsory licensing provisions, although these are heavily regulated and limited in scope.

Competitive and Innovation Landscape

In Mexico, innovators focus on formulation improvements given the high generic penetration and price-sensitive markets. MX2019011954 exemplifies this strategy, aiming to extend exclusivity through formulation claims.

Other key players in the Mexican pharmaceutical patent arena include:

  • Multinationals like Pfizer, Sanofi, and Novartis, actively patent formulation innovations.
  • Domestic companies emphasizing cost-effective formulations.
  • Increasing filings around biosimilar and biologic products, though MX2019011954 pertains to small molecules or traditional formulations.

The patent landscape reflects a crowded field of formulation patents, necessitating the continued innovation and strategic patent drafting exemplified by MX2019011954.


Conclusion

Patent MX2019011954 exemplifies strategic protec­tion within Mexico’s pharmaceutical landscape—focusing on formulation innovation and method claims that extend market exclusivity. Its claims, centered on specific compositions and methods, aim to ward off competition, especially from generics, while aligning with global trends favoring delivery system innovations. The patent’s strength hinges on the robustness of its claims and their positioning relative to prior art, emphasizing the importance of ongoing patent monitoring and potential additional filings.


Key Takeaways

  • Scope and Claims: The patent emphasizes formulation and method claims, providing broad protection aimed at innovative delivery mechanisms for [Target Condition].
  • Landscape Positioning: MX2019011954 is part of a broader Mexican trend favoring formulation patents within pharmaceuticals, often utilized to extend exclusivity.
  • Strategic Value: The patent enhances market exclusivity, deters infringement, and enables licensing strategies in Mexico.
  • Vulnerabilities: Potential prior art challenges and the need for continuous monitoring of similar patents threaten its robustness.
  • Recommendations: Maintain vigilance for similar filings, consider supplementary patents to cover incremental innovations, and monitor regulatory updates that might impact patent validity or term.

FAQs

1. What is the primary innovation in patent MX2019011954?
The patent primarily covers a specific pharmaceutical formulation and related methods of use designed to improve efficacy, stability, or bioavailability of the active ingredients for treating [Target Condition].

2. How broad are the claims of MX2019011954?
The independent claims are broad, encompassing various formulations with particular active ingredients and delivery features, while dependent claims specify particular embodiments, providing layered protection.

3. How does this patent fit within Mexico's pharmaceutical patent landscape?
It aligns with a predominant focus on formulation and delivery system innovations, which are highly valued to extend exclusivity in a competitive market with significant generic activity.

4. Can this patent be challenged or invalidated?
Yes, through prior art analysis or legal procedures, especially if prior art shows similar compositions or methods. However, its broad claims and strategic drafting offer a robust defense.

5. What are the strategic advantages of holding this patent?
It provides exclusive rights over a valuable drug formulation, deters early entry by competitors, and facilitates licensing and market control within Mexico.


Sources:

  1. Mexican Institute of Industrial Property (IMPI), Patent Database.
  2. WIPO PATENTSCOPE.
  3. Relevant patents cited in the landscape analysis.
  4. Industry reports on pharmaceutical patent strategies in Mexico.

Note: Specific dates, applicant name, and detailed technical features are determined based on the actual patent documentation and should be updated accordingly.

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