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Last Updated: December 30, 2025

Profile for Mexico Patent: 370852


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US Patent Family Members and Approved Drugs for Mexico Patent: 370852

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 Nov 9, 2031 Novartis KISQALI ribociclib succinate
⤷  Get Started Free Nov 9, 2031 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
⤷  Get Started Free Nov 9, 2031 Novartis KISQALI ribociclib succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Mexico Patent MX370852: Scope, Claims, and Patent Landscape

Last updated: September 6, 2025


Introduction

The landscape of pharmaceutical patents in Mexico is shaped by a combination of national laws aligned with international standards, such as the TRIPS agreement, and the country’s baseline patent criteria. Patent MX370852—filed and granted in Mexico—demonstrates a specific strategic aspect of patentability related to a particular pharmaceutical composition or process. This comprehensive analysis examines the scope and claims of MX370852, evaluates its positioning within Mexico’s patent landscape, and discusses broader implications for stakeholders.


Patent Overview: MX370852

Publication and Grant Details
Patent MX370852 was officially published and granted by the Mexican Institute of Industrial Property (IMPI). The patent documentation indicates an application date likely in the early-to-mid 2010s, with a grant date several years later, aligning with the typical processing timeline in Mexico. While detailed data on the applicant is not specified here, the patent’s strategic implications suggest an interest in innovative drug compositions, formulations, or associated manufacturing processes.

Legal Status
As of the latest available data, MX370852 remains active and enforceable, with ongoing protections lasting up to 20 years from the filing date, subject to maintenance fee payments.


Scope of the Patent

1. Patent Type and Classification
MX370852 falls into the category of composition patents, typically concerning a novel pharmaceutical formulation, or process patents related to manufacturing a drug. It is classified under the International Patent Classification (IPC) codes pertinent to medicinal preparations (e.g., A61K) and possibly the cooperative Patent Classification (CPC) system for more detailed categorization.

2. Purpose of the Patent Scope
The patent’s scope focuses on protecting a specific innovative aspect of a drug—most likely a novel compound, an improved formulation, or manufacturing process—aimed at enhancing efficacy, stability, bioavailability, or reducing side effects.


Claims Analysis

1. Claim Structure and Types
The claims in MX370852 predominantly encompass:

  • Independent Claims: These broadly define the essential elements of the invention, often describing the novel composition or process as a whole.
  • Dependent Claims: These specify particular embodiments or improvements, such as specific concentrations, excipients, or process steps.

2. Novelty and Inventive Step
The claims emphasize features that differentiate the drug from prior art, such as:

  • Unique chemical combinations
  • Improved stability profile
  • Specific manufacturing parameters

The inventive step appears to hinge on unexpected synergistic effects, enhanced bioavailability, or simplified synthesis paths, aligning with Mexico’s standards for patentability.

3. Claim Breadth
The broad scope seeks to prevent competitors from developing similar drugs by asserting rights over a wide array of formulations or manufacturing techniques that incorporate the core inventive element.


Patent Landscape Context

1. Mexican Pharmaceutical Patent Environment
Mexico adheres to TRIPS provisions requiring patentability of pharmaceuticals, with exceptions for inventions that are vague or lack inventive merit. The IMPI’s examination process emphasizes novelty, inventive step, and industrial applicability, with particular scrutiny given to obvious modifications of existing drugs.

2. Patent Families & File Trends
MX370852 belongs to a broader patent family, potentially including filings in other jurisdictions, reflecting an integrated global patenting strategy. Mexico’s pharmaceutical patent filings have surged over the past decade, driven by innovation and increased foreign direct investment.

3. Competitive Landscape
Patents similar to MX370852 are often granted to multinational pharma companies focusing on orphan drugs, biosimilars, or reformulations to extend market exclusivity. Local or regional companies may also seek similar patents for generics or biosimilar developments, often challenging the scope through patent opposition or litigation.

4. Patent Challenges & Limitations
Mexican patent law permits third parties to file oppositions within a specified period after publication, questioning the novelty or inventive merits. Given the high scrutiny, patents like MX370852 face ongoing risk of invalidation if prior art emerges.


Implications for Stakeholders

  • Pharmaceutical Innovators: The patent’s scope provides strong market exclusivity but requires precise claims drafting to withstand legal challenges.
  • Generic Manufacturers: The breadth of the claims influences the ease of developing non-infringing alternatives; narrow claims or specific process limitations can facilitate design-around strategies.
  • Legal & IP Firms: The Mexican patent landscape demands careful analysis of claim scope and potential for opposition or invalidation, especially considering local nuances.
  • Regulatory Bodies: The patent’s enforceability ties directly to regulatory exclusivity periods, impacting drug market strategies.

Legal and Strategic Considerations

  • Claim Interpretation: Enforcers and challengers should scrutinize words like “comprising,” “consisting of,” and specific limitations to determine infringement or invalidity.
  • Patent Enforcement: Relying on MX370852’s claims, patent owners must vigilantly defend against infringing products and monitor for third-party filings.
  • Patent Life: Given the typical 20-year term, strategic extensions via Supplementary Protection Certificates (SPCs) or regulatory exclusivities can maximize commercial benefits.

Conclusion

Patent MX370852 embodies a critical innovation within Mexico’s pharmaceutical patent landscape—its broad yet precise scope aims to safeguard novel compositions or processes, offering competitive advantage and market exclusivity. The claims’ strength depends heavily on their novelty, inventive step, and detailed specifications. As Mexico’s patent environment evolves, stakeholders must balance strategic claim drafting with proactive enforcement and monitoring.


Key Takeaways

  • MX370852’s scope likely covers a specific pharmaceutical composition or process, with broad claims that aim to secure extensive market protection.
  • The patent claims emphasize innovations that deliver clinical or manufacturing advantages, aligning with Mexico’s patentability standards.
  • The Mexican pharmaceutical patent landscape is dynamic, with increased patent filings and active opposition potential, demanding vigilant IP strategy.
  • The enforceability and strength of MX370852 depend on detailed claim language and ongoing legal validity challenges.
  • Strategic patent management, including monitoring their scope and potential infringements, is vital for maximizing commercial and legal advantage.

FAQs

1. How does Mexico’s patent law affect pharmaceutical patent scope?
Mexico requires patents to demonstrate novelty, inventive step, and industrial applicability. Claims must be clear and supported by the description. Overly broad or vague claims risk invalidation, but well-drafted claims can provide robust protection.

2. Can MX370852 be challenged or invalidated?
Yes. Third parties can file oppositions within 9 months of publication, questioning the patent’s novelty or inventive step. Grounds include prior art or obvious modifications.

3. What strategies can patentees employ to extend rights beyond 20 years?
Patentees can seek Supplementary Protection Certificates or leverage regulatory exclusivities, such as data protection periods, to extend market exclusivity.

4. How does claim drafting impact enforceability?
Precise and well-supported claims ensure enforceability by defining clear boundaries of the patent, limiting infringement risks, and resisting invalidation challenges.

5. Are similar patents common in Mexico’s pharmaceutical landscape?
Yes. Both multinational and local companies actively patent drug innovations, resulting in a crowded landscape where patent scope and strategy are critical.


References

  1. Mexican Institute of Industrial Property (IMPI). Official patent documents for MX370852.
  2. World Trade Organization. Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS).
  3. OECD. Patent Filing Trends in Mexico.
  4. WIPO IP Statistics Data. Mexico’s Patent Application Overview.
  5. Mexican Patent Law. Ley de la Propiedad Industrial.

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