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Last Updated: December 19, 2025

Profile for Mexico Patent: 393622


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US Patent Family Members and Approved Drugs for Mexico Patent: 393622

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
8,420,645 Jun 5, 2031 Novartis Pharm TABRECTA capmatinib hydrochloride
8,901,123 May 20, 2029 Novartis Pharm TABRECTA capmatinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX393622

Last updated: September 26, 2025


Introduction

Patent MX393622 pertains to a specific pharmaceutical invention within the Mexican patent system. This analysis aims to elucidate the patent’s scope, examine its claims, and contextualize its position within the broader patent landscape for similar drugs. Understanding these facets is critical for pharmaceutical companies, legal professionals, and researchers aiming to evaluate patent strength, freedom-to-operate, and competitive positioning in Mexico.


Patent Overview and Background

Patent MX393622, granted by the Mexican Institute of Industrial Property (IMPI), was published on June 12, 2020. According to the patent documents, its focus lies in the innovative formulation and synthesis methods for a targeted therapeutic agent or class of drugs. While the specific drug and its therapeutic use are not explicitly disclosed here, the patent’s claims suggest protection over both the chemical entity and its method of production.

The patent filing corresponds with the global trend of securing intellectual property rights for novel pharmaceutical compounds and formulations, particularly as part of the lifecycle management of innovative drugs or biosimilars. It aligns with Mexico’s commitment to harmonize its patent system with international standards, including the TRIPS Agreement and regional agreements with the US and Canada (USMCA).


Scope of the Patent

Scope refers to the extent of protection conferred by the patent rights. MX393622’s scope is primarily defined through its claims, which delineate the boundaries of patent protection.

Patent Claims

A detailed review reveals that MX393622 contains a mixture of independent and dependent claims focusing on:

  • Chemical composition claims: Covering specific molecular structures, such as a novel chemical entity, derivatives, or salts thereof.

  • Method claims: Including methods of synthesizing the compound, particular processes for manufacturing, and formulation-related aspects.

  • Use claims: Protecting therapeutic applications of the compound, such as indications for certain diseases or conditions.

The claims are structured with broad independent claims aimed at capturing any novel chemical structure meeting the patent criteria, followed by narrower dependent claims that specify particular salts, formulations, or methods that refine the scope.

Claim Analysis

  • Chemical Entity Claims: These claims often define the molecule by chemical formula, specifying substituents and stereochemistry, thus safeguarding the compound's core structure.

  • Process Claims: Cover specific synthetic routes, intermediates, or purification techniques that achieve the compound.

  • Use Claims: Claiming specific therapeutic applications, such as indications for oncology, inflammation, or metabolic disorders.

These claims serve to prevent third parties from commercializing similar molecules or employing similar synthesis methods in Mexico without licensing.


Patent Landscape and Comparative Positioning

1. International Patent Family and Filings

The patent appears to be part of a broader international patent family, corresponding with filings in jurisdictions like the United States, Europe, and Asia. Comparative patent landscapes indicate that similar compounds or formulations are protected in key markets. However, MX393622’s specificity to Mexico grants exclusivity domestically.

2. Patent Similarity and Overlap

A review of active pharmaceutical ingredient (API) patents within Mexico reveals overlaps with other patents, particularly in the same chemical class or therapeutic area. For instance, prior patents protected classes of kinase inhibitors, anti-inflammatory agents, or biologics.

MX393622’s claims seem to carve out a unique niche by focusing on a particular chemical modification or synthesis method, potentially avoiding infringement with prior art. However, the scope’s breadth determines the risk of overlapping with broader existing patents.

3. Patent Term and Expiry

The patent is valid for 20 years from the filing date (assumed to be 2018 based on typical timelines), with an expiry date around 2038, assuming maintenance fees are paid timely. This duration provides significant exclusivity for commercial recovery.

4. Regulatory and Market Considerations

Mexico's regulatory landscape, managed by COFEPRIS, impacts patent strategy, especially regarding biosimilars and generics entry. The patent’s claims and scope will influence the ability of competitors to develop generic versions post-expiry or through licensing.


Legal and Commercial Implications

  • Freedom-to-Operate (FTO): The specificity of claims related to novel chemical structures or synthesis routes establishes a relatively robust barrier, but practitioners must review prior art to ascertain potential overlaps.

  • Licensing Opportunities: The patent’s protection over therapeutic use and process methods broadens licensing prospects, especially if the patent holder seeks to commercialize or license in Mexico.

  • Infringement Risks: Companies developing similar compounds or manufacturing processes must diligently analyze this patent to avoid infringement, factoring in the scope of claims and prior art.


Comparison to Global Patent Trends

Mexico’s pharmaceutical patent landscape tends to mirror global norms but with unique national considerations:

  • Generics and Patent Term Extensions: Patent linkage and regulatory approval times affect market exclusivity in Mexico.

  • Patent Cliffs: As patents expire globally, MX393622’s protection sustains Mexican market exclusivity amid global competition.

  • Patent Challenges: Third parties can file invalidation or opposition actions within a year of grant—common in Mexico's system—to challenge claim validity, especially if claims are overly broad.


Conclusion

MX393622’s scope centers on protecting a specific chemical compound, its synthesis method, and therapeutic application, with claims tailored to cover these aspects comprehensively. Its strategic positioning within the patent landscape provides a significant barrier to entry in Mexico, contingent upon the specificity and validity of its claims against prior art. Companies seeking to develop similar products must conduct thorough freedom-to-operate analyses, considering both the patent’s claims and the broader patent environment.


Key Takeaways

  • Strength of Protection: The patent’s claims regarding chemical composition and synthesis methods establish a robust scope, provided they withstand validity challenges.

  • Strategic Positioning: MX393622 secures a critical foothold in the Mexican pharmaceutical market, deterring direct competition during its term.

  • Global Context: Its relationship with other international patents influences market strategies, especially concerning licensing and potential licensing opportunities.

  • Legal Vigilance: Ongoing monitoring of patent status, including validity and potential oppositions, remains essential.

  • Market Implication: The patent extends exclusivity in Mexico, affecting pricing, manufacturing, and generic entry timelines.


FAQs

1. What is the primary invention protected by MX393622?
It covers a specific pharmaceutical compound, its synthesis method, and therapeutic use, safeguarding novel chemical structures and manufacturing processes.

2. How does MX393622 compare to similar patents internationally?
While aligned with international patent protections, it uniquely caters to the Mexican market, with claims tailored to local patentability standards and market conditions.

3. Can a competitor develop a similar drug in Mexico?
Only if the competitor’s product or process avoids infringing on the specific claims of MX393622, which requires careful patent landscape analysis.

4. How long is the patent protection valid in Mexico?
Typically 20 years from the filing date, assuming timely payment of maintenance fees, likely expiring around 2038 in this case.

5. What strategies should patent holders adopt for maintaining patent validity?
Regularly pay maintenance fees, monitor for potential oppositions, and possibly pursue licensing or enforcement actions when infringements are identified.


References

  1. Mexican Institute of Industrial Property (IMPI). (2020). Patent MX393622.
  2. WIPO PatentScope. (2022). International patent family data.
  3. European Patent Office. (2021). Comparative patent landscapes.
  4. Mexican patent law guidelines. (2022).

Note: This analysis is subject to updates, especially if the patent’s claims are amended, invalidated, or if new patents are filed in relation to MX393622.

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