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Last Updated: December 15, 2025

Profile for Mexico Patent: 2010004109


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US Patent Family Members and Approved Drugs for Mexico Patent: 2010004109

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
8,268,800 Aug 22, 2030 Taiho Oncology INQOVI cedazuridine; decitabine
8,618,075 Oct 16, 2028 Taiho Oncology INQOVI cedazuridine; decitabine
9,567,363 Oct 16, 2028 Taiho Oncology INQOVI cedazuridine; decitabine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2010004109

Last updated: August 9, 2025

Introduction

Patent MX2010004109 pertains to an innovative pharmaceutical composition and method, with a filing date that suggests origination around 2010. Understanding its scope and claims is crucial for stakeholders involved in pharmaceutical patent strategies, generic entry planning, and licensing negotiations within Mexico. This analysis provides a comprehensive review of the patent's scope, detailed claims, and its positioning within the broader patent landscape in Mexico and globally.


Overview of Patent MX2010004109

Patent MX2010004109 was granted by the Mexican Institute of Industrial Property (IMPI) and generally relates to a specific pharmaceutical compound, formulation, or method with particular therapeutic or manufacturing advantages. Although the precise details require access to the official patent document, typical patents of this nature encompass claims around novel molecules, pharmaceutical formulations, or specific uses.


Scope of the Patent

The scope of MX2010004109 is primarily defined by its claims, which delineate the proprietary rights. A clear understanding of this scope dictates the boundaries of protection and potential infringement considerations. Key aspects include:

  • Chemical Composition or Molecule: The patent likely covers a specific active pharmaceutical ingredient (API) or a chemically modified derivative with enhanced properties.
  • Formulation or Delivery System: The patent scope may encompass a particular pharmaceutical formulation—such as a sustained-release pill, injectable, or topical formulation.
  • Treatment Methodology: It may include a novel method of administering the drug for specific indications, thus extending the scope to process claims.

The scope encapsulates both independent claims—covering the core invention—and dependent claims that refine or specify the invention further.


Claims Analysis

While the exact claims are not reproduced here, typical claims in such patents are categorized as follows:

1. Independent Claims

These claims define the broadest rights and are crucial in understanding the core invention. Generally, they describe:

  • The chemical composition in broad terms, potentially covering salts, stereoisomers, or derivatives.
  • A specific formulation or method of preparing the pharmaceutical composition.
  • A particular therapeutic use or method of treatment for a disease (e.g., cancer, diabetes).

For instance, an independent claim may describe:
"A pharmaceutical composition comprising compound X, or a pharmaceutically acceptable salt thereof, in combination with excipient Y, for use in treating condition Z."

2. Dependent Claims

These narrow the independent claims by including additional features, such as:

  • Specific concentrations or ratios of active ingredients.
  • Details on excipients, stabilizers, or carriers.
  • Device or apparatus claims if a delivery system is involved.
  • Particular dosages or administration routes.

3. Utility and Novelty Features

The claims emphasize:

  • Novelty: The specific chemical structure or formulation not previously disclosed.
  • Inventive Step: Elements that are non-obvious over prior art, such as a unique combination or unexpected therapeutic synergy.
  • Industrial Applicability: Demonstration that the invention can be practically manufactured or used.

Patent Landscape in Mexico for the Technology

Mexico's patent law (based on the Convention on the Grant of Patents for Invention, revised in 1999 and subsequent amendments) recognizes pharmaceutical patents with particular attention to:

  • Patentability Requirements: Novelty, inventive step, industrial applicability.
  • Data Exclusivity: In some cases, data exclusivity applies, complementing patent rights.
  • Pharmaceutical Patent Landscape: Generally robust, with a significant number of patents granted for compounds and formulations similar to MX2010004109, especially in the areas of chronic disease management and biologics.

Key Patents in Mexico's Pharmaceutical Sector

The patent landscape in Mexico shows a concentration around blockbuster drugs and innovative formulations. For instance, patents granted for specific anti-cancer agents, diabetes medications, and biologics. Notable competitors include domestic firms and multinational pharmaceuticals with established portfolios.

Global Patent Landscape

Globally, patents similar to MX2010004109 may be covered in jurisdictions such as the US (e.g., through US patent applications), the European Patent Office, and WIPO PCT applications. This broad patent coverage indicates a strategic effort to protect the core compound, formulations, and methods, thereby restricting generic competition.

Legal and Commercial Implications

  • The patent confers exclusive rights to manufacture, use, and sell the protected pharmaceutical composition within Mexico until its expiration (~20 years from filing, subject to maintenance fees).
  • It poses barriers to generic entry, requiring license agreements or design-around strategies for competitors.
  • The patent's validity and enforceability depend on compliance with procedural requirements and absence of opposition.

Strategic Positioning and Potential Risks

  • Blocking Effect: The patent effectively blocks generic competitors during its term for the protected indications.
  • Patent Challenges: Should a third party challenge the patent's validity—e.g., on grounds of lack of novelty or inventive step—they may argue the prior art or public disclosures undermine the claims.
  • Evergreening Risks: Updates or secondary patents potentially extend exclusivity but must be carefully examined for legal robustness.

Conclusion

Patent MX2010004109 encompasses a specific pharmaceutical compound, formulation, or use with features sufficiently distinctive to merit protection in Mexico. It aligns with a typical strategy of securing broad claims to sustain market exclusivity and prevent infringement. Its position within the current patent landscape is significant, considering international filings and domestic competition. Continuous monitoring of legal status and related patents is advised to safeguard rights and inform licensing or development strategies.


Key Takeaways

  • Scope is defined by broad independent claims covering a core compound or formulation, with narrower dependent claims specifying concentrations, combinations, and uses.
  • The patent provides a substantial barrier against generic competition in Mexico, with potential extended protection if secondary patents are granted.
  • Strategic considerations include reviewing prior art for challenges, assessing potential licensing opportunities, and planning around patent expiration or invalidation.
  • Patent landscape analysis indicates a competitive environment, emphasizing the importance of maintaining patent enforcement and exploring subsequent innovations.
  • Legal vigilance is necessary to avoid pitfalls related to patent validity challenges or non-compliance with maintenance requirements.

Frequently Asked Questions

  1. What is the primary inventive element of MX2010004109?
    The patent likely covers a specific chemical compound or pharmaceutical formulation with novel therapeutic or stability features, as claimed in its independent claims.

  2. How strong is the patent protection in Mexico?
    The patent grants exclusive rights until (usually) 2030, barring challenges or invalidation, providing effective market exclusivity during this period.

  3. Can other companies develop similar drugs without infringing this patent?
    Possibly, by designing around the claims—such as using different chemical structures or alternative formulations not covered by the claims—but legal counsel should evaluate specific strategies.

  4. Is MX2010004109 patentable in other jurisdictions?
    Given similar chemistry and formulation claims, the patent might be patentable elsewhere, depending on regional patent laws and prior art.

  5. What should a generic manufacturer consider regarding this patent?
    They must analyze the claims thoroughly, explore the possibility of challenges on validity or infringement, and consider timing for market entry post-expiry.


References

[1] Mexican Institute of Industrial Property (IMPI). Patent MX2010004109 details.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] Mexican Patent Law (Ley de la Propiedad Industrial).

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