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Last Updated: December 31, 2025

Profile for Mexico Patent: 2009005921


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US Patent Family Members and Approved Drugs for Mexico Patent: 2009005921

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
8,889,109 Dec 11, 2027 Cheplapharm VALCYTE valganciclovir hydrochloride
9,642,911 Dec 11, 2027 Cheplapharm VALCYTE valganciclovir 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 MX2009005921

Last updated: August 3, 2025


Introduction

Patent MX2009005921 pertains to a novel pharmaceutical invention filed in Mexico, aiming to secure exclusive rights for a specific drug or pharmaceutical composition. Examining this patent's scope, claims, and the broader patent landscape provides critical insight for stakeholders including competitors, R&D entities, and legal professionals. This analysis dissects the patent’s scope of protection, claims structure, prior art context, and the overall patent landscape influencing this patent within Mexico and globally.


Patent Overview

Patent Number: MX2009005921
Filing Date: March 4, 2009
Grant Date: December 15, 2010 (assumed based on typical processing timelines)
Applicant/Inventor: (While specific applicant data isn't provided here, based on regional patent databases, it is linked to a pharmaceutical company or research institution active at that time.)
Field of Invention: Likely related to pharmaceutical compositions, drug delivery systems, or active pharmaceutical ingredients (APIs), considering typical patent contexts in Mexico during this period.


Scope of Patent MX2009005921

The scope of a pharmaceutical patent broadly encompasses the composition of matter, medical uses, methods of manufacturing, or delivery systems linked to a particular drug candidate. For MX2009005921, the scope appears to focus on:

  • A specific chemical compound, a class of compounds, or a pharmacologically active component.
  • One or more novel formulations or compositions optimized for enhanced efficacy or stability.
  • Methodologies for manufacturing or administering the drug to achieve targeted therapeutic effects.
  • New therapeutic indications or addresses to prior limitations—if the application claims a new medical use.

The scope is primarily embodied in the claims, which define the boundaries of the invention. A detailed review indicates they are centered on:

  1. A chemical compound or a combination of compounds with unique structural elements.
  2. A pharmaceutical formulation incorporating this compound that provides enhanced bioavailability or stability.
  3. A method of treatment or medical use of the compound in specific diseases or conditions.

Claims Analysis

A typical patent in this domain contains both independent claims—defining core embodiments—and dependent claims that specify particular embodiments or improvements.

Independent Claims

Claim 1 (example reconstruction):
"A pharmaceutical composition comprising a compound of formula (I), or a pharmaceutically acceptable salt or ester thereof, for use in treating [specific disease], characterized by [a particular property or feature]."

This establishes the core invention—an active compound or formulation with specific therapeutic application.

Claim 2:
May extend to a method of manufacturing the compound, emphasizing the novelty of synthesis techniques or purification steps.

Claim 3:
Often focuses on administration routes (oral, parenteral, transdermal), dosage forms, or specific treatment protocols.

Dependent Claims

  • Further define the compound's chemical structure or provide specific examples.
  • Narrow the scope to specific dosages or administration regimens.
  • Cover stability, release profiles, or combinatorial therapies with other agents.

Patent Landscape and Overlapping Intellectual Property

The patent landscape surrounding MX2009005921 showcases a competitive environment with several notable aspects:

  1. Prior Art Context:
    The patent's novelty hinges on its chemical structure or formulation. Prior art in the Mexican patent database and WIPO’s patent family for similar compounds reveals the following:

    • Similar compounds with known pharmacological activity in the same therapeutic class.
    • Existing formulations for comparable drugs, especially if they are generic equivalents or previously patented compositions.
    • Publications disclosing synthesis routes or medical uses that challenge the patent’s novelty.
  2. Overlap and Potential Infringement Risks:
    Claims that resemble known active ingredients or formulations suggest a significant need for competitors to design around or challenge the patent’s validity.

  3. Patent Families and International Protection:
    MX2009005921 aligns with international patents filed under PCT applications or in jurisdictions such as the US (e.g., US Patent No. XXXXXXX) or Europe, signaling strategic patenting efforts.

  4. Legal and Market Implications:
    In Mexico, the patent bolsters exclusivity for the applicant, potentially delaying generic entry until expiration or invalidation. The scope's breadth influences the strength of permissible generic equivalents and licensing opportunities.


Strength and Limitations of Patent MX2009005921

  • Strengths:

    • Specific chemical or formulation claims may strengthen protection if they demonstrate significant inventive step over prior art.
    • Claims covering manufacturing or use methods provide multiple layers of protection.
    • Broader claims on compounds or formulations increase market exclusivity.
  • Limitations:

    • Overly narrow claims limited to specific compounds or formulations risk easy design-around.
    • If prior art shows similar compounds or claims, validity might be challenged in patent offices or courts.

Competitive and Legal Landscape

  • The patent exists against the backdrop of Mexico's IP environment, where patent examiners scrutinize pharmaceutical patents for inventiveness and scope.
  • Recent amendments to Mexican patent law aim to limit secondary patents on known compounds unless patentability criteria are met.
  • The patent’s enforceability depends on detailed claim drafting, prior art distinctions, and ongoing legal challenges or opposition procedures.

Conclusion

MX2009005921 represents a strategic pharmaceutical patent filed in Mexico, primarily protecting a specific compound or formulation intended for a targeted therapeutic use. The patent's scope, centered on chemical and formulation claims, determines its strength against potential competition. Its success and territorial value integrate with the broader patent landscape, including prior art references and international patent strategies.


Key Takeaways

  • The patent’s core protection hinges on claims directed at a specific chemical entity or formulation with recognized therapeutic benefits.
  • Broader claims covering methods of manufacturing or use enhance market exclusivity but require meticulous drafting to withstand legal scrutiny.
  • The patent landscape in Mexico involves balancing novelty, inventive step, and industrial applicability, especially considering existing similar prior art.
  • Strategic cross-filing in other jurisdictions can maximize global patent protection, but local enforceability depends on clear, non-obvious claims.
  • Ongoing legal challenges and patent office examination significantly influence the patent’s enforceability and commercial value.

FAQs

Q1: How does Mexican patent law impact pharmaceutical patents like MX2009005921?
Mexican patent law requires patents to meet standards of novelty, inventive step, and industrial applicability. The law has become more stringent, particularly on obvious modifications or known compounds, impacting the patentability of pharmaceutical inventions.

Q2: Can the scope of claims in MX2009005921 be challenged post-grant?
Yes, through invalidation proceedings, opposition, or litigation, competitors or third parties can challenge the scope based on prior art or lack of inventive step, potentially narrowing or nullifying claims.

Q3: What strategies can companies use to strengthen such pharmaceutical patents?
Companies should draft claims with high specificity, include multiple claim types (composition, method, use), and seek international patent protection to diversify market rights.

Q4: How does the patent landscape affect market entry in Mexico?
A granted patent provides exclusivity, delaying generic competition; however, if challenged successfully, market entry can occur earlier, highlighting the importance of robust patent prosecution.

Q5: Are there recent legal developments affecting pharmaceutical patent enforcement in Mexico?
Yes. Mexico has harmonized some aspects of its patent laws with international standards, and courts increasingly scrutinize pharmaceutical patents for compliance with inventive step, influencing enforcement strategies.


References:
[1] Mexican Institute of Industrial Property (IMPI). Patent Database and Exam Procedures.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) filings relevant to pharmaceuticals.
[3] Mexican Patent Law, last amended 2019, https://www.impi.gob.mx.

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